UniProt | Protein Name |
---|---|
Q86X52 |
|
GO Term | Evidence Code | PMID |
---|---|---|
sulfation | ||
chondroitin sulfate biosynthetic process | ||
chondrocyte development | ||
positive regulation of smoothened signaling pathway | ||
response to nutrient levels |
GO Term | Evidence Code | PMID |
---|---|---|
extracellular region | ||
membrane | ||
Golgi cisterna membrane | ||
Golgi membrane |
GO Term | Evidence Code | PMID |
---|---|---|
glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity | ||
N-acetylgalactosaminyl-proteoglycan 3-beta-glucuronosyltransferase activity | ||
metal ion binding |
Species | Protein | mRNA |
---|---|---|
Rattus norvegicus | XP_218759 | XM_218759 |
Drosophila melanogaster | NP_996440 | NM_206717 |
Caenorhabditis elegans | BAC76780 | AB088397 |
Mus musculus | XP_194358 | XM_194358 |
DO ID | Disease Name | Source |
---|---|---|
DOID:0110593 | autosomal dominant nonsyndromic deafness 9 | |
DOID:1115 | sarcoma | |
DOID:11193 | syndactyly | |
DOID:13714 | anodontia | |
DOID:1612 | breast cancer | |
DOID:162 | cancer | |
DOID:3068 | glioblastoma | |
DOID:3070 | high grade glioma | |
DOID:3074 | giant cell glioblastoma | |
DOID:3192 | neurilemmoma |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000160 | Narrow mouth |
HP:0000164 | Abnormality of the dentition |
HP:0000175 | Cleft palate |
HP:0000311 | Round face |
HP:0000316 | Hypertelorism |
HP:0000327 | Hypoplasia of the maxilla |
HP:0000347 | Micrognathia |
HP:0000369 | Low-set ears |
HP:0000517 | Abnormal lens morphology |
Disease ID | Disease Name |
---|---|
OMIM:605282 |
|
ORPHA:363417 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
116450683 | CORMO02523 | ||
115612810 | STRHB23034 |
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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