{ "bcoid": "GLY_000134", "title": "Mouse Protein Function (NCBI Refseq)", "description": "The Mouse Protein Function (NCBI RefSeq) dataset contains biological function annotation of mouse [taxid:10090] ...", "filename": "mouse_protein_function_refseq.csv", "filetype": "csv", "categories": { "species": [ "Mus musculus" ], "molecule": [ "Protein" ], "tag": [ "Protein Function" ], "file_type": [ "csv" ], "status": [ "Reviewed" ], "scope": [ "internal" ] }, "minitable": { "content": [ [ "Q99020-1...", "NP_001041526..." ], [ "Q99020-1...", "NP_001041526..." ] ], "headers": [ "uniprotkb_ca...", "refseq_ac..." ], "colwidth": [ "40%", "20%" ] }, "sampledata": { "type": "table", "data": [ [ { "type": "string", "label": "uniprotkb_canonical_ac" }, { "type": "string", "label": "refseq_ac" }, { "type": "string", "label": "xref_key" }, { "type": "string", "label": "xref_id" }, { "type": "string", "label": "annotation" } ], [ "Q99020-1", "NP_001041526", "protein_xref_refseq", "NP_001041526", "This gene encodes a protein with consensus RNA binding domains present in a number of other RNA binding proteins and a glycine-rich C-terminus. This gene overlaps in a tail-to-tail orientation the gene encoding alanine-glyoxylate aminotransferase 2-like 2. Some of the exons of this gene are interspersed with exons of alanine-glyoxylate aminotransferase 2-like 2. Two alternatively spliced transcript variants that encode distinct proteins have been described for this gene. [provided by RefSeq, Jul 2008]." ], [ "Q99020-1", "NP_001041526", "protein_xref_refseq", "NP_001041526", "Axonal mRNA binding of hnRNP A/B is crucial for axon targeting and maturation of olfactory sensory neurons." ], [ "Q99020-1", "NP_001041526", "protein_xref_pubmed", "37083330", "Axonal mRNA binding of hnRNP A/B is crucial for axon targeting and maturation of olfactory sensory neurons." ], [ "Q99020-1", "NP_001041526", "protein_xref_refseq", "NP_001041526", "Scrutinized the motility of Hnrnpab(-/-) cells and confirmed that the decreases in both cell motility and Eps8 are restored by ectopically coexpressing both alternatively spliced Hnrnpab isoforms, therefore these variants are surprisingly nonredundant for cell motility." ], [ "Q99020-1", "NP_001041526", "protein_xref_pubmed", "30314980", "Scrutinized the motility of Hnrnpab(-/-) cells and confirmed that the decreases in both cell motility and Eps8 are restored by ectopically coexpressing both alternatively spliced Hnrnpab isoforms, therefore these variants are surprisingly nonredundant for cell motility." ], [ "Q99020-1", "NP_001041526", "protein_xref_refseq", "NP_001041526", "Structure and binding of CBF-A (AUF2)" ], [ "Q99020-1", "NP_001041526", "protein_xref_pubmed", "12086581", "Structure and binding of CBF-A (AUF2)" ], [ "Q9JJI8-1", "NP_001041522", "protein_xref_refseq", "NP_001041522", "RPL38 knockdown inhibits the inflammation and apoptosis in chondrocytes through regulating METTL3-mediated SOCS2 m6A modification in osteoarthritis." ], [ "Q9JJI8-1", "NP_001041522", "protein_xref_pubmed", "35596790", "RPL38 knockdown inhibits the inflammation and apoptosis in chondrocytes through regulating METTL3-mediated SOCS2 m6A modification in osteoarthritis." ], [ "Q9JJI8-1", "NP_001041522", "protein_xref_refseq", "NP_001041522", "Ectopic mineralization in the middle ear and chronic otitis media with effusion caused by RPL38 deficiency in the Tail-short (Ts) mouse." ], [ "Q9JJI8-1", "NP_001041522", "protein_xref_pubmed", "21062742", "Ectopic mineralization in the middle ear and chronic otitis media with effusion caused by RPL38 deficiency in the Tail-short (Ts) mouse." ], [ "O35453-1", "NP_001263198", "protein_xref_refseq", "NP_001263198", "This gene encodes a type II transmembrane serine protease that may function in diverse processes, including regulation of cell growth. Deficiency in this gene results in hearing loss. The protein is cleaved into a catalytic serine protease chain and a non-catalytic scavenger receptor cysteine-rich chain, which associate via a single disulfide bond. