Incidental Mutation 'R4935:Dnah3'
ID 380303
Institutional Source Beutler Lab
Gene Symbol Dnah3
Ensembl Gene ENSMUSG00000052273
Gene Name dynein, axonemal, heavy chain 3
Synonyms Dnahc3
MMRRC Submission 042535-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # R4935 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 119521894-119694503 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 119615700 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 1676 (Y1676*)
Ref Sequence ENSEMBL: ENSMUSP00000146895 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046993] [ENSMUST00000209154] [ENSMUST00000213149]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000046993
AA Change: Y1687*
SMART Domains Protein: ENSMUSP00000042857
Gene: ENSMUSG00000052273
AA Change: Y1687*

DomainStartEndE-ValueType
low complexity region 121 133 N/A INTRINSIC
low complexity region 805 820 N/A INTRINSIC
Pfam:DHC_N2 826 1235 3.3e-144 PFAM
AAA 1388 1527 1.59e-1 SMART
low complexity region 1594 1606 N/A INTRINSIC
Blast:AAA 1669 1897 9e-84 BLAST
AAA 2033 2180 1.33e-3 SMART
Pfam:AAA_8 2362 2632 1.5e-63 PFAM
Pfam:MT 2644 2994 7.4e-52 PFAM
Pfam:AAA_9 3015 3240 3.5e-92 PFAM
low complexity region 3338 3349 N/A INTRINSIC
Pfam:Dynein_heavy 3376 4079 4.4e-285 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000209154
AA Change: Y1676*
Predicted Effect probably benign
Transcript: ENSMUST00000213149
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.9%
  • 10x: 94.8%
  • 20x: 86.9%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the dynein family, whose members encode large proteins that are constituents of the microtubule-associated motor protein complex. This complex is composed of dynein heavy, intermediate and light chains, which can be axonemal or cytoplasmic. This protein is an axonemal dynein heavy chain. It is involved in producing force for ciliary beating by using energy from ATP hydrolysis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016]
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A730071L15Rik A G 11: 6,150,442 (GRCm39) *138W probably null Het
Abcb1a T A 5: 8,787,773 (GRCm39) probably null Het
Acp6 T C 3: 97,079,060 (GRCm39) probably null Het
Adcyap1 A T 17: 93,511,541 (GRCm39) I172L probably benign Het
Adgrf1 A C 17: 43,606,130 (GRCm39) I85L probably benign Het
Afdn A T 17: 14,111,228 (GRCm39) T1604S probably benign Het
Angpt2 T C 8: 18,742,131 (GRCm39) Y475C probably damaging Het
Ank2 A G 3: 126,749,713 (GRCm39) S439P probably damaging Het
Ank3 T A 10: 69,812,033 (GRCm39) N366K probably damaging Het
Ankrd11 A G 8: 123,626,922 (GRCm39) S87P probably benign Het
Ano7 T A 1: 93,323,036 (GRCm39) S459T possibly damaging Het
Asxl3 G A 18: 22,656,369 (GRCm39) V1460M probably benign Het
Atg16l1 A C 1: 87,694,764 (GRCm39) N147T possibly damaging Het
Atp10a T C 7: 58,463,512 (GRCm39) V1015A probably damaging Het
Atxn7 T A 14: 14,100,401 (GRCm38) S696T probably benign Het
Babam1 C T 8: 71,852,446 (GRCm39) T184I probably benign Het
Blk A G 14: 63,618,711 (GRCm39) S175P possibly damaging Het
