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UGT1A1
UDP glucuronosyltransferase family 1 member A1
Disorder-associated locus
OMIM: 191740
3 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Crigler-Najjar syndrome type 1
ORPHA:79234
→
Crigler-Najjar syndrome type 2
ORPHA:79235
→
Ген-кандидат
1
Transient familial neonatal hyperbilirubinemia
ORPHA:2312
→
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Редкие заболевания
UGT1A1
🧬
UGT1A1
UDP glucuronosyltransferase family 1 member A1
Disorder-associated locus
OMIM: 191740
3 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
2
Crigler-Najjar syndrome type 1
ORPHA:79234
→
Crigler-Najjar syndrome type 2
ORPHA:79235
→
Ген-кандидат
1
Transient familial neonatal hyperbilirubinemia
ORPHA:2312
→