DISEASES

Disease-gene associations mined from literature

Literature associating HLX and osteogenesis imperfecta type 7

HLX [ENSP00000355870]

H2.0-like homeobox protein; Transcription factor required for TBX21/T-bet-dependent maturation of Th1 cells as well as maintenance of Th1-specific gene expression. Involved in embryogenesis and hematopoiesis (By similarity); Belongs to the H2.0 homeobox family.

Synonyms:  HLX,  F8VWZ5,  Q14774,  F8VWZ5p,  hF8VWZ5 ...

Linkouts:  STRING  Pharos  UniProt  OMIM