Incidental Mutation 'R7231:Dnah9'
ID 562489
Institutional Source Beutler Lab
Gene Symbol Dnah9
Ensembl Gene ENSMUSG00000056752
Gene Name dynein, axonemal, heavy chain 9
Synonyms D11Ertd686e, Dnahc9
MMRRC Submission 045342-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.294) question?
Stock # R7231 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 65831282-66168551 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 65965647 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 2896 (D2896G)
Ref Sequence ENSEMBL: ENSMUSP00000079494 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080665]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000080665
AA Change: D2896G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000079494
Gene: ENSMUSG00000056752
AA Change: D2896G

DomainStartEndE-ValueType
Pfam:DHC_N1 209 787 3.6e-164 PFAM
coiled coil region 788 820 N/A INTRINSIC
low complexity region 1228 1240 N/A INTRINSIC
Pfam:DHC_N2 1290 1699 1.4e-134 PFAM
AAA 1863 1999 4.9e-1 SMART
AAA 2141 2341 1.99e0 SMART
AAA 2468 2614 6.75e-1 SMART
Pfam:AAA_8 2786 3053 1.1e-165 PFAM
Pfam:MT 3065 3408 7.2e-208 PFAM
Pfam:AAA_9 3430 3652 3.2e-87 PFAM
Pfam:Dynein_heavy 3786 4482 1e-241 PFAM
Predicted Effect
SMART Domains Protein: ENSMUSP00000116499
Gene: ENSMUSG00000056752
AA Change: D445G

DomainStartEndE-ValueType
Pfam:AAA_7 1 258 3e-155 PFAM
Pfam:AAA_8 336 603 3.9e-166 PFAM
Pfam:MT 615 958 2.3e-208 PFAM
Pfam:AAA_9 980 1202 1.1e-87 PFAM
Pfam:Dynein_heavy 1336 1514 2.4e-52 PFAM
Pfam:Dynein_heavy 1508 1956 8.6e-155 PFAM
Meta Mutation Damage Score 0.2271 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 98% (78/80)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the heavy chain subunit of axonemal dynein, a large multi-subunit molecular motor. Axonemal dynein attaches to microtubules and hydrolyzes ATP to mediate the movement of cilia and flagella. The gene expresses at least two transcript variants; additional variants have been described, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A T 11: 9,294,175 (GRCm38) T2013S probably benign Het
Ablim3 A G 18: 61,805,064 (GRCm38) probably null Het
Acvrl1 T A 15: 101,136,223 (GRCm38) C206* probably null Het
Adamts15 C A 9: 30,906,158 (GRCm38) R541S probably damaging Het
Add3 A G 19: 53,233,146 (GRCm38) I230V probably benign Het
Ankrd27 A G 7: 35,628,446 (GRCm38) D742G possibly damaging Het
Asxl3 A G 18: 22,517,540 (GRCm38) E862G probably damaging Het
Asxl3 A T 18: 22,411,499 (GRCm38) probably null Het
Atp2b2 G A 6: 113,765,732 (GRCm38) T798M possibly damaging Het
Car12 T C 9: 66,752,317 (GRCm38) I208T probably damaging Het
Cgn T A 3: 94,773,192 (GRCm38) Q600L probably damaging Het
Cgnl1 C T 9: 71,632,645 (GRCm38) A1106T probably benign Het
Cmtr2 T C 8: 110,222,546 (GRCm38) V496A probably benign Het
Cplx4 C A 18: 65,957,052 (GRCm38) D99Y probably damaging Het
Cyfip2 T C 11: 46,224,136 (GRCm38) T915A probably benign Het
Cyp4a32 T C 4: 115,609,697 (GRCm38) L193P probably damaging Het
