人 MYH14 (NM_024729) cDNA克隆

基本信息

Accession: NM_024729
基因名称: MYH14
基因别名: DFNA4; MHC16; MYH17; PNMHH; DFNA4A; myosin; FP17425; NMHC II-C; NMHC-II-C
基因描述: Homo sapiens myosin, heavy chain 14, non-muscle (MYH14), transcript variant 2, mRNA.
种属: Human
CDS区长度: 5988 (查看编码区序列)
翻译后氨基酸长度: 1995 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks two alternate in-frame exons in the 5' coding region, compared to variant 3. The resulting isoform (2) lacks two separate segments in the motor domain, compared to isoform 3.

订购信息

产品编号 产品名称 载体 规格 价格
G165468 人 MYH14 (NM_024729) 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 MYH14 (NM_001077186) cDNA克隆 transcript variant 1
人 MYH14 (NM_024729) cDNA克隆 transcript variant 2
人 MYH14 (NM_001145809) cDNA克隆 transcript variant 3

基因简介

This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin; it should not be confused with the unconventional myosin-14 (MYO14). Myosins are actin-dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene result in one form of autosomal dominant hearing impairment. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

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