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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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Histone-arginine methyltransferase METTL23; Methyltransferase-like protein 23
基因别名: C17orf95; METTL23; MRT44
UniProt ID: (Human) Q86XA0
Entrez Gene ID: (Human) 124512