cvd-logocvd - Molecule ID A5767

geneALDH7A1, ATQ1
nameAldehyde dehydrogenase family 7 member A1
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
AL7A1_HUMANP49419ENSG00000164904501Hs.483239107323, 266100

Functions and classifications

GOC:cytosol, C:mitochondrial matrix, C:nucleus, F:aldehyde dehydrogenase (NAD) activity, F:betaine-aldehyde dehydrogenase activity, F:L-aminoadipate-semialdehyde dehydrogenase activity, P:cellular aldehyde metabolic process, P:cellular nitrogen compound metabolic process, P:glycine betaine biosynthetic process from choline, P:lysine catabolic process, P:sensory perception of sound, F:oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor, F:oxidoreductase activity, C:cytosol, C:mitochondrial matrix, C:nucleus, F:aldehyde dehydrogenase (NAD) activity, F:betaine-aldehyde dehydrogenase activity, F:L-aminoadipate-semialdehyde dehydrogenase activity, P:cellular aldehyde metabolic process, P:cellular nitrogen compound metabolic process, P:glycine betaine biosynthetic process from choline, P:lysine catabolic process, P:sensory perception of sound, F:oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor, F:oxidoreductase activity
UniProt3D-structure, Acetylation, Alternative splicing, Complete proteome, Cytoplasm, Disease mutation, Epilepsy, Mitochondrion, NAD, Nucleus, Oxidoreductase, Polymorphism, Reference proteome, Transit peptide
PADBENZ: enzyme, enzymatic properties

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valueDetectionPubMed/DOI
Exp21417265Homo sapiens17heartmyocardiumDCM (Dilated cardiomyopathy)0.8000.023LC-MS/MS21417265

Compile date 02-09-2018© C/VD project