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CPXCR1


Official Full Name
CPX chromosome region candidate 1
Organism
Homo sapiens
Gene ID
53336
Background
This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]
Synonyms
CT77

Cat.No. Product Name Price
SHH269061 shRNA set against Human CPXCR1 (NM_033048.5) Inquiry
SHG197009 shRNA set against Mouse Cpxcr1(NM_001033471.3) Inquiry
SHH269065 shRNA set against Mouse CPXCR1 (NM_001033471.3) Inquiry
Cat.No. Product Name Price
CDFH004207 Human CPXCR1 cDNA Clone(NM_001184771.1) Inquiry
MiUTR1M-03299 CPXCR1 miRNA 3'UTR clone Inquiry
MiUTR4H-TG02328 CPXCR1 miRNA 3'UTR clone Inquiry
CDCB160366 Human CPXCR1 ORF clone (NM_033048.4) Inquiry
CDCB184739 Rabbit CPXCR1 ORF clone (XM_002720257.2) Inquiry
CDCR050350 Mouse Cpxcr1 ORF clone (NM_001033471.3) Inquiry
CDCR357515 Human CPXCR1 ORF Clone(NM_001184771.1) Inquiry
CDCS409132 Human CPXCR1 ORF Clone (BC027614) Inquiry
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