Incidental Mutation 'R1903:Dnah1'
ID 209991
Institutional Source Beutler Lab
Gene Symbol Dnah1
Ensembl Gene ENSMUSG00000019027
Gene Name dynein, axonemal, heavy chain 1
Synonyms MDHC7, B230373P09Rik, ferf1, G1-415-19, E030034C22Rik, Dnahc1
MMRRC Submission 039923-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1903 (G1)
Quality Score 225
Status Not validated
Chromosome 14
Chromosomal Location 30982332-31045853 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 31041716 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 85 (D85G)
Ref Sequence ENSEMBL: ENSMUSP00000043281 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000048603]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000048603
AA Change: D85G

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000043281
Gene: ENSMUSG00000019027
AA Change: D85G

DomainStartEndE-ValueType
low complexity region 43 59 N/A INTRINSIC
Pfam:DHC_N2 998 1404 6.3e-146 PFAM
AAA 1558 1697 6.02e-1 SMART
AAA 1839 2077 4.66e0 SMART
low complexity region 2149 2157 N/A INTRINSIC
AAA 2204 2353 2.35e-1 SMART
Pfam:AAA_8 2533 2803 7.7e-84 PFAM
Pfam:MT 2815 3165 9.9e-57 PFAM
Pfam:AAA_9 3185 3410 1.1e-93 PFAM
Pfam:Dynein_heavy 3545 4246 2.7e-275 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000226148
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228755
Coding Region Coverage
  • 1x: 97.3%
  • 3x: 96.7%
  • 10x: 95.0%
  • 20x: 91.8%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an inner dynein arm heavy chain that provides structural support between the radial spokes and the outer doublet of the sperm tail. Naturally occurring mutations in this gene are associated with primary ciliary dyskinesia and multiple morphological anomalies of the flagella that result in asthenozoospermia and male infertility. Mice with a homozygous knockout of the orthologous gene are viable but have reduced sperm motility and are infertile. [provided by RefSeq, Feb 2017]
PHENOTYPE: Homozygous mutants are male sterile, and show impaired ciliary and flagellar motility that is also observed in the tracheal cilia. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 120 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017B05Rik A C 9: 57,165,635 (GRCm39) S246R possibly damaging Het
Abca13 C T 11: 9,416,411 (GRCm39) R4058C probably benign Het
Acacb A T 5: 114,303,795 (GRCm39) R73* probably null Het
Adam22 C T 5: 8,184,525 (GRCm39) C489Y probably damaging Het
Agap3 A T 5: 24,698,011 (GRCm39) K460I probably damaging Het
Ak4 T C 4: 101,320,833 (GRCm39) I214T possibly damaging Het
Anpep C T 7: 79,488,004 (GRCm39) E518K probably benign Het
Arrb2 T A 11: 70,328,808 (GRCm39) H221Q probably damaging Het
Atl1 T G 12: 70,006,049 (GRCm39) F452V probably damaging Het
Atp8b5 A G 4: 43,357,063 (GRCm39) T604A probably damaging Het
Bglap3 T C 3: 88,276,068 (GRCm39) I95V probably benign Het
Ccdc88a G T 11: 29,411,788 (GRCm39) M532I probably benign Het
Ccnl1 A G 3: 65,854,332 (GRCm39) S430P possibly damaging Het
Cdhr18 C T 14: 13,829,657 (GRCm38) S695N possibly damaging Het
Cdk5rap2 A T 4: 70,321,791 (GRCm39) probably null Het
