人 XPNPEP3 (NM_022098) cDNA克隆

Accession: NM_022098
基因名称: XPNPEP3
基因别名: APP3; NPHPL1
基因描述: Homo sapiens X-prolyl aminopeptidase (aminopeptidase P) 3, putative (XPNPEP3), transcript variant 1, mRNA.
种属: Human
CDS区长度: 1524 (查看编码区序列)
翻译后氨基酸长度: 507 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1, also known as APP3m). This isoform has been shown to be localized to the mitochondria (PMID:20179356).
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G102189 人 XPNPEP3 (NM_022098) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene belongs to the family of X-pro-aminopeptidases that utilize a metal cofactor, and remove the N-terminal amino acid from peptides with a proline residue in the penultimate position. This protein has been shown to localize to the mitochondria of renal cells, and have a role in ciliary function. Mutations in this gene are associated with nephronophthisis-like nephropathy-1. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene, however, expression of some of these isoforms in vivo is not known.[provided by RefSeq, Mar 2011]