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KIF1B
kinesin family member 1B
gene with protein product
OMIM: 605995
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Hereditary pheochromocytoma-paraganglioma
ORPHA:29072
→
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
ORPHA:99946
→
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Редкие заболевания
KIF1B
🧬
KIF1B
kinesin family member 1B
gene with protein product
OMIM: 605995
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Hereditary pheochromocytoma-paraganglioma
ORPHA:29072
→
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
ORPHA:99946
→