人 BSCL2 (NM_001122955) cDNA克隆

Accession: NM_001122955
基因名称: BSCL2
基因别名: HMN5; SPG17; GNG3LG
基因描述: Homo sapiens Berardinelli-Seip congenital lipodystrophy 2 (seipin) (BSCL2), transcript variant 1, mRNA.
种属: Human
CDS区长度: 1389 (查看编码区序列)
翻译后氨基酸长度: 462 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longer isoform (1).
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G101648 人 BSCL2 (NM_001122955) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes the multi-pass transmembrane protein protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2).[provided by RefSeq, Mar 2011]