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2013]." ], [ "O35453-1", "NP_001263198", "protein_xref_refseq", "NP_001263198", "Hepsin enhances liver metabolism and inhibits adipocyte browning in mice." ], [ "O35453-1", "NP_001263198", "protein_xref_pubmed", "32404422", "Hepsin enhances liver metabolism and inhibits adipocyte browning in mice." ], [ "O35453-1", "NP_001263198", "protein_xref_refseq", "NP_001263198", "Hepsin-mediated Processing of Uromodulin is Crucial for Salt-sensitivity and Thick Ascending Limb Homeostasis. Publication Status: Online-Only" ], [ "O35453-1", "NP_001263198", "protein_xref_pubmed", "31444371", "Hepsin-mediated Processing of Uromodulin is Crucial for Salt-sensitivity and Thick Ascending Limb Homeostasis. Publication Status: Online-Only" ], [ "O35453-1", "NP_001263198", "protein_xref_refseq", "NP_001263198", "Crystal structure of human hepsin, confirming cleavage and association of the two chains" ], [ "O35453-1", "NP_001263198", "protein_xref_pubmed", "12962630", "Crystal structure of human hepsin, confirming cleavage and association of the two chains" ], [ "Q9DBU5-1", "NP_001243014", "protein_xref_refseq", "NP_001243014", "Rnf6 controls cellular LIMK1 concentrations and indicate a new function for the ubiquitin/proteasome system in regulating local growth cone actin dynamics Erratum:[Genes Dev. 2005 Nov 1;19(21):2643]" ], [ "Q9DBU5-1", "NP_001243014", "protein_xref_pubmed", "16204183", "Rnf6 controls cellular LIMK1 concentrations and indicate a new function for the ubiquitin/proteasome system in regulating local growth cone actin dynamics Erratum:[Genes Dev. 2005 Nov 1;19(21):2643]" ], [ "Q3UY90-1", "NP_001186856", "protein_xref_refseq", "NP_001186856", "In mouse embryo fibroblasts (MEFs) obtained from cavin-1-/- or caveolin-1-/- mice, Fam198a precursor was retained in ER and no mature Fam198a could be formed in these cells." ], [ "Q3UY90-1", "NP_001186856", "protein_xref_pubmed", "30188967", "In mouse embryo fibroblasts (MEFs) obtained from cavin-1-/- or caveolin-1-/- mice, Fam198a precursor was retained in ER and no mature Fam198a could be formed in these cells." ], [ "P33434-1", "NP_032636", "protein_xref_refseq", "NP_032636", "This gene encodes a member of the matrix metalloproteinase family of extracellular matrix-degrading enzymes that are involved in tissue remodeling, wound repair, progression of atherosclerosis and tumor invasion. The encoded preproprotein undergoes proteolytic processing to generate a mature, zinc-dependent endopeptidase enzyme that hydrolyzes collagens, gelatins, laminin, fibronectin and elastin. Mice lacking the encoded protein exhibit suppressed angiogenesis and attenuated features of human multicentric osteolysis with arthritis including abnormal skeletal and craniofacial development. [provided by RefSeq, Feb 2016]." ], [ "P33434-1", "NP_032636", "protein_xref_refseq", "NP_032636", "Formin-related protein 1 facilitates proliferation and aggressive phenotype of clear cell renal cell carcinoma through MAPK/MMP2 pathway." ], [ "P33434-1", "NP_032636", "protein_xref_pubmed", "37454877", "Formin-related protein 1 facilitates proliferation and aggressive phenotype of clear cell renal cell carcinoma through MAPK/MMP2 pathway." ], [ "P33434-1", "NP_032636", "protein_xref_refseq", "NP_032636", "Matrix metalloproteinase-2 proteolyzes mitofusin-2 and impairs mitochondrial function during myocardial ischemia-reperfusion injury. Publication Status: Online-Only" ], [ "P33434-1", "NP_032636", "protein_xref_pubmed", "37495895", "Matrix metalloproteinase-2 proteolyzes mitofusin-2 and impairs mitochondrial function during myocardial ischemia-reperfusion injury. Publication Status: Online-Only" ], [ "P33434-1", "NP_032636", "protein_xref_refseq", "NP_032636", "HNF4G stimulates the development of pancreatic cancer by promoting IGF2BP2 transcription." ], [ "P33434-1", "NP_032636", "protein_xref_pubmed", "36607591", "HNF4G