UniProt | Protein Name |
---|---|
Q9BT40 |
|
GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of renal water transport | ||
negative regulation of glucose transmembrane transport |
DO ID | Disease Name | Source |
---|---|---|
DOID:0014667 | disease of metabolism | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0050629 | Aicardi-Goutieres syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000135 | Hypogonadism |
HP:0000252 | Microcephaly |
HP:0000486 | Strabismus |
HP:0000518 | Cataract |
HP:0000639 | Nystagmus |
HP:0000648 | Optic atrophy |
HP:0000768 | Pectus carinatum |
HP:0001156 | Brachydactyly |
HP:0001167 | Abnormal finger morphology |
Disease ID | Disease Name |
---|---|
OMIM:617404 |
|
ORPHA:559 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
454410 | PANTR13179 | ||
100294645 | PONAB11525 | ||
480647 | CANLF19143 | ||
112933092 | VULVU29049 | ||
123777088 | URSAM15043 | ||
100467068 | AILME13999 | ||
101683037 | MUSPF15651 | ||
101085842 | FELCA31778 | ||
118886220 | BALMU11242 | ||
100663160 | LOXAF07794 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024