UniProt | Protein Name |
---|---|
P35579 |
|
GO Term | Evidence Code | PMID |
---|---|---|
meiotic spindle organization | ||
angiogenesis | ||
in utero embryonic development | ||
establishment of T cell polarity | ||
plasma membrane repair |
GO Term | Evidence Code | PMID |
---|---|---|
microfilament motor activity | ||
microfilament motor activity | ||
virus receptor activity | ||
RNA binding | ||
cytoskeletal motor activity |
Gene Ontology |
---|
ATP binding |
actin binding |
actin filament binding |
cytoskeletal motor activity |
nucleotide binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050567 | orofacial cleft | |
DOID:0060651 | MYH-9 related disease | |
DOID:0110032 | autosomal dominant Alport syndrome | |
DOID:0110548 | autosomal dominant nonsyndromic deafness 17 | |
DOID:10003 | sensorineural hearing loss | |
DOID:1588 | thrombocytopenia | |
DOID:576 | proteinuria | |
DOID:783 | end stage renal disease |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
4619 | SGD:S000001065 | ||
4625 | SGD:S000001065 | ||
4627 | Xenbase:XB-GENE-1002222 | ||
4628 | SGD:S000001065 | ||
4629 | SGD:S000001065 | ||
8735 | SGD:S000001065 | ||
17879 | SGD:S000001065 | ||
17882 | SGD:S000001065 | ||
17883 | SGD:S000001065 | ||
17884 | SGD:S000001065 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 7, 2025