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:0110253 | cataract 14 multiple types | |
DOID:0110254 | cataract 25 | |
DOID:0110255 | cataract 5 multiple types | |
DOID:0110256 | cataract 21 multiple types | |
DOID:0110257 | cataract 24 | |
DOID:0110258 | cataract 10 multiple types | |
DOID:0110259 | cataract 43 | |
DOID:0110260 | cataract 7 | |
DOID:0110261 | cataract 35 | |
DOID:0110262 | cataract 45 |
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 |
---|---|---|---|
106580790 | SALSA76764 | ||
115163103 | SALTR98687 | ||
115206054 | SALTR110509 | ||
100708563 | ORENI16445 | ||
115570188 | SPAAU18571 | ||
443677 | Xenbase:XB-GENE-996351 | ||
100127685 | Xenbase:XB-GENE-996350 | ||
101948693 | CHRPI08720 | ||
109317274 | CROPO22363 | ||
103820107 | SERCA16126 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024