Cep126 A T 9: 8,120,748 (GRCm39) Y92N possibly damaging Het
Cfap44 A C 16: 44,242,737 (GRCm39) T714P probably benign Het
Cnga1 T G 5: 72,774,068 (GRCm39) D90A possibly damaging Het
Cnot1 T C 8: 96,469,749 (GRCm39) I1369V possibly damaging Het
Coq3 T C 4: 21,910,466 (GRCm39) S314P probably damaging Het
Crhr1 A G 11: 104,060,675 (GRCm39) R151G probably damaging Het
Crybg2 A G 4: 133,806,167 (GRCm39) I930V probably damaging Het
Ctcf T A 8: 106,402,620 (GRCm39) probably null Het
Dct T C 14: 118,271,690 (GRCm39) N380S probably benign Het
Decr2 A T 17: 26,306,387 (GRCm39) L83Q probably damaging Het
Depdc5 CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT 5: 33,067,751 (GRCm39) probably benign Het
Dgkb T C 12: 38,216,776 (GRCm39) probably null Het
Dnah7a T C 1: 53,574,637 (GRCm39) D1709G probably damaging Het
Dnajc13 A C 9: 104,106,136 (GRCm39) L346R probably damaging Het
Dsc1 A T 18: 20,229,045 (GRCm39) V415D probably damaging Het
Duox2 T A 2: 122,125,832 (GRCm39) I296F probably damaging Het
Ece2 T A 16: 20,463,922 (GRCm39) L890H probably damaging Het
Ecsit A G 9: 21,987,815 (GRCm39) S75P possibly damaging Het
Enpp3 A G 10: 24,654,687 (GRCm39) C664R probably damaging Het
Evpl G T 11: 116,117,854 (GRCm39) D778E probably damaging Het
Eya3 T A 4: 132,448,663 (GRCm39) probably null Het
Fam217b A T 2: 178,062,374 (GRCm39) I113F probably benign Het
Galnt6 G A 15: 100,613,999 (GRCm39) P101S possibly damaging Het
Gm379 G A X: 107,707,870 (GRCm39) Q210* probably null Het
Grk4 A T 5: 34,833,531 (GRCm39) probably null Het
Gtf3c4 A G 2: 28,729,968 (GRCm39) V91A probably benign Het
Hcfc2 G T 10: 82,538,392 (GRCm39) G143V probably damaging Het
Heatr4 A C 12: 84,005,221 (GRCm39) H710Q probably damaging Het
Htr3a A T 9: 48,817,681 (GRCm39) D97E probably damaging Het
Htr4 T G 18: 62,561,193 (GRCm39) F151L probably benign Het
Il22ra1 A T 4: 135,478,219 (GRCm39) Q430L probably damaging Het
Invs T A 4: 48,402,824 (GRCm39) probably null Het
Ip6k1 G A 9: 107,918,195 (GRCm39) E77K possibly damaging Het
Irs1 T C 1: 82,267,182 (GRCm39) S345G probably damaging Het
Kdm4a A G 4: 118,017,596 (GRCm39) V490A probably benign Het
Kif26a C T 12: 112,141,974 (GRCm39) R743C probably damaging Het
Kif28 A G 1: 179,530,088 (GRCm39) V691A possibly damaging Het
Klhl5 T A 5: 65,324,330 (GRCm39) L696Q probably benign Het
Krtap5-1 T C 7: 141,850,084 (GRCm39) probably benign Het
Lama2 A C 10: 27,064,395 (GRCm39) D1195E probably damaging Het
Lamb1 T G 12: 31,379,209 (GRCm39) L1722R probably damaging Het
Lrp11 T A 10: 7,499,544 (GRCm39) L245Q probably damaging Het
Ltbp2 T C 12: 84,876,879 (GRCm39) E422G probably benign Het
Man2b1 T A 8: 85,813,451 (GRCm39) D214E probably damaging Het
Mlxipl A T 5: 135,162,422 (GRCm39) D628V possibly damaging Het
Msantd5f6 T A 4: 73,321,675 (GRCm39) Y120F probably damaging Het
Myo18b G A 5: 112,840,624 (GRCm39) R2390C probably damaging Het
Mypn T A 10: 62,959,176 (GRCm39) R1048S probably benign Het
Napepld A G 5: 21,870,270 (GRCm39) S383P probably damaging Het
Napsa A G 7: 44,231,160 (GRCm39) T130A probably damaging Het
Nbr1 T C 11: 101,465,978 (GRCm39) I716T probably damaging Het
