Incidental Mutation 'R3435:Dnah1'
ID 267166
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 040653-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R3435 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 30982332-31045853 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 31038631 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 150 (D150G)
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: D150G

PolyPhen 2 Score 0.957 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000043281
Gene: ENSMUSG00000019027
AA Change: D150G

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: ENSMUST00000228755
Meta Mutation Damage Score 0.1309 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency 100% (33/33)
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: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933409G03Rik A C 2: 68,432,189 (GRCm39) D91A unknown Het
Abca9 T C 11: 110,045,256 (GRCm39) E359G probably benign Het
Atp7a G A X: 105,138,463 (GRCm39) R563K probably benign Het
Fam47e T A 5: 92,733,221 (GRCm39) V152D probably damaging Het
Gm19965 C A 1: 116,749,353 (GRCm39) H345N possibly damaging Het
Ift74 A G 4: 94,510,089 (GRCm39) probably null Het
Iqgap3 A G 3: 88,001,911 (GRCm39) I384V probably benign Het
Lrrc57 T A 2: 120,439,862 (GRCm39) probably benign Het
Mafk C T 5: 139,786,062 (GRCm39) Q87* probably null Het
Mast2 A T 4: 116,165,292 (GRCm39) S1314T probably benign Het
Mast4 A G 13: 102,923,887 (GRCm39) I508T probably damaging Het
Mdn1 T C 4: 32,733,726 (GRCm39) probably null Het
Mup6 G T 4: 60,004,116 (GRCm39) probably null Het
Neurl1a T C 19: 47,245,964 (GRCm39) V532A probably damaging Het
Nod2 A G 8: 89,390,637 (GRCm39) R293G possibly damaging Het
Notch3 A T 17: 32,377,592 (GRCm39) D161E possibly damaging Het
Or1j1 T A 2: 36,702,690 (GRCm39) Q138L probably benign Het
Osbpl3 A T 6: 50,325,050 (GRCm39) N149K possibly damaging Het
P2rx4 T A 5: 122,863,133 (GRCm39) I202K probably damaging Het
Pbxip1 T C 3: 89,354,543 (GRCm39) L354P probably damaging Het
Pld1 A T 3: 28,178,772 (GRCm39) M889L probably benign Het
Ppp2r2b T A 18: 42,874,174 (GRCm39) Q52L possibly damaging Het
Prob1 T C 18: 35,787,294 (GRCm39) E320G possibly damaging Het
Stard13 A T 5: 150,965,644 (GRCm39) L937Q probably damaging Het
Strn4 T C 7: 16,571,558 (GRCm39) S563P possibly damaging Het
Syne1 T C 10: 5,298,565 (GRCm39) D1114G probably damaging Het
Tmem117 T C 15: 94,992,573 (GRCm39) I411T probably damaging Het
Tmx3 T A 18: 90,546,028 (GRCm39) V203E probably damaging Het
Ttn T C 2: 76,709,062 (GRCm39) probably benign Het
Vmn1r209 A T 13: 22,990,267 (GRCm39) M141K probably benign 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
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'- AACAGTTCCACAGGCTCTG -3'
(R):5'- TAAGTGTCCCATACCCCAGG -3'

Sequencing Primer
(F):5'- GGCTGGCCCCTGATGGTG -3'
(R):5'- GTGTCCCATACCCCAGGCATAC -3'
Posted On 2015-02-18