UniProt | Protein Name |
---|---|
Q3MUY2 |
|
GO Term | Evidence Code | PMID |
---|---|---|
GPI anchor biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum membrane | ||
plasma membrane | ||
glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex |
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylinositol N-acetylglucosaminyltransferase activity | ||
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:540 | strabismus | |
DOID:758 | situs inversus | |
DOID:0050841 | focal hand dystonia | |
DOID:0060216 | Cogan syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060320 | inguinal hernia | |
DOID:0060823 | syndromic X-linked intellectual disability 94 | |
DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | |
DOID:0111338 | isolated elevated serum creatine phosphokinase levels | |
DOID:10293 | monocular esotropia |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000023 | Inguinal hernia |
HP:0000126 | Hydronephrosis |
HP:0000193 | Bifid uvula |
HP:0000218 | High palate |
HP:0000248 | Brachycephaly |
HP:0000280 | Coarse facial features |
HP:0000286 | Epicanthus |
HP:0000289 | Broad philtrum |
HP:0000303 | Mandibular prognathia |
Disease ID | Disease Name |
---|---|
OMIM:616809 |
|
ORPHA:247262 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
103175070 | CALMI06225 | ||
555881 | DANRE27104 | ||
100196164 | SALSA06834 | ||
115197464 | SALTR12399 | ||
103466265 | POERE28738 | ||
108710150 | Xenbase:XB-GENE-17346800 | ||
496649 | Xenbase:XB-GENE-5783232 | ||
101175705 | Xenbase:XB-GENE-17329836 | ||
103305692 | CHRPI11476 | ||
103826050 | SERCA03794 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024