Gene Gene information from NCBI Gene database.
Entrez ID 126133
Gene name Aldehyde dehydrogenase 16 family member A1
Gene symbol ALDH16A1
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19q13.33
Summary 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 z
miRNA miRNA information provided by mirtarbase database.
69
miRTarBase ID miRNA Experiments Reference
MIRT045250 hsa-miR-186-5p CLASH 23622248
MIRT035869 hsa-miR-1247-5p CLASH 23622248
MIRT776895 hsa-miR-4269 CLIP-seq
MIRT776896 hsa-miR-4514 CLIP-seq
MIRT776897 hsa-miR-4692 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0004029 Function Aldehyde dehydrogenase (NAD+) activity IBA
GO:0005515 Function Protein binding IPI 32296183, 33961781, 35271311
GO:0016020 Component Membrane HDA 19946888
GO:0016491 Function Oxidoreductase activity IEA
GO:0016620 Function Oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613358 28114 ENSG00000161618
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IZ83
Protein name Aldehyde dehydrogenase family 16 member A1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00171 Aldedh 48 488 Aldehyde dehydrogenase family Family
PF00171 Aldedh 539 774 Aldehyde dehydrogenase family Family
Sequence
MAATRAGPRAREIFTSLEYGPVPESHACALAWLDTQDRCLGHYVNGKWLKPEHRNSVPCQ
DPITGENLASCLQAQAEDVAAAVEAARMAFKGWSAHPGVVRAQHLTRLAEVIQKHQRLLW
TLESLVTGRAVREVRDGDVQLAQQLLHYHAIQASTQEEALAGWEPMGVIGLILPPTFSFL
EMMWRICPALAVGCTVVALVPPASPAPLLLAQLAGELGPFPGILNVLSGPASLVPILASQ
PGIRKVAFCGAPEEGRALRRSLAGECAELGLALGTESLLLLTDTADVDSAVEGVVDAAWS
DRGPGGLRLLIQESVWDEAMRRLQERMGRLRSGRGLDGAVDMGARGAAACDLVQRFVREA
QSQGAQVFQAGDVPSERPFYPPTLVSNLPPASPCAQVEVPWPVVVASPFRTAKEALLVAN
GTPRGGSASVWSERLGQALELGYGLQVGTVWINAHGLRDPSVPTGGCKESGCSWHGGPDG
LYEYLRPS
GTPARLSCLSKNLNYDTFGLAVPSTLPAGPEIGPSPAPPYGLFVGGRFQAPG
ARSSRPIRDSSGNLHGYVAEGGAKDIRGAVEAAHQAFPGWAGQSPGARAALLWALAAALE
RRKSTLASRLERQGAELKAAEAEVELSARRLRAWGARVQAQGHTLQVAGLRGPVLRLREP
LGVLAVVCPDEWPLLAFVSLLAPALAYGNTVVMVPSAACPLLALEVCQDMATVFPAGLAN
VVTGDRDHLTRCLALHQDVQAMWYFGSAQGSQFVEWASAGNLKPVWASRGCPRA
WDQEAE
GAGPELGLRVARTKALWLPMGD
Sequence length 802
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Colon adenocarcinoma Uncertain significance rs756830979 RCV005937520
Gastric cancer Uncertain significance rs766273860 RCV005928981
Ovarian serous cystadenocarcinoma Uncertain significance rs766273860 RCV005928982
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Glioblastoma Associate 35116021
Gout Associate 28642574
Neoplasms Associate 35116021