{ "uniprot_canonical_ac": "Q9Y5W7-1", "uniprot_ac": "Q9Y5W7", "uniprot_id": "SNX14_HUMAN", "mass": { "chemical_mass": 110182.0, "monoisotopic_mass": 110182.0 }, "refseq": { "ac": "XP_016866579", "name": "sorting nexin-14 isoform X3", "summary": "", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_016866579" }, "gene_names": [ { "name": "SNX14", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprot/Q9Y5W7", "id": "Q9Y5W7" } ], "protein_names": [ { "name": "Sorting nexin-14", "resource": "UniProtKB", "type": "recommended", "url": "", "id": "Q9Y5W7" }, { "name": "sorting nexin-14 isoform X3", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_016866579", "id": "XP_016866579" }, { "name": "sorting nexin-14 isoform c", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543", "id": "NP_001284543" } ], "function": [ { "annotation": "A unique ataxia syndrome due to biallelic SNX14 mutations leading to lysosome-autophagosome dysfunction.", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" }, { "database": "PubMed", "id": "25848753", "url": "https://glygen.org/publication/PubMed/25848753" } ] }, { "annotation": "Here we report on a child with a novel missense mutation in the SNX14 gene that appears to be debilitating for protein conformation, function and review the previously reported cases from 15 families", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" }, { "database": "PubMed", "id": "27913285", "url": "https://glygen.org/publication/PubMed/27913285" } ] }, { "annotation": "Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome. Erratum:[Am J Hum Genet. 2015 Jun 4;96(6):1008-9]", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" }, { "database": "PubMed", "id": "25439728", "url": "https://glygen.org/publication/PubMed/25439728" } ] }, { "annotation": "Plays a role in maintaining normal neuronal excitability and synaptic transmission. May be involved in several stages of intracellular trafficking (By similarity). Required for autophagosome clearance, possibly by mediating the fusion of lysosomes with autophagosomes (Probable). Binds phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2), a key component of late endosomes/lysosomes (PubMed:25848753). Does not bind phosphatidylinositol 3-phosphate (PtdIns(3P)) (PubMed:25848753, PubMed:25148684).", "evidence": [ { "database": "UniProtKB", "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7#function" }, { "database": "UniProtKB", "id": "Q8BHY8", "url": "https://www.uniprot.org/uniprot/Q8BHY8#function" }, { "database": "PubMed", "id": "25848753", "url": "https://glygen.org/publication/PubMed/25848753" }, { "database": "PubMed", "id": "25148684", "url": "https://glygen.org/publication/PubMed/25148684" } ] }, { "annotation": "Snx14, an endoplasmic reticulum-resident protein associated with the cerebellar ataxia SCAR20, localizes to ER-LD contacts following fatty acid treatment, where it promotes lipid droplet maturation.", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" }, { "database": "PubMed", "id": "30765438", "url": "https://glygen.org/publication/PubMed/30765438" } ] }, { "annotation": "This gene encodes a member of the sorting nexin family. Members of this family have a phox (PX) phosphoinositide binding domain and are involved in intracellular trafficking. The encoded protein also contains a regulator of G protein signaling (RGS) domain. Regulator of G protein signaling family members are regulatory molecules that act as GTPase activating proteins for G alpha subunits of heterotrimeric G proteins. Alternate splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014].", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" } ] }, { "annotation": "We therefore identify an important role for SNX14 in neutral lipid homeostasis between the endoplasmic reticulum , lysosomes and lipid droplets that may provide an early intervention target to alleviate the clinical symptoms of autosomal recessive cerebellar ataxia 20 (SCAR20).", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" }, { "database": "PubMed", "id": "29635513", "url": "https://glygen.org/publication/PubMed/29635513" } ] } ], "disease": [ { "disease_id": "DOID:0080066", "recommended_name": { "id": "DOID:0080066", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080066", "name": "autosomal recessive spinocerebellar ataxia 20", "description": "An autosomal recessive cerebellar ataxia that is characterized by severely delayed psychomotor development with poor or absent speech, wide-based or absent gait, coarse facies, and cerebellar atrophy and that has_material_basis_in homozygous mutation in the SNX14 gene on chromosome 6q14." }, "synonyms": [ { "id": "DOID:0080066", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0080066", "name": "SCAR20", "description": "" }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "autosomal recessive spinocerebellar ataxia 20", "description": "Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the SNX14 gene." }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "SCAR20", "description": "" }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "SNX14 autosomal recessive cerebellar ataxia", "description": "" }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "autosomal recessive cerebellar ataxia caused by mutation in SNX14", "description": "" }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "autosomal recessive spinocerebellar ataxia type 20", "description": "" }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "intellectual disability-coarse face-macrocephaly-cerebellar hypoplasia syndrome", "description": "" }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "spinocerebellar ataxia, autosomal recessive type 20", "description": "" }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome", "description": "" }, { "id": "MONDO:0014601", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014601", "name": "spinocerebellar ataxia, autosomal recessive 20", "description": "" }, { "id": "MIM:616354", "resource": "MIM", "url": "https://www.omim.org/entry/616354", "name": "Spinocerebellar ataxia, autosomal recessive, 20", "description": "Spinocerebellar ataxia, autosomal recessive, 20" } ], "evidence": [ { "id": "616354", "database": "MIM", "url": "https://www.omim.org/entry/616354" } ] } ], "snv": [ { "evidence": [ { "id": "Q9Y5W7", "database": "BioMuta", "url": "https://hive.biochemistry.gwu.edu/biomuta/proteinview/Q9Y5W7" } ], "glycoeffect": [], "start_pos": 349, "end_pos": 349, "subjects_tested": "0", "subjects_positive": "0", "frequency": "0.0", "sequence_org": "R", "sequence_mut": "C", "comment": "Somatic mutation passed 1 out of 6 filters: num. of cancers (4).", "chr_id": "6", "chr_pos": "85547175", "ref_nt": "G", "alt_nt": "A", "minor_allelic_frequency": "", "site_lbl": "R349", "disease": [ { "disease_id": "DOID:4159", "recommended_name": { "id": "DOID:4159", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:4159", "name": "skin cancer", "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells." }, "synonyms": [ { "id": "DOID:4159", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:4159", "name": "CA - skin cancer", "description": "" }, { "id": "DOID:4159", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:4159", "name": "malignant neoplasm of skin", "description": "" }, { "id": "DOID:4159", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:4159", "name": "melanoma and Non-melanoma skin cancer", "description": "" } ] }, { "disease_id": "DOID:363", "recommended_name": { "id": "DOID:363", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:363", "name": "uterine cancer", "description": "A female reproductive organ cancer that is located_in the uterus." }, "synonyms": [ { "id": "DOID:363", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:363", "name": "CA - cancer of uterus", "description": "" }, { "id": "DOID:363", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:363", "name": "Tumour of uterus", "description": "" }, { "id": "DOID:363", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:363", "name": "malignant neoplasm of uterus", "description": "" }, { "id": "DOID:363", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:363", "name": "malignant uterine tumor", "description": "" }, { "id": "DOID:363", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:363", "name": "neoplasm of uterus", "description": "" }, { "id": "DOID:363", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:363", "name": "uterine tumor", "description": "" }, { "id": "DOID:363", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:363", "name": "uterus neoplasm", "description": "" } ] }, { "disease_id": "DOID:10534", "recommended_name": { "id": "DOID:10534", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10534", "name": "stomach cancer", "description": "A gastrointestinal system cancer that is located_in the stomach." }, "synonyms": [ { "id": "DOID:10534", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10534", "name": "gastric cancer", "description": "" }, { "id": "DOID:10534", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10534", "name": "gastric neoplasm", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer", "description": "A primary or metastatic malignant neoplasm involving the stomach." }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric neoplasm", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "Ca lesser curvature - stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "cancer of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer risk after h. pylori infection", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer, somatic", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant gastric neoplasm", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant gastric tumor", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant gastric tumour", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant neoplasm of lesser curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant neoplasm of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant neoplasm of the stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant stomach neoplasm", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of body of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of greater curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of lesser curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of the stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumour of body of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumour of greater curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumour of lesser curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumour of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumour of the stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "stomach cancer", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "Ca body - stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "ca greater curvature of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant neoplasm of body of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer, intestinal", "description": "" }, { "id": "MIM:613659", "resource": "MIM", "url": "https://www.omim.org/entry/613659", "name": "Gastric cancer", "description": "Gastric cancer" } ] }, { "disease_id": "DOID:1793", "recommended_name": { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "pancreatic cancer", "description": "An endocrine gland cancer located_in the pancreas." }, "synonyms": [ { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "Ca body of pancreas", "description": "" }, { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "Ca head of pancreas", "description": "" }, { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "Ca tail of pancreas", "description": "" }, { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "malignant neoplasm of body of pancreas", "description": "" }, { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "malignant neoplasm of head of pancreas", "description": "" }, { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "malignant neoplasm of tail of pancreas", "description": "" }, { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "pancreas neoplasm", "description": "" }, { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "pancreatic neoplasm", "description": "" }, { "id": "DOID:1793", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1793", "name": "pancreatic tumor", "description": "" } ] } ], "keywords": [ "biomuta", "somatic", "cancer", "disease" ] } ], "mutagenesis": [], "expression_tissue": [ { "tissue": { "name": "Adult mammalian kidney", "namespace": "UBERON", "id": "0000082", "url": "http://purl.obolibrary.org/obo/UBERON_0000082" }, "score": "92.18", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Oral cavity", "namespace": "UBERON", "id": "0000167", "url": "http://purl.obolibrary.org/obo/UBERON_0000167" }, "score": "83.45", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Stomach", "namespace": "UBERON", "id": "0000945", "url": "http://purl.obolibrary.org/obo/UBERON_0000945" }, "score": "96.44", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Esophagus", "namespace": "UBERON", "id": "0001043", "url": "http://purl.obolibrary.org/obo/UBERON_0001043" }, "score": "94.81", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Rectum", "namespace": "UBERON", "id": "0001052", "url": "http://purl.obolibrary.org/obo/UBERON_0001052" }, "score": "95.89", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Urinary bladder", "namespace": "UBERON", "id": "0001255", "url": "http://purl.obolibrary.org/obo/UBERON_0001255" }, "score": "93.38", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Thyroid gland", "namespace": "UBERON", "id": "0002046", "url": "http://purl.obolibrary.org/obo/UBERON_0002046" }, "score": "95.51", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Liver", "namespace": "UBERON", "id": "0002107", "url": "http://purl.obolibrary.org/obo/UBERON_0002107" }, "score": "93.41", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Prostate gland", "namespace": "UBERON", "id": "0002367", "url": "http://purl.obolibrary.org/obo/UBERON_0002367" }, "score": "96.84", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] }, { "tissue": { "name": "Thoracic mammary gland", "namespace": "UBERON", "id": "0005200", "url": "http://purl.obolibrary.org/obo/UBERON_0005200" }, "score": "94.59", "present": "HIGH", "evidence": [ { "database": "Bgee", "id": "ENSG00000135317", "url": "https://bgee.org/?page=gene&gene_id=ENSG00000135317" } ] } ], "expression_disease": [ { "significant": "Yes", "trend": "down", "name": "Prostate cancer [DO disease name]", "url": "http://disease-ontology.org/term/DOID:10283", "evidence": [ { "database": "BioXpress", "id": "Q9Y5W7", "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/Q9Y5W7" } ], "disease": [ { "disease_id": "DOID:10283", "recommended_name": { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostate cancer", "description": "A male reproductive organ cancer that is located_in the prostate." }, "synonyms": [ { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "NGP - new growth of prostate", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "hereditary prostate cancer", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "malignant tumor of the prostate", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostate cancer, familial", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostate neoplasm", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostatic cancer", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "prostatic neoplasm", "description": "" }, { "id": "DOID:10283", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10283", "name": "tumor of the prostate", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "prostate cancer, hereditary, type 9", "description": "" }, { "id": "MONDO:0012597", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012597", "name": "HPC9", "description": "" }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "prostate cancer, hereditary, 12", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene." }, { "id": "MONDO:0012741", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012741", "name": "EHBP1 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"https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "prostate cancer, hereditary, type 5", "description": "" }, { "id": "MONDO:0012244", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012244", "name": "HPC5", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, hereditary, 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, hereditary, 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, hereditary, type 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "prostate cancer, susceptibility to, 3", "description": "" }, { "id": "MONDO:0012093", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012093", "name": "HPC3", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, type 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, susceptibility to, 4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "HPC4", "description": "" }, { "id": "MONDO:0012094", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012094", "name": "prostate cancer, hereditary, on chromosome 7", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, 13", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene." }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "MSMB familial prostate cancer", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "familial prostate cancer caused by mutation in MSMB", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, 13", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "prostate cancer, hereditary, type 13", "description": "" }, { "id": "MONDO:0012758", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012758", "name": "HPC13", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "prostate cancer, hereditary, 8", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "prostate cancer, hereditary, 8", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "prostate cancer, hereditary, type 8", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "HPC8", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "predisposing for prostate cancer", "description": "" }, { "id": "MONDO:0011270", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011270", "name": "prostate cancer, susceptibility to", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, hereditary, type 6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "HPC6", "description": "" }, { "id": "MONDO:0012300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012300", "name": "prostate cancer, susceptibility to", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "prostate cancer, hereditary, 10", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "HPC10", "description": "" }, { "id": "MONDO:0012620", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012620", "name": "prostate cancer, hereditary, 10", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "familial prostate carcinoma", "description": "Prostate carcinoma that has developed in relatives of patients with a history of prostate carcinoma." }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "familial