{ "uniprot_canonical_ac": "A0A0R4IF73-1", "uniprot_ac": "A0A0R4IF73", "uniprot_id": "A0A0R4IF73_DANRE", "mass": { "chemical_mass": 15127.0, "monoisotopic_mass": 15127.0 }, "refseq": { "ac": "XP_001343826", "name": "protein C19orf12 homolog", "summary": "", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_001343826" }, "gene_names": [ { "name": "si:ch211-260e23.7", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73", "id": "A0A0R4IF73" }, { "name": "si:ch211-260e23.7", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_001343826", "id": "XP_001343826" } ], "protein_names": [ { "name": "Protein C19orf12 homolog", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73/entry#names_and_taxonomy", "id": "A0A0R4IF73" }, { "name": "Si:ch211-260e23.7", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73/entry#names_and_taxonomy", "id": "A0A0R4IF73" }, { "name": "protein C19orf12 homolog", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_001343826", "id": "XP_001343826" } ], "function": [ { "annotation": "##Genome-Annotation-Data-START## Annotation Provider :: NCBI RefSeq Annotation Status :: Full annotation Annotation Name :: GCF_049306965.1-RS_2025_04 Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline Annotation Software Version :: 10.3 Annotation Method :: Best-placed RefSeq; Gnomon; cmsearch; tRNAscan-SE Features Annotated :: Gene; mRNA; CDS; ncRNA Annotation Date :: 04/11/2025 ##Genome-Annotation-Data-END## MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NC_133182) annotated using gene prediction method: Gnomon. Also see: Documentation of NCBI's Annotation Process COMPLETENESS: full length.", "evidence": [ { "database": "RefSeq", "id": "XP_001343826", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_001343826" } ] } ], "disease": [ { "disease_id": "DOID:0110738", "recommended_name": { "id": "DOID:0110738", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110738", "name": "neurodegeneration with brain iron accumulation 4", "description": "A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the C19orf12 gene on chromosome 19q12." }, "synonyms": [ { "id": "DOID:0110738", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110738", "name": "Neurodegeneration with brain iron accumulation due to C19orf12 mutation", "description": "" }, { "id": "DOID:0110738", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110738", "name": "MPAN", "description": "" }, { "id": "DOID:0110738", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110738", "name": "Mitochondrial Protein-Associated Neurodegeneration", "description": "" }, { "id": "DOID:0110738", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110738", "name": "NBIA due to C19orf12 mutation", "description": "" }, { "id": "DOID:0110738", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110738", "name": "NBIA4", "description": "" }, { "id": "DOID:0110738", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110738", "name": "Neurodegeneration with brain iron accumulation type 4", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "neurodegeneration with brain iron accumulation 4", "description": "Mitochondrial membrane protein-sssociated neurodegeneration (MPAN), also known as neurogeneration with brain iron accumulation (NBIA) due to C19orf12 mutations, is an autosomal recessive neurodegenerative disorder characterized by iron accumulation in specific regions of the brain, usually the basal ganglia, and associated with slowly progressive pyramidal (spasticity) and extrapyramidal (dystonia) signs, motor axonal neuropathy, optic atrophy, cognitive decline, and neuropsychiatric abnormalities." }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "C19orf12 neurodegeneration with brain iron accumulation", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "MPAN", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "NBIA due to C19orf12 