ALDH16A1
Identifiers
AliasesALDH16A1, aldehyde dehydrogenase 16 family member A1
External IDsOMIM: 613358 MGI: 1916998 HomoloGene: 34938 GeneCards: ALDH16A1
Orthologs
SpeciesHumanMouse
Entrez

126133

69748

Ensembl

ENSG00000161618

ENSMUSG00000007833

UniProt

Q8IZ83

Q571I9

RefSeq (mRNA)

NM_001145396
NM_153329

NM_145954

RefSeq (protein)

NP_001138868
NP_699160

NP_666066

Location (UCSC)Chr 19: 49.45 – 49.47 MbChr 7: 44.79 – 44.8 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Aldehyde dehydrogenase 16 family, member A1 also known as ALDH16A1 is an aldehyde dehydrogenase gene.

Clinical significance

Mutations in the SPG21 (ACP33/maspardin) gene are associated with the mast syndrome, a type of spastic paraplegia. The protein encoded by the SPG21 gene has been shown to interact with the ALDH16A1 enzyme.[5]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000161618 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000007833 - 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. Hanna MC, Blackstone C (January 2009). "Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1". Neurogenetics. 10 (3): 217–28. doi:10.1007/s10048-009-0172-6. PMC 5585778. PMID 19184135.

Further reading


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.