Col5a1 T A 2: 27,914,754 (GRCm39) F123L probably damaging Het
Csmd3 T C 15: 48,024,480 (GRCm39) Y496C probably damaging Het
Fdxacb1 T A 9: 50,683,243 (GRCm39) M402K probably benign Het
Frmd5 A G 2: 121,393,405 (GRCm39) V141A possibly damaging Het
Gapvd1 G A 2: 34,594,504 (GRCm39) R685* probably null Het
Grik2 A G 10: 49,116,826 (GRCm39) L645P probably damaging Het
H2aj T A 6: 136,785,681 (GRCm39) V115E possibly damaging Het
Hrh3 T C 2: 179,743,061 (GRCm39) Y189C probably damaging Het
Kcnc2 A G 10: 112,108,133 (GRCm39) T175A probably benign Het
Kcnv2 A G 19: 27,300,332 (GRCm39) Y61C probably damaging Het
Kif24 T C 4: 41,394,939 (GRCm39) R645G probably damaging Het
Knl1 A G 2: 118,899,438 (GRCm39) I380V possibly damaging Het
Lamb2 A G 9: 108,364,700 (GRCm39) I1151M possibly damaging Het
Leo1 A G 9: 75,353,159 (GRCm39) D234G probably benign Het
Lrp1b T G 2: 41,388,405 (GRCm39) N407H probably benign Het
Matn2 T C 15: 34,428,831 (GRCm39) S732P probably damaging Het
Mrps30 A T 13: 118,523,431 (GRCm39) F114I possibly damaging Het
Or1l8 T C 2: 36,817,713 (GRCm39) N138D probably benign Het
Or4f17-ps1 G A 2: 111,357,793 (GRCm39) V45I probably damaging Het
Or5b123 T C 19: 13,597,066 (GRCm39) I180T probably benign Het
Oxr1 T C 15: 41,676,980 (GRCm39) V179A probably benign Het
Plaur A T 7: 24,166,141 (GRCm39) S71C possibly damaging Het
Plbd2 T C 5: 120,624,786 (GRCm39) N461D possibly damaging Het
Plcb2 T A 2: 118,549,396 (GRCm39) Y322F probably damaging Het
Prkab2 T C 3: 97,569,671 (GRCm39) V79A probably damaging Het
Ptpn3 A T 4: 57,197,568 (GRCm39) C774S probably damaging Het
Ring1 A C 17: 34,242,016 (GRCm39) L131R probably benign Het
Rxfp2 G A 5: 149,975,097 (GRCm39) probably null Het
Selenbp1 A T 3: 94,845,269 (GRCm39) I122F probably benign Het
Septin7 A G 9: 25,217,468 (GRCm39) H394R probably benign Het
Slc1a7 G A 4: 107,864,758 (GRCm39) V266I probably damaging Het
Slc2a10 A G 2: 165,359,578 (GRCm39) T481A probably benign Het
Spmap2l T C 5: 77,185,200 (GRCm39) probably null Het
Tapbp A G 17: 34,144,596 (GRCm39) M231V probably benign Het
Tbxas1 A T 6: 38,999,981 (GRCm39) N256I probably benign Het
Uimc1 A G 13: 55,240,998 (GRCm39) I30T probably damaging Het
Usp48 C A 4: 137,377,669 (GRCm39) N231K probably benign Het
Zfhx3 T G 8: 109,674,482 (GRCm39) V1844G possibly damaging Het
Znrf3 A T 11: 5,233,422 (GRCm39) C212S probably damaging Het
Other mutations in Dnah3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00650:Dnah3 APN 7 119,538,128 (GRCm39) missense possibly damaging 0.88
IGL01095:Dnah3 APN 7 119,550,820 (GRCm39) missense probably benign 0.02
IGL01329:Dnah3 APN 7 119,622,164 (GRCm39) missense probably damaging 1.00
IGL01380:Dnah3 APN 7 119,525,787 (GRCm39) missense probably damaging 1.00
IGL01410:Dnah3 APN 7 119,566,943 (GRCm39) missense possibly damaging 0.91
IGL01487:Dnah3 APN 7 119,564,753 (GRCm39) nonsense probably null
IGL01843:Dnah3 APN 7 119,542,798 (GRCm39) missense probably benign 0.12
IGL01929:Dnah3 APN 7 119,550,874 (GRCm39) nonsense probably null