Nexn A T 3: 151,953,818 (GRCm39) M212K probably damaging Het
Nlrp9b T A 7: 19,757,182 (GRCm39) S140T probably benign Het
Nxpe2 T C 9: 48,230,906 (GRCm39) T488A probably benign Het
Or10g3 T G 14: 52,610,174 (GRCm39) Q112P possibly damaging Het
Or10v1 A T 19: 11,873,913 (GRCm39) Y176F probably benign Het
Or5ac25 A T 16: 59,182,526 (GRCm39) D18E probably benign Het
Or7g12 A T 9: 18,900,192 (GRCm39) K303* probably null Het
Or8k20 C T 2: 86,106,190 (GRCm39) V214I probably benign Het
Osbpl5 T C 7: 143,256,918 (GRCm39) D404G possibly damaging Het
Pan2 T G 10: 128,144,237 (GRCm39) L162R probably damaging Het
Parp1 G T 1: 180,416,235 (GRCm39) V545F probably damaging Het
Pcdh18 A G 3: 49,709,896 (GRCm39) V473A probably benign Het
Plb1 A T 5: 32,448,582 (GRCm39) N350I probably damaging Het
Polr1a A G 6: 71,944,898 (GRCm39) K1318R probably benign Het
Ppp1r18 C T 17: 36,184,738 (GRCm39) P130S probably damaging Het
Prss48 C T 3: 85,905,614 (GRCm39) W86* probably null Het
Rab3c A T 13: 110,220,744 (GRCm39) I137N probably damaging Het
Rab3gap2 G C 1: 184,954,099 (GRCm39) R57P probably benign Het
Rad54l2 A C 9: 106,570,916 (GRCm39) probably null Het
Ralgapb C A 2: 158,337,483 (GRCm39) N1147K probably benign Het
Rfx7 C T 9: 72,524,093 (GRCm39) R428C probably damaging Het
Robo1 A G 16: 72,757,092 (GRCm39) Q351R probably null Het
Samd4 T C 14: 47,311,585 (GRCm39) F81S probably damaging Het
Shprh T A 10: 11,059,541 (GRCm39) Y1097* probably null Het
Sik3 C G 9: 46,132,387 (GRCm39) H1276Q probably benign Het
Slc24a4 T A 12: 102,097,876 (GRCm39) D79E probably benign Het
Slc7a13 A T 4: 19,839,254 (GRCm39) I286F probably benign Het
Smarca1 G A X: 46,938,840 (GRCm39) Q723* probably null Het
Spata31d1b T C 13: 59,865,882 (GRCm39) L1010P probably damaging Het
Sult2a1 T C 7: 13,569,900 (GRCm39) S111G possibly damaging Het
Tecpr2 C T 12: 110,914,346 (GRCm39) T1219M probably damaging Het
Tesk1 T C 4: 43,446,998 (GRCm39) M462T probably benign Het
Thoc2l T A 5: 104,666,196 (GRCm39) S239R probably benign Het
Tmem171 C A 13: 98,822,924 (GRCm39) G292* probably null Het
Tmtc2 G T 10: 105,025,969 (GRCm39) T833N probably benign Het
Tnc G T 4: 63,918,299 (GRCm39) T1204K probably benign Het
Tnfaip3 T C 10: 18,883,937 (GRCm39) K148E probably benign Het
Tnrc18 G A 5: 142,800,895 (GRCm39) S21F probably damaging Het
Tns4 T C 11: 98,966,401 (GRCm39) T425A probably damaging Het
Tox T A 4: 6,688,948 (GRCm39) Y472F probably damaging Het
Trak2 A T 1: 58,958,014 (GRCm39) probably null Het
Trim33 T A 3: 103,244,760 (GRCm39) Y716N probably damaging Het
Trrap T G 5: 144,752,863 (GRCm39) I1813R probably damaging Het
Ttc29 A G 8: 78,978,361 (GRCm39) E137G probably benign Het
Ube2j2 A G 4: 156,033,483 (GRCm39) K19R probably benign Het
Ubxn2b T C 4: 6,208,889 (GRCm39) I206T possibly damaging Het
Usp40 A G 1: 87,909,778 (GRCm39) F559L probably benign Het
Utp4 T A 8: 107,638,982 (GRCm39) probably null Het
Vac14 A G 8: 111,409,166 (GRCm39) N524S probably benign Het
Vps13c T C 9: 67,801,334 (GRCm39) S605P probably damaging Het
Vwa5b2 G T 16: 20,423,582 (GRCm39) S1165I possibly damaging Het
