ZBTB42
Information ZBTB42
- Description
The protein encoded by this gene is a member of the C2H2 zinc finger protein family. This protein is predicted to have a pox virus and zinc finger (POZ) domain at the N-terminus and four zinc finger domains at the C-terminus. In human and mouse, the protein localizes to the nuclei of skeletal muscle cells. Knockdown of this gene in zebrafish results in abnormal skeletal muscle development and myofibrillar disorganization. A novel homozygous variant of the human gene has been associated with lethal congenital contracture syndrome, an autosomal recessive disorder that results in muscle wasting. [provided by RefSeq, Mar 2015]
- Full Name
zinc finger and BTB domain containing 42
Source NCBI
- Species
Homo sapiens [tax_id: 9606]
- Genome
hg38
ReMap Statistics
- Datasets
- 1
- Biotypes
- 1
- Peaks
- 31,434
- Non-redundant peaks
- 31,434
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- NCBI Gene
- 100128927
- Official Gene Name
- ZBTB42
- JASPAR
- Ensembl
- ENSG00000179627
- UniProt
- B2RXF5
- Genevisible
- B2RXF5
- RefSeq
- NM_001137601
- Aliases
- AL590327.1; ZNF925