IGL01994:Dnah3 APN 7 119,550,437 (GRCm39) missense possibly damaging 0.58
IGL02115:Dnah3 APN 7 119,628,277 (GRCm39) missense probably damaging 1.00
IGL02273:Dnah3 APN 7 119,550,494 (GRCm39) missense probably damaging 1.00
IGL02299:Dnah3 APN 7 119,566,802 (GRCm39) missense probably benign 0.39
IGL02421:Dnah3 APN 7 119,550,215 (GRCm39) missense possibly damaging 0.87
IGL02514:Dnah3 APN 7 119,565,470 (GRCm39) missense probably damaging 1.00
IGL02596:Dnah3 APN 7 119,538,137 (GRCm39) missense probably benign 0.19
IGL02716:Dnah3 APN 7 119,536,246 (GRCm39) missense probably damaging 0.97
IGL02738:Dnah3 APN 7 119,564,720 (GRCm39) missense probably benign
IGL03404:Dnah3 APN 7 119,538,200 (GRCm39) missense probably damaging 1.00
R0964_Dnah3_480 UTSW 7 119,551,962 (GRCm39) splice site probably benign
R1778_Dnah3_238 UTSW 7 119,677,625 (GRCm39) missense probably damaging 1.00
R4658_Dnah3_599 UTSW 7 119,549,874 (GRCm39) missense probably damaging 1.00
BB004:Dnah3 UTSW 7 119,550,494 (GRCm39) missense probably damaging 0.97
BB014:Dnah3 UTSW 7 119,550,494 (GRCm39) missense probably damaging 0.97
R0011:Dnah3 UTSW 7 119,618,924 (GRCm39) missense probably damaging 1.00
R0195:Dnah3 UTSW 7 119,676,998 (GRCm39) critical splice donor site probably null
R0241:Dnah3 UTSW 7 119,521,953 (GRCm39) missense probably damaging 1.00
R0241:Dnah3 UTSW 7 119,521,953 (GRCm39) missense probably damaging 1.00
R0312:Dnah3 UTSW 7 119,644,882 (GRCm39) missense probably damaging 1.00
R0316:Dnah3 UTSW 7 119,564,882 (GRCm39) missense possibly damaging 0.94
R0370:Dnah3 UTSW 7 119,685,943 (GRCm39) missense possibly damaging 0.91
R0426:Dnah3 UTSW 7 119,542,795 (GRCm39) missense probably benign 0.11
R0525:Dnah3 UTSW 7 119,527,977 (GRCm39) missense probably damaging 1.00
R0625:Dnah3 UTSW 7 119,671,110 (GRCm39) missense possibly damaging 0.68
R0627:Dnah3 UTSW 7 119,620,138 (GRCm39) missense probably damaging 1.00
R0632:Dnah3 UTSW 7 119,567,128 (GRCm39) missense probably benign 0.11
R0928:Dnah3 UTSW 7 119,629,274 (GRCm39) missense probably damaging 1.00
R0964:Dnah3 UTSW 7 119,551,962 (GRCm39) splice site probably benign
R0972:Dnah3 UTSW 7 119,634,563 (GRCm39) splice site probably null
R1066:Dnah3 UTSW 7 119,660,232 (GRCm39) missense probably damaging 1.00
R1082:Dnah3 UTSW 7 119,677,668 (GRCm39) missense probably damaging 1.00
R1127:Dnah3 UTSW 7 119,522,253 (GRCm39) missense probably damaging 1.00
R1132:Dnah3 UTSW 7 119,538,227 (GRCm39) missense possibly damaging 0.50
R1222:Dnah3 UTSW 7 119,689,899 (GRCm39) missense probably benign 0.28
R1420:Dnah3 UTSW 7 119,551,202 (GRCm39) missense probably damaging 0.99
R1456:Dnah3 UTSW 7 119,646,853 (GRCm39) missense probably damaging 1.00
R1472:Dnah3 UTSW 7 119,670,181 (GRCm39) missense probably benign 0.12
R1617:Dnah3 UTSW 7 119,689,169 (GRCm39) missense probably benign 0.01
R1624:Dnah3 UTSW 7 119,618,918 (GRCm39) missense probably damaging 0.99
R1654:Dnah3 UTSW 7 119,525,672 (GRCm39) missense probably damaging 1.00
R1673:Dnah3 UTSW 7 119,570,402 (GRCm39) nonsense probably null
