Excel File Text File All mouse models of autosomal dominant nonsyndromic deafness with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      autosomal dominant auditory neuropathy 1 Tg(CAG-Diap3)924Lesp/0 FVB/NJ-Tg(CAG-Diap3)924Lesp J:193237 View
autosomal dominant auditory neuropathy 1 Tg(CAG-Diaph3)771Lesp/0 FVB/NJ-Tg(CAG-Diaph3)771Lesp J:193237 View
autosomal dominant nonsyndromic deafness 9 Cochtm1Mrtn/Cochtm1Mrtn CBACa.129S4-Cochtm1Mrtn J:140594, J:167669 View
autosomal dominant nonsyndromic deafness 12 Tectatm2Gpr/Tecta+ involves: 129S/SvEv * C57BL/6J J:101691 View
autosomal dominant nonsyndromic deafness 12 Tectatm3.1Gpr/Tecta+ involves: 129S/SvEv J:203482 View
autosomal dominant nonsyndromic deafness 12 Tectatm4.1Gpr/Tecta+ involves: 129S/SvEv J:203482 View
autosomal dominant nonsyndromic deafness 12 Tectatm5.1Gpr/Tecta+ involves: 129S/SvEv J:203482 View
autosomal dominant nonsyndromic deafness 13 Col11a2tm1Mne/Col11a2tm1Mne FVB.129-Col11a2tm1Mne J:71948 View
autosomal dominant nonsyndromic deafness 22 Myo6em1Bcgen/Myo6+ involves: C57BL/6J * CBA/CaJ J:288210 View
autosomal dominant nonsyndromic deafness 22 Myo6sv/Myo6sv involves: B10.HA/(33NX)Sn * C57BL/6J J:29898 View
autosomal dominant nonsyndromic deafness 25 Slc17a8tm1Selm/Slc17a8tm1Selm involves: 129/Sv * C57BL/6 J:139493 View
autosomal dominant nonsyndromic deafness 36 Tmc1dn/Tmc1dn involves: STOCK Grhl3ct * M. m. molossinus J:22445 View
autosomal dominant nonsyndromic deafness 36 Tmc1dn/Tmc1dn STOCK Grhl3ct/J J:236 View
autosomal dominant nonsyndromic deafness 36 Tmc1Mhdabth/Tmc1+ C3HeB/FeJ-Tmc1Mhdabth/Ieg J:86685 View
autosomal dominant nonsyndromic deafness 41 P2rx2em1Xzl/P2rx2+ CBA/J-P2rx2em1Xzl J:315007 View
autosomal dominant nonsyndromic deafness 67 Osbpl2em1Cya/Osbpl2em1Cya C57BL/6-Osbpl2em1Cya J:324115 View
      autosomal dominant nonsyndromic deafness 4A Ceacam16tm1Wzm/Ceacam16tm1Wzm BALB/cJ-Ceacam16tm1Wzm J:187537 View
autosomal dominant nonsyndromic deafness 25 Trpv4tm1Msz/Trpv4tm1Msz involves: 129X1/SvJ * C57BL/6 J:104851 View

       
No similarity to the expected human disease phenotype was found.
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
NOT Models      autosomal dominant nonsyndromic deafness 2A Gjb3tm1Kwi/Gjb3tm1Kwi involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:68014 View
autosomal dominant nonsyndromic deafness 15 Pou4f3tm1Rsd/Pou4f3+ involves: 129S4/SvJae * C57BL/6 J:57149 View
autosomal dominant nonsyndromic deafness 65 Cdh23Ahl+/Cdh23Ahl+
Tbc1d24em4Tbf/Tbc1d24em4Tbf		 B6.Cg-Cdh23Ahl+ Tbc1d24em4Tbf J:299025 View
autosomal dominant nonsyndromic deafness 65 Tbc1d24em4Tbf/Tbc1d24em4Tbf C57BL/6J-Tbc1d24em4Tbf J:299025 View