MYNN (myoneurin)
| Gene | |
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
55892 |
|
Gene name
Gene Name - the full gene name approved by the HGNC.
|
Myoneurin |
|
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
MYNN |
|
Synonyms (NCBI Gene)
Gene synonyms aliases
|
OSZF, SBBIZ1, ZBTB31, ZNF902 |
|
Chromosome
Chromosome number
|
3 |
|
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
3q26.2 |
|
Summary
Summary of gene provided in NCBI Entrez Gene.
|
This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome |
|
miRNA
miRNA information provided by mirtarbase database.
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|||||||
|
|||||||
| Protein | ||||||||||||||||||||||||||||||||||||||||||||||
| UniProt ID | Q9NPC7 | |||||||||||||||||||||||||||||||||||||||||||||
| Protein name | Myoneurin (Zinc finger and BTB domain-containing protein 31) | |||||||||||||||||||||||||||||||||||||||||||||
| PDB | 2VPK | |||||||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
|
|||||||||||||||||||||||||||||||||||||||||||||
| Tissue specificity | TISSUE SPECIFICITY: Mainly expressed in the neuromuscular system. Located in and around synaptic myonuclei in adult muscle. Expression is dysregulated after nerve injury. Also found in the testis, ovary and placenta. {ECO:0000269|PubMed:10873615, ECO:0000 | |||||||||||||||||||||||||||||||||||||||||||||
| Sequence |
|
|||||||||||||||||||||||||||||||||||||||||||||
| Sequence length | 610 | |||||||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||||||||||||||||||||||
|
Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
|
|||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||