VEZF1 (vascular endothelial zinc finger 1)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 7716 |
| Gene name | Vascular endothelial zinc finger 1 |
| Gene symbol | VEZF1 |
| Synonyms (NCBI Gene) |
CMD1OODB1ZNF161
|
| Chromosome | 17 |
| Chromosome location | 17q22 |
| Summary | Transcriptional regulatory proteins containing tandemly repeated zinc finger domains are thought to be involved in both normal and abnormal cellular proliferation and differentiation. ZNF161 is a C2H2-type zinc finger protein (Koyano-Nakagawa et al., 1994 |
|
miRNA
miRNA information provided by mirtarbase database.
994
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Protein
Protein information from UniProt database.
|
||||||||||||||||||||||||||
|
UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
|
Q14119 | |||||||||||||||||||||||||
| Protein name | Vascular endothelial zinc finger 1 (Putative transcription factor DB1) (Zinc finger protein 161) | |||||||||||||||||||||||||
| Protein function | Possible transcription factor. Specifically binds to the CT/GC-rich region of the interleukin-3 promoter and mediates tax transactivation of IL-3. | |||||||||||||||||||||||||
| Family and domains |
Pfam
|
|||||||||||||||||||||||||
| Tissue specificity | TISSUE SPECIFICITY: Ubiquitously expressed. Highest levels in skeletal muscle and kidney. {ECO:0000269|PubMed:8035792}. | |||||||||||||||||||||||||
| Sequence |
|
|||||||||||||||||||||||||
| Sequence length | 521 | |||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||
|
Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
8
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||