help  | about  | cite  | software

Gene : ACADSB Homo sapiens

Name  ? acyl-CoA dehydrogenase short/branched chain Cytological Location  10q26.13
Brief Description  acyl-CoA dehydrogenase short/branched chain
description  Short/branched chain acyl-CoA dehydrogenase(ACADSB) is a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. Substrate specificity is the primary characteristic used to define members of this gene family. The ACADSB gene product has the greatest activity towards the short branched chain acyl-CoA derivative, (S)-2-methylbutyryl-CoA, but also reacts significantly with other 2-methyl branched chain substrates and with short straight chain acyl-CoAs. The cDNA encodes for a mitochondrial precursor protein which is cleaved upon mitochondrial import and predicted to yield a mature peptide of approximately 43.7-KDa. [provided by RefSeq, Jul 2008]
  • synonyms:
  • SBCAD,
  • ACAD7,
  • U12778,
  • HGNC:91,
  • OTTHUMG00000019200,
  • uc001lhb.4,
  • ACAD7,
  • 2-MEBCAD,
  • acyl-Coenzyme A dehydrogenase, short/branched chain,
  • SBCAD,
  • NM_001609,
  • ACADSB
  • identifiers:
  • 36,
  • ENSG00000196177,
  • ACADSB

Genome feature

Region: gene ? Length: 49378  
Location: 10:123008913-123058290 Cyto location: 10q26.13


Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer

Function

Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

Homologue Displayer

Gene --> Orthologues

Interactions

Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

808 SN Ps

5 Cross References

19 Data Sets

13 Homologues

0 Located Features

90 Rna Seq Results