UniProt | Protein Name |
---|---|
Q9BT40 |
|
GO Term | Evidence Code | PMID |
---|---|---|
cellular response to insulin stimulus | ||
phosphatidylinositol dephosphorylation | ||
in utero embryonic development | ||
cellular response to epidermal growth factor stimulus | ||
negative regulation of calcium ion transport |
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity | ||
inositol trisphosphate phosphatase activity | ||
phosphatidylinositol trisphosphate phosphatase activity | ||
inositol bisphosphate phosphatase activity | ||
phosphatidylinositol phosphate 5-phosphatase activity |
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:0002167 | Abnormality of speech or vocalization |
HP:0002334 | Abnormal cerebellar vermis morphology |
HP:0002650 | Scoliosis |
HP:0002673 | Coxa valga |
HP:0002808 | Kyphosis |
HP:0002827 | Hip dislocation |
HP:0003198 | Myopathy |
HP:0003202 | Skeletal muscle atrophy |
HP:0003236 | Elevated circulating creatine kinase concentration |
HP:0003241 | External genital hypoplasia |
Disease ID | Disease Name |
---|---|
OMIM:617404 |
|
ORPHA:559 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
110222149 | PHACI22919 | ||
101041430 | SAIBB15775 | ||
101597543 | JACJA19705 | ||
102440108 | MYOLU11610 | ||
117013726 | RHIFE07175 | ||
100231908 | TAEGU07512 | ||
103242115 | CHLSB05056 | ||
108524657 | RHIBE17304 | ||
104670313 | RHIRO24550 | ||
100601583 | NOMLE16260 |
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Last updated: August 19, 2024