UniProt | Protein Name |
---|---|
A8K8F9 |
|
A0A384MR47 |
|
P51178 |
|
GO Term | Evidence Code | PMID |
---|---|---|
release of sequestered calcium ion into cytosol | ||
phosphatidylinositol metabolic process | ||
phosphatidylinositol-mediated signaling | ||
lipid catabolic process | ||
phospholipid metabolic process |
|
GO Term | Evidence Code | PMID |
---|---|---|
cytoplasm | ||
plasma membrane |
|
|
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
GTPase activating protein binding | ||
phosphatidylinositol-4,5-bisphosphate binding | ||
calcium ion binding | ||
protein binding | ||
phosphatidylinositol phospholipase C activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050819 | obsolete Matthew-Wood syndrome | |
DOID:0050865 | tongue squamous cell carcinoma | |
DOID:0080070 | mucolipidosis II alpha/beta | |
DOID:0080081 | nonsyndromic congenital nail disorder 3 | |
DOID:0080199 | colorectal carcinoma | |
DOID:0080324 | tuberous sclerosis 1 | |
DOID:10141 | obsolete asthenopia | |
DOID:10534 | stomach cancer | |
DOID:10629 | microphthalmia | |
DOID:10652 | Alzheimer's disease |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000498 | Blepharitis |
HP:0000499 | Abnormal eyelash morphology |
HP:0000613 | Photophobia |
HP:0000787 | Nephrolithiasis |
HP:0001231 | Abnormal fingernail morphology |
HP:0001595 | Abnormal hair morphology |
HP:0001598 | Concave nail |
HP:0001820 | Leukonychia |
Disease ID | Disease Name |
---|---|
OMIM:151600 |
|
ORPHA:2387 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115157572 | SALTR61799 | ||
115183969 | SALTR51152 | ||
115195303 | SALTR96967 | ||
115537216 | GADMO36043 | ||
115548723 | GADMO59023 | ||
101163204 | ORYLA06716 | ||
101167907 | ORYLA09153 | ||
100691757 | ORENI29356 | ||
100710733 | ORENI74960 | ||
115570241 | SPAAU47200 |
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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