prosaposin

Summary
Gene Symbol
  • PSAP
Aliases
  • saposin-A
  • saposin-B
  • saposin-C
  • saposin-D
  • variant Gaucher disease and variant metachromatic leukodystrophy
Organism
Homo sapiens (human)
External Links
NCBI Gene
5660
HGNC
9498
KEGG Gene ID
hsa:5660
PubChem
5660
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • Gangliosidosis
  • Gaucher disease
  • Glycoprotein
  • Lysosome
  • Metachromatic leukodystrophy
  • Neurodegeneration
  • Parkinson disease
  • Parkinsonism
  • Reference proteome
  • Repeat
  • Secreted
  • Signal
  • Sphingolipid metabolism
Proteins
Displaying 1 entry
UniProt Protein Name
P07602
  • Proactivator polypeptide
Gene Ontology (GO)
GO Hierarchy
Displaying entry 11 - 11 of 11 in total
GO Term Evidence Code PMID
late endosome
GO Hierarchy
GO Hierarchy
Human Protein Atlas
ENSG00000197746

soft tissue soft tissue blood blood blood blood blood blood blood blood blood blood blood blood blood blood lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node kidney kidney adrenal gland adrenal gland breast breast duodenum stomach small intestine colon rectum appendix esophagus eye eye salivary gland nasopharynx nasopharynx tongue tonsil tonsil tonsil hair skin adipose tissue adipose tissue adipose tissue spinal cord oral mucosa lung lung heart bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus liver pancreas thyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland spleen gallbladder ductus deferens ductus deferens seminal vesicle seminal vesicle seminal vesicle seminal vesicle testis testis epididymis epididymis brain smooth muscle urinary bladder prostate bone marrow skeletal muscle skeletal muscle skeletal muscle skeletal muscle skeletal muscle thymus thymus cartilage sole of foot sole of foot soft tissue blood blood blood blood blood blood blood blood blood blood blood blood lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lactating breast lactating breast kidney kidney adrenal gland adrenal gland duodenum stomach small intestine colon rectum appendix esophagus eye eye salivary gland salivary gland salivary gland salivary gland salivary gland salivary gland nasopharynx tongue tonsil tonsil hair skin adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue spinal cord oral mucosa lung lung heart bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus liver pancreas thyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland spleen gallbladder brain skeletal muscle skeletal muscle skeletal muscle skeletal muscle skeletal muscle thymus thymus smooth muscle urinary bladder vagina ovary ovary fallopian tube fallopian tube endometrium placenta cervix cervix bone marrow cartilage sole of foot sole of foot olfactory region cerebral cortex cerebellum medulla pons midbrain pituitary gland hypothalamus amygdala thalamus choroid plexus choroid plexus corpus callosum basal ganglia substantia nigra dorsal raphe dorsal raphe dorsal raphe dorsal raphe dorsal raphe dorsal raphe caudate hippocampus retina retina

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

KEGG BRITE Database
Orthology
K12382
Name
saposin
References
Disease
Disease Ontology
Displaying entries 101 - 110 of 267 in total
DO ID Disease Name Source
DOID:0110542 autosomal dominant nonsyndromic deafness 10
DOID:0110543 autosomal dominant nonsyndromic deafness 11
DOID:0110544 autosomal dominant nonsyndromic deafness 12
DOID:0110545 autosomal dominant nonsyndromic deafness 13
DOID:0110546 autosomal dominant nonsyndromic deafness 15
DOID:0110547 autosomal dominant nonsyndromic deafness 16
DOID:0110548 autosomal dominant nonsyndromic deafness 17
DOID:0110549 autosomal dominant nonsyndromic deafness 18
DOID:0110550 autosomal dominant nonsyndromic deafness 20
DOID:0110551 autosomal dominant nonsyndromic deafness 21
The Human Phenotype Ontology
Displaying entries 51 - 60 of 148 in total
HPO ID HPO Term
HP:0001971 Hypersplenism
HP:0002013 Vomiting
HP:0002015 Dysphagia
HP:0002020 Gastroesophageal reflux
HP:0002061 Lower limb spasticity
HP:0002063 Rigidity
HP:0002066 Gait ataxia
HP:0002069 Bilateral tonic-clonic seizure
HP:0002072 Chorea
HP:0002079 Hypoplasia of the corpus callosum
Displaying all 10 entries
Disease ID Disease Name
OMIM:611721
  • combined PSAP deficiency
ORPHA:139406
  • combined PSAP deficiency
ORPHA:309271
  • metachromatic leukodystrophy, adult form
OMIM:611722
  • Krabbe disease due to saposin A deficiency
ORPHA:206436
  • infantile Krabbe disease
ORPHA:309263
  • metachromatic leukodystrophy, juvenile form
OMIM:610539
  • Gaucher disease due to saposin C deficiency
ORPHA:309256
  • metachromatic leukodystrophy, late infantile form
OMIM:619491
  • Parkinson disease 24, autosomal dominant, susceptibility to
OMIM:249900
  • metachromatic leukodystrophy due to saposin B deficiency
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP002838
Gene Name
prosaposin

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024