人 OTX2 (NM_021728) cDNA克隆

Accession: NM_021728
基因名称: OTX2
基因别名: CPHD6; MCOPS5
基因描述: Homo sapiens orthodenticle homeobox 2 (OTX2), transcript variant 1, mRNA.
种属: Human
CDS区长度: 894 (查看编码区序列)
翻译后氨基酸长度: 297 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longer isoform (a). Variants 1 and 5 encode the same protein (isoform a).
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G100201 人 OTX2 (NM_021728) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a member of the bicoid subfamily of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and plays a role in brain, craniofacial, and sensory organ development. The encoded protein also influences the proliferation and differentiation of dopaminergic neuronal progenitor cells during mitosis. Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6). This gene is also suspected of having an oncogenic role in medulloblastoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Pseudogenes of this gene are known to exist on chromosomes two and nine. [provided by RefSeq, Jul 2012]