prostate cancer", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "hereditary prostate cancer", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "hereditary prostate carcinoma", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "prostate cancer, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "prostate cancer, familial, susceptibility to, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "prostate cancer, somatic", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "prostate cancer, susceptibility to, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "prostate cancer, familial", "description": "" }, { "id": "MONDO:0023122", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0023122", "name": "prostate cancer, hereditary", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer, hereditary, 7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "HPC7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer, hereditary, 7", "description": "" }, { "id": "MONDO:0012470", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012470", "name": "prostate cancer aggressiveness", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "prostate cancer, hereditary, 1", "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene." }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "RNASEL familial prostate cancer", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "familial prostate cancer caused by mutation in RNASEL", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "prostate cancer 1", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "prostate cancer, hereditary, 1", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "prostate cancer, hereditary, type 1", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "HPC1", "description": "" }, { "id": "MONDO:0011098", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011098", "name": "Prca1", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "prostate cancer, hereditary, 11", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "HPC11", "description": "" }, { "id": "MONDO:0012768", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012768", "name": "prostate cancer, hereditary, 11", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "prostate cancer, hereditary, 14", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "HPC14", "description": "" }, { "id": "MONDO:0012769", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012769", "name": "prostate cancer, hereditary, 14", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "prostate cancer, hereditary, 15", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "HPC15", "description": "" }, { "id": "MONDO:0012770", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012770", "name": "prostate cancer, hereditary, 15", "description": "" }, { "id": "MONDO:0010257", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010257", "name": "prostate cancer, hereditary, X-linked 1", "description": "" }, { "id": "MONDO:0010257", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010257", "name": "HPCX1", "description": "" }, { "id": "MONDO:0010257", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010257", "name": "prostate cancer, hereditary, X-linked 1", "description": "" }, { "id": "MONDO:0010257", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010257", "name": "prostate cancer susceptibility, X-linked", "description": "" }, { "id": "MONDO:0010405", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010405", "name": "prostate cancer, hereditary, X-linked 2", "description": "" }, { "id": "MONDO:0010405", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010405", "name": "HPCX2", "description": "" }, { "id": "MONDO:0010405", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010405", "name": "prostate cancer, hereditary, X-linked 2", "description": "" }, { "id": "MIM:611868", "resource": "MIM", "url": "https://www.omim.org/entry/611868", "name": "Prostate cancer, hereditary, 12", "description": "Prostate cancer, hereditary, 12" }, { "id": "MIM:611928", "resource": "MIM", "url": "https://www.omim.org/entry/611928", "name": "Prostate cancer, hereditary, 13", "description": "Prostate cancer, hereditary, 13" }, { "id": "MIM:176807", "resource": "MIM", "url": "https://www.omim.org/entry/176807", "name": "Prostate cancer", "description": "Prostate cancer" }, { "id": "MIM:601518", "resource": "MIM", "url": "https://www.omim.org/entry/601518", "name": "Prostate cancer, hereditary, 1", "description": "Prostate cancer, hereditary, 1" }, { "id": "MIM:611955", "resource": "MIM", "url": "https://www.omim.org/entry/611955", "name": "Prostate cancer, hereditary, 11", "description": "Prostate cancer, hereditary, 11" } ] } ] }, { "significant": "No", "trend": "up", "name": "Stomach cancer [DO disease name]", "url": "http://disease-ontology.org/term/DOID:10534", "evidence": [ { "database": "BioXpress", "id": "Q9Y5W7", "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/Q9Y5W7" } ], "disease": [ { "disease_id": "DOID:10534", "recommended_name": { "id": "DOID:10534", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10534", "name": "stomach cancer", "description": "A gastrointestinal system cancer that is located_in the stomach." }, "synonyms": [ { "id": "DOID:10534", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10534", "name": "gastric cancer", "description": "" }, { "id": "DOID:10534", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:10534", "name": "gastric neoplasm", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer", "description": "A primary or metastatic malignant neoplasm involving the stomach." }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric neoplasm", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "Ca lesser curvature - stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "cancer of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer risk after h. pylori infection", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer, somatic", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant gastric neoplasm", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant gastric tumor", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant gastric tumour", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant neoplasm of lesser curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant neoplasm of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant neoplasm of the stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant stomach neoplasm", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of body of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of greater curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of lesser curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumor of the stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumour of body of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant tumour of greater curve of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": 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"MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "malignant neoplasm of body of stomach", "description": "" }, { "id": "MONDO:0001056", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001056", "name": "gastric cancer, intestinal", "description": "" }, { "id": "MIM:613659", "resource": "MIM", "url": "https://www.omim.org/entry/613659", "name": "Gastric cancer", "description": "Gastric cancer" } ] } ] }, { "significant": "No", "trend": "up", "name": "Urinary bladder cancer [DO disease name]", "url": "http://disease-ontology.org/term/DOID:11054", "evidence": [ { "database": "BioXpress", "id": "Q9Y5W7", "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/Q9Y5W7" } ], "disease": [ { "disease_id": "DOID:11054", "recommended_name": { "id": "DOID:11054", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:11054", "name": "urinary bladder cancer", "description": "An urinary system cancer that 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"https://monarchinitiative.org/disease/MONDO:0001187", "name": "bladder cancer, somatic", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "cancer of urinary bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant bladder neoplasm", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant bladder tumor", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant bladder tumour", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant neoplasm of bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant neoplasm of the bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant neoplasm of the urinary bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant neoplasm of urinary bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant neoplasm, bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant neoplasm, urinary bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant tumor of bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant tumor of the bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant tumor of the urinary bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant tumor of urinary bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant tumor, urinary bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant tumour of bladder", "description": "" }, { "id": "MONDO:0001187", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0001187", "name": "malignant tumour of the 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{ "id": "DOID:1612", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1612", "name": "malignant neoplasm of breast", "description": "" }, { "id": "DOID:1612", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1612", "name": "malignant