VGLL2 (vestigial like family member 2)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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245806 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Vestigial like family member 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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VGLL2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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VGL2, VITO1 |
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Chromosome
Chromosome number
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6 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6q22.1 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a protein with a transcriptional enhancer factor 1 (TEF-1) interaction domain. The encoded protein may act as a co-factor of TEF-1 regulated gene expression during skeletal muscle development. Alternatively spliced transcript variants en |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||
| UniProt ID | Q8N8G2 | ||||||||||
| Protein name | Transcription cofactor vestigial-like protein 2 (Vgl-2) (Protein VITO1) | ||||||||||
| Protein function | May act as a specific coactivator for the mammalian TEFs. May play a role in the development of skeletal muscles. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Skeletal muscle. {ECO:0000269|PubMed:12617818}. | ||||||||||
| Sequence |
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| Sequence length | 317 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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