STAT3 — signal transducer and activator of transcription 3 | MEDLIB

gene with protein productOMIM: 1025827 заболеваний

GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)2

Autosomal dominant hyper-IgE syndrome due to STAT3 deficiencyORPHA:2314

Chronic lymphoproliferative disorder of natural killer cellsORPHA:512017

Disease-causing germline mutation(s) (gain of function) in2

STAT3-related early-onset multisystem autoimmune diseaseORPHA:438159

Isolated permanent neonatal diabetes mellitusORPHA:99885

Часть слитого гена2

Acute promyelocytic leukemiaORPHA:520

Breast implant-associated anaplastic large cell lymphomaORPHA:667662

Соматическая мутация (причина)2

T-cell large granular lymphocyte leukemiaORPHA:86872

Breast implant-associated anaplastic large cell lymphomaORPHA:667662

gene with protein productOMIM: 1025827 заболеваний

GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)2

Autosomal dominant hyper-IgE syndrome due to STAT3 deficiencyORPHA:2314

Chronic lymphoproliferative disorder of natural killer cellsORPHA:512017

Disease-causing germline mutation(s) (gain of function) in2

STAT3-related early-onset multisystem autoimmune diseaseORPHA:438159

Isolated permanent neonatal diabetes mellitusORPHA:99885

Часть слитого гена2

Acute promyelocytic leukemiaORPHA:520

Breast implant-associated anaplastic large cell lymphomaORPHA:667662

Соматическая мутация (причина)2

T-cell large granular lymphocyte leukemiaORPHA:86872

Breast implant-associated anaplastic large cell lymphomaORPHA:667662