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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| METTL23-20-RE | 20 (40 μL) | 200 μL |  |
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| METTL23-20-OR | 20 (40 μL) | 200 μL |  |
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| METTL23-20-GO | 20 (40 μL) | 200 μL |  |
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| METTL23-20-GR | 20 (40 μL) | 200 μL |  |
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| METTL23-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : METTL23
Gene Name : Methyltransferase like 23
Chromosome : CHR 17: 767,258,73-767,338,80
Locus : 17q25.1
Alt. Genes : CTDSP2
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