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Gene : ALDH16A1 Homo sapiens

Name  ? aldehyde dehydrogenase 16 family member A1 Cytological Location  19q13.33
Brief Description  aldehyde dehydrogenase 16 family member A1
Description  This gene encodes a member of the aldehyde dehydrogenase superfamily. The family members act on aldehyde substrates and use nicotinamide adenine dinucleotide phosphate (NADP) as a cofactor. This gene is conserved in chimpanzee, dog, cow, mouse, rat, and zebrafish. The protein encoded by this gene interacts with maspardin, a protein that when truncated is responsible for Mast syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2010]
  • synonyms:
  • uc002pnt.4,
  • OTTHUMG00000183163,
  • NM_153329,
  • aldehyde dehydrogenase 16 family, member A1,
  • MGC10204,
  • ALDH16A1,
  • AY007096,
  • HGNC:28114
  • identifiers:
  • 126133,
  • ENSG00000161618,
  • ALDH16A1

Genome feature

Region: gene ? Length: 17826  
Location: 19:49453225-49471050 Cyto location: 19q13.33

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3740 SNPs

5 Cross References

15 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results