G2Cdb::Human Disease report

Disease id
D00000102
Name
Paediatric acute myeloid leukaemia
Nervous system disease
no

Genes (1)

Gene Name/Description Mutations Found Literature Mutations Type Genetic association?
G00001453 PTPN11
protein tyrosine phosphatase, non-receptor type 11
Y (16115145) Unknown (?) ?

References

  • Differences in the prevalence of PTPN11 mutations in FAB M5 paediatric acute myeloid leukaemia.

    Goemans BF, Zwaan CM, Martinelli S, Harrell P, de Lange D, Carta C, Reinhardt D, Hählen K, Creutzig U, Tartaglia M, Heinrich MC and Kaspers GJ

    British journal of haematology 2005;130;5;801-3

Literature (1)

Pubmed - human_disease

  • Differences in the prevalence of PTPN11 mutations in FAB M5 paediatric acute myeloid leukaemia.

    Goemans BF, Zwaan CM, Martinelli S, Harrell P, de Lange D, Carta C, Reinhardt D, Hählen K, Creutzig U, Tartaglia M, Heinrich MC and Kaspers GJ

    British journal of haematology 2005;130;5;801-3

© G2C 2014. The Genes to Cognition Programme received funding from The Wellcome Trust and the EU FP7 Framework Programmes:
EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).

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