BHLHA9

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)
End	1,271,815 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	76,564,502 bp
RNA expression pattern
	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
	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
	727857
	320522
	ENSG00000205899
	ENSMUSG00000044243
	Q7RTU4
	Q5RJB0
	NM_001164405
	NM_177182
	NP_001157877
	NP_796156
	Wikidata
View/Edit Human	View/Edit Mouse

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