- accession:NM_001141974
- 基因别名:ATP13A2
- 基因描述:Homo sapiens ATPase type 13A2 (ATP13A2), transcript variant 3, mRNA.
- 载体: 现货载体
- CDS区长度:3477
- 翻译后氨基酸长度:1158
- TranscriptVariant:This variant (3) uses an alternate in-frame splice site in the 5' coding region, and lacks two alternate exons in the 3' coding region which results in a frameshift, compared to variant 1. The resulting protein (isoform 3) is shorter and has a distinct C-terminus, compared to isoform 1. The transcript contains an upstream ORF that could encode a 103aa protein and may modulate translation from the downstream ORF encoding isoform 3.
- 基因简介:This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008]
- 载体信息:自有图片地址
- 规格:10ul 质粒
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