stimulates the development of pancreatic cancer by promoting IGF2BP2 transcription." ], [ "P33434-1", "NP_032636", "protein_xref_refseq", "NP_032636", "Amelioration of Pulmonary Fibrosis by Matrix Metalloproteinase-2 Overexpression. Publication Status: Online-Only" ], [ "P33434-1", "NP_032636", "protein_xref_pubmed", "37047672", "Amelioration of Pulmonary Fibrosis by Matrix Metalloproteinase-2 Overexpression. Publication Status: Online-Only" ], [ "O70138-1", "NP_032637", "protein_xref_refseq", "NP_032637", "This gene encodes a member of the matrix metalloproteinase family of extracellular matrix-degrading enzymes that are involved in tissue remodeling, wound repair, progression of atherosclerosis and tumor invasion. The encoded preproprotein undergoes proteolytic processing to generate a mature, zinc-dependent endopeptidase enzyme that degrades types I, II and III collagens. Mice lacking the encoded protein exhibit abnormalities in the inflammatory responses to various agents. This gene is located in a cluster of other matrix metalloproteinase genes on chromosome 9. [provided by RefSeq, Feb 2016]." ], [ "O70138-1", "NP_032637", "protein_xref_refseq", "NP_032637", "Lab-Attenuated Rabies Virus Facilitates Opening of the Blood-Brain Barrier by Inducing Matrix Metallopeptidase 8." ], [ "O70138-1", "NP_032637", "protein_xref_pubmed", "36005758", "Lab-Attenuated Rabies Virus Facilitates Opening of the Blood-Brain Barrier by Inducing Matrix Metallopeptidase 8." ], [ "O70138-1", "NP_032637", "protein_xref_refseq", "NP_032637", "A Novel Protective Role for Matrix Metalloproteinase-8 in the Pulmonary Vasculature." ], [ "O70138-1", "NP_032637", "protein_xref_pubmed", "34550870", "A Novel Protective Role for Matrix Metalloproteinase-8 in the Pulmonary Vasculature." ], [ "P53690-1", "NP_032634", "protein_xref_refseq", "NP_032634", "This gene encodes a member of the matrix metalloproteinase family of extracellular matrix-degrading enzymes that are involved in tissue remodeling, wound repair, progression of atherosclerosis and tumor invasion. The encoded preproprotein undergoes proteolytic processing to generate a mature, zinc-dependent endopeptidase enzyme. Mice lacking the encoded protein exhibit craniofacial dysmorphism, arthritis, osteopenia, dwarfism, and fibrosis of soft tissues. [provided by RefSeq, Feb 2016]." ], [ "P53690-1", "NP_032634", "protein_xref_refseq", "NP_032634", "Global, but not chondrocyte-specific, MT1-MMP deficiency in adult mice causes inflammatory arthritis." ], [ "P53690-1", "NP_032634", "protein_xref_pubmed", "37598898", "Global, but not chondrocyte-specific, MT1-MMP deficiency in adult mice causes inflammatory arthritis." ], [ "P53690-1", "NP_032634", "protein_xref_refseq", "NP_032634", "MMP14 cleaves PTH1R in the chondrocyte-derived osteoblast lineage, curbing signaling intensity for proper bone anabolism. Publication Status: Online-Only" ], [ "P53690-1", "NP_032634", "protein_xref_pubmed", "36892459", "MMP14 cleaves PTH1R in the chondrocyte-derived osteoblast lineage, curbing signaling intensity for proper bone anabolism. Publication Status: Online-Only" ], [ "O54732-1", "NP_032635", "protein_xref_refseq", "NP_032635", "This gene encodes a member of the matrix metalloproteinase family of extracellular matrix-degrading enzymes that are involved in tissue remodeling, wound repair, progression of atherosclerosis and tumor invasion. The encoded preproprotein undergoes proteolytic processing to generate a mature, zinc-dependent endopeptidase enzyme. A deficiency of the encoded protein in mice is compatible with normal development and postnatal growth. [provided by RefSeq, Feb 2016]." ], [ "P33435-1", "NP_032633", "protein_xref_refseq", "NP_032633", "This gene encodes a member of the matrix metalloproteinase family that plays a role in wound healing, skeletal development and bone remodeling. The encoded protein is activated by the removal of an N-terminal activation peptide