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MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint for

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MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint forThis gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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Description

The chromosome 22 breakpoint for this translocation is located within the BCR gene (BCR

in the conversion of tyrosine to melanin

Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA receptors

The members of this family are ubiquitously expressed and are generally most abundant in mitochondria-enriched tissues such as heart

It may also be related to the P2Y receptors

MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint forThis gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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