tumor of the breast", "description": "" }, { "id": "DOID:1612", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1612", "name": "mammary cancer", "description": "" }, { "id": "DOID:1612", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1612", "name": "mammary tumor", "description": "" }, { "id": "DOID:1612", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1612", "name": "primary breast cancer", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "hereditary breast carcinoma", "description": "Breast carcinoma that has developed in relatives of patients with history of breast carcinoma." }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer susceptibility, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, invasive ductal, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, lobular, somatic", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, male, susceptibility to, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, protection against, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, somatic", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, susceptibility to, autosomal dominant, somatic mutation", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "familial breast cancer", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "familial breast carcinoma", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "familial cancer of breast", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "familial cancer of the breast", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "hereditary breast cancer", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "hereditary breast carcinoma", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, familial", "description": "" }, { "id": "MONDO:0016419", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0016419", "name": "breast cancer, familial Male", "description": "" }, { "id": "MIM:114480", "resource": "MIM", "url": "https://www.omim.org/entry/114480", "name": "Breast cancer", "description": "Breast cancer" } ] } ] }, { "significant": "Yes", "trend": "up", "name": "Thyroid cancer [DO disease name]", "url": "http://disease-ontology.org/term/DOID:1781", "evidence": [ { "database": "BioXpress", "id": "Q9Y5W7", "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/Q9Y5W7" } ], "disease": [ { "disease_id": "DOID:1781", "recommended_name": { "id": "DOID:1781", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1781", "name": "thyroid cancer", "description": "An endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage." }, "synonyms": [ { "id": "DOID:1781", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1781", "name": "thyroid gland cancer", "description": "" }, { "id": "DOID:1781", "resource": "Disease Ontology", 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"database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HJS3", "url": "https://www.uniprot.org/uniprot/A0A804HJS3", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HJS3-1", "url": "https://www.uniprot.org/uniprot/A0A804HJS3-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HJT4", "url": "https://www.uniprot.org/uniprot/A0A804HJT4", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HJT4-1", "url": "https://www.uniprot.org/uniprot/A0A804HJT4-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HJW4", "url": "https://www.uniprot.org/uniprot/A0A804HJW4", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HJW4-1", "url": "https://www.uniprot.org/uniprot/A0A804HJW4-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HJZ4", "url": "https://www.uniprot.org/uniprot/A0A804HJZ4", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HJZ4-1", "url": "https://www.uniprot.org/uniprot/A0A804HJZ4-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HK22", "url": "https://www.uniprot.org/uniprot/A0A804HK22", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HK22-1", "url": "https://www.uniprot.org/uniprot/A0A804HK22-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HK24", "url": "https://www.uniprot.org/uniprot/A0A804HK24", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HK24-1", "url": "https://www.uniprot.org/uniprot/A0A804HK24-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HK55", "url": "https://www.uniprot.org/uniprot/A0A804HK55", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HK55-1", "url": "https://www.uniprot.org/uniprot/A0A804HK55-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKA3", "url": "https://www.uniprot.org/uniprot/A0A804HKA3", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKA3-1", "url": "https://www.uniprot.org/uniprot/A0A804HKA3-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKC6", "url": "https://www.uniprot.org/uniprot/A0A804HKC6", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKC6-1", "url": "https://www.uniprot.org/uniprot/A0A804HKC6-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKD6", "url": "https://www.uniprot.org/uniprot/A0A804HKD6", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKD6-1", "url": "https://www.uniprot.org/uniprot/A0A804HKD6-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKH6", "url": "https://www.uniprot.org/uniprot/A0A804HKH6", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKH6-1", "url": "https://www.uniprot.org/uniprot/A0A804HKH6-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKJ3", "url": "https://www.uniprot.org/uniprot/A0A804HKJ3", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKJ3-1", "url": "https://www.uniprot.org/uniprot/A0A804HKJ3-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKN0", "url": "https://www.uniprot.org/uniprot/A0A804HKN0", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKN0-1", "url": "https://www.uniprot.org/uniprot/A0A804HKN0-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKN4", "url": "https://www.uniprot.org/uniprot/A0A804HKN4", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKN4-1", "url": "https://www.uniprot.org/uniprot/A0A804HKN4-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKP6", "url": "https://www.uniprot.org/uniprot/A0A804HKP6", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKP6-1", "url": "https://www.uniprot.org/uniprot/A0A804HKP6-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKT4", "url": "https://www.uniprot.org/uniprot/A0A804HKT4", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKT4-1", "url": "https://www.uniprot.org/uniprot/A0A804HKT4-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKY3", "url": "https://www.uniprot.org/uniprot/A0A804HKY3", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKY3-1", "url": "https://www.uniprot.org/uniprot/A0A804HKY3-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKZ1", "url": "https://www.uniprot.org/uniprot/A0A804HKZ1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HKZ1-1", "url": "https://www.uniprot.org/uniprot/A0A804HKZ1-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HL41", "url": "https://www.uniprot.org/uniprot/A0A804HL41", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HL41-1", "url": "https://www.uniprot.org/uniprot/A0A804HL41-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HL44", "url": "https://www.uniprot.org/uniprot/A0A804HL44", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HL44-1", "url": "https://www.uniprot.org/uniprot/A0A804HL44-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HL53", "url": "https://www.uniprot.org/uniprot/A0A804HL53", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HL53-1", "url": "https://www.uniprot.org/uniprot/A0A804HL53-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HLC7", "url": "https://www.uniprot.org/uniprot/A0A804HLC7", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HLC7-1", "url": "https://www.uniprot.org/uniprot/A0A804HLC7-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HLH9", "url": "https://www.uniprot.org/uniprot/A0A804HLH9", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A804HLH9-1", "url": "https://www.uniprot.org/uniprot/A0A804HLH9-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6RBA7", "url": "https://www.uniprot.org/uniprot/D6RBA7", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6RBA7-1", "url": "https://www.uniprot.org/uniprot/D6RBA7-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6RDA6", "url": "https://www.uniprot.org/uniprot/D6RDA6", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6RDA6-1", "url": "https://www.uniprot.org/uniprot/D6RDA6-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6RDH9", "url": "https://www.uniprot.org/uniprot/D6RDH9", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6RDH9-1", "url": "https://www.uniprot.org/uniprot/D6RDH9-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6REK1", "url": "https://www.uniprot.org/uniprot/D6REK1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6REK1-1", "url": "https://www.uniprot.org/uniprot/D6REK1-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6RJG9", "url": "https://www.uniprot.org/uniprot/D6RJG9", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D6RJG9-1", "url": "https://www.uniprot.org/uniprot/D6RJG9-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "E2QRM8", "url": "https://www.uniprot.org/uniprot/E2QRM8", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "E2QRM8-1", "url": "https://www.uniprot.org/uniprot/E2QRM8-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "H0Y926", "url": "https://www.uniprot.org/uniprot/H0Y926", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "H0Y926-1", "url": "https://www.uniprot.org/uniprot/H0Y926-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q5JRQ0", "url": "https://www.uniprot.org/uniprot/Q5JRQ0", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q5JRQ0-1", "url": "https://www.uniprot.org/uniprot/Q5JRQ0-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q9Y5W7-1", "url": "https://www.uniprot.org/uniprot/Q9Y5W7-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q9Y5W7-2", "url": "https://www.uniprot.org/uniprot/Q9Y5W7-2", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q9Y5W7-3", "url": "https://www.uniprot.org/uniprot/Q9Y5W7-3", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q9Y5W7-4", "url": "https://www.uniprot.org/uniprot/Q9Y5W7-4", "database": "UniProtKB", "categories": [ "Protein" ] } ], "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 946, "header": "sp|Q9Y5W7-1|SNX14_HUMAN Isoform 1 of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=3 CANONICAL=Q9Y5W7-1" }, "isoforms": [ { "isoform_ac": "A0A804HHR7-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSE", "length": 139, "header": "tr|A0A804HHR7-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85572137, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682034.1", "url": "https://www.ensembl.org/id/ENST00000682034.