Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11112
Gene name Gene Name - the full gene name approved by the HGNC.
3-hydroxyisobutyrate dehydrogenase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HIBADH
Synonyms (NCBI Gene) Gene synonyms aliases
NS5ATP1
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p15.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a mitochondrial 3-hydroxyisobutyrate dehydrogenase enzyme. The encoded protein plays a critical role in the catabolism of L-valine by catalyzing the oxidation of 3-hydroxyisobutyrate to methylmalonate semialdehyde. [provided by RefSeq, N
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT024585 hsa-miR-215-5p Microarray 19074876
MIRT025320 hsa-miR-34a-5p Proteomics 21566225
MIRT026367 hsa-miR-192-5p Microarray 19074876
MIRT649445 hsa-miR-1228-3p HITS-CLIP 23824327
MIRT649444 hsa-miR-520f-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IBA
GO:0005739 Component Mitochondrion IEA
GO:0005739 Component Mitochondrion IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608475 4907 ENSG00000106049
Protein
UniProt ID P31937
Protein name 3-hydroxyisobutyrate dehydrogenase, mitochondrial (HIBADH) (EC 1.1.1.31)
PDB 2GF2 , 2I9P
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03446 NAD_binding_2 41 200 NAD binding domain of 6-phosphogluconate dehydrogenase Domain
PF14833 NAD_binding_11 203 330 NAD-binding of NADP-dependent 3-hydroxyisobutyrate dehydrogenase Domain
Tissue specificity TISSUE SPECIFICITY: Detected in skin fibroblasts. {ECO:0000269|PubMed:16466957}.
Sequence
Sequence length 336
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Valine, leucine and isoleucine degradation
Metabolic pathways
  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)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Prostate cancer Prostate cancer N/A N/A GWAS
Urolithiasis Urolithiasis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Diabetes Mellitus Type 2 Associate 24455749
Obesity Associate 26474449
Schizophrenia Associate 26474449