Gene Gene information from NCBI Gene database.
Entrez ID 8659
Gene name Aldehyde dehydrogenase 4 family member A1
Gene symbol ALDH4A1
Synonyms (NCBI Gene)
ALDH4P5CDP5CDh
Chromosome 1
Chromosome location 1p36.13
Summary 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.
6
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.
168
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0003842 Function L-glutamate gamma-semialdehyde dehydrogenase activity IBA
GO:0003842 Function L-glutamate gamma-semialdehyde dehydrogenase activity IEA
GO:0003842 Function L-glutamate gamma-semialdehyde dehydrogenase activity TAS 8621661
GO:0004029 Function Aldehyde dehydrogenase (NAD+) activity IDA 4015840
GO:0004029 Function Aldehyde dehydrogenase (NAD+) activity TAS 8621661
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606811 406 ENSG00000159423
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
304
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hyperprolinemia type 2 Likely pathogenic; Pathogenic rs756807746, rs2100593635, rs2522599015, rs779536510, rs387906314, rs2522617063, rs78532707, rs1557620472 RCV001808041
RCV002052047
RCV002481176
RCV000004209
RCV000004211
RCV003389279
RCV000505674
RCV000692385
See cases Likely pathogenic rs1429118574 RCV002252974
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ALDH4A1-related disorder Likely benign; Benign; Conflicting classifications of pathogenicity rs202214117, rs2230709, rs138788183, rs9426679, rs149414160, rs145243354, rs139640415, rs9426797, rs2522598185, rs780190351, rs1239440212, rs370813324, rs1360449246, rs371491394, rs150762865
View all (2 more)
RCV003968563
RCV003982997
RCV003920191
RCV003977831
RCV003967830
RCV003920190
RCV003920192
RCV003967831
RCV003921776
RCV003894216
RCV003964022
RCV003969335
RCV003946923
RCV003962232
RCV003965757
RCV003908276
RCV003973062
Hyperprolinemia Uncertain significance; Likely benign rs774289867, rs112566606, rs559524012, rs886045708, rs878956441, rs551988232, rs11311839 RCV000363145
RCV000297129
RCV000261728
RCV000400845
RCV000356587
RCV000312285
RCV000321565
Intellectual disability Conflicting classifications of pathogenicity; Uncertain significance; Likely benign rs147600006, rs139640415, rs756299719, rs923744167, rs774464848, rs371321697, rs150027463 RCV001252139
RCV001252138
RCV001252133
RCV001252136
RCV001252135
RCV001252134
RCV001252137
Melanoma Benign rs11740 RCV005891561
Associations from Text MiningDisease associations identified through Pubtator
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