mutation", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "NBIA4", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "mitochondrial Protein-associated neurodegeneration", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "neurodegeneration with brain iron accumulation 4", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "neurodegeneration with brain iron accumulation caused by mutation in C19orf12", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "neurodegeneration with brain iron accumulation due to C19orf12 mutation", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "neurodegeneration with brain iron accumulation type 4", "description": "" }, { "id": "MONDO:0013674", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013674", "name": "mitochondrial membrane protein-associated neurodegeneration", "description": "" }, { "id": "MIM:614298", "resource": "MIM", "url": "https://www.omim.org/entry/614298", "name": "Neurodegeneration with brain iron accumulation 4", "description": "Neurodegeneration with brain iron accumulation 4" } ], "unlinked_id_list": [], "evidence": [ { "id": "0110738", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:0110738" } ] }, { "disease_id": "DOID:0110795", "recommended_name": { "id": "DOID:0110795", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110795", "name": "hereditary spastic paraplegia 43", "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12." }, "synonyms": [ { "id": "DOID:0110795", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110795", "name": "SPG43", "description": "" }, { "id": "DOID:0110795", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110795", "name": "autosomal recessive spastic paraplegia 43", "description": "" }, { "id": "DOID:0110795", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110795", "name": "autosomal recessive spastic paraplegia type 43", "description": "" }, { "id": "MONDO:0014024", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014024", "name": "hereditary spastic paraplegia 43", "description": "Autosomal recessive spastic paraplegia type 43 is a rare, complex hereditary spastic paraplegia characterized by a childhood to adolescent onset of progressive lower limb spasticity, associated with mild to severe gait disturbances, extensor plantar responses, muscle weakness and severe distal atrophy, frequently with upper limb involvement. Additional features may include joint contractures, distal sensory loss and brisk or absent deep tendon reflexes. Other signs, such as depression, memory loss, optic atrophy (with vision loss) and brain iron deposition (revealed by brain imagery), have also been reported." }, { "id": "MONDO:0014024", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014024", "name": "C19orf12 autosomal recessive complex spastic paraplegia", "description": "" }, { "id": "MONDO:0014024", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014024", "name": "SPG43", "description": "" }, { "id": "MONDO:0014024", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014024", "name": "autosomal recessive complex spastic paraplegia caused by mutation in C19orf12", "description": "" }, { "id": "MONDO:0014024", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014024", "name": "autosomal recessive spastic paraplegia 43", "description": "" }, { "id": "MONDO:0014024", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014024", "name": "autosomal recessive spastic paraplegia type 43", "description": "" }, { "id": "MONDO:0014024", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014024", "name": "hereditary spastic paraplegia type 43", "description": "" }, { "id": "MONDO:0014024", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014024", "name": "spastic paraplegia 43, autosomal recessive", "description": "" }, { "id": "MIM:615043", "resource": "MIM", "url": "https://www.omim.org/entry/615043", "name": "Spastic paraplegia 43, autosomal recessive", "description": "Spastic paraplegia 43, autosomal recessive" } ], "unlinked_id_list": [], "evidence": [ { "id": "0110795", "database": "AGR", "url": "https://www.alliancegenome.org/disease/DOID:0110795" } ] } ], "snv": [], "mutagenesis": [], "expression_tissue": [], "expression_disease": [], "species": [ { "name": "Danio rerio", "taxid": 7955, "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IF73", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73" } ], "common_name": "Zebrafish", "glygen_name": "Zebrafish", "reference_species": "Danio rerio [7955]" } ], "gene": [ { "name": "si:ch211-260e23.7", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73", "locus": {} } ], "crossref": [ { "id": "ZFIN:ZDB-GENE-141216-158", "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-141216-158", "database": "AGR", "categories": [ "Protein Classification" ] }, { "id": "ENSDARG00000104856", "url": "https://bgee.org/?page=gene&gene_id=ENSDARG00000104856", "database": "Bgee", "categories": [ "Gene Expression" ] }, { "id": "100004554", "url": "https://www.ncbi.nlm.nih.gov/gene/100004554", "database": "GeneID", "categories": [ "Genome Annotation" ] }, { "id": "IPR033369", "url": "https://www.ebi.ac.uk/interpro/entry/IPR033369", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "dre:100004554", "url": "https://www.genome.jp/dbget-bin/www_bget?dre:100004554", "database": "KEGG Pathway", "categories": [ "Enzyme and Pathway" ] }, { "id": "CHISKVK", "url": "https://omabrowser.org/oma/group/CHISKVK/", "database": "OMA", "categories": [ "Protein Classification" ] }, { "id": "A0A0R4IF73", "url": "https://www.orthodb.org/?gene=A0A0R4IF73", "database": "OrthoDB", "categories": [ "Protein Classification" ] }, { "id": "PTHR31493", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR31493", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PTHR31493:SF1", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR31493:SF1", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PF20721", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF20721", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "XP_001343826", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_001343826", "database": "RefSeq", "categories": [ "Protein" ] }, { "id": "A0A0R4IF73", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A0R4IF73-1", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "ZDB-GENE-141216-158", "url": "https://zfin.org/ZDB-GENE-141216-158", "database": "ZFIN", "categories": [ "Protein", "Organism-specific" ] } ], "sequence": { "sequence": "MNRQIDDVMGLCCRVSESRQIKAALQNSSKGAAAAGGGAFVGGLLGGPPGIFIGGALGGAFGWWMTSGKFHPLHQIIMEMPPQQKNKLYSEVMAVLGNLDWVDMAQLILLVMGNSSLQMRVLTTLISFATKELGAKIEYGQN", "length": 142, "header": "tr|A0A0R4IF73-1|A0A0R4IF73_DANRE Isoform 1 of Si:ch211-260e23.7 OS=Danio rerio OX=7955 GN=si:ch211-260e23.7 PE=3 SV=1 CANONICAL=A0A0R4IF73-1" }, "isoforms": [ { "isoform_ac": "A0A0R4IF73-1", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73/entry#A0A0R4IF73-1", "sequence": { "sequence": "MNRQIDDVMGLCCRVSESRQIKAALQNSSKGAAAAGGGAFVGGLLGGPPGIFIGGALGGAFGWWMTSGKFHPLHQIIMEMPPQQKNKLYSEVMAVLGNLDWVDMAQLILLVMGNSSLQMRVLTTLISFATKELGAKIEYGQN", "length": 142, "header": "tr|A0A0R4IF73-1|A0A0R4IF73_DANRE Isoform 1 of Si:ch211-260e23.7 OS=Danio rerio OX=7955 GN=si:ch211-260e23.7 PE=3 SV=1 CANONICAL=A0A0R4IF73-1" }, "locus": {} } ], "glycosylation": [], "phosphorylation": [], "glycation": [], "keywords": [], "publication": [ { "title": "The zebrafish reference genome sequence and its relationship to the human genome.", "journal": "Nature", "date": "2013", "authors": "Howe Kerstin, Clark Matthew D, Torroja Carlos F, Torrance James, Berthelot Camille, Muffato Matthieu, Collins John E, Humphray Sean, McLaren Karen, Matthews Lucy, McLaren Stuart, Sealy Ian, Caccamo Mario, Churcher Carol, Scott Carol, Barrett Jeffrey C, Koch Romke, Rauch Gerd-J\u00f6rg, White Simon, Chow William, Kilian Britt, Quintais Leonor T, Guerra-Assun\u00e7\u00e3o Jos\u00e9 A, Zhou Yi, Gu Yong, Yen Jennifer, Vogel Jan-Hinnerk, Eyre Tina, Redmond