Zdhhc19 C T 16: 32,317,231 (GRCm39) R28* probably null Het
Zfp106 T C 2: 120,357,329 (GRCm39) I1189V probably benign Het
Zfp189 C T 4: 49,529,511 (GRCm39) Q205* probably null Het
Other mutations in Dnah1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00090:Dnah1 APN 14 31,009,830 (GRCm39) missense probably benign 0.01
IGL00227:Dnah1 APN 14 31,008,853 (GRCm39) missense probably damaging 1.00
IGL00491:Dnah1 APN 14 30,983,796 (GRCm39) missense probably damaging 1.00
IGL00787:Dnah1 APN 14 31,022,020 (GRCm39) missense possibly damaging 0.91
IGL00809:Dnah1 APN 14 31,022,766 (GRCm39) nonsense probably null
IGL00911:Dnah1 APN 14 31,026,391 (GRCm39) splice site probably null
IGL00949:Dnah1 APN 14 31,029,047 (GRCm39) missense probably benign 0.00
IGL00976:Dnah1 APN 14 31,000,095 (GRCm39) missense probably damaging 1.00
IGL01484:Dnah1 APN 14 31,021,897 (GRCm39) missense probably damaging 0.98
IGL01629:Dnah1 APN 14 31,014,277 (GRCm39) missense probably damaging 1.00
IGL01716:Dnah1 APN 14 30,985,335 (GRCm39) missense probably benign 0.34
IGL01893:Dnah1 APN 14 30,988,427 (GRCm39) missense probably damaging 1.00
IGL01933:Dnah1 APN 14 31,032,872 (GRCm39) missense probably benign 0.40
IGL01938:Dnah1 APN 14 31,005,844 (GRCm39) missense probably benign
IGL02032:Dnah1 APN 14 30,996,326 (GRCm39) missense probably benign
IGL02052:Dnah1 APN 14 30,990,743 (GRCm39) missense probably damaging 0.99
IGL02097:Dnah1 APN 14 31,026,958 (GRCm39) missense possibly damaging 0.92
IGL02127:Dnah1 APN 14 31,026,885 (GRCm39) missense probably benign 0.00
IGL02143:Dnah1 APN 14 31,005,246 (GRCm39) missense probably damaging 1.00
IGL02158:Dnah1 APN 14 31,022,924 (GRCm39) missense probably benign 0.00
IGL02442:Dnah1 APN 14 31,009,835 (GRCm39) missense probably damaging 1.00
IGL02525:Dnah1 APN 14 31,027,790 (GRCm39) missense probably benign 0.05
IGL02558:Dnah1 APN 14 30,996,336 (GRCm39) missense possibly damaging 0.96
IGL02633:Dnah1 APN 14 31,006,772 (GRCm39) missense probably benign 0.05
IGL02720:Dnah1 APN 14 30,984,177 (GRCm39) missense probably damaging 0.96
IGL02728:Dnah1 APN 14 31,005,955 (GRCm39) missense probably benign 0.44
IGL02738:Dnah1 APN 14 31,014,597 (GRCm39) missense probably benign 0.27
IGL02863:Dnah1 APN 14 31,017,250 (GRCm39) missense probably damaging 0.99
IGL02944:Dnah1 APN 14 31,022,828 (GRCm39) missense possibly damaging 0.88
IGL03110:Dnah1 APN 14 30,988,674 (GRCm39) missense probably benign 0.40
IGL03201:Dnah1 APN 14 31,022,906 (GRCm39) missense probably benign 0.13
IGL03215:Dnah1 APN 14 30,996,348 (GRCm39) missense probably damaging 1.00
IGL03230:Dnah1 APN 14 30,992,023 (GRCm39) missense probably damaging 1.00
IGL03248:Dnah1 APN 14 30,991,846 (GRCm39) missense probably damaging 1.00
IGL03267:Dnah1 APN 14 31,008,545 (GRCm39) missense probably benign 0.00
IGL03299:Dnah1 APN 14 31,037,079 (GRCm39) nonsense probably null
IGL03301:Dnah1 APN 14 31,014,649 (GRCm39) missense probably damaging 1.00
ergonomic UTSW 14 31,022,705 (GRCm39) missense possibly damaging 0.91
Faraday UTSW 14 31,032,839 (GRCm39) missense probably null 0.05
K3955:Dnah1 UTSW 14 30,988,416 (GRCm39) missense probably benign
