Incidental Mutation 'R7241:Dnah1'
ID 563234
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 045348-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7241 (G1)
Quality Score 225.009
Status Not validated
Chromosome 14
Chromosomal Location 30982332-31045853 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 30986896 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 3632 (H3632R)
Ref Sequence ENSEMBL: ENSMUSP00000043281 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022458] [ENSMUST00000048603]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000022458
SMART Domains Protein: ENSMUSP00000022458
Gene: ENSMUSG00000021901

DomainStartEndE-ValueType
Pfam:Peptidase_C12 5 215 3e-70 PFAM
low complexity region 282 293 N/A INTRINSIC
low complexity region 396 407 N/A INTRINSIC
low complexity region 577 596 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000048603
AA Change: H3632R

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000043281
Gene: ENSMUSG00000019027
AA Change: H3632R

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
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
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: 81 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca14 A G 7: 119,846,184 (GRCm39) T612A probably damaging Het
Acacb G A 5: 114,383,161 (GRCm39) A2115T possibly damaging Het
Adam32 T C 8: 25,388,510 (GRCm39) K398R probably benign Het
Adam9 T A 8: 25,441,002 (GRCm39) I824F possibly damaging Het
Ahnak A G 19: 8,986,395 (GRCm39) I2560V possibly damaging Het
Ank3 G A 10: 69,542,644 (GRCm39) M1I probably null Het
Anks1b T G 10: 90,348,699 (GRCm39) I789S probably damaging Het
Ap2b1 T A 11: 83,241,931 (GRCm39) N641K probably benign Het
Arhgap33 A G 7: 30,228,146 (GRCm39) L412P probably damaging Het
Atp13a3 T A 16: 30,171,095 (GRCm39) M317L possibly damaging Het
B4galt5 A G 2: 167,148,617 (GRCm39) L167P probably damaging Het
Bace2 T C 16: 97,237,998 (GRCm39) I483T possibly damaging Het
C2cd3 A C 7: 100,056,257 (GRCm39) K177T Het
Ccr4 T C 9: 114,322,024 (GRCm39) T14A probably benign Het
Cep250 A T 2: 155,833,472 (GRCm39) H1799L probably benign Het
Cgnl1 T C 9: 71,632,052 (GRCm39) Q433R probably benign Het
Copb1 C T 7: 113,836,591 (GRCm39) V384M probably damaging Het
Cyp2c50 T A 19: 40,079,012 (GRCm39) N118K probably benign Het
Cyp4a32 A G 4: 115,459,499 (GRCm39) I78V probably benign Het
Cyth4 A G 15: 78,491,245 (GRCm39) K108R probably benign Het
Dnah3 T C 7: 119,542,856 (GRCm39) I540V probably benign Het
Dock4 A G 12: 40,844,859 (GRCm39) Y1174C probably damaging Het
Drd5 A G 5: 38,477,879 (GRCm39) T291A probably damaging Het
Eeig1 A G 2: 32,448,076 (GRCm39) R62G probably benign Het
Fbn1 T C 2: 125,148,415 (GRCm39) N2611S possibly damaging Het
Fcsk A G 8: 111,622,529 (GRCm39) I133T probably benign Het
Fhod3 A G 18: 25,193,409 (GRCm39) E640G probably damaging Het
Flvcr2 T A 12: 85,852,013 (GRCm39) D522E probably benign Het
Ganc T A 2: 120,272,010 (GRCm39) I556K probably damaging Het
Gjc2 T A 11: 59,067,960 (GRCm39) E174V unknown Het
Gzmd G A 14: 56,368,799 (GRCm39) R32C probably damaging Het
Hltf T A 3: 20,119,556 (GRCm39) H200Q probably benign Het
Ift88 A G 14: 57,717,454 (GRCm39) I559M probably damaging Het
