人 ALPL (NM_001127501) cDNA克隆

Accession: NM_001127501
基因名称: ALPL
基因别名: HOPS; TNAP; APTNAP; TNSALP; AP-TNAP
基因描述: Homo sapiens alkaline phosphatase, liver/bone/kidney (ALPL), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1410 (查看编码区序列)
翻译后氨基酸长度: 469 (查看氨基酸序列)
Transcript Variant: This variant (2) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (2) is shorter than isoform 1.
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G122073 人 ALPL (NM_001127501) cDNA克隆 pDONR223 2ug质粒 点击询价

There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. The exact physiological function of the alkaline phosphatases is not known. A proposed function of this form of the enzyme is matrix mineralization; however, mice that lack a functional form of this enzyme show normal skeletal development. This enzyme has been linked directly to hypophosphatasia, a disorder that is characterized by hypercalcemia and includes skeletal defects. The character of this disorder can vary, however, depending on the specific mutation since this determines age of onset and severity of symptoms. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]