to generate a zinc-dependent endopeptidase enzyme that can cleave various native collagens, including types I - IV, X and XIV. Mice lacking the encoded protein display profound defects in growth plate cartilage as well as a delay in the endochondral bone development. Lack of the encoded protein also impairs the wound healing process due to reduced keratinocyte migration and vascular density at the wound site. This gene is located in a cluster of other matrix metalloproteinase genes on chromosome 9. [provided by RefSeq, Jun 2015]." ], [ "P33435-1", "NP_032633", "protein_xref_refseq", "NP_032633", "Matrix Metalloproteinase-1 Expression in Fibroblasts Accelerates Dermal Aging and Promotes Papilloma Development in Mouse Skin." ], [ "P33435-1", "NP_032633", "protein_xref_pubmed", "36914001", "Matrix Metalloproteinase-1 Expression in Fibroblasts Accelerates Dermal Aging and Promotes Papilloma Development in Mouse Skin." ], [ "P33435-1", "NP_032633", "protein_xref_refseq", "NP_032633", "The Expression of MMP1 and MMP7 in Mice Liver after Exposure to Aflatoxin B1 Using Immunohistochemistry Technique. Publication Status: Online-Only" ], [ "P33435-1", "NP_032633", "protein_xref_pubmed", "37312734", "The Expression of MMP1 and MMP7 in Mice Liver after Exposure to Aflatoxin B1 Using Immunohistochemistry Technique. Publication Status: Online-Only" ], [ "P51949-1", "NP_032638", "protein_xref_refseq", "NP_032638", "MAT1 serves as a promoter in the lung metastasis of osteosarcoma through increasing AKT1 expression." ], [ "P51949-1", "NP_032638", "protein_xref_pubmed", "31421084", "MAT1 serves as a promoter in the lung metastasis of osteosarcoma through increasing AKT1 expression." ], [ "P51949-1", "NP_032638", "protein_xref_refseq", "NP_032638", "Deletion of the TFIIH kinase subunit Mat1 in mouse fibroblasts leads to dramatically reduced RNA polymerase II Ser5 phosphorylation." ], [ "P51949-1", "NP_032638", "protein_xref_pubmed", "21385826", "Deletion of the TFIIH kinase subunit Mat1 in mouse fibroblasts leads to dramatically reduced RNA polymerase II Ser5 phosphorylation." ], [ "P51949-1", "NP_032638", "protein_xref_refseq", "NP_032638", "Investigated the function of the Cdk7.cyclin H.Mat1 complex in murine embryonic stem (ES) cells and preimplantation embryos to determine whether it regulates the unique cell cycle structure and transcriptional network of pluripotent cells" ], [ "P51949-1", "NP_032638", "protein_xref_pubmed", "20231280", "Investigated the function of the Cdk7.cyclin H.Mat1 complex in murine embryonic stem (ES) cells and preimplantation embryos to determine whether it regulates the unique cell cycle structure and transcriptional network of pluripotent cells" ], [ "P51949-1", "NP_032638", "protein_xref_refseq", "NP_032638", "This study demonstrates a requirement for MAT1 in the operation of PGC-1 coactivators that control cell metabolism." ], [ "P51949-1", "NP_032638", "protein_xref_pubmed", "17276355", "This study demonstrates a requirement for MAT1 in the operation of PGC-1 coactivators that control cell metabolism." ], [ "Q61884-1", "NP_032639", "protein_xref_refseq", "NP_032639", "BBOF1 is required for sperm motility and male fertility by stabilizing the flagellar axoneme in mice. Publication Status: Online-Only" ], [ "Q61884-1", "NP_032639", "protein_xref_pubmed", "37198331", "BBOF1 is required for sperm motility and male fertility by stabilizing the flagellar axoneme in mice. Publication Status: Online-Only" ], [ "Q61884-1", "NP_032639", "protein_xref_refseq", "NP_032639", "Prenatal alcohol exposure Mns1(-/-) fetuses with severe eye defects also presented with craniofacial dysmorphologies characteristic of fetal alcohol syndrome and midline tissue loss in the brain, palate, and nasal septum" ], [ "Q61884-1", "NP_032639", "protein_xref_pubmed", "30129265", "Prenatal alcohol exposure Mns1(-/-) fetuses with severe eye defects also presented with craniofacial dysmorphologies characteristic of fetal alcohol