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RAB39B
RAB39B, member RAS oncogene family
gene with protein product
OMIM: 300774
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Early-onset parkinsonism-intellectual disability syndrome
ORPHA:2379
→
X-linked non-syndromic intellectual disability
ORPHA:777
→
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Редкие заболевания
RAB39B
🧬
RAB39B
RAB39B, member RAS oncogene family
gene with protein product
OMIM: 300774
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Early-onset parkinsonism-intellectual disability syndrome
ORPHA:2379
→
X-linked non-syndromic intellectual disability
ORPHA:777
→