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000506724.1", "url": "https://www.ensembl.org/id/ENSP00000506724.1" } ] } }, { "isoform_ac": "A0A804HHX8-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTRNLMIEFYDQNYQMMKCCLFMKNCRRFIKHTVWMKVLTKLDLIPSL", "length": 362, "header": "tr|A0A804HHX8-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85543623, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682776.1", "url": "https://www.ensembl.org/id/ENST00000682776.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507490.1", "url": "https://www.ensembl.org/id/ENSP00000507490.1" } ] } }, { "isoform_ac": "A0A804HHZ6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNSS", "length": 48, "header": "tr|A0A804HHZ6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85572371, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683873.1", "url": "https://www.ensembl.org/id/ENST00000683873.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000506829.1", "url": "https://www.ensembl.org/id/ENSP00000506829.1" } ] } }, { "isoform_ac": "A0A804HI30-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 849, "header": "tr|A0A804HI30-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684647.1", "url": "https://www.ensembl.org/id/ENST00000684647.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000506873.1", "url": "https://www.ensembl.org/id/ENSP00000506873.1" } ] } }, { "isoform_ac": "A0A804HI47-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRQQDQPLLFSLPSVKTMKMKTFVIIHFHLIQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 891, "header": "tr|A0A804HI47-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683898.1", "url": "https://www.ensembl.org/id/ENST00000683898.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000506897.1", "url": "https://www.ensembl.org/id/ENSP00000506897.1" } ] } }, { "isoform_ac": "A0A804HI51-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 850, "header": "tr|A0A804HI51-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682939.1", "url": "https://www.ensembl.org/id/ENST00000682939.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000506902.1", "url": "https://www.ensembl.org/id/ENSP00000506902.1" } ] } }, { "isoform_ac": "A0A804HIA1-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 850, "header": "tr|A0A804HIA1-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682491.1", "url": "https://www.ensembl.org/id/ENST00000682491.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000506970.1", "url": "https://www.ensembl.org/id/ENSP00000506970.1" } ] } }, { "isoform_ac": "A0A804HIC5-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKSFALSPRLEYSGMISAHCNLRLPGSSDSPASASRVAGTTGICHHARLIFCIFSRDRVSPC", "length": 242, "header": "tr|A0A804HIC5-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85564802, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683698.1", "url": "https://www.ensembl.org/id/ENST00000683698.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507000.1", "url": "https://www.ensembl.org/id/ENSP00000507000.1" } ] } }, { "isoform_ac": "A0A804HIC6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPAFLRVCIMPCAL", "length": 895, "header": "tr|A0A804HIC6-1|A0A804HIC6_HUMAN Computationally mapped isoform of Sorting nexin 14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85508279, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682133.1", "url": "https://www.ensembl.org/id/ENST00000682133.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507001.1", "url": "https://www.ensembl.org/id/ENSP00000507001.1" } ] } }, { "isoform_ac": "A0A804HID3-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVGEAYLCILRKGI", "length": 381, "header": "tr|A0A804HID3-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85543754, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683481.1", "url": "https://www.ensembl.org/id/ENST00000683481.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507015.1", "url": "https://www.ensembl.org/id/ENSP00000507015.1" } ] } }, { "isoform_ac": "A0A804HID8-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLAKISLLHQSNKRLLHSKGNKQQSEETTCRMGGNIYGYFTWKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 985, "header": "tr|A0A804HID8-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684717.1", "url": "https://www.ensembl.org/id/ENST00000684717.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507024.1", "url": "https://www.ensembl.org/id/ENSP00000507024.1" } ] } }, { "isoform_ac": "A0A804HIJ3-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTRNLMIEFYDQNYQMMKCCLFMKNCRRFIKHTVWMKVLTKLDLIPSL", "length": 414, "header": "tr|A0A804HIJ3-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85543623, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682688.1", "url": "https://www.ensembl.org/id/ENST00000682688.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507097.1", "url": "https://www.ensembl.org/id/ENSP00000507097.1" } ] } }, { "isoform_ac": "A0A804HIK6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVTEKQ", "length": 938, "header": "tr|A0A804HIK6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85507218, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683541.1", "url": "https://www.ensembl.org/id/ENST00000683541.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507116.1", "url": "https://www.ensembl.org/id/ENSP00000507116.1" } ] } }, { "isoform_ac": "A0A804HIM9-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHSDLVV", "length": 117, "header": "tr|A0A804HIM9-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85572230, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684422.1", "url": "https://www.ensembl.org/id/ENST00000684422.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507146.1", "url": "https://www.ensembl.org/id/ENSP00000507146.1" } ] } }, { "isoform_ac": "A0A804HIR3-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 901, "header": "tr|A0A804HIR3-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683785.1", "url": "https://www.ensembl.org/id/ENST00000683785.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507188.1", "url": "https://www.ensembl.org/id/ENSP00000507188.1" } ] } }, { "isoform_ac": "A0A804HIV6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVVVWARRSGSCLQSQHFGRPRQVDHLKSGVRDQPGQHSETLSRQKYKN", "length": 416, "header": "tr|A0A804HIV6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85545850, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682455.1", "url": "https://www.ensembl.org/id/ENST00000682455.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507586.1", "url": "https://www.ensembl.org/id/ENSP00000507586.1" } ] } }, { "isoform_ac": "A0A804HIW9-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNS", "length": 47, "header": "tr|A0A804HIW9-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85572371, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682854.1", "url": "https://www.ensembl.org/id/ENST00000682854.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507257.1", "url": "https://www.ensembl.org/id/ENSP00000507257.1" } ] } }, { "isoform_ac": "A0A804HIX9-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFLDTSLNIGLSIEDILNSMYLNQN", "length": 559, "header": "tr|A0A804HIX9-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85530207, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683073.1", "url": "https://www.ensembl.org/id/ENST00000683073.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507270.1", "url": "https://www.ensembl.org/id/ENSP00000507270.1" } ] } }, { "isoform_ac": "A0A804HIZ9-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEVSIWNLLS", "length": 723, "header": "tr|A0A804HIZ9-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85517848, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684581.1", "url": "https://www.ensembl.org/id/ENST00000684581.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507294.1", "url": "https://www.ensembl.org/id/ENSP00000507294.1" } ] } }, { "isoform_ac": "A0A804HJ02-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKDL", "length": 212, "header": "tr|A0A804HJ02-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85548372, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682412.1", "url": "https://www.ensembl.org/id/ENST00000682412.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507297.1", "url": "https://www.ensembl.org/id/ENSP00000507297.1" } ] } }, { "isoform_ac": "A0A804HJ61-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKKKLSRFGGKCL", "length": 945, "header": "tr|A0A804HJ61-1|A0A804HJ61_HUMAN Computationally mapped isoform of Sorting nexin 14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85506457, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683479.1", "url": "https://www.ensembl.org/id/ENST00000683479.