UniProt | Protein Name |
---|---|
Q9Y6A1 |
|
A0A140VKE0 |
|
GO Term | Evidence Code | PMID |
---|---|---|
protein O-linked glycosylation | ||
protein O-linked mannosylation | ||
positive regulation of protein O-linked glycosylation | ||
extracellular matrix organization |
GO Term | Evidence Code | PMID |
---|---|---|
membrane | ||
endoplasmic reticulum membrane | ||
sarcoplasmic reticulum | ||
endoplasmic reticulum | ||
acrosomal vesicle |
GO Term | Evidence Code | PMID |
---|---|---|
protein binding | ||
metal ion binding | ||
mannosyltransferase activity | ||
dolichyl-phosphate-mannose-protein mannosyltransferase activity |
Gene Ontology |
---|
dolichyl-phosphate-mannose-protein mannosyltransferase activity |
mannosyltransferase activity |
protein O-linked glycosylation |
protein O-linked mannosylation |
transferase activity |
InterPro |
---|
Glycosyl transferase family 39/83 |
Glycosyltransferase 39-like |
MIR motif |
Mir domain superfamily |
Protein O-mannosyl-transferase, C-terminal four TM domain |
Species | Protein | mRNA |
---|---|---|
Saccharomyces cerevisiae | NP_010188 | NC_001136.6 |
Drosophila melanogaster | NP_524025 | NM_079301 |
Rattus norvegicus | NP_445858 | NM_053406 |
Mus musculus | NP_660127 | NM_145145 |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050453 | lissencephaly | |
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0050700 | cardiomyopathy | |
DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | |
DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | |
DOID:0112374 | muscular dystrophy-dystroglycanopathy | |
DOID:9296 | cleft lip | |
DOID:9884 | muscular dystrophy |
HPO ID | HPO Term |
---|---|
HP:0000478 | Abnormality of the eye |
HP:0000482 | Microcornea |
HP:0000485 | Megalocornea |
HP:0000486 | Strabismus |
HP:0000501 | Glaucoma |
HP:0000505 | Visual impairment |
HP:0000518 | Cataract |
HP:0000519 | Developmental cataract |
HP:0000525 | Abnormality iris morphology |
HP:0000528 | Anophthalmia |
Disease ID | Disease Name |
---|---|
ORPHA:370959 |
|
OMIM:236670 |
|
OMIM:609308 |
|
ORPHA:588 |
|
ORPHA:899 |
|
OMIM:613155 |
|
ORPHA:370980 |
|
ORPHA:370968 |
|
ORPHA:86812 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
39297 | FB:FBgn0003292 | |||
84430 | RGD:620078 | RATNO26952 | ||
99011 | MGI:2138994 | MOUSE33831 | ||
448433 | Xenbase:XB-GENE-944435 | |||
473076 | 9598_0:0029bc | PANTR45088 | ||
569769 | ZFIN:ZDB-GENE-060929-966 | DANRE37025 | ||
608039 | CANLF19342 | |||
617609 | BOVIN03326 | |||
722387 | MACMU13135 | |||
853608 | SGD:S000003904 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024