ZBTB47 (zinc finger and BTB domain containing 47)

2014-11-01  

Identity

HGNC
LOCATION
3p22.1
LOCUSID
ALIAS
ZNF651

Other Information

Locus ID:

NCBI: 92999
HGNC: 26955
Ensembl: ENSG00000114853

Variants:

dbSNP: 92999
ClinVar: 92999
TCGA: ENSG00000114853
COSMIC: ZBTB47

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000114853ENST00000232974Q9UFB7
ENSG00000114853ENST00000505904D6RDG5

Expression (GTEx)

0
10
20
30
40
50
60
70
80
90
100

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
377437822024De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities.0
377437822024De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities.0
201163762010CBFA2T3-ZNF651, like CBFA2T3-ZNF652, functions as a transcriptional corepressor complex.7
201163762010CBFA2T3-ZNF651, like CBFA2T3-ZNF652, functions as a transcriptional corepressor complex.7

Citation

Dessen P

ZBTB47 (zinc finger and BTB domain containing 47)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/75869/zbtb47-(zinc-finger-and-btb-domain-containing-47)