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ALX1

Official Full Name
ALX homeobox 1
Organism
Homo sapiens
GeneID
8092
Background
The specific function of this gene has yet to be determined in humans; however, in rodents, it is necessary for survival of the forebrain mesenchyme and may also be involved in development of the cervix. Mutations in the mouse gene lead to neural tube defects such as acrania and meroanencephaly. [provided by RefSeq, Jul 2008]
Synonyms
FND3; CART1; HEL23;

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