人 WBSCR16 (NM_148842) cDNA克隆

Accession: NM_148842
基因名称: WBSCR16
基因描述: Homo sapiens Williams-Beuren syndrome chromosome region 16 (WBSCR16), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1365 (查看编码区序列)
翻译后氨基酸长度: 454 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks the 3' coding exon and contains an alternate 3' exon, resulting in a distinct 3' coding region and 3' UTR, compared to variant 1. The encoded isoform (2) is shorter and has a distinct C-terminus, compared to isoform 1.
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G165927 人 WBSCR16 (NM_148842) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a protein containing regulator of chromosome condensation 1-like repeats. The encoded protein may function as a guanine nucleotide exchange factor. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]