BHLHA9

Basic helix-loop-helix family, member a9 is a protein in humans that is encoded by the BHLHA9 gene.^[5]

BHLHA9
Identifiers
Aliases	BHLHA9, BHLHF42, basic helix-loop-helix family member a9, CCSPD
External IDs	OMIM: 615416; MGI: 2444198; HomoloGene: 82363; GeneCards: BHLHA9; OMA:BHLHA9 - orthologs
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 gonad Brodmann area 9 prefrontal cortex right frontal lobe primary visual cortex superior frontal gyrus anterior cingulate cortex hypothalamus temporal lobe amygdala Top expressed in spinal ganglia lip female urethra embryo embryo dentate gyrus of hippocampal formation granule cell tail of embryo skin of limb autopod skin skin of abdomen 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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