Seth, Banerjee Ruby, Chi Jianxiang, Fu Beiyuan, Langley Elizabeth, Maguire Sean F, Laird Gavin K, Lloyd David, Kenyon Emma, Donaldson Sarah, Sehra Harminder, Almeida-King Jeff, Loveland Jane, Trevanion Stephen, Jones Matt, Quail Mike, Willey Dave, Hunt Adrienne, Burton John, Sims Sarah, McLay Kirsten, Plumb Bob, Davis Joy, Clee Chris, Oliver Karen, Clark Richard, Riddle Clare, Elliot David, Eliott David, Threadgold Glen, Harden Glenn, Ware Darren, Begum Sharmin, Mortimore Beverley, Mortimer Beverly, Kerry Giselle, Heath Paul, Phillimore Benjamin, Tracey Alan, Corby Nicole, Dunn Matthew, Johnson Christopher, Wood Jonathan, Clark Susan, Pelan Sarah, Griffiths Guy, Smith Michelle, Glithero Rebecca, Howden Philip, Barker Nicholas, Lloyd Christine, Stevens Christopher, Harley Joanna, Holt Karen, Panagiotidis Georgios, Lovell Jamieson, Beasley Helen, Henderson Carl, Gordon Daria, Auger Katherine, Wright Deborah, Collins Joanna, Raisen Claire, Dyer Lauren, Leung Kenric, Robertson Lauren, Ambridge Kirsty, Leongamornlert Daniel, McGuire Sarah, Gilderthorp Ruth, Griffiths Coline, Manthravadi Deepa, Nichol Sarah, Barker Gary, Whitehead Siobhan, Kay Michael, Brown Jacqueline, Murnane Clare, Gray Emma, Humphries Matthew, Sycamore Neil, Barker Darren, Saunders David, Wallis Justene, Babbage Anne, Hammond Sian, Mashreghi-Mohammadi Maryam, Barr Lucy, Martin Sancha, Wray Paul, Ellington Andrew, Matthews Nicholas, Ellwood Matthew, Woodmansey Rebecca, Clark Graham, Cooper James D, Cooper James, Tromans Anthony, Grafham Darren, Skuce Carl, Pandian Richard, Andrews Robert, Harrison Elliot, Kimberley Andrew, Garnett Jane, Fosker Nigel, Hall Rebekah, Garner Patrick, Kelly Daniel, Bird Christine, Palmer Sophie, Gehring Ines, Berger Andrea, Dooley Christopher M, Ersan-\u00dcr\u00fcn Z\u00fcbeyde, Eser Cigdem, Geiger Horst, Geisler Maria, Karotki Lena, Kirn Anette, Konantz Judith, Konantz Martina, Oberl\u00e4nder Martina, Rudolph-Geiger Silke, Teucke Mathias, Lanz Christa, Raddatz G\u00fcnter, Osoegawa Kazutoyo, Zhu Baoli, Rapp Amanda, Widaa Sara, Langford Cordelia, Yang Fengtang, Schuster Stephan C, Carter Nigel P, Harrow Jennifer, Ning Zemin, Herrero Javier, Searle Steve M J, Enright Anton, Geisler Robert, Plasterk Ronald H A, Lee Charles, Westerfield Monte, de Jong Pieter J, Zon Leonard I, Postlethwait John H, N\u00fcsslein-Volhard Christiane, Hubbard Tim J P, Roest Crollius Hugues, Rogers Jane, Stemple Derek L", "evidence": [ { "database": "UniProtKB", "id": "A0A0R4IF73", "url": "https://www.uniprot.org/uniprotkb/A0A0R4IF73" } ], "reference": [ { "type": "PubMed", "id": "23594743", "url": "https://glygen.org/publication/PubMed/23594743" } ] } ], "pathway": [ { "id": "dre:100004554", "name": "", "url": "https://www.genome.jp/dbget-bin/www_bget?dre:100004554", "resource": "KEGG Pathway" } ], "orthologs": [ { "uniprot_canonical_ac": "A0A8M1RM27-1", "protein_name": "Protein C19orf12 homolog", "gene_name": "si:ch211-260e23.8", "tax_id": 7955, "organism": "Danio rerio", "sequence": { "sequence": "MTMSSRVDDVMQLCCEVSASRKIKAAVKSSGKGAAAAGGGAFVGGMVGGPAGIAVGGTLGGLLGTWITSGQFKPFPEIIEELPPKYKEVLYSDIMAALSSLNWTDVASLIALVMGSVTLQEQVLAAIHTFATKELNAELQYGK", "length": 143 }, "evidence": [ { "id": "FB:FBgn0023530", "url": "https://alliancegenome.org/gene/FB:FBgn0023530#orthology", "database": "AGR" }, { "id": "RGD:1585208", "url": "https://alliancegenome.org/gene/RGD:1585208#orthology", "database": "AGR" }, { "id": "MGI:1919494", "url": "https://alliancegenome.org/gene/MGI:1919494#orthology", "database": "AGR" }, { "id": "HGNC:25443", "url": "https://alliancegenome.org/gene/HGNC:25443#orthology", "database": "AGR" } ], "glygen_name": "Zebrafish", "common_name": "Zebrafish" }, { "uniprot_canonical_ac": "D3ZWS2-1", "protein_name": "Similar to human chromosome 19 open reading frame 12", "gene_name": "C1h19orf12", "tax_id": 10116, "organism": "Rattus