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Mirror-image polydactyly gene 1 protein

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Below are the list of possible Mirror-image polydactyly gene 1 protein products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Mirror-image polydactyly gene 1 protein

 Mirror-image polydactyly gene 1 protein ELISA Kit
 Mirror-image polydactyly gene 1 protein Recombinant
 Mirror-image polydactyly gene 1 protein Antibody
MIPOL1: A chromosomal aberration involving MIPOL1 is found in a patient with mirror-image polydactyly of hands and feet without other anomalies (MIP). Translocation t(2;14)(p23.3;q13). MIP is a very rare congenital anomaly characterized by mirror- image duplication of digits. MIP is occasionally associated with dimelia of the ulna and fibula, tibial and/or fibular hypoplasia, nasal abnormality and
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other malformations. Most MIP cases are sporadic, but very rare parent-child transmissions observed in familial cases suggest an autosomal mode of inheritance. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Unknown function

Chromosomal Location of Human Ortholog: 14q13.3

Cellular Component: nucleus

Molecular Function: identical protein binding; protein binding

Disease: Laurin-sandrow Syndrome
 MIPOL1 ELISA Kit
 MIPOL1 Recombinant
 MIPOL1 Antibody
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Mirror-image polydactyly gene 1 protein homolog

 Mirror-image polydactyly gene 1 protein homolog ELISA Kit
 Mirror-image polydactyly gene 1 protein homolog Recombinant
 Mirror-image polydactyly gene 1 protein homolog Antibody
MIPOL1: A chromosomal aberration involving MIPOL1 is found in a patient with mirror-image polydactyly of hands and feet without other anomalies (MIP). Translocation t(2;14)(p23.3;q13). MIP is a very rare congenital anomaly characterized by mirror- image duplication of digits. MIP is occasionally associated with dimelia of the ulna and fibula, tibial and/or fibular hypoplasia, nasal abnormality and
>>>
other malformations. Most MIP cases are sporadic, but very rare parent-child transmissions observed in familial cases suggest an autosomal mode of inheritance. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Unknown function

Cellular Component: nucleus
 Mipol1 ELISA Kit
 Mipol1 Recombinant
 Mipol1 Antibody
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