Dennd5b C T 6: 149,044,604 (GRCm38) R503Q probably damaging Het
Depdc5 C A 5: 32,901,865 (GRCm38) Q303K possibly damaging Het
Dlx1 T A 2: 71,532,496 (GRCm38) M249K possibly damaging Het
Dnah10 A T 5: 124,813,828 (GRCm38) E3218V probably benign Het
Dtx4 C A 19: 12,469,658 (GRCm38) G557* probably null Het
Eps8l2 A G 7: 141,360,392 (GRCm38) N512D probably damaging Het
Fam20a T C 11: 109,721,375 (GRCm38) D114G possibly damaging Het
Fbln1 T C 15: 85,206,152 (GRCm38) S7P unknown Het
Fli1 T C 9: 32,424,188 (GRCm38) E316G probably damaging Het
Fmn2 CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC 1: 174,609,203 (GRCm38) probably benign Het
Haus8 G A 8: 71,253,137 (GRCm38) T302I probably benign Het
Hmcn1 T C 1: 150,638,876 (GRCm38) I3582V probably benign Het
Hnrnpul1 G A 7: 25,748,417 (GRCm38) Q161* probably null Het
Hsf4 C T 8: 105,272,147 (GRCm38) A223V probably damaging Het
Ighg2c A G 12: 113,288,016 (GRCm38) W164R Het
Isl1 A G 13: 116,303,290 (GRCm38) V174A probably benign Het
Itih4 A T 14: 30,896,614 (GRCm38) I661F probably benign Het
Klhl14 A T 18: 21,652,136 (GRCm38) L78Q probably damaging Het
L3mbtl3 T A 10: 26,339,282 (GRCm38) I177F unknown Het
Lingo3 T A 10: 80,835,104 (GRCm38) T331S possibly damaging Het
Lrrc36 T C 8: 105,461,057 (GRCm38) V535A possibly damaging Het
Mapk8ip2 T G 15: 89,458,076 (GRCm38) S497A probably benign Het
Mbip A G 12: 56,337,762 (GRCm38) probably null Het
Nelfa C T 5: 33,898,825 (GRCm38) G498D probably damaging Het
Nlrc5 T A 8: 94,521,805 (GRCm38) probably null Het
Olfr1312 A T 2: 112,042,366 (GRCm38) V222D probably damaging Het
Olfr679 T C 7: 105,085,787 (GRCm38) S24P possibly damaging Het
Olfr701 A T 7: 106,818,443 (GRCm38) Y120F probably damaging Het
Olfr863-ps1 T A 9: 19,941,559 (GRCm38) T294S unknown Het
Pde2a A G 7: 101,505,953 (GRCm38) Y567C probably damaging Het
Pdia4 A T 6: 47,800,957 (GRCm38) F367Y probably benign Het
Pkdrej C A 15: 85,816,188 (GRCm38) C1849F possibly damaging Het
Plekhj1 T G 10: 80,797,658 (GRCm38) T52P probably damaging Het
Ppp2r5d A T 17: 46,684,060 (GRCm38) Y572N probably benign Het
Prkcq T A 2: 11,290,451 (GRCm38) Y570* probably null Het
Ptpn3 T A 4: 57,245,062 (GRCm38) D226V probably damaging Het
Rab1b A G 19: 5,105,201 (GRCm38) S22P probably damaging Het
Ralgapa1 A G 12: 55,604,191 (GRCm38) S2060P probably damaging Het
Rnf148 G T 6: 23,654,891 (GRCm38) S35R probably benign Het
Runx2 G A 17: 44,814,192 (GRCm38) P80L probably damaging Het
Samd15 T A 12: 87,201,044 (GRCm38) S168T possibly damaging Het
Slc26a4 T A 12: 31,547,946 (GRCm38) N167I probably damaging Het
Slc39a1 C A 3: 90,251,790 (GRCm38) H141Q probably benign Het
Slc9a3r2 C T 17: 24,650,104 (GRCm38) R16H probably damaging Het
Snx21 T C 2: 164,786,201 (GRCm38) S46P probably benign Het
Strip2 A G 6: 29,944,487 (GRCm38) S657G probably damaging Het
Stxbp3 G A 3: 108,800,809 (GRCm38) P392L probably damaging Het
Suclg1 G A 6: 73,263,971 (GRCm38) R161H probably benign Het
