DISC1 (NM_001164546) Human 3' UTR Clone

Specifications

Product Data
Product Name	DISC1 (NM_001164546) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	C1orf136; SCZD9
ACCN	NM_001164546
Insert Size	666 bp
Sequence Data	Insert Sequence (showhide) >SC208284 3' UTR clone of NM_001164546 The sequence shown below is from the reference sequence of NM_001164546. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC AAACAAGTGTGAAGGAAAATACTATGAAGTACATGGAAACACTTAAGAATAAACTGTGCAGGTAAGGATA ATAATTTCTGTATTTCAGACTCCGTAGCACATCTAGATTCTTTATTATAACAGAATTTAGTTAAATCGAT GAAAAAGGCTGGCCAGTTTCTCTAATAAATTAACAAAGAAAGACACAAAAAAGCCTTTTGAACCCCATCA GTGAAAGAGCAGGTGCCAGCCCTCATCTTGTCTTTTAAAAAGTAAGTAGATTAAGATGTTTAAAAGTGTC TTGGAGAGATCACAGGAGAGTTTTCATGTTCCATAAGAGAAGAATCTTCTTTACTATATTAAATTCAGAA TTCATTCCTTAGTCTGTTTTTCCCTTTTTTAAACTTTAGTGTTTGAGGGGGGTCTTAAGGATTTTAAGGC GGTTTATACATGGTTTGGAATAATATAGAAATGCACGTCTTAGGTTCTGTTTTGAATCCTGAATCAAAAC CAGCATGAAAATTTCTGGTTGCTTTTTTTAAAACCCAATTAGGAATTCATCTTTGAGAAATGTCAGGGAT GCTGCAGCATGACAAGATGTTTCTGGCTTTTGTGGATGTGTGCTTAGGAAAATAAATCCCAGTCATCAGA ATCTGTTCCTAATTAAGGCAACAAGTACTAGAGTGG ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_001164546.1
Synonyms	C1orf136; SCZD9
Summary	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]
Locus ID	27185

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