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:0060058 | lymphoma | |
DOID:0060180 | colitis | |
DOID:0060189 | ileitis | |
DOID:0060190 | ileocolitis | |
DOID:0060248 | Simpson-Golabi-Behmel syndrome type 1 | |
DOID:0060284 | paroxysmal nocturnal hemoglobinuria | |
DOID:0060318 | acute promyelocytic leukemia | |
DOID:0060474 | familial erythrocytosis 2 | |
DOID:0060705 | X-linked lymphoproliferative syndrome 1 | |
DOID:0060706 | X-linked lymphoproliferative syndrome 2 |
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 |
---|---|---|---|
100555105 | ANOCA11715 | ||
103670322 | URSMA16091 | ||
103672979 | URSMA26214 | ||
102544742 | VICPA01860 | ||
100950751 | OTOGA05955 | ||
105732276 | AOTNA36506 | ||
101053337 | SAIBB18644 | ||
101955334 | ICTTR01046 | ||
118319434 | SCOMX06085 | ||
102441052 | MYOLU00690 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024