UniProt | Protein Name |
---|---|
A0A0S2A4E4 |
|
P35573 |
|
GO Term | Evidence Code | PMID |
---|---|---|
glycogen catabolic process | ||
response to glucocorticoid | ||
response to nutrient | ||
glycogen biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
polysaccharide binding | ||
polyubiquitin modification-dependent protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0014667 | disease of metabolism | |
DOID:0050440 | familial partial lipodystrophy | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050700 | cardiomyopathy | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060318 | acute promyelocytic leukemia | |
DOID:0060689 | atrichia with papular lesions | |
DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |
DOID:0080092 | myofibrillar myopathy 1 | |
DOID:0080094 | myofibrillar myopathy 3 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000219 | Thin upper lip vermilion |
HP:0000233 | Thin vermilion border |
HP:0000272 | Malar flattening |
HP:0000293 | Full cheeks |
HP:0000455 | Broad nasal tip |
HP:0000490 | Deeply set eye |
HP:0001256 | Intellectual disability, mild |
HP:0001324 | Muscle weakness |
HP:0001395 | Hepatic fibrosis |
Disease ID | Disease Name |
---|---|
OMIM:232400 |
|
ORPHA:366 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100478160 | AILME11215 | ||
101687415 | MUSPF03702 | ||
101086077 | FELCA18120 | ||
122228128 | PANLE11221 | ||
118888497 | BALMU23435 | ||
100659336 | LOXAF15232 | ||
100050695 | HORSE33979 | ||
517397 | BOVIN26443 | ||
102178874 | CAPHI22143 | ||
101111501 | SHEEP00562 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024