UniProt | Protein Name |
---|---|
A0A140VJL3 |
|
P00492 |
|
GO Term | Evidence Code | PMID |
---|---|---|
central nervous system neuron development | ||
lymphocyte proliferation | ||
dendrite morphogenesis | ||
purine nucleotide biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
hypoxanthine phosphoribosyltransferase activity | ||
magnesium ion binding | ||
protein binding | ||
guanine phosphoribosyltransferase activity | ||
nucleotide binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110758 | type 1 diabetes mellitus 21 | |
DOID:0110759 | type 1 diabetes mellitus 22 | |
DOID:0110760 | type 1 diabetes mellitus 23 | |
DOID:0110761 | type 1 diabetes mellitus 24 | |
DOID:0110843 | xeroderma pigmentosum group A | |
DOID:0110844 | xeroderma pigmentosum group C | |
DOID:0110845 | xeroderma pigmentosum group D | |
DOID:0110846 | xeroderma pigmentosum group E | |
DOID:0110847 | xeroderma pigmentosum variant type | |
DOID:0110848 | xeroderma pigmentosum group F |
HPO ID | HPO Term |
---|---|
HP:0000029 | Testicular atrophy |
HP:0000083 | Renal insufficiency |
HP:0000112 | Nephropathy |
HP:0000121 | Nephrocalcinosis |
HP:0000707 | Abnormality of the nervous system |
HP:0000708 | Atypical behavior |
HP:0000742 | Self-mutilation |
HP:0000787 | Nephrolithiasis |
HP:0000790 | Hematuria |
HP:0000791 | Uric acid nephrolithiasis |
Disease ID | Disease Name |
---|---|
ORPHA:510 |
|
ORPHA:79233 |
|
OMIM:300322 |
|
OMIM:300323 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
108700178 | Xenbase:XB-GENE-17330668 | ||
394936 | Xenbase:XB-GENE-1014679 | ||
109310997 | CROPO18605 | ||
113446755 | PSETE20102 | ||
100548399 | MELGA12936 | ||
103824492 | SERCA22104 | ||
791108 | ORNAN23438 | ||
100406827 | CALJA47571 | ||
105586233 | CERAT20119 | ||
709186 | MACMU47279 |
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Last updated: August 19, 2024