Tas1r3 T C 4: 155,862,826 (GRCm38) Y134C probably damaging Het
Tgif1 T A 17: 70,846,173 (GRCm38) Q114L probably damaging Het
Tll2 A G 19: 41,086,234 (GRCm38) F964L probably benign Het
Tmem181a T C 17: 6,297,920 (GRCm38) S247P possibly damaging Het
Trav23 A T 14: 53,977,568 (GRCm38) R79S probably damaging Het
Trf C A 9: 103,225,148 (GRCm38) C177F probably damaging Het
Triml1 T C 8: 43,136,371 (GRCm38) Y260C probably benign Het
Tulp4 T C 17: 6,236,235 (GRCm38) F1513L probably benign Het
Umodl1 G A 17: 30,986,116 (GRCm38) V562I probably damaging Het
Ush2a A G 1: 188,759,763 (GRCm38) K3083R possibly damaging Het
Vmn1r74 A T 7: 11,846,961 (GRCm38) I63F probably benign Het
Vmn2r38 C T 7: 9,097,638 (GRCm38) C43Y possibly damaging Het
Vmn2r50 A T 7: 10,053,083 (GRCm38) N32K probably benign Het
Vps13d A G 4: 145,057,462 (GRCm38) V3914A Het
Vwa5b2 A G 16: 20,604,128 (GRCm38) T984A probably benign Het
Zc3h3 C T 15: 75,840,382 (GRCm38) V77M probably damaging Het
Zfp397 A T 18: 23,960,358 (GRCm38) H300L probably damaging Het
Zfp950 G A 19: 61,119,212 (GRCm38) R478C probably benign Het
Other mutations in Dnah9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00696:Dnah9 APN 11 65,841,238 (GRCm38) splice site probably benign
IGL00805:Dnah9 APN 11 65,881,695 (GRCm38) missense probably benign 0.00
IGL00826:Dnah9 APN 11 65,989,942 (GRCm38) missense probably damaging 1.00
IGL01108:Dnah9 APN 11 65,849,980 (GRCm38) missense possibly damaging 0.93
IGL01152:Dnah9 APN 11 66,072,056 (GRCm38) missense probably damaging 1.00
IGL01353:Dnah9 APN 11 66,080,571 (GRCm38) missense probably damaging 1.00
IGL01364:Dnah9 APN 11 66,155,459 (GRCm38) missense probably damaging 1.00
IGL01479:Dnah9 APN 11 65,955,717 (GRCm38) missense probably benign 0.14
IGL01537:Dnah9 APN 11 65,947,680 (GRCm38) missense probably benign
IGL01565:Dnah9 APN 11 66,033,829 (GRCm38) missense possibly damaging 0.95
IGL01597:Dnah9 APN 11 66,118,830 (GRCm38) missense probably damaging 1.00
IGL01619:Dnah9 APN 11 65,831,615 (GRCm38) nonsense probably null
IGL01625:Dnah9 APN 11 66,044,645 (GRCm38) missense probably damaging 1.00
IGL01803:Dnah9 APN 11 66,118,829 (GRCm38) missense probably damaging 1.00
IGL01819:Dnah9 APN 11 66,108,126 (GRCm38) missense probably benign 0.33
IGL01896:Dnah9 APN 11 66,130,666 (GRCm38) missense possibly damaging 0.89
IGL01922:Dnah9 APN 11 66,075,034 (GRCm38) splice site probably benign
IGL01923:Dnah9 APN 11 66,125,235 (GRCm38) splice site probably benign
IGL02059:Dnah9 APN 11 66,072,958 (GRCm38) missense probably damaging 1.00
IGL02068:Dnah9 APN 11 66,061,045 (GRCm38) missense probably damaging 1.00
IGL02135:Dnah9 APN 11 66,117,492 (GRCm38) missense possibly damaging 0.63
IGL02146:Dnah9 APN 11 65,927,700 (GRCm38) missense probably damaging 1.00
IGL02264:Dnah9 APN 11 66,080,488 (GRCm38) splice site probably benign
IGL02325:Dnah9 APN 11 65,834,217 (GRCm38) missense probably damaging 1.00
IGL02426:Dnah9 APN 11 66,125,153 (GRCm38) missense probably benign
