BHLHA9
Identifiers
Aliases	BHLHA9, BHLHF42, basic helix-loop-helix family member a9, CCSPD
External IDs	OMIM: 615416 MGI: 2444198 HomoloGene: 82363 GeneCards: BHLHA9
Gene location (Human) Chr. Chromosome 17 (human)[1] Band 17p13.3 Start 1,270,444 bp[1] End 1,271,815 bp[1]
Gene location (Mouse) Chr. Chromosome 11 (mouse)[2] Band 11|11 B5 Start 76,563,296 bp[2] End 76,564,502 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in Brodmann area 9 prefrontal cortex superior frontal gyrus hypothalamus temporal lobe amygdala hippocampus proper liver right lobe of liver substantia nigra Top expressed in spinal ganglia lip female urethra skin of limb autopod skin skin of abdomen skin of back abdominal wall superior frontal gyrus hippocampus proper More reference expression data BioGPS n/a
Gene ontology Molecular function DNA binding protein binding protein dimerization activity protein heterodimerization activity DNA-binding transcription factor activity, RNA polymerase II-specific Cellular component cytoplasm nucleus Biological process multicellular organism development regulation of transcription, DNA-templated transcription, DNA-templated regulation of transcription by RNA polymerase II Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 727857 320522 Ensembl ENSG00000205899 ENSMUSG00000044243 UniProt Q7RTU4 Q5RJB0 RefSeq (mRNA) NM_001164405 NM_177182 RefSeq (protein) NP_001157877 NP_796156 Location (UCSC) Chr 17: 1.27 – 1.27 Mb Chr 11: 76.56 – 76.56 Mb PubMed search [3] [4]
Wikidata
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Basic helix-loop-helix family, member a9 is a protein in humans that is encoded by the BHLHA9 gene.^[5]