R1677:Dnah3 UTSW 7 119,527,963 (GRCm39) missense probably damaging 1.00
R1687:Dnah3 UTSW 7 119,645,009 (GRCm39) splice site probably null
R1711:Dnah3 UTSW 7 119,677,794 (GRCm39) missense probably damaging 1.00
R1738:Dnah3 UTSW 7 119,634,582 (GRCm39) missense probably damaging 1.00
R1778:Dnah3 UTSW 7 119,677,625 (GRCm39) missense probably damaging 1.00
R1866:Dnah3 UTSW 7 119,528,079 (GRCm39) splice site probably null
R1883:Dnah3 UTSW 7 119,677,142 (GRCm39) missense probably benign 0.06
R1894:Dnah3 UTSW 7 119,685,557 (GRCm39) missense probably benign 0.05
R1929:Dnah3 UTSW 7 119,574,352 (GRCm39) missense probably benign 0.10
R1988:Dnah3 UTSW 7 119,567,182 (GRCm39) missense probably damaging 0.99
R1988:Dnah3 UTSW 7 119,566,793 (GRCm39) missense possibly damaging 0.92
R2010:Dnah3 UTSW 7 119,694,400 (GRCm39) start codon destroyed probably benign 0.00
R2022:Dnah3 UTSW 7 119,550,465 (GRCm39) missense probably damaging 1.00
R2026:Dnah3 UTSW 7 119,638,629 (GRCm39) missense probably damaging 1.00
R2063:Dnah3 UTSW 7 119,551,132 (GRCm39) missense probably damaging 0.96
R2131:Dnah3 UTSW 7 119,566,982 (GRCm39) missense possibly damaging 0.93
R2152:Dnah3 UTSW 7 119,551,236 (GRCm39) missense probably benign 0.02
R2199:Dnah3 UTSW 7 119,550,792 (GRCm39) missense possibly damaging 0.89
R2271:Dnah3 UTSW 7 119,574,352 (GRCm39) missense probably benign 0.10
R2350:Dnah3 UTSW 7 119,645,011 (GRCm39) splice site probably null
R2567:Dnah3 UTSW 7 119,551,920 (GRCm39) missense possibly damaging 0.83
R2848:Dnah3 UTSW 7 119,567,161 (GRCm39) missense probably benign 0.01
R2902:Dnah3 UTSW 7 119,550,722 (GRCm39) missense possibly damaging 0.61
R2926:Dnah3 UTSW 7 119,550,338 (GRCm39) missense probably damaging 1.00
R2944:Dnah3 UTSW 7 119,550,333 (GRCm39) missense probably damaging 1.00
R3022:Dnah3 UTSW 7 119,677,704 (GRCm39) missense possibly damaging 0.93
R3401:Dnah3 UTSW 7 119,566,879 (GRCm39) missense probably benign 0.00
R3402:Dnah3 UTSW 7 119,566,879 (GRCm39) missense probably benign 0.00
R3403:Dnah3 UTSW 7 119,566,879 (GRCm39) missense probably benign 0.00
R3919:Dnah3 UTSW 7 119,550,303 (GRCm39) missense probably damaging 1.00
R3972:Dnah3 UTSW 7 119,685,943 (GRCm39) missense probably damaging 0.99
R4162:Dnah3 UTSW 7 119,522,061 (GRCm39) missense probably damaging 1.00
R4184:Dnah3 UTSW 7 119,682,516 (GRCm39) missense probably damaging 1.00
R4198:Dnah3 UTSW 7 119,522,061 (GRCm39) missense probably damaging 1.00
R4199:Dnah3 UTSW 7 119,522,061 (GRCm39) missense probably damaging 1.00
R4200:Dnah3 UTSW 7 119,522,061 (GRCm39) missense probably damaging 1.00
R4239:Dnah3 UTSW 7 119,628,248 (GRCm39) nonsense probably null
R4478:Dnah3 UTSW 7 119,671,086 (GRCm39) missense probably benign 0.00
R4579:Dnah3 UTSW 7 119,608,554 (GRCm39) missense probably damaging 1.00
R4600:Dnah3 UTSW 7 119,689,169 (GRCm39) missense probably benign
R4649:Dnah3 UTSW 7 119,646,921 (GRCm39) missense probably damaging 1.00
R4658:Dnah3 UTSW 7 119,549,874 (GRCm39) missense probably damaging 1.00
R4728:Dnah3 UTSW 7 119,658,589 (GRCm39) missense probably damaging 0.99