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507368.1", "url": "https://www.ensembl.org/id/ENSP00000507368.1" } ] } }, { "isoform_ac": "A0A804HJ76-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEGCDR", "length": 143, "header": "tr|A0A804HJ76-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85565408, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684451.1", "url": "https://www.ensembl.org/id/ENST00000684451.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507384.1", "url": "https://www.ensembl.org/id/ENSP00000507384.1" } ] } }, { "isoform_ac": "A0A804HJ79-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHK", "length": 183, "header": "tr|A0A804HJ79-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85565332, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682454.1", "url": "https://www.ensembl.org/id/ENST00000682454.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507851.1", "url": "https://www.ensembl.org/id/ENSP00000507851.1" } ] } }, { "isoform_ac": "A0A804HJ91-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 893, "header": "tr|A0A804HJ91-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682171.1", "url": "https://www.ensembl.org/id/ENST00000682171.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508327.1", "url": "https://www.ensembl.org/id/ENSP00000508327.1" } ] } }, { "isoform_ac": "A0A804HJA7-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVVFQTTFKRCRITNTQFKIEQR", "length": 389, "header": "tr|A0A804HJA7-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85538862, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682374.1", "url": "https://www.ensembl.org/id/ENST00000682374.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507425.1", "url": "https://www.ensembl.org/id/ENSP00000507425.1" } ] } }, { "isoform_ac": "A0A804HJC6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 902, "header": "tr|A0A804HJC6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683643.1", "url": "https://www.ensembl.org/id/ENST00000683643.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507444.1", "url": "https://www.ensembl.org/id/ENSP00000507444.1" } ] } }, { "isoform_ac": "A0A804HJD1-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYSKKYRVFTASCFRRIWSRASCCFEKSKR", "length": 129, "header": "tr|A0A804HJD1-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85549798, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683878.1", "url": "https://www.ensembl.org/id/ENST00000683878.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507449.1", "url": "https://www.ensembl.org/id/ENSP00000507449.1" } ] } }, { "isoform_ac": "A0A804HJF4-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKTEFCSVAQAGVQWHDLSSLQPPPPRFK", "length": 158, "header": "tr|A0A804HJF4-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85564905, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682174.1", "url": "https://www.ensembl.org/id/ENST00000682174.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507248.1", "url": "https://www.ensembl.org/id/ENSP00000507248.1" } ] } }, { "isoform_ac": "A0A804HJG1-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 821, "header": "tr|A0A804HJG1-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684680.1", "url": "https://www.ensembl.org/id/ENST00000684680.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507491.1", "url": "https://www.ensembl.org/id/ENSP00000507491.1" } ] } }, { "isoform_ac": "A0A804HJH5-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKSFALSPRLEYSGMISAHCNLRLPGSSDSPASASRVAGTTGICHHARLIFCIFSRDRVSPC", "length": 243, "header": "tr|A0A804HJH5-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85564802, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683126.1", "url": "https://www.ensembl.org/id/ENST00000683126.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507507.1", "url": "https://www.ensembl.org/id/ENSP00000507507.1" } ] } }, { "isoform_ac": "A0A804HJI4-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPAFLRVCIMPCAL", "length": 852, "header": "tr|A0A804HJI4-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85508279, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683577.1", "url": "https://www.ensembl.org/id/ENST00000683577.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507516.1", "url": "https://www.ensembl.org/id/ENSP00000507516.1" } ] } }, { "isoform_ac": "A0A804HJK3-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 859, "header": "tr|A0A804HJK3-1|A0A804HJK3_HUMAN Computationally mapped isoform of Sorting nexin 14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682660.1", "url": "https://www.ensembl.org/id/ENST00000682660.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507539.1", "url": "https://www.ensembl.org/id/ENSP00000507539.1" } ] } }, { "isoform_ac": "A0A804HJL8-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRLKKVLL", "length": 489, "header": "tr|A0A804HJL8-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85533782, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683097.1", "url": "https://www.ensembl.org/id/ENST00000683097.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507556.1", "url": "https://www.ensembl.org/id/ENSP00000507556.1" } ] } }, { "isoform_ac": "A0A804HJS3-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPAFLRVCIMPCAL", "length": 896, "header": "tr|A0A804HJS3-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85508279, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682464.1", "url": "https://www.ensembl.org/id/ENST00000682464.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507625.1", "url": "https://www.ensembl.org/id/ENSP00000507625.1" } ] } }, { "isoform_ac": "A0A804HJT4-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPAFLRVCIMPCAL", "length": 844, "header": "tr|A0A804HJT4-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85508279, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684299.1", "url": "https://www.ensembl.org/id/ENST00000684299.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507637.1", "url": "https://www.ensembl.org/id/ENSP00000507637.1" } ] } }, { "isoform_ac": "A0A804HJW4-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 918, "header": "tr|A0A804HJW4-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000681981.1", "url": "https://www.ensembl.org/id/ENST00000681981.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507672.1", "url": "https://www.ensembl.org/id/ENSP00000507672.1" } ] } }, { "isoform_ac": "A0A804HJZ4-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 919, "header": "tr|A0A804HJZ4-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683754.1", "url": "https://www.ensembl.org/id/ENST00000683754.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507707.1", "url": "https://www.ensembl.org/id/ENSP00000507707.1" } ] } }, { "isoform_ac": "A0A804HK22-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 882, "header": "tr|A0A804HK22-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682738.1", "url": "https://www.ensembl.org/id/ENST00000682738.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507742.1", "url": "https://www.ensembl.org/id/ENSP00000507742.1" } ] } }, { "isoform_ac": "A0A804HK24-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEGCDR", "length": 90, "header": "tr|A0A804HK24-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85565408, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683726.1", "url": "https://www.ensembl.org/id/ENST00000683726.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507744.1", "url": "https://www.ensembl.org/id/ENSP00000507744.1" } ] } }, { "isoform_ac": "A0A804HK55-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 891, "header": "tr|A0A804HK55-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682682.1", "url": "https://www.ensembl.org/id/ENST00000682682.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507777.1", "url": "https://www.ensembl.org/id/ENSP00000507777.1" } ] } }, { "isoform_ac": "A0A804HKA3-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPAFLRVCIMPCAL", "length": 843, "header": "tr|A0A804HKA3-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85508279, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682633.1", "url": "https://www.ensembl.org/id/ENST00000682633.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507843.1", "url": "https://www.ensembl.org/id/ENSP00000507843.1" } ] } }, { "isoform_ac": "A0A804HKC6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 945, "header": "tr|A0A804HKC6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682497.1", "url": "https://www.ensembl.org/id/ENST00000682497.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507869.1", "url": "https://www.ensembl.org/id/ENSP00000507869.1" } ] } }, { "isoform_ac": "A0A804HKD6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRWIFHLL", "length": 53, "header": "tr|A0A804HKD6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85558042, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682057.1", "url": "https://www.ensembl.org/id/ENST00000682057.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507883.1", "url": "https://www.ensembl.org/id/ENSP00000507883.1" } ] } }, { "isoform_ac": "A0A804HKH6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 829, "header": "tr|A0A804HKH6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684281.1", "url": "https://www.ensembl.org/id/ENST00000684281.