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chromosomal translocation t(8;11)(p11.2;p15) (childhood acute myeloid leukemia)
chromosomal translocation t(8;11)(p11.2;p15) involving WHSC1L1 with NUP98 found in childhood acute myeloid leukemia
Properties
GENERAL: chromosomal translocation
FORM: t8p11.2:11p15
LOCUS: human chromosome-8 P11.2
human chromosome-11 P15
PATHOLOGY: acute leukemia
ABERRANT-GENE: WHSC1L1P
nucleoporin Nup98
COMPARTMENT: cell nucleus
MOTIF: calponin homology domain
NAME: calponin homology domain
SITE: 7-480
glutamate residue {890-894} (5)
References
UniProt :accession Q9BZ95