人 ASPH (NM_001164755) cDNA克隆

Accession: NM_001164755
基因名称: ASPH
基因别名: AAH; BAH; HAAH; JCTN; junctin; CASQ2BP1
基因描述: Homo sapiens aspartate beta-hydroxylase (ASPH), transcript variant 11, mRNA.
种属: Human
CDS区长度: 813 (查看编码区序列)
翻译后氨基酸长度: 270 (查看氨基酸序列)
Transcript Variant: This variant (11) lacks an alternate in-frame exon and uses a distinct 3' splice pattern that lacks many coding exons, compared to variant 1. The resulting isoform (k) lacks an internal segment and has a substantially shorter and distinct C-terminus, compared to isoform a.
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G115854 人 ASPH (NM_001164755) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene is thought to play an important role in calcium homeostasis. The gene is expressed from two promoters and undergoes extensive alternative splicing. The encoded set of proteins share varying amounts of overlap near their N-termini but have substantial variations in their C-terminal domains resulting in distinct functional properties. The longest isoforms (a and f) include a C-terminal Aspartyl/Asparaginyl beta-hydroxylase domain that hydroxylates aspartic acid or asparagine residues in the epidermal growth factor (EGF)-like domains of some proteins, including protein C, coagulation factors VII, IX, and X, and the complement factors C1R and C1S. Other isoforms differ primarily in the C-terminal sequence and lack the hydroxylase domain, and some have been localized to the endoplasmic and sarcoplasmic reticulum. Some of these isoforms are found in complexes with calsequestrin, triadin, and the ryanodine receptor, and have been shown to regulate calcium release from the sarcoplasmic reticulum. Some isoforms have been implicated in metastasis. [provided by RefSeq, Sep 2009]