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TMEM237

transmembrane protein 237

gene with protein productOMIM: 6144234 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3
Joubert syndrome with oculorenal defectORPHA:2318
→
Isolated Joubert syndromeORPHA:475
→
Joubert syndrome with renal defectORPHA:220497
→
Disease-causing germline mutation(s) (loss of function) in1
Meckel syndromeORPHA:564
→
Данные: Orphadata (CC-BY-4.0)