BTBD9

BTBD9
Identifiers
AliasesBTBD9, dJ322I12.1, BTB domain containing 9
External IDsOMIM: 611237; MGI: 1916625; HomoloGene: 14995; GeneCards: BTBD9; OMA:BTBD9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

114781

224671

Ensembl

ENSG00000183826

ENSMUSG00000062202

UniProt

Q96Q07

Q8C726

RefSeq (mRNA)

NM_001099272
NM_001172418
NM_052893
NM_152733

NM_027060
NM_172618

RefSeq (protein)

NP_001092742
NP_001165889
NP_443125
NP_689946

NP_081336
NP_766206

Location (UCSC)Chr 6: 38.17 – 38.64 MbChr 17: 30.43 – 30.8 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

BTB domain containing 9 is a protein that in humans is encoded by the BTBD9 gene.

BTBD9 is in a subgroup of BTB(POZ) proteins, which contribute to the forming of limbs and determination of cell fate in developing Drosophila melanogaster. BTB(POZ) proteins also play a role in cellular functions such as: cytoskeleton regulation, transcription regulation, the gating and assembly of ion channels, and ubiquitination of proteins. BTBD9 is highly expressed throughout the brain and shows variable levels of expression in most other body tissues.

The gene is located on the short arm of chromosome 6 and the domain contains eight exons and seven introns. The chromosome 6 locational domain that codes for BTB(POZ) proteins is understood to contain genes encoding protein-protein interactions. BTBD9 is a protein located in cellular cytosol and also expressed within Human embryonic kidney cell lineages. There is also evidence suggesting that BTBD9 is highly expressed within the human nervous system from comparison analysis to Drosophila and human cell studies.