syndrome and midline tissue loss in the brain, palate, and nasal septum" ], [ "Q61884-1", "NP_032639", "protein_xref_refseq", "NP_032639", "Compared to other embryonic tissues at this developmental stage, Mns1 expression is strongly enriched in the ventral node. Publication Status: Online-Only" ], [ "Q61884-1", "NP_032639", "protein_xref_pubmed", "30148830", "Compared to other embryonic tissues at this developmental stage, Mns1 expression is strongly enriched in the ventral node. Publication Status: Online-Only" ], [ "Q61884-1", "NP_032639", "protein_xref_refseq", "NP_032639", "These results demonstrate that MNS1 is essential for spermiogenesis, the assembly of sperm flagella, and motile ciliary functions. GeneRIF: MNS1 is an integral component of sperm flagella. Mice lacking MNS1 exhibit male sterility as evidenced by abnormal assembly of flagella. MNS1-deficient mice also display defects in left-right asymmetry patterning of internal organs and hydrocephalus." ], [ "Q61884-1", "NP_032639", "protein_xref_pubmed", "22396656", "These results demonstrate that MNS1 is essential for spermiogenesis, the assembly of sperm flagella, and motile ciliary functions. GeneRIF: MNS1 is an integral component of sperm flagella. Mice lacking MNS1 exhibit male sterility as evidenced by abnormal assembly of flagella. MNS1-deficient mice also display defects in left-right asymmetry patterning of internal organs and hydrocephalus." ], [ "Q920G9-1", "NP_035948", "protein_xref_refseq", "NP_035948", "MGCL-1 is a factor modulating MDM2-p53 axis by enhanced degradation of MDM2" ], [ "Q920G9-1", "NP_035948", "protein_xref_pubmed", "12927808", "MGCL-1 is a factor modulating MDM2-p53 axis by enhanced degradation of MDM2" ], [ "Q920G9-1", "NP_035948", "protein_xref_refseq", "NP_035948", "The mgcl-1 gene product appears to be essential for appropriate nuclear-lamina organization, which in turn is essential for normal sperm morphogenesis and chromatin remodeling." ], [ "Q920G9-1", "NP_035948", "protein_xref_pubmed", "12556490", "The mgcl-1 gene product appears to be essential for appropriate nuclear-lamina organization, which in turn is essential for normal sperm morphogenesis and chromatin remodeling." ], [ "Q920G9-1", "NP_035948", "protein_xref_refseq", "NP_035948", "Gmcl1 interacts with the DP component of the E2F transcription factor." ], [ "Q920G9-1", "NP_035948", "protein_xref_pubmed", "9878064", "Gmcl1 interacts with the DP component of the E2F transcription factor." ], [ "Q9WVR4-1", "NP_035944", "protein_xref_refseq", "NP_035944", "This protein shows high expression in brain and testis. The protein was tested in a behavioral test battery in knockout mice. The mice showed behavioral abnormalities." ], [ "Q9WVR4-1", "NP_035944", "protein_xref_pubmed", "11875043", "This protein shows high expression in brain and testis. The protein was tested in a behavioral test battery in knockout mice. The mice showed behavioral abnormalities." ], [ "Q9Z111-1", "NP_035947", "protein_xref_refseq", "NP_035947", "Gadd45g, A Novel Antidepressant Target, Mediates Metformin-Induced Neuronal Differentiation of Neural Stem Cells Via DNA Demethylation." ], [ "Q9Z111-1", "NP_035947", "protein_xref_pubmed", "35511865", "Gadd45g, A Novel Antidepressant Target, Mediates Metformin-Induced Neuronal Differentiation of Neural Stem Cells Via DNA Demethylation." ], [ "Q9WVH9-1", "NP_035942", "protein_xref_refseq", "NP_035942", "Compromised Cardiopulmonary Function in Fibulin-5 Deficient Mice." ], [ "Q9WVH9-1", "NP_035942", "protein_xref_pubmed", "35171214", "Compromised Cardiopulmonary Function in Fibulin-5 Deficient Mice." ], [ "Q9WVH9-1", "NP_035942", "protein_xref_refseq", "NP_035942", "Role of fibulin-5 insufficiency and prolapse progression on murine vaginal biomechanical function. Publication Status: Online-Only" ], [ "Q9WVH9-1", "NP_035942", "protein_xref_pubmed", "34697337", "Role of fibulin-5 insufficiency and prolapse progression on murine vaginal biomechanical