norvegicus", "sequence": { "sequence": "MSAEMPIMVDDIMKLLCSICQEKKMKAAVKHSGRGAVVVGAMAFVGGLVGGPPGLAVGGTVGGLLGAWMTSGQFKPVPQILMELPPAEQQKLVNEATAIIRNLDWTDAVQLTALVMSNQAMQQKLLAMLTTYVTKELQAEIRYDD", "length": 145 }, "evidence": [ { "id": "FB:FBgn0023530", "url": "https://alliancegenome.org/gene/FB:FBgn0023530#orthology", "database": "AGR" }, { "id": "ZFIN:ZDB-GENE-141216-158", "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-141216-158#orthology", "database": "AGR" }, { "id": "RGD:1585208", "url": "https://alliancegenome.org/gene/RGD:1585208#orthology", "database": "AGR" }, { "id": "MGI:1919494", "url": "https://alliancegenome.org/gene/MGI:1919494#orthology", "database": "AGR" }, { "id": "HGNC:25443", "url": "https://alliancegenome.org/gene/HGNC:25443#orthology", "database": "AGR" } ], "glygen_name": "Rat", "common_name": "Rat" }, { "uniprot_canonical_ac": "Q1L990-1", "protein_name": "Protein C19orf12 homolog", "gene_name": "", "tax_id": 7955, "organism": "Danio rerio", "sequence": { "sequence": "MPPHVDDVMKLCCELSANQQVKTAVKQSGKGAAAAGGLAFAGGLIGGPLGIAVGGAVGGLLGCWMKSGQFKPLPQVIMELTPDQQARLYEDIVAILGSITWTDVAQLTALVMGNASLQQQVTAALLSYIHKELQAEVHYID", "length": 141 }, "evidence": [ { "id": "FB:FBgn0023530", "url": "https://alliancegenome.org/gene/FB:FBgn0023530#orthology", "database": "AGR" }, { "id": "RGD:1585208", "url": "https://alliancegenome.org/gene/RGD:1585208#orthology", "database": "AGR" }, { "id": "MGI:1919494", "url": "https://alliancegenome.org/gene/MGI:1919494#orthology", "database": "AGR" }, { "id": "HGNC:25443", "url": "https://alliancegenome.org/gene/HGNC:25443#orthology", "database": "AGR" } ], "glygen_name": "Zebrafish", "common_name": "Zebrafish" }, { "uniprot_canonical_ac": "Q66ID9-1", "protein_name": "Zgc:101715", "gene_name": "c19orf12b2", "tax_id": 7955, "organism": "Danio rerio", "sequence": { "sequence": "MANRKDDIIKFCCEISADKKIQAAFKGSAKGAAVAGGGAFVGGLIGGPAGIALGAAVGGALGAWMTSGQFRPLPEILMELTPSQQDKLYSDVMAIVGSLKWTDVPQLMAQVHGNSSLQEQVLGAILSYTKNQLKAEVKFED", "length": 141 }, "evidence": [ { "id": "FB:FBgn0023530", "url": "https://alliancegenome.org/gene/FB:FBgn0023530#orthology", "database": "AGR" }, { "id": "RGD:1585208", "url": "https://alliancegenome.org/gene/RGD:1585208#orthology", "database": "AGR" }, { "id": "MGI:1919494", "url": "https://alliancegenome.org/gene/MGI:1919494#orthology", "database": "AGR" }, { "id": "HGNC:25443", "url": "https://alliancegenome.org/gene/HGNC:25443#orthology", "database": "AGR" } ], "glygen_name": "Zebrafish", "common_name": "Zebrafish" }, { "uniprot_canonical_ac": "Q8WUR0-1", "protein_name": "Protein C19orf12 homolog", "gene_name": "", "tax_id": 10090, "organism": "Mus musculus", "sequence": { "sequence": "MPIMVDDIMRLLCSISQERKMKAAVKHSGKGAMVAGAMAFVGGLVGGPPGIAVGGTVGGLLGAWMTSGQFKPVPQILMELPPAEQRKLVNEAMAIIGNLDWTDAVQLTALVMSNQAMQQRLLAMLTTYVTKELQAEIRYED", "length": 141 }, "evidence": [ { "id": "FB:FBgn0023530", "url": "https://alliancegenome.org/gene/FB:FBgn0023530#orthology", "database": "AGR" }, { "id": "ZFIN:ZDB-GENE-141216-158", "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-141216-158#orthology", "database": "AGR" }, { "id": "RGD:1585208", "url": "https://alliancegenome.org/gene/RGD:1585208#orthology", "database": "AGR" }, { "id": "MGI:1919494", "url": "https://alliancegenome.org/gene/MGI:1919494#orthology", "database": "AGR" }, { "id": "HGNC:25443", "url": "https://alliancegenome.org/gene/HGNC:25443#orthology", "database": "AGR" } ], "glygen_name": "Mouse", "common_name": "Mouse" }, { "uniprot_canonical_ac": "Q9NSK7-4", "protein_name": "Protein C19orf12", "gene_name": "C19orf12", "tax_id": 9606, "organism": "Homo sapiens", "sequence": { "sequence": "MTIMVEDIMKLLCSLSGERKMKAAVKHSGKGALVTGAMAFVGGLVGGPPGLAVGGAVGGLLGAWMTSGQFKPVPQILMELPPAEQQRLFNEAAAIIRHLEWTDAVQLTALVMGSEALQQQLLAMLVNYVTKELRAEIQYDD", "length": 141 }, "evidence": [ { "id": "FB:FBgn0023530", "url": "https://alliancegenome.org/gene/FB:FBgn0023530#orthology", "database": "AGR" }, { "id": "ZFIN:ZDB-GENE-141216-158", 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