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：C57BL/6Smoc-Tsc1tm1(flox)Smoc
維持形態：Repository Live | SMOC番号：NM-CKO-200231
病気の予測：tuberous sclerosis, autism spectrum disorder, anterior segment dysgenesis
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系統名：C57BL/6Smoc-Tsc2tm1(flox)Smoc
維持形態：Sperm cryopreservation | SMOC番号：NM-CKO-2102032
病気の予測：uterine fibroid, tuberous sclerosis
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系統名：C57BL/6Smoc-Tubb4Aem1Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KO-191131
応用分野：Low myelinated leukocyte dystrophy 6, autosomal dominant tonic dystonia 4,
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系統名：C57BL/6Smoc-Ube3aem1Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KO-200599
病気の予測：Angelman syndrome
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系統名：C57BL/6Smoc-Uoxem1Smoc
維持形態：Repository Live | SMOC番号：NM-KO-191205
病気の予測：nephrogenic diabetes insipidus
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系統名：C57BL/6Smoc-Usp1em1(flox)Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-CKO-200052
病気の予測：Fanconi anemia complementation group D2
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系統名：C57BL/6Smoc-Wasem1Smoc
維持形態：Developing | SMOC番号：NM-KO-190725
病気の予測：Wiskott-Aldrich syndrome
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系統名：C57BL/6Smoc-Zmpste24em1Smoc
維持形態：Repository Live | SMOC番号：NM-KO-18011
病気の予測：achalasia, familial partial lipodystrophy, progeria
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