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All mouse models of diarrhea with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | congenital diarrhea 5 with tufting enteropathy | EpcamGt(RST412)Byg/EpcamGt(RST412)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:195002 | View | |||
| congenital secretory chloride diarrhea 1 | Slc26a3tm1Sole/Slc26a3tm1Sole | involves: 129S6/SvEvTac * C57BL/6 | J:117587 | View | ||||
| microvillus inclusion disease |
Myo5btm1.1Cle/Myo5btm1.1Cle Tg(Vil1-cre/ERT2)23Syr/0 |
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * DBA/2 | J:227079 | View | ||||
| microvillus inclusion disease | Myo5btm1a(KOMP)Wtsi/Myo5btm1a(KOMP)Wtsi | C57BL/6N-Myo5btm1a(KOMP)Wtsi | J:229427 | View | ||||
| | microvillus inclusion disease |
Cdc42tm1Brak/Cdc42tm1Brak Tg(Vil1-cre)997Gum/0 |
involves: C57BL/6J * SJL | J:184563 | View | |||
| | congenital secretory sodium diarrhea 3 |
Prss8em1Bug/Prss8em1Bug Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg |
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * NIH Black Swiss | J:261068 | View | |||