R4739:Dnah3 UTSW 7 119,677,169 (GRCm39) missense possibly damaging 0.54
R4758:Dnah3 UTSW 7 119,678,629 (GRCm39) missense probably benign 0.00
R4785:Dnah3 UTSW 7 119,567,047 (GRCm39) missense probably benign 0.29
R4789:Dnah3 UTSW 7 119,610,295 (GRCm39) missense probably damaging 1.00
R4930:Dnah3 UTSW 7 119,550,904 (GRCm39) nonsense probably null
R4946:Dnah3 UTSW 7 119,530,783 (GRCm39) missense probably damaging 1.00
R4981:Dnah3 UTSW 7 119,555,424 (GRCm39) missense probably benign 0.03
R4984:Dnah3 UTSW 7 119,528,002 (GRCm39) missense probably benign 0.04
R5025:Dnah3 UTSW 7 119,671,128 (GRCm39) missense probably benign 0.02
R5046:Dnah3 UTSW 7 119,550,803 (GRCm39) missense probably damaging 1.00
R5056:Dnah3 UTSW 7 119,620,169 (GRCm39) missense probably damaging 1.00
R5068:Dnah3 UTSW 7 119,632,013 (GRCm39) missense probably benign
R5069:Dnah3 UTSW 7 119,632,013 (GRCm39) missense probably benign
R5154:Dnah3 UTSW 7 119,551,642 (GRCm39) missense probably damaging 1.00
R5208:Dnah3 UTSW 7 119,631,861 (GRCm39) missense probably damaging 1.00
R5323:Dnah3 UTSW 7 119,620,234 (GRCm39) missense probably damaging 1.00
R5330:Dnah3 UTSW 7 119,542,871 (GRCm39) missense probably benign 0.00
R5385:Dnah3 UTSW 7 119,524,126 (GRCm39) missense probably damaging 1.00
R5391:Dnah3 UTSW 7 119,689,299 (GRCm39) missense probably benign 0.02
R5564:Dnah3 UTSW 7 119,570,689 (GRCm39) critical splice donor site probably null
R5594:Dnah3 UTSW 7 119,570,844 (GRCm39) missense possibly damaging 0.89
R5610:Dnah3 UTSW 7 119,538,288 (GRCm39) splice site probably null
R5673:Dnah3 UTSW 7 119,550,812 (GRCm39) missense possibly damaging 0.91
R5678:Dnah3 UTSW 7 119,677,074 (GRCm39) missense probably benign 0.00
R5737:Dnah3 UTSW 7 119,658,421 (GRCm39) missense probably benign 0.03
R5766:Dnah3 UTSW 7 119,577,445 (GRCm39) missense probably damaging 1.00
R5769:Dnah3 UTSW 7 119,689,175 (GRCm39) nonsense probably null
R5789:Dnah3 UTSW 7 119,542,822 (GRCm39) missense possibly damaging 0.70
R5791:Dnah3 UTSW 7 119,530,696 (GRCm39) missense probably benign 0.00
R5841:Dnah3 UTSW 7 119,550,244 (GRCm39) utr 3 prime probably benign
R5843:Dnah3 UTSW 7 119,550,244 (GRCm39) utr 3 prime probably benign
R5844:Dnah3 UTSW 7 119,550,244 (GRCm39) utr 3 prime probably benign
R5846:Dnah3 UTSW 7 119,550,244 (GRCm39) utr 3 prime probably benign
R5851:Dnah3 UTSW 7 119,638,585 (GRCm39) missense possibly damaging 0.51
R5853:Dnah3 UTSW 7 119,538,056 (GRCm39) missense probably damaging 1.00
R5857:Dnah3 UTSW 7 119,550,244 (GRCm39) utr 3 prime probably benign
R5865:Dnah3 UTSW 7 119,574,331 (GRCm39) missense probably benign 0.00
R5885:Dnah3 UTSW 7 119,668,927 (GRCm39) missense probably benign 0.10
R5898:Dnah3 UTSW 7 119,677,724 (GRCm39) missense probably benign 0.37
R5917:Dnah3 UTSW 7 119,615,749 (GRCm39) missense probably damaging 1.00
R5964:Dnah3 UTSW 7 119,522,103 (GRCm39) missense probably benign 0.00
R5990:Dnah3 UTSW 7 119,672,764 (GRCm39) missense probably benign
R6004:Dnah3 UTSW 7 119,685,520 (GRCm39) missense probably benign 0.10