IGL02440:Dnah9 APN 11 65,955,246 (GRCm38) missense probably damaging 1.00
IGL02471:Dnah9 APN 11 65,947,618 (GRCm38) nonsense probably null
IGL02496:Dnah9 APN 11 66,029,363 (GRCm38) missense probably damaging 1.00
IGL02672:Dnah9 APN 11 65,927,601 (GRCm38) missense probably benign 0.02
IGL02718:Dnah9 APN 11 65,886,640 (GRCm38) missense probably damaging 0.99
IGL02832:Dnah9 APN 11 66,040,346 (GRCm38) missense probably damaging 1.00
IGL02851:Dnah9 APN 11 66,037,744 (GRCm38) splice site probably benign
IGL02859:Dnah9 APN 11 65,881,619 (GRCm38) splice site probably benign
IGL02864:Dnah9 APN 11 66,061,003 (GRCm38) missense probably damaging 1.00
IGL02954:Dnah9 APN 11 66,118,967 (GRCm38) missense probably damaging 1.00
IGL02987:Dnah9 APN 11 65,841,273 (GRCm38) missense probably benign 0.23
IGL02987:Dnah9 APN 11 65,855,272 (GRCm38) missense probably damaging 0.98
IGL03160:Dnah9 APN 11 66,108,054 (GRCm38) missense probably damaging 0.98
IGL03171:Dnah9 APN 11 65,981,241 (GRCm38) missense probably benign 0.13
IGL03180:Dnah9 APN 11 65,886,639 (GRCm38) missense probably damaging 0.99
IGL03388:Dnah9 APN 11 65,947,542 (GRCm38) missense probably damaging 1.00
anarchy UTSW 11 65,955,248 (GRCm38) missense probably damaging 0.99
sacco UTSW 11 66,168,079 (GRCm38) missense possibly damaging 0.82
Tweed UTSW 11 66,072,072 (GRCm38) missense probably damaging 0.99
vanzetti UTSW 11 65,855,372 (GRCm38) nonsense probably null
IGL02837:Dnah9 UTSW 11 65,874,196 (GRCm38) missense probably damaging 1.00
PIT4280001:Dnah9 UTSW 11 66,005,013 (GRCm38) missense probably benign 0.44
R0021:Dnah9 UTSW 11 65,969,979 (GRCm38) missense probably benign 0.36
R0021:Dnah9 UTSW 11 65,969,979 (GRCm38) missense probably benign 0.36
R0025:Dnah9 UTSW 11 65,969,955 (GRCm38) splice site probably benign
R0025:Dnah9 UTSW 11 65,969,955 (GRCm38) splice site probably benign
R0070:Dnah9 UTSW 11 66,160,040 (GRCm38) missense probably benign 0.10
R0164:Dnah9 UTSW 11 65,918,804 (GRCm38) nonsense probably null
R0164:Dnah9 UTSW 11 65,918,804 (GRCm38) nonsense probably null
R0180:Dnah9 UTSW 11 66,147,290 (GRCm38) missense probably damaging 1.00
R0195:Dnah9 UTSW 11 65,895,905 (GRCm38) missense probably benign 0.30
R0230:Dnah9 UTSW 11 65,855,315 (GRCm38) missense probably damaging 1.00
R0243:Dnah9 UTSW 11 65,911,852 (GRCm38) missense possibly damaging 0.91
R0279:Dnah9 UTSW 11 65,911,789 (GRCm38) critical splice donor site probably null
R0288:Dnah9 UTSW 11 66,025,134 (GRCm38) critical splice donor site probably null
R0309:Dnah9 UTSW 11 66,026,972 (GRCm38) splice site probably benign
R0356:Dnah9 UTSW 11 66,130,562 (GRCm38) critical splice donor site probably null
R0403:Dnah9 UTSW 11 66,084,789 (GRCm38) missense possibly damaging 0.90
R0413:Dnah9 UTSW 11 66,108,135 (GRCm38) missense probably damaging 1.00
R0448:Dnah9 UTSW 11 65,918,713 (GRCm38) splice site probably benign
R0496:Dnah9 UTSW 11 66,075,135 (GRCm38) missense probably null 1.00
R0557:Dnah9 UTSW 11 66,084,666 (GRCm38) missense probably damaging 1.00
