GO Term | Evidence Code | PMID |
---|---|---|
nervous system development | ||
purine nucleobase metabolic process | ||
ribonucleoside monophosphate biosynthetic process | ||
hypoxanthine biosynthetic process | ||
5-phosphoribose 1-diphosphate biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
ribose phosphate diphosphokinase complex | ||
cytosol |
|
|
cytoplasm |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:26 | pancreas disease | |
DOID:10003 | sensorineural hearing loss | |
DOID:10554 | meningoencephalitis | |
DOID:10584 | retinitis pigmentosa | |
DOID:1059 | intellectual disability | |
DOID:10595 | Charcot-Marie-Tooth disease | |
DOID:1074 | kidney failure | |
DOID:1142 | alternating exotropia | |
DOID:1143 | exotropia | |
DOID:11771 | spontaneous ocular nystagmus |
HPO ID | HPO Term |
---|---|
HP:0000028 | Cryptorchidism |
HP:0000047 | Hypospadias |
HP:0000083 | Renal insufficiency |
HP:0000154 | Wide mouth |
HP:0000218 | High palate |
HP:0000268 | Dolichocephaly |
HP:0000286 | Epicanthus |
HP:0000316 | Hypertelorism |
HP:0000325 | Triangular face |
HP:0000365 | Hearing impairment |
Disease ID | Disease Name |
---|---|
ORPHA:423479 |
|
OMIM:311070 |
|
ORPHA:411543 |
|
OMIM:301835 |
|
OMIM:304500 |
|
ORPHA:1187 |
|
ORPHA:411536 |
|
OMIM:300661 |
|
ORPHA:99014 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
781227 | BOVIN36697 | ||
102173923 | CAPHI32016 | ||
101115347 | SHEEP20244 | ||
105991379 | DIPOR14153 | ||
105992816 | DIPOR14153 | ||
19139 | MGI:97775 | MOUSE65845 | |
328099 | MOUSE07952 | ||
29562 | RGD:61955 | RATNO35265 | |
314140 | RGD:1359636 | RATNO35265 | |
100725562 | CAVPO16703 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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