TBL1XR1
Information TBL1XR1
- Description
This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. [provided by RefSeq, Mar 2016]
- Full Name
TBL1X receptor 1
Source NCBI
- Species
Homo sapiens [tax_id: 9606]
- Genome
hg38
ReMap Statistics
- Datasets
- 4
- Biotypes
- 3
- Peaks
- 63,194
- Non-redundant peaks
- 49,919
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- NCBI Gene
- 79718
- Official Gene Name
- TBL1XR1
- JASPAR
- Ensembl
- ENSG00000177565
- UniProt
- Q9BZK7
- Genevisible
- Q9BZK7
- RefSeq
- NM_001321193
- Aliases
- C21; DC42; FLJ12894; IRA1; TBLR1
Datasets Table for TBL1XR1
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| TBL1XR1 | K-562 | ENCODE | Homo sapiens | ENCSR000EGB | 18,781 | |||
| TBL1XR1 | K-562 | ENCODE | Homo sapiens | ENCSR000EGA | 9,052 | |||
| TBL1XR1 | Hep-G2 | ENCODE | Homo sapiens | ENCSR101FJS | 33,213 | |||
| TBL1XR1 | GM12878 | ENCODE | Homo sapiens | ENCSR000DYZ | 2,148 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |