HLXB9
MIM.142994 7q36
Homeobox gene.
germline mutations in the HLXB9 gene
- in type IV form of caudal regression syndromes (CRS) characterized by hemisacrum (some cases of Currarino syndrome)
HLXB9-ETV6 fusion protein by t(7;12)(q36;p13) in infant acute myeloid leukemia (#11454678#, #12939747#)
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