function. Publication Status: Online-Only" ], [ "Q9WVH9-1", "NP_035942", "protein_xref_refseq", "NP_035942", "FBLN-5 is a novel TGF-beta-inducible target gene that regulates cell growth and motility in a context-specific manner and affects protein kinase activation by TGF-beta." ], [ "Q9WVH9-1", "NP_035942", "protein_xref_pubmed", "12021267", "FBLN-5 is a novel TGF-beta-inducible target gene that regulates cell growth and motility in a context-specific manner and affects protein kinase activation by TGF-beta." ], [ "Q9WVH9-1", "NP_035942", "protein_xref_refseq", "NP_035942", "Fibulin-5 is a calcium-dependent, elastin-binding protein that localizes to the surface of elastic fibres in vivo." ], [ "Q9WVH9-1", "NP_035942", "protein_xref_pubmed", "11805834", "Fibulin-5 is a calcium-dependent, elastin-binding protein that localizes to the surface of elastic fibres in vivo." ], [ "Q8BJW6-1", "NP_001005509", "protein_xref_refseq", "NP_001005509", "Bridging Energy Need and Feeding Behavior: The Impact of eIF2alpha Phosphorylation in AgRP Neurons." ], [ "Q8BJW6-1", "NP_001005509", "protein_xref_pubmed", "37478284", "Bridging Energy Need and Feeding Behavior: The Impact of eIF2alpha Phosphorylation in AgRP Neurons." ], [ "Q8BJW6-1", "NP_001005509", "protein_xref_refseq", "NP_001005509", "Oxidized phospholipids facilitate calcific aortic valve disease by elevating ATF4 through the PERK/eIF2alpha axis." ] ] }, "readme": "Name\n - Mouse Protein Function (NCBI Refseq)\n\nVersion\n - v-2.3.1\n\nCreated on\n - 2019-03-16T15:38:06.344586\n\nModified on\n - 2022-09-26T08:56:48.530675\n\nCreated by\n - Jeet Vora [jeetvora@gwu.edu], Robel Kahsay [rykahsay@gwu.edu], Karina Martinez [karinamartinez@gwu.edu], Jingyue Wu [jingyue.wu@email.gwu.edu]\n\nAuthors\n - Maria Martin [martin@ebi.ac.uk], Preethi Vasudev [pvasudev@ebi.ac.uk]\n\nChecksum\n - \n\nUsability Domain\n - The Mouse Protein Function (NCBI RefSeq) dataset contains biological function annotation of mouse [taxid:10090] genes from GeneRIF section in the NCBI RefSeq database. The dataset is derived from NCBI RefSeq Release 96, September 9, 2019. If you use this dataset please provide proper attribution to NCBI RefSeq and GlyGen. \n\nDescription Domain\n Keywords\n - protein function\n - NCBI RefSeq\n - geneRIF\n - PMID\n\n Pipeline Steps\n - Step-1: The script extract-from-gp.py extracts protein function information from NCBI RefSeq gpff format files and maps it to the UniProtKb canonical accessions for a final dataset output in a csv format. \n\nExecution Domain\n Scripts - https://github.com/glygener/glygen-backend-integration/blob/master/dataset-maker/extract-from-endpoint.py\n\n\n Software Prerequisites\n Name: Python\n Version: 2.7.5\n URI: https://www.python.org/download/releases/2.7.5/\n\nI/O Domain\n Input Subdomain\n Name: mouse_protein_xref_refseq.csv\n URI: https:/data.glygen.org/ln2releases/data/v-2.3.1/reviewed/mouse_protein_xref_refseq.csv\n Name: refseq_protein_all_10090.gpff\n URI: https:/data.glygen.org/ln2downloads/ncbi/refseq/2023_10_12/refseq_protein_all_10090.gpff\n Output Subdomain\n Name: mouse_protein_function_refseq.csv\n URI: https:/data.glygen.org/ln2releases/data/v-2.3.1/reviewed/mouse_protein_function_refseq.csv\n Name: mouse_protein_function_refseq.stat.csv\n URI: https:/data.glygen.org/ln2releases/data/v-2.3.1/reviewed/mouse_protein_function_refseq.stat.csv\n\nFields\n Name: \"uniprotkb_canonical_ac\"\n Description: \"\"\n Unique Values: \"13391\"\n Name: \"refseq_ac\"\n Description: \"Accession in the NCBI RefSeq database\"\n Unique Values: \"15372\"\n Name: \"xref_key\"\n Description: \"Source key associated to the xref_id\"\n Unique Values: \"2\"\n Name: \"xref_id\"\n Description: \"ID of the X-ref\"\n Unique Values: \"46724\"\n Name: \"annotation\"\n Description: \"Function annotation from UniProtKB|RefSeq database\"\n Unique Values: \"33096\"", "downloadurl": "/ln2data/releases/data/v-2.3.1/reviewed/mouse_protein_function_refseq.csv" }