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: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 |
---|---|---|---|
110222149 | PHACI22919 | ||
101041430 | SAIBB15775 | ||
101597543 | JACJA19705 | ||
102440108 | MYOLU11610 | ||
117013726 | RHIFE07175 | ||
100231908 | TAEGU07512 | ||
103242115 | CHLSB05056 | ||
108524657 | RHIBE17304 | ||
104670313 | RHIRO24550 | ||
100601583 | NOMLE16260 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024