R6033:Dnah3 UTSW 7 119,670,870 (GRCm39) missense probably benign 0.00
R6033:Dnah3 UTSW 7 119,670,870 (GRCm39) missense probably benign 0.00
R6045:Dnah3 UTSW 7 119,566,745 (GRCm39) missense probably damaging 0.99
R6056:Dnah3 UTSW 7 119,629,254 (GRCm39) missense probably damaging 1.00
R6133:Dnah3 UTSW 7 119,685,469 (GRCm39) missense probably benign 0.10
R6229:Dnah3 UTSW 7 119,564,711 (GRCm39) missense probably benign 0.11
R6237:Dnah3 UTSW 7 119,608,607 (GRCm39) missense probably damaging 1.00
R6333:Dnah3 UTSW 7 119,653,856 (GRCm39) missense probably damaging 1.00
R6408:Dnah3 UTSW 7 119,522,191 (GRCm39) splice site probably null
R6447:Dnah3 UTSW 7 119,522,277 (GRCm39) missense probably benign 0.12
R6606:Dnah3 UTSW 7 119,660,179 (GRCm39) missense probably benign 0.02
R6666:Dnah3 UTSW 7 119,670,172 (GRCm39) missense probably benign 0.16
R6733:Dnah3 UTSW 7 119,522,197 (GRCm39) missense probably benign 0.22
R6815:Dnah3 UTSW 7 119,570,950 (GRCm39) missense probably benign
R6882:Dnah3 UTSW 7 119,570,407 (GRCm39) missense possibly damaging 0.95
R6934:Dnah3 UTSW 7 119,653,824 (GRCm39) critical splice donor site probably null
R6966:Dnah3 UTSW 7 119,631,977 (GRCm39) missense probably damaging 1.00
R7025:Dnah3 UTSW 7 119,629,233 (GRCm39) missense possibly damaging 0.90
R7207:Dnah3 UTSW 7 119,570,312 (GRCm39) missense probably damaging 1.00
R7214:Dnah3 UTSW 7 119,521,965 (GRCm39) missense probably damaging 1.00
R7222:Dnah3 UTSW 7 119,670,746 (GRCm39) missense probably benign 0.00
R7235:Dnah3 UTSW 7 119,631,893 (GRCm39) missense probably damaging 1.00
R7241:Dnah3 UTSW 7 119,542,856 (GRCm39) missense probably benign 0.03
R7313:Dnah3 UTSW 7 119,580,567 (GRCm39) missense probably benign 0.39
R7342:Dnah3 UTSW 7 119,629,208 (GRCm39) missense probably damaging 1.00
R7368:Dnah3 UTSW 7 119,628,239 (GRCm39) missense probably benign
R7375:Dnah3 UTSW 7 119,550,900 (GRCm39) missense probably damaging 1.00
R7395:Dnah3 UTSW 7 119,660,183 (GRCm39) missense probably benign 0.00
R7395:Dnah3 UTSW 7 119,565,474 (GRCm39) missense
R7431:Dnah3 UTSW 7 119,650,967 (GRCm39) missense probably damaging 1.00
R7499:Dnah3 UTSW 7 119,660,135 (GRCm39) missense probably damaging 0.99
R7515:Dnah3 UTSW 7 119,672,815 (GRCm39) missense probably benign 0.21
R7564:Dnah3 UTSW 7 119,570,817 (GRCm39) missense probably benign
R7618:Dnah3 UTSW 7 119,577,601 (GRCm39) missense probably damaging 0.97
R7697:Dnah3 UTSW 7 119,566,657 (GRCm39) missense
R7728:Dnah3 UTSW 7 119,538,051 (GRCm39) missense probably damaging 1.00
R7757:Dnah3 UTSW 7 119,570,438 (GRCm39) splice site probably null
R7757:Dnah3 UTSW 7 119,670,793 (GRCm39) missense probably benign
R7774:Dnah3 UTSW 7 119,550,975 (GRCm39) nonsense probably null
R7804:Dnah3 UTSW 7 119,610,235 (GRCm39) missense probably damaging 1.00
R7804:Dnah3 UTSW 7 119,551,841 (GRCm39) missense probably damaging 1.00
R7857:Dnah3 UTSW 7 119,550,927 (GRCm39) missense probably damaging 1.00
R7871:Dnah3 UTSW 7 119,566,775 (GRCm39) missense
R7903:Dnah3 UTSW 7 119,641,351 (GRCm39) missense probably damaging 1.00