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507932.1", "url": "https://www.ensembl.org/id/ENSP00000507932.1" } ] } }, { "isoform_ac": "A0A804HKJ3-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQELFPELNKVQKEVTSVTSWM", "length": 934, "header": "tr|A0A804HKJ3-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684118.1", "url": "https://www.ensembl.org/id/ENST00000684118.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507950.1", "url": "https://www.ensembl.org/id/ENSP00000507950.1" } ] } }, { "isoform_ac": "A0A804HKN0-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEVSIWNLLS", "length": 724, "header": "tr|A0A804HKN0-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85517848, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683085.1", "url": "https://www.ensembl.org/id/ENST00000683085.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507993.1", "url": "https://www.ensembl.org/id/ENSP00000507993.1" } ] } }, { "isoform_ac": "A0A804HKN4-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKTEFCSVAQAGVQWHDLSSLQPPPPRFK", "length": 210, "header": "tr|A0A804HKN4-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85564905, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682023.1", "url": "https://www.ensembl.org/id/ENST00000682023.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000507998.1", "url": "https://www.ensembl.org/id/ENSP00000507998.1" } ] } }, { "isoform_ac": "A0A804HKP6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRWIFHLL", "length": 160, "header": "tr|A0A804HKP6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85558042, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683857.1", "url": "https://www.ensembl.org/id/ENST00000683857.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508015.1", "url": "https://www.ensembl.org/id/ENSP00000508015.1" } ] } }, { "isoform_ac": "A0A804HKT4-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKRQGFTVLARMVSIS", "length": 197, "header": "tr|A0A804HKT4-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85564779, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684273.1", "url": "https://www.ensembl.org/id/ENST00000684273.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508063.1", "url": "https://www.ensembl.org/id/ENSP00000508063.1" } ] } }, { "isoform_ac": "A0A804HKY3-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKGFTLLPRLECSGVISAHCNLCLPGSSDSPTSASRVAGITGL", "length": 224, "header": "tr|A0A804HKY3-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85561218, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682022.1", "url": "https://www.ensembl.org/id/ENST00000682022.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508118.1", "url": "https://www.ensembl.org/id/ENSP00000508118.1" } ] } }, { "isoform_ac": "A0A804HKZ1-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRLTEVPPWWCWIKSGRILWITRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 967, "header": "tr|A0A804HKZ1-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000684570.1", "url": "https://www.ensembl.org/id/ENST00000684570.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508127.1", "url": "https://www.ensembl.org/id/ENSP00000508127.1" } ] } }, { "isoform_ac": "A0A804HL41-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSE", "length": 87, "header": "tr|A0A804HL41-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85572137, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683195.1", "url": "https://www.ensembl.org/id/ENST00000683195.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508190.1", "url": "https://www.ensembl.org/id/ENSP00000508190.1" } ] } }, { "isoform_ac": "A0A804HL44-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 873, "header": "tr|A0A804HL44-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000682991.1", "url": "https://www.ensembl.org/id/ENST00000682991.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508193.1", "url": "https://www.ensembl.org/id/ENSP00000508193.1" } ] } }, { "isoform_ac": "A0A804HL53-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTRNLMIEFYDQNYQMMKCCLFMKNCRRFIKHTVWMKVLTKLDLIPSL", "length": 370, "header": "tr|A0A804HL53-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85543623, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683458.1", "url": "https://www.ensembl.org/id/ENST00000683458.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508204.1", "url": "https://www.ensembl.org/id/ENSP00000508204.1" } ] } }, { "isoform_ac": "A0A804HLC7-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHK", "length": 131, "header": "tr|A0A804HLC7-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85565332, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683196.1", "url": "https://www.ensembl.org/id/ENST00000683196.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508297.1", "url": "https://www.ensembl.org/id/ENSP00000508297.1" } ] } }, { "isoform_ac": "A0A804HLH9-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEGCDR", "length": 91, "header": "tr|A0A804HLH9-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85565408, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000683880.1", "url": "https://www.ensembl.org/id/ENST00000683880.1" }, { "database": "Ensembl Peptide", "id": "ENSP00000508357.1", "url": "https://www.ensembl.org/id/ENSP00000508357.1" } ] } }, { "isoform_ac": "D6RBA7-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDELFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 653, "header": "tr|D6RBA7-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=2 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000509338.6", "url": "https://www.ensembl.org/id/ENST00000509338.6" }, { "database": "Ensembl Peptide", "id": "ENSP00000424302.2", "url": "https://www.ensembl.org/id/ENSP00000424302.2" } ] } }, { "isoform_ac": "D6RDA6-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSESLTLSPRLVYSGNILAHCNLCLSGSSDTPASAPQIAGNTGS", "length": 180, "header": "tr|D6RDA6-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=2 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85567573, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000514419.6", "url": "https://www.ensembl.org/id/ENST00000514419.6" }, { "database": "Ensembl Peptide", "id": "ENSP00000425387.2", "url": "https://www.ensembl.org/id/ENSP00000425387.2" } ] } }, { "isoform_ac": "D6RDH9-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRRKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 665, "header": "tr|D6RDH9-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=1 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000513865.5", "url": "https://www.ensembl.org/id/ENST00000513865.5" }, { "database": "Ensembl Peptide", "id": "ENSP00000420938.1", "url": "https://www.ensembl.org/id/ENSP00000420938.1" } ] } }, { "isoform_ac": "D6REK1-1", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSE", "length": 86, "header": "tr|D6REK1-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=2 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85572137, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000513869.2", "url": "https://www.ensembl.org/id/ENST00000513869.2" }, { "database": "Ensembl Peptide", "id": "ENSP00000426806.2", "url": "https://www.ensembl.org/id/ENSP00000426806.2" } ] } }, { "isoform_ac": "D6RJG9-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQELFPELNKVQKEVTSVTSWM", "length": 935, "header": "tr|D6RJG9-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=2 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000515216.6", "url": "https://www.ensembl.org/id/ENST00000515216.6" }, { "database": "Ensembl Peptide", "id": "ENSP00000425630.2", "url": "https://www.ensembl.org/id/ENSP00000425630.2" } ] } }, { "isoform_ac": "E2QRM8-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVGEAYLCILRKGI", "length": 337, "header": "tr|E2QRM8-1|E2QRM8_HUMAN Computationally mapped isoform of Sorting nexin 14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=2 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85543754, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000369635.7", "url": "https://www.ensembl.org/id/ENST00000369635.7" }, { "database": "Ensembl Peptide", "id": "ENSP00000358649.3", "url": "https://www.ensembl.org/id/ENSP00000358649.3" } ] } }, { "isoform_ac": "H0Y926-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVTEKQ", "length": 939, "header": "tr|H0Y926-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=2 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85507218, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000508658.6", "url": "https://www.ensembl.org/id/ENST00000508658.6" }, { "database": "Ensembl Peptide", "id": "ENSP00000422814.2", "url": "https://www.ensembl.org/id/ENSP00000422814.2" } ] } }, { "isoform_ac": "Q5JRQ0-1", "url": "", "sequence": { "sequence": "YVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 322, "header": "tr|Q5JRQ0-1|SNX14_HUMAN Computationally mapped isoform of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=2 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85530225, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000418862.2", "url": "https://www.ensembl.org/id/ENST00000418862.2" }, { "database": "Ensembl Peptide", "id": "ENSP00000391981.2", "url": "https://www.ensembl.org/id/ENSP00000391981.2" } ] } }, { "isoform_ac": "Q9Y5W7-1", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 946, "header": "sp|Q9Y5W7-1|SNX14_HUMAN Isoform 1 of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=3 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000314673.8", "url": "https://www.ensembl.org/id/ENST00000314673.8" }, { "database": "Ensembl