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Gene: PSAP (prosaposin) Canis lupus familiaris
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Symbol: PSAP
Name: prosaposin
Description: ENCODES a protein that exhibits beta-galactosidase activity (inferred); G protein-coupled receptor binding (inferred); ganglioside GM1 binding (inferred); INVOLVED IN antigen processing and presentation (inferred); cellular response to organic substance (inferred); cerebellar Purkinje cell differentiation (inferred); ASSOCIATED WITH atypical Gaucher's disease due to saposin C deficiency (ortholog); combined saposin deficiency (ortholog); genetic disease (ortholog); FOUND IN aggresome (inferred); late endosome (inferred); lysosome (inferred)
Type: protein-coding
RefSeq Status: MODEL
Also known as: prosaposin (variant Gaucher disease and variant metachromatic leukodystrophy)
Orthologs:
Homo sapiens (human) : PSAP (prosaposin)  HGNC  Alliance
Mus musculus (house mouse) : Psap (prosaposin)  MGI  Alliance
Rattus norvegicus (Norway rat) : Psap (prosaposin)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Psap (prosaposin)
Pan paniscus (bonobo/pygmy chimpanzee) : PSAP (prosaposin)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Psap (prosaposin)
Sus scrofa (pig) : PSAP (prosaposin)
Chlorocebus sabaeus (African green monkey) : PSAP (prosaposin)
Heterocephalus glaber (naked mole-rat) : Psap (prosaposin)
more info ...
Latest Assembly: CanFam3.1 - Dog CanFam3.1 Assembly
Position:
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl422,572,153 - 22,603,848 (-)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.1422,571,095 - 22,603,880 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Genomics

Comparative Map Data

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
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Additional Information

External Database Links
 
More on PSAP
NCBI Gene
Ensembl Gene
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 12386781
Created: 2017-01-24
Species: Canis lupus familiaris
Last Modified: 2020-02-26
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.