PIT1430001:Dnah1 UTSW 14 30,984,537 (GRCm39) missense probably damaging 1.00
PIT4382001:Dnah1 UTSW 14 31,006,412 (GRCm39) missense probably damaging 1.00
R0043:Dnah1 UTSW 14 30,996,362 (GRCm39) missense probably damaging 0.97
R0092:Dnah1 UTSW 14 30,993,566 (GRCm39) missense probably benign 0.00
R0100:Dnah1 UTSW 14 30,984,109 (GRCm39) critical splice donor site probably null
R0100:Dnah1 UTSW 14 30,984,109 (GRCm39) critical splice donor site probably null
R0101:Dnah1 UTSW 14 31,005,856 (GRCm39) missense probably damaging 1.00
R0119:Dnah1 UTSW 14 30,998,115 (GRCm39) missense probably damaging 1.00
R0136:Dnah1 UTSW 14 30,998,115 (GRCm39) missense probably damaging 1.00
R0144:Dnah1 UTSW 14 30,989,831 (GRCm39) splice site probably benign
R0279:Dnah1 UTSW 14 31,024,332 (GRCm39) missense possibly damaging 0.94
R0299:Dnah1 UTSW 14 30,998,115 (GRCm39) missense probably damaging 1.00
R0316:Dnah1 UTSW 14 31,000,108 (GRCm39) missense probably benign 0.00
R0739:Dnah1 UTSW 14 30,987,872 (GRCm39) nonsense probably null
R0789:Dnah1 UTSW 14 31,026,548 (GRCm39) missense probably benign
R0826:Dnah1 UTSW 14 31,025,864 (GRCm39) missense probably benign 0.02
R1102:Dnah1 UTSW 14 31,018,414 (GRCm39) nonsense probably null
R1116:Dnah1 UTSW 14 31,029,824 (GRCm39) missense probably benign 0.13
R1229:Dnah1 UTSW 14 31,032,808 (GRCm39) missense probably benign 0.11
R1447:Dnah1 UTSW 14 31,028,855 (GRCm39) missense probably benign 0.06
R1449:Dnah1 UTSW 14 30,985,908 (GRCm39) missense probably damaging 1.00
R1462:Dnah1 UTSW 14 30,990,738 (GRCm39) splice site probably benign
R1482:Dnah1 UTSW 14 31,016,831 (GRCm39) missense probably damaging 1.00
R1500:Dnah1 UTSW 14 31,038,715 (GRCm39) missense probably benign
R1512:Dnah1 UTSW 14 31,014,994 (GRCm39) missense probably damaging 1.00
R1591:Dnah1 UTSW 14 30,994,289 (GRCm39) missense probably benign 0.01
R1598:Dnah1 UTSW 14 31,023,219 (GRCm39) missense probably benign 0.07
R1644:Dnah1 UTSW 14 31,024,249 (GRCm39) splice site probably benign
R1672:Dnah1 UTSW 14 30,998,157 (GRCm39) missense probably damaging 1.00
R1713:Dnah1 UTSW 14 31,001,139 (GRCm39) missense probably damaging 1.00
R1769:Dnah1 UTSW 14 31,032,839 (GRCm39) missense probably null 0.05
R1796:Dnah1 UTSW 14 30,983,050 (GRCm39) missense probably benign 0.00
R1902:Dnah1 UTSW 14 31,041,716 (GRCm39) missense probably damaging 0.99
R1905:Dnah1 UTSW 14 30,986,587 (GRCm39) missense probably benign 0.06
R1908:Dnah1 UTSW 14 30,984,515 (GRCm39) missense probably damaging 1.00
R1972:Dnah1 UTSW 14 30,987,348 (GRCm39) nonsense probably null
R1973:Dnah1 UTSW 14 30,987,348 (GRCm39) nonsense probably null
R2004:Dnah1 UTSW 14 31,023,813 (GRCm39) missense possibly damaging 0.79
R2051:Dnah1 UTSW 14 31,001,080 (GRCm39) missense probably damaging 1.00
R2062:Dnah1 UTSW 14 30,993,086 (GRCm39) missense probably damaging 1.00
R2188:Dnah1 UTSW 14 31,001,121 (GRCm39) missense probably damaging 0.98
R2240:Dnah1 UTSW 14 31,021,931 (GRCm39) missense probably benign 0.00
R2862:Dnah1 UTSW 14 31,006,719 (GRCm39) missense probably benign 0.21
R2894:Dnah1 UTSW 14 31,020,718 (GRCm39) missense possibly damaging 0.67
R3120:Dnah1 UTSW 14 30,988,779 (GRCm39) nonsense probably null
R3410:Dnah1 UTSW 14 30,991,774 (GRCm39) missense possibly damaging 0.55
R3411:Dnah1 UTSW 14 30,991,774 (GRCm39) missense possibly damaging 0.55
R3435:Dnah1 UTSW 14 31,038,631 (GRCm39) missense probably damaging 0.96
R3615:Dnah1 UTSW 14 31,037,105 (GRCm39) missense possibly damaging 0.92
R3616:Dnah1 UTSW 14 31,037,105 (GRCm39) missense possibly damaging 0.92
R3741:Dnah1 UTSW 14 30,987,424 (GRCm39) splice site probably benign
R3805:Dnah1 UTSW 14 31,016,720 (GRCm39) missense possibly damaging 0.67
R3894:Dnah1 UTSW 14 31,028,985 (GRCm39) missense probably benign
R4007:Dnah1 UTSW 14 31,025,741 (GRCm39) splice site probably benign
R4201:Dnah1 UTSW 14 30,984,227 (GRCm39) missense probably benign 0.00
R4232:Dnah1 UTSW 14 31,026,873 (GRCm39) missense probably benign
R4372:Dnah1 UTSW 14 31,026,879 (GRCm39) missense probably damaging 1.00
R4391:Dnah1 UTSW 14 31,016,792 (GRCm39) missense probably damaging 1.00
R4423:Dnah1 UTSW 14 31,006,718 (GRCm39) missense probably benign 0.00
R4526:Dnah1 UTSW 14 31,007,955 (GRCm39) missense probably benign 0.05
R4650:Dnah1 UTSW 14 31,006,844 (GRCm39) splice site probably null
R4723:Dnah1 UTSW 14 30,994,899 (GRCm39) missense probably damaging 1.00
R4748:Dnah1 UTSW 14 31,041,902 (GRCm39) missense probably benign
R4783:Dnah1 UTSW 14 30,985,436 (GRCm39) missense probably damaging 1.00
R4784:Dnah1 UTSW 14 30,985,436 (GRCm39) missense probably damaging 1.00
R4785:Dnah1 UTSW 14 30,985,436 (GRCm39) missense probably damaging 1.00
R4843:Dnah1 UTSW 14 30,986,920 (GRCm39) missense probably damaging 1.00
R4879:Dnah1 UTSW 14 31,022,705 (GRCm39) missense possibly damaging 0.91
R4897:Dnah1 UTSW 14 30,989,496 (GRCm39) missense probably damaging 1.00
R4911:Dnah1 UTSW 14 31,017,280 (GRCm39) missense probably damaging 1.00
R4985:Dnah1 UTSW 14 31,008,855 (GRCm39) missense probably null 1.00
R5070:Dnah1 UTSW 14 31,004,375 (GRCm39) missense probably benign 0.05
R5128:Dnah1 UTSW 14 31,018,152 (GRCm39) splice site probably null
R5409:Dnah1 UTSW 14 30,985,212 (GRCm39) missense probably damaging 1.00
R5436:Dnah1 UTSW 14 31,038,704 (GRCm39) missense probably benign
R5481:Dnah1 UTSW 14 31,030,828 (GRCm39) missense possibly damaging 0.55
R5550:Dnah1 UTSW 14 31,038,665 (GRCm39) missense probably benign 0.00
R5555:Dnah1 UTSW 14 31,012,776 (GRCm39) missense probably damaging 0.99
R5566:Dnah1 UTSW 14 30,996,323 (GRCm39) missense probably benign 0.35
R5623:Dnah1 UTSW 14 31,007,980 (GRCm39) missense possibly damaging 0.62
R5701:Dnah1 UTSW 14 30,996,001 (GRCm39) missense probably damaging 1.00
R5751:Dnah1 UTSW 14 31,032,863 (GRCm39) missense probably benign 0.00
R5823:Dnah1 UTSW 14 30,988,375 (GRCm39) missense possibly damaging 0.92
R6030:Dnah1 UTSW 14 30,989,984 (GRCm39) missense probably damaging 1.00
R6030:Dnah1 UTSW 14 30,989,984 (GRCm39) missense probably damaging 1.00
R6090:Dnah1 UTSW 14 30,991,382 (GRCm39) missense possibly damaging 0.83
R6139:Dnah1 UTSW 14 31,007,984 (GRCm39) missense probably benign 0.02
R6145:Dnah1 UTSW 14 31,022,927 (GRCm39) missense probably benign 0.07
R6306:Dnah1 UTSW 14 31,026,544 (GRCm39) missense probably damaging 0.97
R6376:Dnah1 UTSW 14 30,997,565 (GRCm39) missense probably damaging 1.00
R6451:Dnah1 UTSW 14 31,022,765 (GRCm39) missense probably benign 0.08
R6549:Dnah1 UTSW 14 30,991,340 (GRCm39) missense probably damaging 1.00
R6748:Dnah1 UTSW 14 31,021,945 (GRCm39) missense probably damaging 0.99
R6826:Dnah1 UTSW 14 31,008,247 (GRCm39) missense probably benign 0.00
R6870:Dnah1 UTSW 14 30,993,018 (GRCm39) nonsense probably null
R6932:Dnah1 UTSW 14 31,009,733 (GRCm39) missense probably damaging 1.00
R6944:Dnah1 UTSW 14 30,990,861 (GRCm39) missense probably damaging 1.00
R7033:Dnah1 UTSW 14 30,986,882 (GRCm39) missense probably damaging 1.00
R7078:Dnah1 UTSW 14 31,019,067 (GRCm39) missense probably damaging 1.00
R7133:Dnah1 UTSW 14 31,008,033 (GRCm39) missense probably benign
R7136:Dnah1 UTSW 14 31,020,613 (GRCm39) missense probably damaging 1.00
R7203:Dnah1 UTSW 14 30,996,339 (GRCm39) missense probably benign
R7241:Dnah1 UTSW 14 30,986,896 (GRCm39) missense probably benign 0.00
R7260:Dnah1 UTSW 14 30,991,343 (GRCm39) missense probably damaging 1.00
R7264:Dnah1 UTSW 14 30,991,851 (GRCm39) missense probably benign
R7291:Dnah1 UTSW 14 31,020,662 (GRCm39) missense probably damaging 1.00
R7293:Dnah1 UTSW 14 31,009,820 (GRCm39) missense probably damaging 1.00
R7300:Dnah1 UTSW 14 30,991,798 (GRCm39) missense probably benign 0.05
R7319:Dnah1 UTSW 14 31,018,551 (GRCm39) missense probably benign 0.02
R7323:Dnah1 UTSW 14 31,020,664 (GRCm39) missense probably damaging 1.00
R7472:Dnah1 UTSW 14 31,022,748 (GRCm39) missense possibly damaging 0.80
R7472:Dnah1 UTSW 14 30,983,547 (GRCm39) missense probably damaging 1.00
R7499:Dnah1 UTSW 14 31,037,079 (GRCm39) nonsense probably null
R7526:Dnah1 UTSW 14 31,009,833 (GRCm39) missense possibly damaging 0.49
R7560:Dnah1 UTSW 14 31,026,940 (GRCm39) missense probably benign
R7574:Dnah1 UTSW 14 31,041,865 (GRCm39) missense probably benign 0.00
R7617:Dnah1 UTSW 14 31,006,739 (GRCm39) missense possibly damaging 0.80
R7620:Dnah1 UTSW 14 31,025,863 (GRCm39) missense possibly damaging 0.47
R7692:Dnah1 UTSW 14 31,014,295 (GRCm39) missense probably benign 0.00
R7702:Dnah1 UTSW 14 31,032,866 (GRCm39) missense probably benign
R7786:Dnah1 UTSW 14 30,984,478 (GRCm39) missense probably damaging 1.00
R7984:Dnah1 UTSW 14 30,989,772 (GRCm39) missense probably damaging 1.00
R8002:Dnah1 UTSW 14 31,020,679 (GRCm39) missense probably damaging 1.00
R8022:Dnah1 UTSW 14 30,986,971 (GRCm39) missense probably damaging 1.00
R8032:Dnah1 UTSW 14 30,993,505 (GRCm39) missense probably damaging 1.00
R8099:Dnah1 UTSW 14 31,024,321 (GRCm39) missense probably benign 0.00
R8171:Dnah1 UTSW 14 31,019,067 (GRCm39) missense probably damaging 1.00
R8263:Dnah1 UTSW 14 31,015,134 (GRCm39) missense probably damaging 1.00
R8274:Dnah1 UTSW 14 31,017,531 (GRCm39) missense probably benign 0.00
R8345:Dnah1 UTSW 14 30,986,551 (GRCm39) missense probably damaging 1.00
R8348:Dnah1 UTSW 14 31,015,682 (GRCm39) missense probably damaging 1.00
R8353:Dnah1 UTSW 14 31,005,159 (GRCm39) missense probably benign
