UniProt | Protein Name |
---|---|
Q9BT40 |
|
GO Term | Evidence Code | PMID |
---|---|---|
protein localization to plasma membrane | ||
negative regulation of glycogen biosynthetic process | ||
negative regulation of single stranded viral RNA replication via double stranded DNA intermediate | ||
negative regulation of protein phosphorylation | ||
positive regulation of transcription, DNA-templated |
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:0110231 | cataract 1 multiple types | |
DOID:0110232 | cataract 29 | |
DOID:0110233 | cataract 27 | |
DOID:0110234 | cataract 4 multiple types | |
DOID:0110235 | cataract 2 multiple types | |
DOID:0110236 | cataract 39 multiple types | |
DOID:0110237 | cataract 42 | |
DOID:0110238 | cataract 18 | |
DOID:0110239 | cataract 12 multiple types | |
DOID:0110240 | cataract 20 multiple types |
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 |
---|---|---|---|
103275954 | CARSF20523 | ||
115601883 | STRHB05464 |
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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