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CPXCR1
CPX chromosome region candidate 1CT77
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]
Top validated antibodies |
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| LSBio |  LS-C399590 |
Polyclonal |
WB
EL
IHC
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| Biorbyt | orb2104 |
Polyclonal |
WB
EL
ICC
IHC
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| Invitrogen Antibodies | 26005-1-AP |
Polyclonal |
WB
IP
OA
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| NovoPro Bioscience Inc. | 109534 |
Polyclonal |
WB
EL
IP
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| Proteintech Group | 26005-1-AP |
Polyclonal |
WB
EL
IP
|
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