R0584:Dnah9 UTSW 11 65,990,489 (GRCm38) missense probably damaging 1.00
R0598:Dnah9 UTSW 11 66,118,877 (GRCm38) missense probably benign 0.02
R0599:Dnah9 UTSW 11 65,965,689 (GRCm38) missense probably damaging 1.00
R0606:Dnah9 UTSW 11 65,841,333 (GRCm38) missense probably damaging 1.00
R0666:Dnah9 UTSW 11 66,085,458 (GRCm38) missense probably benign 0.01
R0715:Dnah9 UTSW 11 66,081,248 (GRCm38) splice site probably benign
R0726:Dnah9 UTSW 11 65,965,681 (GRCm38) missense probably damaging 1.00
R0737:Dnah9 UTSW 11 66,107,898 (GRCm38) missense probably damaging 1.00
R0763:Dnah9 UTSW 11 66,155,530 (GRCm38) missense probably benign 0.30
R0792:Dnah9 UTSW 11 65,896,001 (GRCm38) missense possibly damaging 0.84
R0829:Dnah9 UTSW 11 66,005,176 (GRCm38) missense probably benign 0.00
R0973:Dnah9 UTSW 11 66,005,837 (GRCm38) splice site probably null
R0974:Dnah9 UTSW 11 66,005,837 (GRCm38) splice site probably null
R1055:Dnah9 UTSW 11 66,160,011 (GRCm38) missense probably damaging 1.00
R1081:Dnah9 UTSW 11 66,084,877 (GRCm38) missense probably damaging 0.99
R1184:Dnah9 UTSW 11 66,084,612 (GRCm38) critical splice donor site probably null
R1225:Dnah9 UTSW 11 65,871,060 (GRCm38) missense possibly damaging 0.94
R1304:Dnah9 UTSW 11 65,927,588 (GRCm38) missense probably damaging 0.98
R1417:Dnah9 UTSW 11 65,955,747 (GRCm38) missense probably damaging 0.96
R1439:Dnah9 UTSW 11 65,874,132 (GRCm38) missense probably benign 0.22
R1447:Dnah9 UTSW 11 66,108,482 (GRCm38) missense possibly damaging 0.65
R1450:Dnah9 UTSW 11 65,927,786 (GRCm38) missense probably damaging 1.00
R1470:Dnah9 UTSW 11 65,927,822 (GRCm38) missense probably benign 0.11
R1470:Dnah9 UTSW 11 65,927,822 (GRCm38) missense probably benign 0.11
R1486:Dnah9 UTSW 11 65,834,272 (GRCm38) missense probably damaging 1.00
R1519:Dnah9 UTSW 11 65,881,761 (GRCm38) missense probably damaging 0.96
R1570:Dnah9 UTSW 11 66,112,330 (GRCm38) missense probably benign
R1617:Dnah9 UTSW 11 65,895,921 (GRCm38) missense probably damaging 1.00
R1623:Dnah9 UTSW 11 66,037,637 (GRCm38) missense probably damaging 1.00
R1626:Dnah9 UTSW 11 66,085,267 (GRCm38) missense probably benign 0.05
R1671:Dnah9 UTSW 11 65,927,963 (GRCm38) missense probably damaging 0.99
R1694:Dnah9 UTSW 11 65,954,824 (GRCm38) nonsense probably null
R1701:Dnah9 UTSW 11 65,911,924 (GRCm38) missense probably damaging 1.00
R1702:Dnah9 UTSW 11 66,085,195 (GRCm38) missense possibly damaging 0.72
R1708:Dnah9 UTSW 11 65,915,154 (GRCm38) missense probably benign 0.11
R1718:Dnah9 UTSW 11 66,168,079 (GRCm38) missense possibly damaging 0.82
R1729:Dnah9 UTSW 11 66,085,020 (GRCm38) missense possibly damaging 0.51
R1760:Dnah9 UTSW 11 65,981,222 (GRCm38) missense probably benign 0.31
R1784:Dnah9 UTSW 11 66,085,020 (GRCm38) missense possibly damaging 0.51
R1793:Dnah9 UTSW 11 66,119,594 (GRCm38) critical splice donor site probably null
R1801:Dnah9 UTSW 11 65,955,297 (GRCm38) missense probably damaging 0.99
