UniProt | Protein Name |
---|---|
Q8TEQ8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
GPI anchor biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
mannose-ethanolamine phosphotransferase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:10293 | monocular esotropia | |
DOID:10487 | Hirschsprung's disease | |
DOID:10488 | imperforate anus | |
DOID:1059 | intellectual disability | |
DOID:11111 | hydronephrosis | |
DOID:11832 | visual epilepsy | |
DOID:12215 | oligohydramnios | |
DOID:1270 | hereditary hemorrhagic telangiectasia | |
DOID:1271 | capillary disease | |
DOID:1272 | telangiectasis |
HPO ID | HPO Term |
---|---|
HP:0002558 | Supernumerary nipple |
HP:0002650 | Scoliosis |
HP:0002696 | Abnormal parietal bone morphology |
HP:0002714 | Downturned corners of mouth |
HP:0003155 | Elevated circulating alkaline phosphatase concentration |
HP:0003196 | Short nose |
HP:0003577 | Congenital onset |
HP:0004969 | Peripheral pulmonary artery stenosis |
HP:0006118 | Shortening of all distal phalanges of the fingers |
HP:0006808 | Cerebral hypomyelination |
Disease ID | Disease Name |
---|---|
OMIM:614749 |
|
ORPHA:247262 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115532330 | GADMO25222 | ||
103474015 | POERE05659 | ||
102300593 | HAPBU30383 | ||
113025961 | ASTCA37075 | ||
115592739 | SPAAU33164 | ||
444225 | Xenbase:XB-GENE-5945147 | ||
100145458 | Xenbase:XB-GENE-5945117 | ||
101941736 | CHRPI26192 | ||
109307798 | CROPO12297 | ||
113449710 | PSETE23581 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024