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.
|
|
系統名：C57BL/6Smoc-Slc6a1em2(S295L)Smoc
維持形態：Repository Live | SMOC番号：NM-KI-190014
応用分野：Nervous system, Immune system, Genetic epilepsy, Rare disease
|
|
|
|
||
|
|
系統名：C57BL/6Smoc-Spink1em1c.197+2t>cSmoc
維持形態：Sperm cryopreservation | SMOC番号：NM-KI-232249
|
|
|
|
||
|
|
||
|
|
系統名：C57BL/6Smoc-Tcf4em(QGQSVSSGSSEIKSDDEGD502-518QSQSVSSSSSEIKSDDESD)Smoc
維持形態：Sperm cryopreservation | SMOC番号：NM-KI-220595
|
|
|
|
||
|
|
系統名：C57BL/6Smoc-tm6sf2em1(E167K)Smoc
維持形態：Embryo cryopreservation | SMOC番号：NM-KI-200002
応用分野：Myocardial infarction and total cholesterol related
|
|
|
|
系統名：C57BL/6Smoc-Tmem173em(V154M)Smoc
維持形態：Sperm cryopreservation | SMOC番号：NM-KI-225039
応用分野：STING-associated vasculopathy with onset in infancy (SAVI)
|
|
|
|