R1827:Dnah9 UTSW 11 65,850,061 (GRCm38) missense probably damaging 0.97
R1836:Dnah9 UTSW 11 66,118,841 (GRCm38) missense probably benign 0.10
R1840:Dnah9 UTSW 11 65,834,198 (GRCm38) nonsense probably null
R1847:Dnah9 UTSW 11 65,834,386 (GRCm38) missense probably damaging 1.00
R1872:Dnah9 UTSW 11 66,037,490 (GRCm38) missense probably benign 0.16
R1929:Dnah9 UTSW 11 65,976,398 (GRCm38) missense probably benign 0.05
R1969:Dnah9 UTSW 11 65,848,371 (GRCm38) missense probably damaging 1.00
R1971:Dnah9 UTSW 11 65,848,371 (GRCm38) missense probably damaging 1.00
R2027:Dnah9 UTSW 11 65,955,338 (GRCm38) missense probably benign 0.11
R2049:Dnah9 UTSW 11 66,044,683 (GRCm38) missense probably damaging 1.00
R2064:Dnah9 UTSW 11 66,145,435 (GRCm38) missense probably benign 0.31
R2104:Dnah9 UTSW 11 66,061,124 (GRCm38) missense probably damaging 1.00
R2109:Dnah9 UTSW 11 66,037,585 (GRCm38) missense probably damaging 1.00
R2160:Dnah9 UTSW 11 66,117,483 (GRCm38) missense probably damaging 1.00
R2172:Dnah9 UTSW 11 66,072,779 (GRCm38) missense probably damaging 1.00
R2198:Dnah9 UTSW 11 65,859,499 (GRCm38) missense possibly damaging 0.50
R2271:Dnah9 UTSW 11 66,112,362 (GRCm38) missense probably benign 0.37
R2272:Dnah9 UTSW 11 66,112,362 (GRCm38) missense probably benign 0.37
R2396:Dnah9 UTSW 11 66,085,158 (GRCm38) missense probably benign 0.01
R2398:Dnah9 UTSW 11 65,915,203 (GRCm38) missense probably damaging 1.00
R2418:Dnah9 UTSW 11 66,095,415 (GRCm38) nonsense probably null
R2419:Dnah9 UTSW 11 66,095,415 (GRCm38) nonsense probably null
R2510:Dnah9 UTSW 11 66,005,169 (GRCm38) missense probably damaging 1.00
R2680:Dnah9 UTSW 11 66,033,925 (GRCm38) missense probably benign 0.00
R2875:Dnah9 UTSW 11 66,168,461 (GRCm38) missense possibly damaging 0.89
R2979:Dnah9 UTSW 11 66,117,588 (GRCm38) missense possibly damaging 0.89
R3236:Dnah9 UTSW 11 65,954,989 (GRCm38) missense probably benign 0.11
R3237:Dnah9 UTSW 11 65,954,989 (GRCm38) missense probably benign 0.11
R3433:Dnah9 UTSW 11 66,075,112 (GRCm38) missense possibly damaging 0.85
R3737:Dnah9 UTSW 11 66,156,908 (GRCm38) nonsense probably null
R3820:Dnah9 UTSW 11 65,851,003 (GRCm38) critical splice donor site probably null
R3821:Dnah9 UTSW 11 65,851,003 (GRCm38) critical splice donor site probably null
R3822:Dnah9 UTSW 11 65,851,003 (GRCm38) critical splice donor site probably null
R3861:Dnah9 UTSW 11 66,052,994 (GRCm38) splice site probably benign
R3918:Dnah9 UTSW 11 65,870,974 (GRCm38) missense possibly damaging 0.54
R4011:Dnah9 UTSW 11 65,834,464 (GRCm38) missense probably damaging 0.98
R4044:Dnah9 UTSW 11 66,133,635 (GRCm38) missense probably benign 0.03
R4072:Dnah9 UTSW 11 66,084,904 (GRCm38) missense probably benign 0.00
R4076:Dnah9 UTSW 11 66,084,904 (GRCm38) missense probably benign 0.00
R4097:Dnah9 UTSW 11 65,990,459 (GRCm38) missense probably damaging 1.00
R4409:Dnah9 UTSW 11 66,085,477 (GRCm38) missense possibly damaging 0.51
R4410:Dnah9 UTSW 11 66,085,477 (GRCm38) missense possibly damaging 0.51
