CC2D1A
Information CC2D1A
- Description
This gene encodes a transcriptional repressor that binds to a conserved 14-bp 5'-repressor element and regulates expression of the 5-hydroxytryptamine (serotonin) receptor 1A gene in neuronal cells. The DNA binding and transcriptional repressor activities of the protein are inhibited by calcium. A mutation in this gene results in a nonsyndromic form of cognitive disability (MRT3). [provided by RefSeq, Jul 2017]
- Full Name
coiled-coil and C2 domain containing 1A
- Source NCBI
ReMap Statistics
- Datasets
- 1
- Biotypes
- 1
- Peaks
- 20,325
- Non-redundant peaks
- 20,325
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- JASPAR
- Ensembl
- ENSG00000132024
- UniProt
- Q6P1N0
- Genevisible
- Q6P1N0
- RefSeq
- NM_017721
- Aliases
- FLJ20241; Freud-1; MRT3
Datasets Table for CC2D1A
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| CC2D1A | K-562 | ENCODE | Homo sapiens | ENCSR343IFJ | 20,325 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |