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SIN3B
SIN3 transcription regulator family member B
gene with protein product
OMIM: 607777
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
SIN3-related intellectual disability syndrome due to a point mutation
ORPHA:500166
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Редкие заболевания
SIN3B
🧬
SIN3B
SIN3 transcription regulator family member B
gene with protein product
OMIM: 607777
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
SIN3-related intellectual disability syndrome due to a point mutation
ORPHA:500166
→