UniProt | Protein Name |
---|---|
Q9BT40 |
|
GO Term | Evidence Code | PMID |
---|---|---|
negative regulation of peptidyl-threonine phosphorylation | ||
ruffle assembly | ||
negative regulation of stress fiber assembly | ||
phosphatidylinositol biosynthetic process |
|
|
negative regulation of insulin 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:539 | ophthalmoplegia | |
DOID:540 | strabismus | |
DOID:543 | dystonia | |
DOID:5517 | stomach carcinoma | |
DOID:5723 | optic atrophy | |
DOID:574 | peripheral nervous system disease | |
DOID:591 | phobic disorder | |
DOID:6713 | cerebrovascular disease | |
DOID:680 | tauopathy | |
DOID:684 | hepatocellular carcinoma |
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 |
---|---|---|---|
100462756 | PIGXX03051 | ||
514123 | BOVIN12494 | ||
102177657 | CAPHI10179 | ||
101115806 | SHEEP02601 | ||
100358289 | RABIT07350 | ||
105985678 | DIPOR12245 | ||
100764873 | CRIGR15776 | ||
19062 | MGI:1194899 | MOUSE03320 | |
287533 | RGD:1359130 | RATNO02210 | |
101568699 | OCTDE13579 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024