R4417:Dnah9 UTSW 11 65,981,214 (GRCm38) missense possibly damaging 0.75
R4420:Dnah9 UTSW 11 66,118,749 (GRCm38) missense probably benign 0.00
R4434:Dnah9 UTSW 11 66,108,075 (GRCm38) missense possibly damaging 0.67
R4451:Dnah9 UTSW 11 65,881,641 (GRCm38) missense probably benign 0.07
R4452:Dnah9 UTSW 11 66,027,082 (GRCm38) missense probably damaging 0.96
R4454:Dnah9 UTSW 11 66,147,389 (GRCm38) missense probably damaging 0.96
R4551:Dnah9 UTSW 11 65,841,366 (GRCm38) missense probably damaging 1.00
R4552:Dnah9 UTSW 11 65,841,366 (GRCm38) missense probably damaging 1.00
R4590:Dnah9 UTSW 11 66,040,392 (GRCm38) missense probably damaging 1.00
R4595:Dnah9 UTSW 11 66,168,152 (GRCm38) missense probably benign
R4655:Dnah9 UTSW 11 65,955,732 (GRCm38) missense probably benign 0.00
R4667:Dnah9 UTSW 11 66,155,531 (GRCm38) missense probably benign
R4718:Dnah9 UTSW 11 66,085,473 (GRCm38) missense probably benign
R4720:Dnah9 UTSW 11 66,076,358 (GRCm38) missense probably damaging 1.00
R4734:Dnah9 UTSW 11 65,834,115 (GRCm38) missense probably damaging 1.00
R4749:Dnah9 UTSW 11 65,834,115 (GRCm38) missense probably damaging 1.00
R4765:Dnah9 UTSW 11 65,927,726 (GRCm38) missense probably damaging 1.00
R4905:Dnah9 UTSW 11 65,874,124 (GRCm38) nonsense probably null
R4963:Dnah9 UTSW 11 66,084,611 (GRCm38) splice site probably null
R5074:Dnah9 UTSW 11 65,850,040 (GRCm38) missense probably damaging 1.00
R5230:Dnah9 UTSW 11 66,084,666 (GRCm38) missense probably damaging 0.99
R5262:Dnah9 UTSW 11 66,112,333 (GRCm38) missense probably benign 0.34
R5364:Dnah9 UTSW 11 65,881,696 (GRCm38) missense possibly damaging 0.93
R5370:Dnah9 UTSW 11 66,029,354 (GRCm38) missense probably damaging 1.00
R5386:Dnah9 UTSW 11 66,029,356 (GRCm38) missense probably damaging 1.00
R5389:Dnah9 UTSW 11 66,095,314 (GRCm38) nonsense probably null
R5541:Dnah9 UTSW 11 66,145,336 (GRCm38) missense probably damaging 1.00
R5560:Dnah9 UTSW 11 65,881,740 (GRCm38) missense probably benign 0.00
R5576:Dnah9 UTSW 11 65,834,096 (GRCm38) splice site probably null
R5648:Dnah9 UTSW 11 65,927,755 (GRCm38) missense probably benign 0.00
R5653:Dnah9 UTSW 11 65,849,980 (GRCm38) missense probably damaging 0.99
R5713:Dnah9 UTSW 11 66,025,223 (GRCm38) missense possibly damaging 0.92
R5763:Dnah9 UTSW 11 65,955,239 (GRCm38) missense probably damaging 1.00
R5825:Dnah9 UTSW 11 66,126,601 (GRCm38) missense probably benign 0.01
R5831:Dnah9 UTSW 11 66,108,121 (GRCm38) missense probably benign 0.00
R5847:Dnah9 UTSW 11 66,095,240 (GRCm38) frame shift probably null
R5870:Dnah9 UTSW 11 66,085,210 (GRCm38) missense probably benign 0.01
R5902:Dnah9 UTSW 11 66,025,187 (GRCm38) missense probably benign 0.08
R5918:Dnah9 UTSW 11 65,834,199 (GRCm38) missense probably damaging 1.00
R5979:Dnah9 UTSW 11 65,834,481 (GRCm38) missense probably damaging 1.00
R6065:Dnah9 UTSW 11 66,145,397 (GRCm38) missense possibly damaging 0.65
R6065:Dnah9 UTSW 11 65,855,338 (GRCm38) missense probably benign 0.05
