ALDH16A1

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ALDH16A1
Identifiers
Aliases ALDH16A1, aldehyde dehydrogenase 16 family member A1
External IDs MGI: 1916998 HomoloGene: 34938 GeneCards: ALDH16A1
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001145396
NM_153329

NM_145954

RefSeq (protein)

NP_001138868
NP_699160

NP_666066.1
NP_666066

Location (UCSC) Chr 19: 49.45 – 49.47 Mb Chr 7: 45.14 – 45.15 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

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

Clinical significance[edit]

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.[3]

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ 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. PMID 19184135. 

External links[edit]

Further reading[edit]