R8356:Dnah1 UTSW 14 30,994,972 (GRCm39) missense probably benign 0.00
R8376:Dnah1 UTSW 14 31,023,303 (GRCm39) missense probably damaging 1.00
R8448:Dnah1 UTSW 14 31,015,682 (GRCm39) missense probably damaging 1.00
R8461:Dnah1 UTSW 14 31,027,915 (GRCm39) missense probably benign 0.00
R8534:Dnah1 UTSW 14 31,023,805 (GRCm39) missense probably benign 0.16
R8544:Dnah1 UTSW 14 30,990,861 (GRCm39) missense probably damaging 1.00
R8679:Dnah1 UTSW 14 30,989,767 (GRCm39) missense possibly damaging 0.77
R8716:Dnah1 UTSW 14 30,989,941 (GRCm39) critical splice donor site probably benign
R8750:Dnah1 UTSW 14 31,026,924 (GRCm39) missense probably benign 0.30
R8790:Dnah1 UTSW 14 31,018,232 (GRCm39) missense possibly damaging 0.89
R8808:Dnah1 UTSW 14 31,008,771 (GRCm39) missense probably benign
R8821:Dnah1 UTSW 14 31,018,455 (GRCm39) missense probably benign
R8887:Dnah1 UTSW 14 31,032,997 (GRCm39) missense probably damaging 1.00
R8948:Dnah1 UTSW 14 31,012,396 (GRCm39) missense probably damaging 1.00
R8950:Dnah1 UTSW 14 31,012,396 (GRCm39) missense probably damaging 1.00
R8955:Dnah1 UTSW 14 31,007,950 (GRCm39) missense probably benign
R8987:Dnah1 UTSW 14 31,033,704 (GRCm39) missense possibly damaging 0.93
R8998:Dnah1 UTSW 14 31,018,235 (GRCm39) missense probably benign 0.12
R8999:Dnah1 UTSW 14 31,018,235 (GRCm39) missense probably benign 0.12
R9015:Dnah1 UTSW 14 30,986,316 (GRCm39) missense probably damaging 0.96
R9031:Dnah1 UTSW 14 31,001,128 (GRCm39) missense probably benign
R9088:Dnah1 UTSW 14 30,987,970 (GRCm39) missense probably benign 0.04
R9096:Dnah1 UTSW 14 30,983,027 (GRCm39) missense probably damaging 0.99
R9117:Dnah1 UTSW 14 31,033,581 (GRCm39) splice site probably benign
R9157:Dnah1 UTSW 14 30,987,970 (GRCm39) missense probably damaging 0.97
R9296:Dnah1 UTSW 14 30,996,011 (GRCm39) critical splice acceptor site probably null
R9313:Dnah1 UTSW 14 30,987,970 (GRCm39) missense probably damaging 0.97
R9325:Dnah1 UTSW 14 30,998,160 (GRCm39) missense possibly damaging 0.69
R9352:Dnah1 UTSW 14 31,038,620 (GRCm39) missense probably benign 0.00
R9411:Dnah1 UTSW 14 31,018,256 (GRCm39) missense probably damaging 1.00
R9429:Dnah1 UTSW 14 30,997,499 (GRCm39) nonsense probably null
R9452:Dnah1 UTSW 14 31,018,448 (GRCm39) missense probably benign 0.35
R9562:Dnah1 UTSW 14 30,986,394 (GRCm39) missense probably damaging 1.00
R9565:Dnah1 UTSW 14 30,986,394 (GRCm39) missense probably damaging 1.00
R9616:Dnah1 UTSW 14 31,026,400 (GRCm39) missense probably null 0.20
R9621:Dnah1 UTSW 14 31,016,772 (GRCm39) missense probably damaging 1.00
R9677:Dnah1 UTSW 14 31,029,821 (GRCm39) missense probably benign 0.00
R9723:Dnah1 UTSW 14 30,987,946 (GRCm39) missense probably damaging 1.00
R9758:Dnah1 UTSW 14 30,985,395 (GRCm39) missense probably damaging 0.98
RF006:Dnah1 UTSW 14 31,029,832 (GRCm39) missense probably benign 0.08
Z1088:Dnah1 UTSW 14 31,026,768 (GRCm39) missense probably benign 0.17
Predicted Primers PCR Primer
(F):5'- TGCTAGGGGATTTCCAGAGG -3'
(R):5'- GGTTCCTGAAAGCCATGACC -3'

Sequencing Primer
(F):5'- TAGGGGATTTCCAGAGGCCATC -3'
(R):5'- CATGACCTGGAGAAGATATTACAAG -3'
Posted On 2014-06-30