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:0070309 | absence epilepsy | |
DOID:0050428 | nonepidermolytic palmoplantar keratoderma | |
DOID:0050841 | focal hand dystonia | |
DOID:0060216 | Cogan syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060823 | syndromic X-linked intellectual disability 94 | |
DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | |
DOID:0080199 | colorectal carcinoma | |
DOID:0110213 | isolated cleft palate | |
DOID:10003 | sensorineural hearing loss |
HPO ID | HPO Term |
---|---|
HP:0000729 | Autistic behavior |
HP:0000750 | Delayed speech and language development |
HP:0000767 | Pectus excavatum |
HP:0001009 | Telangiectasia |
HP:0001195 | Single umbilical artery |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001251 | Ataxia |
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
Disease ID | Disease Name |
---|---|
OMIM:614749 |
|
ORPHA:247262 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100654772 | LOXAF17368 | ||
100624832 | PIGXX15658 | ||
783989 | BOVIN34514 | ||
102174206 | CAPHI29089 | ||
101118666 | SHEEP09036 | ||
100339282 | RABIT00154 | ||
105993407 | DIPOR16500 | ||
100774971 | CRIGR13522 | ||
56703 | MGI:1861452 | MOUSE42804 | |
313341 | RGD:1309498 | RATNO33777 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024