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:3355 | fibrosarcoma | |
DOID:0040085 | bacterial sepsis | |
DOID:0050427 | xeroderma pigmentosum | |
DOID:0050461 | aspartylglucosaminuria | |
DOID:0050589 | inflammatory bowel disease | |
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0050681 | Borjeson-Forssman-Lehmann syndrome | |
DOID:0050776 | non-syndromic X-linked intellectual disability | |
DOID:0050841 | focal hand dystonia | |
DOID:0060022 | CD40 ligand deficiency |
HPO ID | HPO Term |
---|---|
HP:0001347 | Hyperreflexia |
HP:0001419 | X-linked recessive inheritance |
HP:0001854 | Podagra |
HP:0001889 | Megaloblastic anemia |
HP:0001903 | Anemia |
HP:0001919 | Acute kidney injury |
HP:0001997 | Gout |
HP:0002013 | Vomiting |
HP:0002015 | Dysphagia |
HP:0002071 | Abnormality of extrapyramidal motor function |
Disease ID | Disease Name |
---|---|
ORPHA:510 |
|
ORPHA:79233 |
|
OMIM:300322 |
|
OMIM:300323 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
281229 | BOVIN36339 | ||
510369 | BOVIN27145 | ||
102183404 | CAPHI31190 | ||
101109657 | SHEEP00217 | ||
100126071 | RABIT13907 | ||
100769768 | CRIGR10776 | ||
15452 | MGI:96217 | MOUSE65554 | |
24465 | RGD:2826 | RATNO45109 | |
100727355 | CAVPO23095 | ||
101574393 | OCTDE11027 |
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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