{ "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", "tags": "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", "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", "Study identified mutations of the Ribosomal Protein L38 (Rpl38) gene in mice exhibiting surprising tissue-specific patterning defects, including pronounced homeotic transformations of the axial skeleton." ], [ "Q9JJI8-1", "NP_001041522", "protein_xref_pubmed", "21529712", "Study identified mutations of the Ribosomal Protein L38 (Rpl38) gene in mice exhibiting surprising tissue-specific patterning defects, including pronounced homeotic transformations of the axial skeleton." ], [ "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", "MMP2 Modulates Inflammatory Response during Axonal Regeneration in the Murine Visual System. Publication Status: Online-Only" ], [ "P33434-1", "NP_032636", "protein_xref_pubmed", "34359839", "MMP2 Modulates Inflammatory Response during Axonal Regeneration in the Murine Visual System. Publication Status: Online-Only" ], [ "P33434-1", "NP_032636", "protein_xref_refseq", "NP_032636", "MMP-2 is a novel histone H3 N-terminal protease necessary for myogenic gene activation. Publication Status: Online-Only" ], [ "P33434-1", "NP_032636", "protein_xref_pubmed", "34001241", "MMP-2 is a novel histone H3 N-terminal protease necessary for myogenic gene activation. 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", "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." ], [ "O70138-1", "NP_032637", "protein_xref_refseq", "NP_032637", "NPY promotes macrophage migration by upregulating matrix metalloproteinase-8 expression." ], [ "O70138-1", "NP_032637", "protein_xref_pubmed", "32710469", "NPY promotes macrophage migration by upregulating matrix metalloproteinase-8 expression." ], [ "O70138-1", "NP_032637", "protein_xref_refseq", "NP_032637", "Endogenous Collagenases Regulate Osteoclast Fusion. Publication Status: Online-Only" ], [ "O70138-1", "NP_032637", "protein_xref_pubmed", "32370054", "Endogenous Collagenases Regulate Osteoclast Fusion. Publication Status: Online-Only" ], [ "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", "Extracellular Matrix Remodeling by Fibroblast-MMP14 Regulates Melanoma Growth. Publication Status: Online-Only" ], [ "P53690-1", "NP_032634", "protein_xref_pubmed", "34830157", "Extracellular Matrix Remodeling by Fibroblast-MMP14 Regulates Melanoma Growth. Publication Status: Online-Only" ], [ "P53690-1", "NP_032634", "protein_xref_refseq", "NP_032634", "Collagen denaturation in the infarcted myocardium involves temporally distinct effects of MT1-MMP-dependent proteolysis and mechanical tension." ], [ "P53690-1", "NP_032634", "protein_xref_pubmed", "34048934", "Collagen denaturation in the infarcted myocardium involves temporally distinct effects of MT1-MMP-dependent proteolysis and mechanical tension." ], [ "P53690-1", "NP_032634", "protein_xref_refseq", "NP_032634", "Loss of MT1-MMP in Alveolar Epithelial Cells Exacerbates Pulmonary Fibrosis. Publication Status: Online-Only" ], [ "P53690-1", "NP_032634", "protein_xref_pubmed", "33805743", "Loss of MT1-MMP in Alveolar Epithelial Cells Exacerbates Pulmonary Fibrosis. Publication Status: Online-Only" ], [ "P53690-1", "NP_032634", "protein_xref_refseq", "NP_032634", "Macrophages promote endothelial-to-mesenchymal transition via MT1-MMP/TGFbeta1 after myocardial infarction. Publication Status: Online-Only" ], [ "P53690-1", "NP_032634", "protein_xref_pubmed", "33063665", "Macrophages promote endothelial-to-mesenchymal transition via MT1-MMP/TGFbeta1 after myocardial infarction. 