ZNF687
Information ZNF687
- Description
This gene encodes C2H2 zinc finger protein. The encoded protein may play a role in bone differentiation and development. Mutations in this gene are the cause of Paget disease of bone-6. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]
- Full Name
zinc finger protein 687
Source NCBI
- Species
Homo sapiens [tax_id: 9606]
- Genome
hg38
ReMap Statistics
- Datasets
- 2
- Biotypes
- 2
- Peaks
- 51,335
- Non-redundant peaks
- 46,610
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- NCBI Gene
- 57592
- Official Gene Name
- ZNF687
- JASPAR
- Ensembl
- ENSG00000143373
- UniProt
- Q8N1G0
- Genevisible
- Q8N1G0
- RefSeq
- NM_001304763
- Aliases
- KIAA1441
Datasets Table for ZNF687
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| ZNF687 | MCF-7 | ENCODE | Homo sapiens | ENCSR899BKM | 24,653 | |||
| ZNF687 | GM12878 | ENCODE | Homo sapiens | ENCSR859FDL | 26,682 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |