GO Term | Evidence Code | PMID |
---|---|---|
cell morphogenesis | ||
mitochondrion organization | ||
sensory perception of mechanical stimulus | ||
protein lipidation | ||
skeletal muscle organ development |
GO Term | Evidence Code | PMID |
---|---|---|
protein-containing complex | ||
mitochondrion |
|
|
lysosome |
GO Term | Evidence Code | PMID |
---|---|---|
collagen binding | ||
platelet-derived growth factor binding | ||
protein binding | ||
extracellular matrix structural constituent conferring tensile strength |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050558 | Ullrich congenital muscular dystrophy | |
DOID:0050663 | Bethlem myopathy | |
DOID:9884 | muscular dystrophy |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100978062 | PANPA23215 | ||
100460129 | PONAB21474 | ||
1291 | HGNC:2211 | HUMAN58982 | |
403668 | CANLF12958 | ||
100464071 | AILME12938 | ||
101692352 | MUSPF01381 | ||
101081156 | FELCA22117 | ||
122229790 | PANLE07673 | ||
101329745 | TURTR00451 | ||
118894224 | BALMU18776 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024