HPSE2

Last updated

HPSE2
Identifiers
Aliases HPSE2 , HPA2, HPR2, UFS, UFS1, heparanase 2 (inactive)
External IDs OMIM: 613469; MGI: 2685814; HomoloGene: 19680; GeneCards: HPSE2; OMA:HPSE2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001166244
NM_001166245
NM_001166246
NM_021828

NM_001081257

RefSeq (protein)

NP_001159716
NP_001159717
NP_001159718
NP_068600

NP_001074726

Location (UCSC) Chr 10: 98.46 – 99.24 Mb Chr 19: 42.77 – 43.38 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Heparanase-2 is an enzyme that in humans is encoded by the HPSE2 gene. [5] [6]


It may be associated with urofacial syndrome. [7]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000172987 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000074852 Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. McKenzie E, Tyson K, Stamps A, Smith P, Turner P, Barry R, Hircock M, Patel S, Barry E, Stubberfield C, Terrett J, Page M (Oct 2000). "Cloning and expression profiling of Hpa2, a novel mammalian heparanase family member". Biochem Biophys Res Commun. 276 (3): 1170–7. doi:10.1006/bbrc.2000.3586. PMID   11027606.
  6. "Entrez Gene: HPSE2 heparanase 2".
  7. Daly SB, Urquhart JE, Hilton E, et al. (June 2010). "Mutations in HPSE2 Cause Urofacial Syndrome". Am J Hum Genet. 86 (6): 963–969. doi:10.1016/j.ajhg.2010.05.006. PMC   3032078 . PMID   20560210.

Further reading