ALX homeobox protein 1 is a protein that in humans is encoded by the ALX1 gene.
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].
via MyGene.info
ALX homeobox protein 1 is a protein that in humans is encoded by the ALX1 gene.
== Function ==
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).