UniProt | Protein Name |
---|---|
Q9BT40 |
|
GO Term | Evidence Code | PMID |
---|---|---|
negative regulation of protein kinase activity | ||
negative regulation of peptidyl-serine phosphorylation | ||
actin cytoskeleton organization |
|
|
regulation of glycogen biosynthetic process | ||
G protein-coupled receptor signaling pathway |
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:3459 | breast carcinoma | |
DOID:3571 | liver cancer | |
DOID:4007 | bladder carcinoma | |
DOID:4090 | agnosia | |
DOID:4159 | skin cancer | |
DOID:423 | myopathy | |
DOID:4407 | phototoxic dermatitis | |
DOID:4480 | achondroplasia | |
DOID:4964 | neurotic disorder | |
DOID:5162 | arteriolosclerosis |
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 |
---|---|---|---|
114585335 | PODMU11698 | ||
107582245 | SINGR27478 | ||
105291862 | PTEVA08444 | ||
115401181 | SALFA47570 | ||
113487016 | ATHCN17509 | ||
105817364 | PROCO27097 | ||
109081047 | CYPCA113968 | ||
109086627 | CYPCA92633 | ||
103730507 | NANGA08234 | ||
116453889 | CORMO10037 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024