人 PHF6 (NM_032458) cDNA克隆

Accession: NM_032458
基因名称: PHF6
基因别名: BFLS; BORJ; CENP-31
基因描述: Homo sapiens PHD finger protein 6 (PHF6), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1098 (查看编码区序列)
翻译后氨基酸长度: 365 (查看氨基酸序列)
Transcript Variant: This variant (2, also called the 'PHF6b' variant) differs in the 3' UTR compared to variant 1. Both variants 1 and 2 encode the same isoform (1).
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G121603 人 PHF6 (NM_032458) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by mental retardation, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010]