Incidental Mutation 'R6030:Dnah1'
ID 480360
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 044202-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6030 (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 A at 30989984 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 3219 (I3219F)
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: I3219F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000043281
Gene: ENSMUSG00000019027
AA Change: I3219F

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: ENSMUST00000228429
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228755
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228927
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.4%
  • 10x: 96.1%
  • 20x: 86.0%
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: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 A G 7: 120,133,021 (GRCm39) N1317D probably benign Het
Abhd8 T A 8: 71,910,794 (GRCm39) Y338F possibly damaging Het
Actg2 G T 6: 83,493,346 (GRCm39) N297K probably damaging Het
Agap1 A G 1: 89,558,156 (GRCm39) D148G probably damaging Het
Alox12 T C 11: 70,145,417 (GRCm39) D52G possibly damaging Het
Ano5 T A 7: 51,224,573 (GRCm39) S496T probably damaging Het
Arl6ip4 T C 5: 124,255,968 (GRCm39) probably null Het
Atp4a G C 7: 30,421,941 (GRCm39) E826Q probably damaging Het
Bbs7 T C 3: 36,657,060 (GRCm39) D256G probably damaging Het
Bckdha T A 7: 25,330,866 (GRCm39) D50V probably damaging Het
Cast A G 13: 74,844,056 (GRCm39) S693P possibly damaging Het
Cfap251 C T 5: 123,412,267 (GRCm39) T532M probably damaging Het
Col6a1 T C 10: 76,545,700 (GRCm39) Y924C unknown Het
Crkl A G 16: 17,270,604 (GRCm39) Y88C probably damaging Het
Cse1l T C 2: 166,761,541 (GRCm39) F32L probably benign Het
Dmxl2 C T 9: 54,300,957 (GRCm39) V2385I probably benign Het
Dnah17 C T 11: 117,916,375 (GRCm39) R4266H probably benign Het
Efcab5 A G 11: 77,012,088 (GRCm39) L722P probably damaging Het
Emilin3 C A 2: 160,751,105 (GRCm39) V215L probably benign Het
Entr1 T C 2: 26,276,983 (GRCm39) D249G possibly damaging Het
Esr1 A T 10: 4,696,622 (GRCm39) N157I possibly damaging Het
Esrrg A G 1: 187,930,904 (GRCm39) M309V probably benign Het
Fam120b G A 17: 15,622,172 (GRCm39) R50Q probably damaging Het
Fat2 G T 11: 55,201,129 (GRCm39) Y648* probably null Het
Gbp2b T A 3: 142,309,414 (GRCm39) I175N probably benign Het
Gm1043 T A 5: 37,311,952 (GRCm39) probably benign Het
Gm21060 A G 19: 61,285,411 (GRCm39) C33R possibly damaging Het
Gpx6 C T 13: 21,496,510 (GRCm39) S28L probably benign Het
Hyls1 G A 9: 35,472,480 (GRCm39) S312F probably benign Het
Ifi44 T C 3: 151,455,195 (GRCm39) Q10R probably benign Het
Impa2 T C 18: 67,451,498 (GRCm39) V264A probably benign Het
Khdc1a A T 1: 21,421,108 (GRCm39) M98L probably benign Het
Lrrc45 T A 11: 120,611,474 (GRCm39) L616* probably null Het
Mios A T 6: 8,215,704 (GRCm39) H300L probably benign Het
Mllt6 A T 11: 97,568,051 (GRCm39) T827S probably damaging Het
Mrc1 C A 2: 14,321,712 (GRCm39) D1068E probably benign Het
Ndst3 T C 3: 123,346,168 (GRCm39) Y702C probably damaging Het
Nek11 T A 9: 105,082,087 (GRCm39) probably null Het
Nek4 T C 14: 30,678,890 (GRCm39) F138S probably damaging Het
Nfatc4 T A 14: 56,069,897 (GRCm39) Y688* probably null Het
Nlrx1 C T 9: 44,175,057 (GRCm39) V240M probably damaging Het
Npy6r A T 18: 44,409,149 (GRCm39) Y190F probably benign Het
Or10ab5 A C 7: 108,245,433 (GRCm39) S117A possibly damaging Het
Or10d4b T C 9: 39,534,637 (GRCm39) F71L probably damaging Het
Or1j10 T G 2: 36,267,556 (GRCm39) L256R probably damaging Het
Or52b4i C A 7: 102,191,817 (GRCm39) R225S probably benign Het
Or5p52 A G 7: 107,502,620 (GRCm39) E232G probably benign Het
Or6c68 A T 10: 129,158,238 (GRCm39) T249S probably benign Het
Osbpl7 A C 11: 96,943,087 (GRCm39) H113P probably benign Het
Pam16l C T 10: 43,400,252 (GRCm39) A30V probably benign Het
Pck1 A G 2: 172,996,650 (GRCm39) E188G probably benign Het
Pimreg A G 11: 71,936,576 (GRCm39) D213G probably benign Het
Pkd1l2 A G 8: 117,769,976 (GRCm39) I1160T probably damaging Het
Ppargc1b G A 18: 61,441,005 (GRCm39) Q622* probably null Het
Ppfia2 T A 10: 106,742,338 (GRCm39) C1044S probably damaging Het
Ppp4r3a A G 12: 101,024,659 (GRCm39) V280A probably damaging Het
Ptprf T C 4: 118,068,245 (GRCm39) N1764D probably benign Het
Pygm C T 19: 6,438,842 (GRCm39) R311C possibly damaging Het
Rab7b A G 1: 131,626,299 (GRCm39) K109R probably damaging Het
Rsf1 GGCG GGCGACGGCTGCG 7: 97,229,113 (GRCm39) probably benign Het
Setbp1 T G 18: 78,900,926 (GRCm39) I914L probably benign Het
Shprh A C 10: 11,027,735 (GRCm39) Q114P probably benign Het
Slc5a9 T C 4: 111,742,725 (GRCm39) I456V possibly damaging Het
Slc8b1 T C 5: 120,657,985 (GRCm39) probably null Het
Spin1 T A 13: 51,293,552 (GRCm39) Y87* probably null Het
Spring1 T C 5: 118,393,798 (GRCm39) W59R probably damaging Het
Srebf2 T C 15: 82,061,477 (GRCm39) probably null Het
Sufu T C 19: 46,463,978 (GRCm39) Y397H probably damaging Het
Tgfb3 A C 12: 86,110,624 (GRCm39) V242G probably benign Het
Tgm3 A T 2: 129,883,920 (GRCm39) Y526F probably damaging Het
Tmem209 A G 6: 30,482,967 (GRCm39) L508P probably damaging Het
Tmem67 T C 4: 12,063,799 (GRCm39) D454G probably benign Het
Ttn T C 2: 76,646,943 (GRCm39) E3280G possibly damaging Het
Tusc3 G C 8: 39,538,560 (GRCm39) G200R probably damaging Het
Umps A G 16: 33,782,508 (GRCm39) V138A probably benign Het
Ypel1 A G 16: 16,902,377 (GRCm39) probably null Het
Zdhhc19 T A 16: 32,317,860 (GRCm39) L63Q 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
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
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
Posted On 2017-06-26