Aliases for METTL23 Gene
External Ids for METTL23 Gene
Previous HGNC Symbols for METTL23 Gene
Previous GeneCards Identifiers for METTL23 Gene
The protein encoded by this gene functions as a transcription factor regulator in the transcriptional pathway for human cognition. It is a partner of the alpha subunit of the GA-binding protein transcription factor. Mutations in this gene cause mild autosomal recessive intellectual disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]
GeneCards Summary for METTL23 Gene
METTL23 (Methyltransferase Like 23) is a Protein Coding gene. Diseases associated with METTL23 include Mental Retardation, Autosomal Recessive 44 and Autosomal Recessive Non-Syndromic Intellectual Disability. Gene Ontology (GO) annotations related to this gene include methyltransferase activity. An important paralog of this gene is METTL21C.
UniProtKB/Swiss-Prot Summary for METTL23 Gene