人 DISC1 (NM_001164537) cDNA克隆

基本信息

Accession: NM_001164537
基因名称: DISC1
基因别名: SCZD9; C1orf136
基因描述: Homo sapiens disrupted in schizophrenia 1 (DISC1), transcript variant a, mRNA.
种属: Human
CDS区长度: 2661 (查看编码区序列)
翻译后氨基酸长度: 886 (查看氨基酸序列)
Transcript Variant: This variant (a) has an additional exon in the 5' coding region, as compared to variant L. The reading frame is not changed, but the resulting isoform (a, also known as isoform 8) is longer than isoform L.

订购信息

产品编号 产品名称 载体 规格 价格
G145054 人 DISC1 (NM_001164537) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 DISC1 (NM_001164537) cDNA克隆 transcript variant a
人 DISC1 (NM_001164538) cDNA克隆 transcript variant b
人 DISC1 (NM_001164539) cDNA克隆 transcript variant c
人 DISC1 (NM_001164540) cDNA克隆 transcript variant d
人 DISC1 (NM_001164541) cDNA克隆 transcript variant e
人 DISC1 (NM_001012958) cDNA克隆 transcript variant Es
人 DISC1 (NM_001164542) cDNA克隆 transcript variant f
人 DISC1 (NM_001164544) cDNA克隆 transcript variant g
人 DISC1 (NM_001164545) cDNA克隆 transcript variant h
人 DISC1 (NM_001164546) cDNA克隆 transcript variant i
人 DISC1 (NM_001164547) cDNA克隆 transcript variant j
人 DISC1 (NM_001164548) cDNA克隆 transcript variant k
人 DISC1 (NM_001164549) cDNA克隆 transcript variant l
人 DISC1 (NM_018662) cDNA克隆 transcript variant L
人 DISC1 (NM_001012957) cDNA克隆 transcript variant Lv
人 DISC1 (NM_001164550) cDNA克隆 transcript variant m
人 DISC1 (NM_001164551) cDNA克隆 transcript variant n
人 DISC1 (NM_001164552) cDNA克隆 transcript variant o
人 DISC1 (NM_001164553) cDNA克隆 transcript variant p
人 DISC1 (NM_001164554) cDNA克隆 transcript variant q
人 DISC1 (NM_001164555) cDNA克隆 transcript variant r
人 DISC1 (NM_001012959) cDNA克隆 transcript variant S
人 DISC1 (NM_001164556) cDNA克隆 transcript variant t

基因简介

This gene encodes a protein with multiple coiled coil motifs which is located in the nucleus, cytoplasm and mitochondria. The protein is involved in neurite outgrowth and cortical development through its interaction with other proteins. This gene is disrupted in a t(1;11)(q42.1;q14.3) translocation which segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

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