Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8659
Gene name Gene Name - the full gene name approved by the HGNC.
Aldehyde dehydrogenase 4 family member A1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ALDH4A1
Synonyms (NCBI Gene) Gene synonyms aliases
ALDH4, P5CD, P5CDh
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.13
Summary Summary of gene provided in NCBI Entrez Gene.
This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. D
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs78532707 C>A,G,T Conflicting-interpretations-of-pathogenicity Splice donor variant, intron variant
rs137852937 G>A,C Pathogenic Non coding transcript variant, missense variant, coding sequence variant
rs149414160 A>G Uncertain-significance, conflicting-interpretations-of-pathogenicity Intron variant, missense variant, coding sequence variant, non coding transcript variant
rs387906314 C>- Likely-pathogenic Genic upstream transcript variant, frameshift variant, coding sequence variant, non coding transcript variant
rs779536510 ->A Pathogenic Coding sequence variant, frameshift variant, non coding transcript variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022075 hsa-miR-128-3p Microarray 17612493
MIRT777420 hsa-miR-125a-5p CLIP-seq
MIRT777421 hsa-miR-125b CLIP-seq
MIRT777422 hsa-miR-128 CLIP-seq
MIRT777423 hsa-miR-183 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003842 Function 1-pyrroline-5-carboxylate dehydrogenase activity IBA 21873635
GO:0004029 Function Aldehyde dehydrogenase (NAD+) activity IDA 4015840
GO:0005515 Function Protein binding IPI 32814053
GO:0005739 Component Mitochondrion IDA
GO:0005759 Component Mitochondrial matrix TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606811 406 ENSG00000159423
Protein
UniProt ID P30038
Protein name Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial (P5C dehydrogenase) (EC 1.2.1.88) (Aldehyde dehydrogenase family 4 member A1) (L-glutamate gamma-semialdehyde dehydrogenase)
Protein function Irreversible conversion of delta-1-pyrroline-5-carboxylate (P5C), derived either from proline or ornithine, to glutamate. This is a necessary step in the pathway interconnecting the urea and tricarboxylic acid cycles. The preferred substrate is
PDB 3V9G , 3V9H , 3V9I , 4OE5 , 8RKQ , 8RKR
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00171 Aldedh 74 547 Aldehyde dehydrogenase family Family
Tissue specificity TISSUE SPECIFICITY: Highest expression is found in liver followed by skeletal muscle, kidney, heart, brain, placenta, lung and pancreas.
Sequence
Sequence length 563
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Hyperprolinemia hyperprolinemia type 2 GenCC
Anorexia Anorexia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Bipolar Disorder Associate 32065947
Cardiomyopathy Dilated Associate 27711126
Hyperprolinemia type 2 Associate 31884946
Insulin Resistance Associate 30678306
Nasopharyngeal Carcinoma Associate 34680942
Non alcoholic Fatty Liver Disease Inhibit 29718361
Schizophrenia Stimulate 32065947
Seizures Associate 31884946
Vitamin B 6 Deficiency Associate 31884946