Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 5660
  • Symbol: PSAP
  • Description: prosaposin

Export (tab separated) Export to Excel

Disease_Term Source Rank Other Values
Gaucher disease, atypical, 610539 (3) OMIM high
  • Genome region : 10q22.1
  • OMIM_ID : 176801 OMIM gene ID
  • OMIM_ID : 610539 OMIM phenotype ID
Krabbe disease, atypical, 611722 (3) OMIM high
  • Genome region : 10q22.1
  • OMIM_ID : 176801 OMIM gene ID
  • OMIM_ID : 611722 OMIM phenotype ID
Metachromatic leukodystrophy due to SAP-b deficiency, 249900 (3) OMIM high
  • Genome region : 10q22.1
  • OMIM_ID : 176801 OMIM gene ID
  • OMIM_ID : 249900 OMIM phenotype ID
Combined SAP deficiency, 611721 (3) OMIM high
  • Genome region : 10q22.1
  • OMIM_ID : 176801 OMIM gene ID
  • OMIM_ID : 611721 OMIM phenotype ID
Asthma (childhood onset) GWAS high