人 DYX1C1 (NM_001033559) cDNA克隆

Accession: NM_001033559
基因名称: DYX1C1
基因别名: RD; DYX1; EKN1; DYXC1; CILD25
基因描述: Homo sapiens dyslexia susceptibility 1 candidate 1 (DYX1C1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1131 (查看编码区序列)
翻译后氨基酸长度: 376 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an alternate exon that causes a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (b) has a distinct and shorter C-terminus, compared to isoform a.
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G117421 人 DYX1C1 (NM_001033559) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene. [provided by RefSeq, Mar 2011]