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 |
---|---|---|
4-alpha-glucanotransferase activity | ||
beta-maltose 4-alpha-glucanotransferase activity | ||
glycogen debranching enzyme activity | ||
protein binding | ||
amylo-alpha-1,6-glucosidase activity |
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:0001638 | Cardiomyopathy |
HP:0001714 | Ventricular hypertrophy |
HP:0001943 | Hypoglycemia |
HP:0002155 | Hypertriglyceridemia |
HP:0002240 | Hepatomegaly |
HP:0002721 | Immunodeficiency |
HP:0002910 | Elevated circulating hepatic transaminase concentration |
HP:0003077 | Hyperlipidemia |
HP:0003198 | Myopathy |
HP:0003236 | Elevated circulating creatine kinase concentration |
Disease ID | Disease Name |
---|---|
OMIM:232400 |
|
ORPHA:366 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115153237 | SALTR00628 | ||
115156796 | SALTR61810 | ||
115169902 | SALTR41359 | ||
115549217 | GADMO58192 | ||
103479203 | POERE11927 | ||
101163765 | ORYLA06378 | ||
100703226 | ORENI29914 | ||
113010983 | ASTCA16973 | ||
115572875 | SPAAU35929 | ||
779381 | Xenbase:XB-GENE-6252447 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024