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CHRDL1 Monoclonal Antibody, 50ul Custom DNA Oligos Mutations in this gene cause

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CHRDL1 Monoclonal Antibody, 50ul Custom DNA Oligos Mutations in this gene causeThis gene encodes an antagonist of bone morphogenetic protein 4. The encoded protein may play a role in topographic retinotectal projection and in the regulation of retinal angiogenesis in response to hypoxia. Alternatively spliced transcript variants encoding different isoforms have been described.

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Description

Mutations in this gene cause cerebellar ataxia in humans

ZNF691 (Zinc Finger Protein 691) is a Protein Coding gene

chromatin structure and gene expression

is present in 3 forms with respect to ability to bind interleukin 2

The protein encoded by CNTNAP3 may play a role in cell recognition within the nervous system

CHRDL1 Monoclonal Antibody, 50ul Custom DNA Oligos Mutations in this gene causeThis gene encodes an antagonist of bone morphogenetic protein 4. The encoded protein may play a role in topographic retinotectal projection and in the regulation of retinal angiogenesis in response to hypoxia. Alternatively spliced transcript variants encoding different isoforms have been described.

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