GO Term | Evidence Code | PMID |
---|---|---|
Ras protein signal transduction |
|
|
phospholipid catabolic process | ||
cellular response to nutrient | ||
small GTPase mediated signal transduction |
|
|
phosphatidic acid biosynthetic process |
|
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
endosome | ||
endocytic vesicle | ||
endoplasmic reticulum membrane |
|
|
late endosome membrane |
GO Term | Evidence Code | PMID |
---|---|---|
phospholipase D activity | ||
N-acylphosphatidylethanolamine-specific phospholipase D activity | ||
phosphatidylinositol binding | ||
protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0002116 | pterygium | |
DOID:0040085 | bacterial sepsis | |
DOID:0050387 | nonpapillary renal cell carcinoma | |
DOID:0050819 | obsolete Matthew-Wood syndrome | |
DOID:0060180 | colitis | |
DOID:0060189 | ileitis | |
DOID:0060190 | ileocolitis | |
DOID:0060320 | inguinal hernia | |
DOID:0060538 | purpura fulminans | |
DOID:0060891 | Parkinson's disease 19A |
HPO ID | HPO Term |
---|---|
HP:0010446 | Tricuspid stenosis |
HP:0011555 | Double inlet left ventricle |
HP:0011591 | Left aortic arch with cervical origin of the right subclavian artery |
HP:0011623 | Muscular ventricular septal defect |
HP:0011662 | Tricuspid atresia |
Disease ID | Disease Name |
---|---|
OMIM:212093 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115179121 | SALTR05523 | ||
115196210 | SALTR05523 | ||
115537366 | GADMO37094 | ||
101175514 | ORYLA08831 | ||
100699552 | ORENI31270 | ||
115597398 | SPAAU05079 | ||
100191021 | Xenbase:XB-GENE-948469 | ||
108718097 | Xenbase:XB-GENE-17330722 | ||
100379682 | Xenbase:XB-GENE-948465 | ||
101931414 | CHRPI04063 |
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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