Ighv1-62-1 C A 12: 115,350,322 (GRCm39) C115F probably damaging Het
Impdh2 A G 9: 108,440,636 (GRCm39) N279S possibly damaging Het
Itpr1 T C 6: 108,494,581 (GRCm39) probably null Het
Kansl1l T C 1: 66,840,787 (GRCm39) N171S possibly damaging Het
Kif14 T A 1: 136,396,491 (GRCm39) C266S probably benign Het
Kif19b A G 5: 140,447,943 (GRCm39) T137A probably damaging Het
Lrriq1 A C 10: 103,051,834 (GRCm39) V306G probably damaging Het
Mast4 G A 13: 103,470,508 (GRCm39) R65W possibly damaging Het
Mex3d T C 10: 80,223,091 (GRCm39) D55G Het
Mrps27 A T 13: 99,547,788 (GRCm39) K233* probably null Het
Myo1f A G 17: 33,798,902 (GRCm39) N189S probably damaging Het
Nbn A T 4: 15,991,190 (GRCm39) K729N probably benign Het
Or1e35 T C 11: 73,798,058 (GRCm39) S87G probably benign Het
Or8k35 C A 2: 86,424,498 (GRCm39) V225F possibly damaging Het
Pgghg T C 7: 140,525,633 (GRCm39) S479P Het
Plaat5 A G 19: 7,591,946 (GRCm39) T121A probably benign Het
Polr1e A C 4: 45,029,340 (GRCm39) H315P probably damaging Het
Pou6f2 A G 13: 18,299,874 (GRCm39) V595A Het
Prdm15 T C 16: 97,596,941 (GRCm39) D960G possibly damaging Het
Prkcz A T 4: 155,353,516 (GRCm39) M460K probably benign Het
Prkd2 G T 7: 16,591,730 (GRCm39) R587L probably benign Het
Prkn C A 17: 12,073,748 (GRCm39) N355K possibly damaging Het
Rabep1 C A 11: 70,830,815 (GRCm39) T829N probably damaging Het
Rptn A G 3: 93,303,261 (GRCm39) E198G probably benign Het
Ryr2 A T 13: 11,680,799 (GRCm39) I3182N possibly damaging Het
Sectm1a T A 11: 120,960,708 (GRCm39) I36F possibly damaging Het
Sez6l T C 5: 112,621,346 (GRCm39) S243G probably benign Het
Spata31h1 T C 10: 82,122,876 (GRCm39) E3378G probably benign Het
Taf2 T A 15: 54,925,537 (GRCm39) H235L probably benign Het
Tbc1d7 T C 13: 43,306,493 (GRCm39) Q161R probably benign Het
Tfcp2 T C 15: 100,416,468 (GRCm39) T271A possibly damaging Het
Thrsp G T 7: 97,066,295 (GRCm39) T139K probably damaging Het
Timm10 T A 2: 84,660,333 (GRCm39) *91R probably null Het
Tlr11 T A 14: 50,599,598 (GRCm39) I528N possibly damaging Het
Tnnt2 T A 1: 135,779,444 (GRCm39) L278Q probably damaging Het
Toe1 A T 4: 116,664,715 (GRCm39) M1K probably null Het
Trpv5 G A 6: 41,652,242 (GRCm39) R148* probably null Het
Ttll13 A C 7: 79,903,911 (GRCm39) K280Q probably damaging Het
Ttn A G 2: 76,783,550 (GRCm39) V860A unknown Het
Txnip T C 3: 96,466,991 (GRCm39) Y222H probably damaging Het
Ubr4 G A 4: 139,170,725 (GRCm39) S1600N probably damaging Het
Uhrf1 T C 17: 56,622,193 (GRCm39) Y364H probably damaging Het
Unc5a A T 13: 55,138,833 (GRCm39) T71S probably damaging Het
Vmn1r123 A T 7: 20,896,537 (GRCm39) Y143F possibly damaging Het
Vmn1r180 T A 7: 23,651,891 (GRCm39) I18N probably damaging Het
Washc2 A G 6: 116,185,168 (GRCm39) M1V probably null Het
Zfp174 C A 16: 3,666,111 (GRCm39) H125Q probably benign Het
Zfpl1 T C 19: 6,131,943 (GRCm39) H227R possibly damaging 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
R1903: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
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'- AGATGCTGAGACCACACGAG -3'
(R):5'- CAGTGGTTTCCTGTAGGCAG -3'

Sequencing Primer
(F):5'- TGAGACCACACGAGGCTGG -3'
(R):5'- CTGTAGGCAGGCTCTGAGG -3'
Posted On 2019-06-26