人 NSD1 (NM_172349) cDNA克隆

Accession: NM_172349
基因名称: NSD1
基因别名: STO; KMT3B; SOTOS; ARA267; SOTOS1
基因描述: Homo sapiens nuclear receptor binding SET domain protein 1 (NSD1), transcript variant 1, mRNA.
种属: Human
CDS区长度: 7284 (查看编码区序列)
翻译后氨基酸长度: 2427 (查看氨基酸序列)
Transcript Variant: This variant (1), also known as ARA267-alpha, differs in the 5' UTR and coding region, compared to variant 2. It encodes a shorter isoform (a), that has a distinct N-terminus compared to isoform b.
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G157875 人 NSD1 (NM_172349) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]