Rare diseases are those that affect only a small percentage of the world’s population. Most rare diseases are genetic. We provide many gene-engineered mouse models which are helpful for new therapies exploration and orphan drug development.
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系統名：FVB-Abcb4em1Smoc
維持形態：Repository Live | SMOC番号：NM-KO-200584
病気の予測：cholecystitis, cholestasis, hepatocellular carcinoma, intrahepatic cholestasis, primary sclerosing cholangitis
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系統名：C57BL/6Smoc-Abcd1em1Smoc
維持形態：Sperm cryopreservation | SMOC番号：NM-KO-2106014
病気の予測：adrenoleukodystrophy
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系統名：C57BL/6Smoc-Abcg2em1Smoc
維持形態：Repository Live | SMOC番号：NM-KO-18013
病気の予測：erythropoietic protoporphyria, hyperuricemia
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系統名：C57BL/6Smoc-Abcg8em1Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KO-200906
病気の予測：sitosterolemia
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系統名：C57BL/6Smoc-Acadlem1Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KO-201235
病気の予測：very long chain acyl-CoA dehydrogenase deficiency
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系統名：C57BL/6Smoc-Acadmem1(E8-10 repeat)Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KI-200239
病気の予測：medium chain acyl-CoA dehydrogenase deficiency
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系統名：C57BL/6Smoc-Acadvlem1Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KO-200908
病気の予測：very long chain acyl-CoA dehydrogenase deficiency
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系統名：C57BL/6Smoc-Adh7em1Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KO-201121
病気の予測：Parkinson's disease
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系統名：C57BL/6Smoc-Agxtem1Smoc
維持形態：Repository Live | SMOC番号：NM-KO-210152
病気の予測：primary hyperoxaluria type 1
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