Peptide", "id": "ENSP00000313121.3", "url": "https://www.ensembl.org/id/ENSP00000313121.3" } ] } }, { "isoform_ac": "Q9Y5W7-2", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 893, "header": "sp|Q9Y5W7-2|SNX14_HUMAN Isoform 2 of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=3 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000346348.7", "url": "https://www.ensembl.org/id/ENST00000346348.7" }, { "database": "Ensembl Peptide", "id": "ENSP00000257769.3", "url": "https://www.ensembl.org/id/ENSP00000257769.3" } ] } }, { "isoform_ac": "Q9Y5W7-3", "url": "", "sequence": { "sequence": "MIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRGSLSLDDFRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 894, "header": "sp|Q9Y5W7-3|SNX14_HUMAN Isoform 3 of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=3 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85574362, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000505648.5", "url": "https://www.ensembl.org/id/ENST00000505648.5" }, { "database": "Ensembl Peptide", "id": "ENSP00000427380.1", "url": "https://www.ensembl.org/id/ENSP00000427380.1" } ] } }, { "isoform_ac": "Q9Y5W7-4", "url": "", "sequence": { "sequence": "MVPWVRTMGQKLKQRLRLDVGREICRQYPLFCFLLLCLSAASLLLNRYIHILMIFWSFVAGVVTFYCSLGPDSLLPNIFFTIKYKPKQLGLQELFPQGHSCAVCGKVKCKRHRPSLLLENYQPWLDLKISSKVDASLSEVLELVLENFVYPWYRDVTDDESFVDELRITLRFFASVLIRRIHKVDIPSIITKKLLKAAMKHIEVIVKARQKVKNTEFLQQAALEEYGPELHVALRSRRDELHYLRKLTELLFPYILPPKATDCRSLTLLIREILSGSVFLPSLDFLADPDTVNHLLIIFIDDSPPEKATEPASPLVPFLQKFAEPRNKKPSVLKLELKQIREQQDLLFRFMNFLKQEGAVHVLQFCLTVEEFNDRILRPELSNDEMLSLHEELQKIYKTYCLDESIDKIRFDPFIVEEIQRIAEGPYIDVVKLQTMRCLFEAYEHVLSLLENVFTPMFCHSDEYFRQLLRGAESPTRNSKLNRNTQKRGESFGISRIGSKIKGVFKSTTMEGAMLPNYGVAEGEDDFIEEGIVVMEDDSPVEAVSTPNTPRNLAAWKISIPYVDFFEDPSSERKEKKERIPVFCIDVERNDRRAVGHEPEHWSVYRRYLEFYVLESKLTEFHGAFPDAQLPSKRIIGPKNYEFLKSKREEFQEYLQKLLQHPELSNSQLLADFLSPNGGETQFLDKILPDVNLGKIIKSVPGKLMKEKGQHLEPFIMNFINSCESPKPKPSRPELTILSPTSENNKKLFNDLFKNNANRAENTERKQNQNYFMEVMTVEGVYDYLMYVGRVVFQVPDWLHHLLMGTRILFKNTLEMYTDYYLQCKLEQLFQEHRLVSLITLLRDAIFCENTEPRSLQDKQKGAKQTFEEMMNYIPDLLVKCIGEETKYESIRLLFDGLQQPVLNKQLTYVLLDIVIQELFPELNKVQKEVTSVTSWM", "length": 937, "header": "sp|Q9Y5W7-4|SNX14_HUMAN Isoform 4 of Sorting nexin-14 OS=Homo sapiens OX=9606 GN=SNX14 PE=1 SV=3 CANONICAL=Q9Y5W7-1" }, "locus": { "chromosome": "6", "start_pos": 85593718, "end_pos": 85505970, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENST00000369627.6", "url": "https://www.ensembl.org/id/ENST00000369627.6" }, { "database": "Ensembl Peptide", "id": "ENSP00000358641.2", "url": "https://www.ensembl.org/id/ENSP00000358641.2" } ] } } ], "glycosylation": [ { "glytoucan_ac": "G49108TO", "type": "O-linked", "subtype": "O-GlcNAcylation", "site_category": "reported_with_glycan", "site_seq": "", "relation": "attached", "comment": "O-GlcNAcylation", "evidence": [ { "id": "Q9Y5W7", "database": "O-GlcNAc Database", "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q9Y5W7" }, { "id": "29485866", "database": "PubMed", "url": "https://glygen.org/publication/PubMed/29485866" } ] } ], "phosphorylation": [ { "start_pos": 548, "end_pos": 548, "kinase_uniprot_canonical_ac": "", "kinase_gene_name": "", "residue": "Ser", "comment": "Phosphoserine", "evidence": [ { "database": "UniProtKB", "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7" }, { "database": "PubMed", "id": "24275569", "url": "https://glygen.org/publication/PubMed/24275569" }, { "database": "iPTMnet", "id": "Q9Y5W7", "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/Q9Y5W7" } ], "site_lbl": "Ser548" } ], "glycation": [], "keywords": [ "glycoprotein", "glycoprotein_reported_with_glycan" ], "publication": [ { "title": "A large family of endosome-localized proteins related to sorting nexin 1.", "journal": "Biochem. J.", "date": "2001", "authors": "Gleeson P.A., Teasdale R.D., Karlsson L., Houghton F., Loci D.", "evidence": [ { "database": "UniProtKB", "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7" } ], "reference": [ { "type": "PubMed", "id": "11485546", "url": "https://glygen.org/publication/PubMed/11485546" } ] }, { "title": "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.", "journal": "Journal of proteomics", "date": "2014", "authors": "Bian Y, Song C, Cheng K, Dong M, Wang F, Huang J, Sun D, Wang L, Ye M, Zou H", "evidence": [ { "database": "UniProtKB", "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7" }, { "database": "iPTMnet", "id": "Q9Y5W7", "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/Q9Y5W7" } ], "reference": [ { "type": "PubMed", "id": "24275569", "url": "https://glygen.org/publication/PubMed/24275569" } ] }, { "title": "Structural basis for different phosphoinositide specificities of the PX domains of sorting nexins regulating G-protein signaling.", "journal": "J. Biol. Chem.", "date": "2014", "authors": "Mas C, Norwood SJ, Bugarcic A, Kinna G, Leneva N, Kovtun O, Ghai R, Ona Yanez LE, Davis JL, Teasdale RD, Collins BM", "evidence": [ { "database": "UniProtKB", "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7" } ], "reference": [ { "type": "PubMed", "id": "25148684", "url": "https://glygen.org/publication/PubMed/25148684" } ] }, { "title": "Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome.", "journal": "Am. J. Hum. Genet.", "date": "2014", "authors": "Thomas AC, Williams H, Seto-Salvia N, Bacchelli C, Jenkins D, O'Sullivan M, Mengrelis K, Ishida M, Ocaka L, Chanudet E, James C, Lescai F, Anderson G, Morrogh D, Ryten M, Duncan AJ, Pai YJ, Saraiva JM, Ramos F, Farren B, Saunders D, Vernay B, Gissen P, Straatmaan-Iwanowska A, Baas F, Wood NW, Hersheson J, Houlden H, Hurst J, Scott R, Bitner-Glindzicz M, Moore GE, Sousa SB, Stanier P", "evidence": [ { "database": "UniProtKB", "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7" }, { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" } ], "reference": [ { "type": "PubMed", "id": "25439728", "url": "https://glygen.org/publication/PubMed/25439728" } ] }, { "title": "Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.", "journal": "Nat. Genet.", "date": "2015", "authors": "Akizu N, Cantagrel V, Zaki MS, Al-Gazali L, Wang X, Rosti RO, Dikoglu E, Gelot AB, Rosti B, Vaux KK, Scott EM, Silhavy JL, Schroth J, Copeland B, Schaffer AE, Gordts PL, Esko JD, Buschman MD, Field SJ, Napolitano G, Abdel-Salam GM, Ozgul RK, Sagiroglu MS, Azam M, Ismail S, Aglan M, Selim L, Mahmoud IG, Abdel-Hadi S, Badawy AE, Sadek AA, Mojahedi F, Kayserili H, Masri A, Bastaki L, Temtamy S, Muller U, Desguerre I, Casanova JL, Dursun A, Gunel M, Gabriel SB, de Lonlay P, Gleeson JG", "evidence": [ { "database": "UniProtKB", "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7" }, { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" } ], "reference": [ { "type": "PubMed", "id": "25848753", "url": "https://glygen.org/publication/PubMed/25848753" } ] }, { "title": "Exome Sequencing and Linkage Analysis Identified Novel Candidate Genes in Recessive Intellectual Disability Associated with Ataxia.", "journal": "Arch. Iran. Med.", "date": "2015", "authors": "Jazayeri R, Hu H, Fattahi Z, Musante L, Abedini SS, Hosseini M, Wienker TF, Ropers HH, Najmabadi H, Kahrizi K", "evidence": [ { "database": "UniProtKB", "id": "Q9Y5W7", "url": "https://www.uniprot.org/uniprot/Q9Y5W7" } ], "reference": [ { "type": "PubMed", "id": "26443249", "url": "https://glygen.org/publication/PubMed/26443249" } ] }, { "title": "Autosomal recessive spinocerebellar ataxia 20: Report of a new patient and review of literature.", "journal": "European journal of medical genetics", "date": "2017", "authors": "Shukla A, Upadhyai P, Shah J, Neethukrishna K, Bielas S, Girisha KM", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" } ], "reference": [ { "type": "PubMed", "id": "27913285", "url": "https://glygen.org/publication/PubMed/27913285" } ] }, { "title": "O-GlcNAc Transferase Recognizes Protein Substrates Using an Asparagine Ladder in the Tetratricopeptide Repeat (TPR) Superhelix.", "journal": "Journal of the American Chemical Society", "date": "2018", "authors": "Levine ZG, Fan C, Melicher MS, Orman M, Benjamin T, Walker S", "evidence": [ { "database": "O-GlcNAc Database", "id": "Q9Y5W7", "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q9Y5W7" } ], "reference": [ { "type": "PubMed", "id": "29485866", "url": "https://glygen.org/publication/PubMed/29485866" } ] }, { "title": "SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20.", "journal": "Human molecular genetics", "date": "2018", "authors": "Bryant D, Liu Y, Datta S, Hariri H, Seda M, Anderson G, Peskett E, Demetriou C, Sousa S, Jenkins D, Clayton P, Bitner-Glindzicz M, Moore GE, Henne WM, Stanier P", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" } ], "reference": [ { "type": "PubMed", "id": "29635513", "url": "https://glygen.org/publication/PubMed/29635513" } ] }, { "title": "Cerebellar ataxia disease-associated Snx14 promotes lipid droplet growth at ER-droplet contacts.", "journal": "The Journal of cell biology", "date": "2019", "authors": "Datta S, Liu Y, Hariri H, Bowerman J, Henne WM", "evidence": [ { "database": "RefSeq", "id": "NP_001284543", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001284543" } ], "reference": [ { "type": "PubMed", "id": "30765438", "url": "https://glygen.org/publication/PubMed/30765438" } ] } ], "pathway": [ { "id": "hsa:57231", "name": "", "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+hsa:57231", "resource": "KEGG Pathway" } ], "orthologs": [ { "uniprot_canonical_ac": "Q8BHY8-1", "protein_name": "Sorting nexin-14", "gene_name": "Snx14", "tax_id": 10090, "organism": "Mus musculus", "sequence": { "sequence": 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