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: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 |
---|---|---|---|
101076491 | TAKRU44074 | ||
102784167 | NEOBR15574 | ||
102014348 | CHILA16899 | ||
108232564 | KRYMA06692 | ||
105724577 | AOTNA27924 | ||
101031661 | SAIBB38743 | ||
111237493 | SERDU26906 | ||
108427252 | PYGNA09048 | ||
101972860 | ICTTR00593 | ||
103129807 | POEFO22371 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024