人 C19orf12 (NM_001282931) cDNA克隆

基本信息

Accession: NM_001282931
基因名称: C19orf12
基因别名: NBIA3; NBIA4; SPG43
基因描述: Homo sapiens chromosome 19 open reading frame 12 (C19orf12), transcript variant 7, mRNA.
种属: Human
CDS区长度: 234 (查看编码区序列)
翻译后氨基酸长度: 77 (查看氨基酸序列)
Transcript Variant: This variant (7) uses an alternate 5' structure and thus differs in the 5' UTR and 5' coding region compared to variant 1. These differences cause translation initiation at a downstream AUG and result in an isoform (4) with a shorter N-terminus, compared to isoform. Variants 5, 6, and 7 encode the same isoform (4).

订购信息

产品编号 产品名称 载体 规格 价格
G117113 人 C19orf12 (NM_001282931) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 C19orf12 (NM_001031726) cDNA克隆 transcript variant 1
人 C19orf12 (NM_031448) cDNA克隆 transcript variant 2
人 C19orf12 (NM_001256046) cDNA克隆 transcript variant 3
人 C19orf12 (NM_001256047) cDNA克隆 transcript variant 4
人 C19orf12 (NM_001282929) cDNA克隆 transcript variant 5
人 C19orf12 (NM_001282930) cDNA克隆 transcript variant 6
人 C19orf12 (NM_001282931) cDNA克隆 transcript variant 7

基因简介

This gene encodes a small transmembrane protein. Mutations in this gene are a cause of neurodegeneration with brain iron accumulation-4 (NBIA4), but the specific function of the encoded protein is unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

相关产品