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LYL1

Involvement in disease

A chromosomal aberration involving LYL1 may be a cause of a form of T-cell acute lymphoblastic leukemia (T-ALL). Translocation t(7;19)(q35;p13) with TCRB.

Cellular localization

Alternative names

BHLHA18, LYL1, Protein lyl-1, Class A basic helix-loop-helix protein 18, Lymphoblastic leukemia-derived sequence 1, bHLHa18

swissprot:P12980 entrezGene:4066 omim:151440