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MNX1

Official Full Name
motor neuron and pancreas homeobox 1
Organism
Homo sapiens
GeneID
3110
Background
This 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. [provided by RefSeq, Sep 2009]
Synonyms
HB9; HLXB9; SCRA1; HOXHB9;

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