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TMEM216
transmembrane protein 216
gene with protein product
OMIM: 613277
4 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
3
Meckel syndrome
ORPHA:564
→
Joubert syndrome with oculorenal defect
ORPHA:2318
→
Orofaciodigital syndrome type 6
ORPHA:2754
→
Disease-causing germline mutation(s) (loss of function) in
1
Retinitis pigmentosa
ORPHA:791
→
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Редкие заболевания
TMEM216
🧬
TMEM216
transmembrane protein 216
gene with protein product
OMIM: 613277
4 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
3
Meckel syndrome
ORPHA:564
→
Joubert syndrome with oculorenal defect
ORPHA:2318
→
Orofaciodigital syndrome type 6
ORPHA:2754
→
Disease-causing germline mutation(s) (loss of function) in
1
Retinitis pigmentosa
ORPHA:791
→