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CTNNB1

catenin beta 1

gene with protein productOMIM: 11680612 заболеваний
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Соматическая мутация (причина)5
Adrenocortical carcinomaORPHA:1501
→
Desmoid tumorORPHA:873
→
CraniopharyngiomaORPHA:54595
→
PilomatrixomaORPHA:91414
→
Adenoid ameloblastomaORPHA:689430
→
Ген-кандидат3
Adult hepatocellular carcinomaORPHA:210159
→
Microcystic stromal tumorORPHA:569248
→
Pediatric hepatocellular carcinomaORPHA:33402
→
Disease-causing germline mutation(s) (gain of function) in2
Acrofacial dysostosis, Weyers typeORPHA:952
→
Osteopathia striata-cranial sclerosis syndromeORPHA:2780
→
Disease-causing germline mutation(s) (loss of function) in1
Familial exudative vitreoretinopathyORPHA:891
→
Герминативная мутация (причина)1
Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndromeORPHA:404473
→
Данные: Orphadata (CC-BY-4.0)