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]." ], [ "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", "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", "We discovered that FXR1P-deficient aNSCs have altered expression of a select number of cell-cycle genes, and we identified the mRNA of cyclin-dependent kinase inhibitor 1A (Cdkn1a, p21) as a direct target of FXR1P." ], [ "Q9WVR4-1", "NP_035944", "protein_xref_pubmed", "28204491", "We discovered that FXR1P-deficient aNSCs have altered expression of a select number of cell-cycle genes, and we identified the mRNA of cyclin-dependent kinase inhibitor 1A (Cdkn1a, p21) as a direct target of FXR1P." ], [ "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", "MicroRNA-128-1-5p attenuates myocardial ischemia/reperfusion injury by suppressing Gadd45g-mediated apoptotic signaling." ], [ "Q9Z111-1", "NP_035947", "protein_xref_pubmed", "32828305", "MicroRNA-128-1-5p attenuates myocardial ischemia/reperfusion injury by suppressing Gadd45g-mediated apoptotic signaling." ], [ "Q9Z111-1", "NP_035947", "protein_xref_refseq", "NP_035947", "Mimicking Age-Associated Gadd45gamma Dysregulation Results in Memory Impairments in Young Adult Mice." ], [ "Q9Z111-1", "NP_035947", "protein_xref_pubmed", "31826946", "Mimicking Age-Associated Gadd45gamma Dysregulation Results in Memory Impairments in Young Adult Mice." ], [ "Q9Z111-1", "NP_035947", "protein_xref_refseq", "NP_035947", "During fear learning, Gadd45gamma serves to act as a coordinator of immediate early gene expression and subsequent memory consolidation by directing temporally specific changes in active DNA demethylation at the promoter of plasticity-related immediate early genes Erratum:[J Neurosci. 2019 May 15;39(20):3993. PMID: 31092609]" ], [ "Q9Z111-1", "NP_035947", "protein_xref_pubmed", "30545945", "During fear learning, Gadd45gamma serves to act as a coordinator of immediate early gene expression and subsequent memory consolidation by directing temporally specific changes in active DNA demethylation at the promoter of plasticity-related immediate early genes Erratum:[J Neurosci. 2019 May 15;39(20):3993. PMID: 31092609]" ], [ "Q9WVH9-1", "NP_035942", "protein_xref_refseq", "NP_035942", "Upregulation of PTK7 and beta-catenin after vaginal mechanical dilatation: an examination of fibulin-5 knockout mice." ], [ "Q9WVH9-1", "NP_035942", "protein_xref_pubmed", "33547906", "Upregulation of PTK7 and beta-catenin after vaginal mechanical dilatation: an examination of fibulin-5 knockout 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", "PAD2-mediated citrullination of Fibulin-5 promotes elastogenesis." ], [ "Q9WVH9-1", "NP_035942", "protein_xref_pubmed", "34274450", "PAD2-mediated citrullination of Fibulin-5 promotes elastogenesis." ], [ "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", "Double-stranded RNA-dependent protein kinase phosphorylation of the alpha-subunit of eukaryotic translation initiation factor 2 mediates apoptosis" ] ] }, "readme": "Name\n - Mouse Protein Function (NCBI Refseq)\n\nVersion\n - v-x.x.x\n\nCreated on\n - 2019-03-16T15:38:06.344586\n\nModified on\n - 2022-01-19T11:17:18.850708\n\nCreated by\n - Jeet Vora [jeetvora@gwu.edu], Rahi Navelkar [rsn13@gwu.edu], Robel Kahsay [rykahsay@gwu.edu], Xavier Holmes [xavierh@email.gwu.edu], Karina Martinez [karinamartinez@gwu.edu], Amanda Bell [amandab2140@gwu.edu], Jonathon Keeney [keeneyjg@gwu.edu], Millicent Quartey [mquartey@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-2.0.1/reviewed/mouse_protein_xref_refseq.csv\n Name: refseq_protein_all_10090.gpff\n URI: https:/data.glygen.org/ln2downloads/ncbi/refseq/2022_02/refseq_protein_all_10090.gpff\n Output Subdomain\n Name: mouse_protein_function_refseq.csv\n URI: https:/data.glygen.org/ln2releases/data/v-2.0.1/reviewed/mouse_protein_function_refseq.csv\n Name: mouse_protein_function_refseq.stat.csv\n URI: https:/data.glygen.org/ln2releases/data/v-2.0.1/reviewed/mouse_protein_function_refseq.stat.csv\n\nFields\n Name: \"uniprotkb_canonical_ac\"\n Description: \"\"\n Unique Values: \"13519\"\n Name: \"refseq_ac\"\n Description: \"Accession in the NCBI RefSeq database\"\n Unique Values: \"15556\"\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: \"47102\"\n Name: \"annotation\"\n Description: \"Function annotation from UniProtKB|RefSeq database\"\n Unique Values: \"33385\"", "downloadurl": "/ln2data/releases/data/v-2.0.1/reviewed/mouse_protein_function_refseq.csv" }