Point mutant knockin mouse model is a mouse in which one or more nucleotides are replaced by mutant nucleotides in the genome. This may result in amino acid changes within the protein sequence, and transcription terminated, thereby significantly affecting the normal function of the protein. Point mutation mouse models are widely used to study the role of specific nucleotides or amino acids in genetic elements or proteins, as well as to mimic human genetic diseases.
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系統名：C57BL/6Smoc-Abcc8 tm1（L1050R/S1051N/P1052C/A1053*）Smoc
維持形態：Sperm cryopreservation | SMOC番号：NM-KI-232146
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系統名：C57BL/6Smoc-Abcc8 tm1（Abcc8-V1049Q/L1050S/S1051*）Smoc
維持形態：Sperm cryopreservation | SMOC番号：NM-KI-232145
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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-Apcem1(L850X)Smoc
維持形態：Repository Live | SMOC番号：NM-KI-200001
病気の予測：familial adenomatous polyposis, colorectal cancer, Lynch syndrome
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系統名：C57BL/6Smoc-Apobem1(Q1388H)Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KI-00056
応用分野：lipid metabolism studies, cardiovascular disease research
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