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KIF1B

kinesin family member 1B

gene with protein productOMIM: 6059952 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in2
Hereditary pheochromocytoma-paragangliomaORPHA:29072
→
Autosomal dominant Charcot-Marie-Tooth disease type 2A1ORPHA:99946
→
Данные: Orphadata (CC-BY-4.0)