R7927:Dnah3 UTSW 7 119,550,494 (GRCm39) missense probably damaging 0.97
R7989:Dnah3 UTSW 7 119,677,012 (GRCm39) missense probably benign
R8142:Dnah3 UTSW 7 119,660,189 (GRCm39) missense probably benign 0.00
R8164:Dnah3 UTSW 7 119,566,837 (GRCm39) missense probably damaging 1.00
R8237:Dnah3 UTSW 7 119,525,636 (GRCm39) missense probably benign 0.01
R8313:Dnah3 UTSW 7 119,550,375 (GRCm39) missense probably benign 0.38
R8338:Dnah3 UTSW 7 119,671,104 (GRCm39) missense probably benign 0.01
R8355:Dnah3 UTSW 7 119,551,431 (GRCm39) missense probably damaging 1.00
R8408:Dnah3 UTSW 7 119,551,728 (GRCm39) missense probably damaging 1.00
R8411:Dnah3 UTSW 7 119,610,253 (GRCm39) missense probably damaging 1.00
R8455:Dnah3 UTSW 7 119,551,431 (GRCm39) missense probably damaging 1.00
R8483:Dnah3 UTSW 7 119,536,253 (GRCm39) missense probably benign 0.00
R8531:Dnah3 UTSW 7 119,550,591 (GRCm39) missense probably damaging 1.00
R8885:Dnah3 UTSW 7 119,561,375 (GRCm39) missense
R8912:Dnah3 UTSW 7 119,689,869 (GRCm39) missense probably benign 0.06
R8966:Dnah3 UTSW 7 119,549,881 (GRCm39) nonsense probably null
R8982:Dnah3 UTSW 7 119,536,294 (GRCm39) missense probably damaging 1.00
R9043:Dnah3 UTSW 7 119,551,272 (GRCm39) missense probably benign
R9053:Dnah3 UTSW 7 119,618,987 (GRCm39) missense possibly damaging 0.67
R9059:Dnah3 UTSW 7 119,684,368 (GRCm39) missense probably benign 0.01
R9182:Dnah3 UTSW 7 119,684,351 (GRCm39) missense probably damaging 0.98
R9365:Dnah3 UTSW 7 119,566,859 (GRCm39) missense
R9383:Dnah3 UTSW 7 119,646,819 (GRCm39) missense probably benign 0.23
R9430:Dnah3 UTSW 7 119,628,205 (GRCm39) missense probably damaging 1.00
R9449:Dnah3 UTSW 7 119,551,473 (GRCm39) missense probably benign 0.12
R9462:Dnah3 UTSW 7 119,551,523 (GRCm39) missense probably benign 0.05
R9505:Dnah3 UTSW 7 119,644,912 (GRCm39) missense probably damaging 1.00
R9559:Dnah3 UTSW 7 119,650,951 (GRCm39) missense probably benign 0.07
R9562:Dnah3 UTSW 7 119,610,114 (GRCm39) missense probably benign 0.05
R9565:Dnah3 UTSW 7 119,610,114 (GRCm39) missense probably benign 0.05
R9609:Dnah3 UTSW 7 119,670,236 (GRCm39) missense probably damaging 0.98
R9622:Dnah3 UTSW 7 119,561,356 (GRCm39) missense
R9633:Dnah3 UTSW 7 119,550,216 (GRCm39) missense probably benign
R9654:Dnah3 UTSW 7 119,641,396 (GRCm39) nonsense probably null
R9665:Dnah3 UTSW 7 119,644,981 (GRCm39) missense probably benign 0.01
R9681:Dnah3 UTSW 7 119,677,611 (GRCm39) missense probably benign 0.04
R9717:Dnah3 UTSW 7 119,574,299 (GRCm39) missense probably damaging 1.00
Z1088:Dnah3 UTSW 7 119,610,096 (GRCm39) missense probably null 1.00
Z1088:Dnah3 UTSW 7 119,685,520 (GRCm39) missense probably benign 0.00
Z1176:Dnah3 UTSW 7 119,567,026 (GRCm39) missense
Z1177:Dnah3 UTSW 7 119,607,085 (GRCm39) missense probably benign
Z1177:Dnah3 UTSW 7 119,567,124 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- ACATTTGTGTGCCGTGCTC -3'
(R):5'- AGGCAATCTAAGGCATGTCTAAC -3'

Sequencing Primer
(F):5'- GCCGTGCTCTGCTTTTAATG -3'
(R):5'- GACCACTAAAAGGGCTTCAGCTTATG -3'
Posted On 2016-04-15