Aliases for MYNN Gene
External Ids for MYNN Gene
Previous GeneCards Identifiers for MYNN 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 14. [provided by RefSeq, Jun 2010]
GeneCards Summary for MYNN Gene
MYNN (Myoneurin) is a Protein Coding gene. Diseases associated with MYNN include Cogan-Reese Syndrome. Gene Ontology (GO) annotations related to this gene include DNA-binding transcription factor activity. An important paralog of this gene is ZBTB17.