Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4329
Gene name Gene Name - the full gene name approved by the HGNC.
Aldehyde dehydrogenase 6 family member A1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ALDH6A1
Synonyms (NCBI Gene) Gene synonyms aliases
MMSADHA, MMSDH
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q24.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the aldehyde dehydrogenase protein family. The encoded protein is a mitochondrial methylmalonate semialdehyde dehydrogenase that plays a role in the valine and pyrimidine catabolic pathways. This protein catalyzes the irrever
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT052812 hsa-miR-320e CLASH 23622248
MIRT705799 hsa-miR-3126-3p HITS-CLIP 23313552
MIRT705798 hsa-miR-3937 HITS-CLIP 23313552
MIRT705797 hsa-miR-4794 HITS-CLIP 23313552
MIRT705796 hsa-miR-664a-5p HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22658674
GO:0004491 Function Methylmalonate-semialdehyde dehydrogenase (acylating, NAD) activity IBA
GO:0004491 Function Methylmalonate-semialdehyde dehydrogenase (acylating, NAD) activity IEA
GO:0004491 Function Methylmalonate-semialdehyde dehydrogenase (acylating, NAD) activity IMP 23835272
GO:0004491 Function Methylmalonate-semialdehyde dehydrogenase (acylating, NAD) activity ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603178 7179 ENSG00000119711
Protein
UniProt ID Q02252
Protein name Methylmalonate-semialdehyde/malonate-semialdehyde dehydrogenase [acylating], mitochondrial (MMSDH) (EC 1.2.1.27) (Aldehyde dehydrogenase family 6 member A1) (Malonate-semialdehyde dehydrogenase [acylating])
Protein function Malonate and methylmalonate semialdehyde dehydrogenase involved in the catabolism of valine, thymine, and compounds catabolized by way of beta-alanine, including uracil and cytidine.
PDB 8XXQ , 9IZU , 9IZV , 9IZW , 9IZX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00171 Aldedh 48 512 Aldehyde dehydrogenase family Family
Sequence
Sequence length 535
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Valine, leucine and isoleucine degradation
beta-Alanine metabolism
Inositol phosphate metabolism
Propanoate metabolism
Metabolic pathways
Carbon metabolism
  Branched-chain amino acid catabolism
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Methylmalonate Semialdehyde Dehydrogenase Deficiency methylmalonate semialdehyde dehydrogenase deficiency rs72552258, rs879255579, rs796065046, rs367863044, rs869320672 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 32711556
Carcinoma Hepatocellular Associate 28430663
Carcinoma Renal Cell Associate 30793530, 31746384, 32737333, 33686951, 35096270, 39348357
Carcinoma Renal Cell Inhibit 32093682
Colorectal Neoplasms Associate 24555920
Demyelinating Diseases Associate 23835272
Insulin Resistance Associate 29986096
Methylmalonate Semialdehyde Dehydrogenase Deficiency Associate 23835272
Methylmalonic acidemia Associate 23835272
Neoplasm Metastasis Associate 28430663, 37379245