prosaposin
| UniProt | Protein Name |
|---|---|
| P07602 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| sphingolipid metabolic process | ||
| lysosomal transport | ||
| lysosomal transport | ||
| adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway | ||
| regulation of autophagy |
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| azurophil granule membrane | ||
| lysosomal lumen | ||
| intracellular membrane-bounded organelle | ||
| collagen-containing extracellular matrix |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protease binding | ||
| protein binding | ||
| phospholipid binding | ||
| enzyme activator activity | ||
| identical protein binding |
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 |
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000020 | Urinary incontinence |
| HP:0000365 | Hearing impairment |
| HP:0000467 | Neck muscle weakness |
| HP:0000496 | Abnormality of eye movement |
| HP:0000508 | Ptosis |
| HP:0000572 | Visual loss |
| HP:0000605 | Supranuclear gaze palsy |
| HP:0000613 | Photophobia |
| Disease ID | Disease Name |
|---|---|
| OMIM:611722 |
|
| OMIM:249900 |
|
| ORPHA:309271 |
|
| OMIM:611721 |
|
| ORPHA:309263 |
|
| ORPHA:206436 |
|
| ORPHA:309256 |
|
| OMIM:619491 |
|
| ORPHA:139406 |
|
| OMIM:610539 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: April 6, 2026