UniProt | Protein Name |
---|---|
P07602 |
|
GO Term | Evidence Code | PMID |
---|---|---|
adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway | ||
ganglioside GM1 transport to membrane | ||
prostate gland growth | ||
epithelial cell differentiation involved in prostate gland development | ||
regulation of autophagy |
GO Term | Evidence Code | PMID |
---|---|---|
ganglioside GP1c binding | ||
protein binding | ||
ganglioside GM3 binding | ||
enzyme activator activity | ||
ganglioside GT1b binding |
Gene Ontology |
---|
lipid metabolic process |
sphingolipid metabolic process |
InterPro |
---|
Saposin B type domain |
Saposin B type, region 2 |
Saposin-like type B, region 1 |
Saposin-like |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060892 | late onset Parkinson's disease | |
DOID:0110961 | atypical Gaucher's disease due to saposin c deficiency | |
DOID:0111330 | combined saposin deficiency | |
DOID:10581 | metachromatic leukodystrophy | |
DOID:10587 | Krabbe disease | |
DOID:3211 | lysosomal storage disease | |
DOID:9455 | lipid storage disease |
HPO ID | HPO Term |
---|---|
HP:0001336 | Myoclonus |
HP:0001347 | Hyperreflexia |
HP:0001508 | Failure to thrive |
HP:0001522 | Death in infancy |
HP:0001601 | Laryngomalacia |
HP:0001744 | Splenomegaly |
HP:0001873 | Thrombocytopenia |
HP:0001903 | Anemia |
HP:0001939 | Abnormality of metabolism/homeostasis |
HP:0001955 | Unexplained fevers |
Disease ID | Disease Name |
---|---|
OMIM:249900 |
|
OMIM:610539 |
|
ORPHA:309256 |
|
OMIM:619491 |
|
OMIM:611721 |
|
ORPHA:309271 |
|
ORPHA:309263 |
|
ORPHA:206436 |
|
ORPHA:139406 |
|
OMIM:611722 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
129006859 | 9600_0:002ad7 |
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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