UniProt | Protein Name |
---|---|
Q9BT40 |
|
GO Term | Evidence Code | PMID |
---|---|---|
negative regulation of protein phosphorylation | ||
negative regulation of MAP kinase activity | ||
negative regulation of glycogen (starch) synthase activity | ||
actin cytoskeleton organization |
|
|
negative regulation of stress fiber assembly |
GO Term | Evidence Code | PMID |
---|---|---|
inositol bisphosphate phosphatase activity | ||
phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity | ||
inositol-1,3,4,5-tetrakisphosphate 5-phosphatase activity | ||
vasopressin receptor activity | ||
inositol-1,4,5-trisphosphate 5-phosphatase activity |
Gene Ontology |
---|
inositol-polyphosphate 5-phosphatase activity |
phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity |
InterPro |
---|
Endonuclease/exonuclease/phosphatase superfamily |
Inositol polyphosphate-related phosphatase |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0080197 | congenital muscular dystrophy with cataracts and intellectual disability |
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 | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
100467068 | AILME13999 | |||
100601583 | NOMLE16260 | |||
100619651 | MONDO15625 | |||
100663160 | LOXAF07794 | |||
100708563 | ORENI16445 | |||
100764873 | CRIGR15776 | |||
100945090 | OTOGA04234 | |||
100976910 | 9597_0:0043da | PANPA15978 | ||
101011974 | PAPAN14773 | |||
101041430 | SAIBB15775 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024