about
P688
Characterisation of recombinant human fatty aldehyde dehydrogenase: implications for Sjögren-Larsson syndromeSjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneHuman liver fatty aldehyde dehydrogenase: microsomal localization, purification, and biochemical characterizationIdentification of fatty aldehyde dehydrogenase in the breakdown of phytol to phytanic acidA gatekeeper helix determines the substrate specificity of Sjögren-Larsson Syndrome enzyme fatty aldehyde dehydrogenase
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Aldehyde dehydrogenase 3 family member A2
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Aldehyde dehydrogenase 3 family member A2
@en
Aldehyde dehydrogenase 3 family member A2
@nl
type
label
Aldehyde dehydrogenase 3 family member A2
@en
Aldehyde dehydrogenase 3 family member A2
@nl
altLabel
ALDH3A2
@en
aldehyde dehydrogenase 10
@en
aldehyde dehydrogenase family 3 member A2
@en
fatty aldehyde dehydrogenase
@en
microsomal aldehyde dehydrogenase
@en
prefLabel
Aldehyde dehydrogenase 3 family member A2
@en
Aldehyde dehydrogenase 3 family member A2
@nl
P361
P527
P637
P680
P681
P682
P705
P352
P637
P638
P31
P352
P361
P527
P637
NP_001026976
NP_001356065
NP_001356066
NP_001356067
NP_001356068
NP_001356075
NP_001356077
XP_024306419
P680
P681
P682
P702
P703
P705
ENSP00000176643
ENSP00000345774
ENSP00000378942
ENSP00000458397
ENSP00000458942
ENSP00000459977
ENSP00000461235
ENSP00000461916
ENSP00000462933
ENSP00000462964