GBA2

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GBA2
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_020944
NM_001330660

NM_172692

RefSeq (protein)

NP_001317589
NP_065995

NP_766280

Location (UCSC)Chr 9: 35.74 – 35.75 MbChr 4: 43.57 – 43.58 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

GBA2 is the gene that encodes the enzyme non-lysosomal glucosylceramidase in humans.[5][6] It has glucosylceramidase (EC 3.2.1.45) activity.

Function

This gene encodes a microsomal beta-glucosidase that catalyzes the hydrolysis of bile acid 3-O-glucosides as endogenous compounds. Studies to determine subcellular localization of this protein in the liver indicated that the enzyme was mainly enriched in the microsomal fraction where it appeared to be confined to the endoplasmic reticulum. This putative transmembrane protein is thought to play a role in carbohydrate transport and metabolism.[6]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000070610Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028467Ensembl, 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. PMID 11489889
    .
  6. ^ a b "Entrez Gene: GBA2 glucosidase, beta (bile acid) 2".

Further reading


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