- accession:NM_001171617
- 基因别名:PREPL
- 基因描述:Homo sapiens prolyl endopeptidase-like (PREPL), transcript variant 7, mRNA.
- 载体:现货载体
- CDS区长度:1917
- 翻译后氨基酸长度:638
- TranscriptVariant:This variant (7, also known as variant B) contains an alternate exon at the 5' end compared to variant 1, resulting in translation initiation from an in-frame downstream AUG and a shorter isoform (4) compared to isoform 1. Variants 6 and 7 encode the same isoform.
- 基因简介:The protein encoded by this gene belongs to the prolyl oligopeptidase subfamily of serine peptidases. Mutations in this gene have been associated with hypotonia-cystinuria syndrome, also known as the 2p21 deletion syndrome. Several alternatively spliced transcript variants encoding either the same or different isoforms have been described for this gene.[provided by RefSeq, Jan 2010]
- 规格:10ul 质粒
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