人 KCNJ13 (NM_001172417) cDNA克隆

基本信息

Accession: NM_001172417
基因名称: KCNJ13
基因别名: SVD; LCA16; KIR1.4; KIR7.1
基因描述: Homo sapiens potassium inwardly-rectifying channel, subfamily J, member 13 (KCNJ13), transcript variant 3, mRNA.
种属: Human
CDS区长度: 843 (查看编码区序列)
翻译后氨基酸长度: 280 (查看氨基酸序列)
Transcript Variant: This variant (3) uses an alternate splice site in the 5' UTR and uses a downstream start codon, compared to variant 1. It encodes isoform 3, which has a shorter N-terminus, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G106159 人 KCNJ13 (NM_001172417) 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 KCNJ13 (NM_002242) cDNA克隆 transcript variant 1
人 KCNJ13 (NM_001172416) cDNA克隆 transcript variant 2
人 KCNJ13 (NM_001172417) cDNA克隆 transcript variant 3

基因简介

This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]

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