- accession:NM_016489
- 基因别名:NT5C3A
- 基因描述:Homo sapiens 5'-nucleotidase, cytosolic IIIA (NT5C3A), transcript variant 3, mRNA.
- 载体:现货载体
- CDS区长度:894
- 翻译后氨基酸长度:297
- TranscriptVariant:This variant (3) differs in the 5' UTR, includes an alternate internal exon in the 5' region, and initiates translation at an alternate start codon, compared to variant 1. Variants 2 and 3 encode the same isoform (2), which is shorter and has a distinct N-terminus, compared to isoform 1.
- 基因简介:This gene encodes a member of the 5'-nucleotidase family of enzymes that catalyze the dephosphorylation of nucleoside 5'-monophosphates. The encoded protein is the type 1 isozyme of pyrimidine 5' nucleotidase and catalyzes the dephosphorylation of pyrimidine 5' monophosphates. Mutations in this gene are a cause of hemolytic anemia due to uridine 5-prime monophosphate hydrolase deficiency. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and pseudogenes of this gene are located on the long arm of chromosomes 3 and 4. [provided by RefSeq, Mar 2012]
- 规格:10ul 质粒
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