R6086:Dnah9 UTSW 11 66,085,174 (GRCm38) missense probably benign
R6086:Dnah9 UTSW 11 65,989,915 (GRCm38) missense probably damaging 0.99
R6102:Dnah9 UTSW 11 65,990,516 (GRCm38) missense probably damaging 0.97
R6120:Dnah9 UTSW 11 66,147,399 (GRCm38) missense probably benign
R6154:Dnah9 UTSW 11 65,855,338 (GRCm38) missense probably benign 0.00
R6262:Dnah9 UTSW 11 65,881,805 (GRCm38) splice site probably null
R6265:Dnah9 UTSW 11 66,168,094 (GRCm38) missense probably benign 0.04
R6290:Dnah9 UTSW 11 65,841,375 (GRCm38) missense probably damaging 1.00
R6345:Dnah9 UTSW 11 66,037,693 (GRCm38) missense probably damaging 0.97
R6357:Dnah9 UTSW 11 65,874,196 (GRCm38) missense probably damaging 1.00
R6534:Dnah9 UTSW 11 65,955,248 (GRCm38) missense probably damaging 0.99
R6574:Dnah9 UTSW 11 66,168,281 (GRCm38) missense probably benign 0.37
R6582:Dnah9 UTSW 11 66,061,097 (GRCm38) missense probably damaging 1.00
R6700:Dnah9 UTSW 11 65,955,366 (GRCm38) missense probably damaging 1.00
R6800:Dnah9 UTSW 11 66,072,739 (GRCm38) critical splice donor site probably null
R6812:Dnah9 UTSW 11 65,981,329 (GRCm38) missense probably damaging 0.99
R6931:Dnah9 UTSW 11 66,117,626 (GRCm38) missense possibly damaging 0.63
R6944:Dnah9 UTSW 11 66,085,149 (GRCm38) missense possibly damaging 0.91
R6958:Dnah9 UTSW 11 66,076,341 (GRCm38) missense probably damaging 1.00
R6977:Dnah9 UTSW 11 66,107,909 (GRCm38) missense probably benign 0.37
R7021:Dnah9 UTSW 11 65,981,231 (GRCm38) missense probably benign
R7161:Dnah9 UTSW 11 65,855,372 (GRCm38) nonsense probably null
R7175:Dnah9 UTSW 11 66,133,637 (GRCm38) missense probably benign 0.03
R7199:Dnah9 UTSW 11 66,118,944 (GRCm38) missense probably benign 0.04
R7284:Dnah9 UTSW 11 65,990,476 (GRCm38) missense probably damaging 0.99
R7314:Dnah9 UTSW 11 65,989,851 (GRCm38) missense probably benign 0.00
R7350:Dnah9 UTSW 11 66,080,578 (GRCm38) missense probably damaging 1.00
R7420:Dnah9 UTSW 11 66,117,407 (GRCm38) critical splice donor site probably null
R7427:Dnah9 UTSW 11 65,955,219 (GRCm38) missense probably benign
R7477:Dnah9 UTSW 11 65,992,731 (GRCm38) missense probably damaging 0.98
R7515:Dnah9 UTSW 11 65,841,414 (GRCm38) missense probably benign 0.01
R7521:Dnah9 UTSW 11 65,989,837 (GRCm38) missense probably damaging 0.98
R7573:Dnah9 UTSW 11 66,125,215 (GRCm38) missense probably benign 0.43
R7659:Dnah9 UTSW 11 65,989,780 (GRCm38) missense probably damaging 0.99
R7707:Dnah9 UTSW 11 66,118,958 (GRCm38) missense probably damaging 1.00
R7749:Dnah9 UTSW 11 65,911,830 (GRCm38) missense probably damaging 1.00
R7792:Dnah9 UTSW 11 65,850,013 (GRCm38) missense probably damaging 1.00
R7808:Dnah9 UTSW 11 66,005,805 (GRCm38) nonsense probably null
R7814:Dnah9 UTSW 11 66,005,660 (GRCm38) missense probably damaging 1.00
R7818:Dnah9 UTSW 11 66,025,211 (GRCm38) missense possibly damaging 0.64
R7890:Dnah9 UTSW 11 66,072,072 (GRCm38) missense probably damaging 0.99
R7976:Dnah9 UTSW 11 65,841,401 (GRCm38) missense possibly damaging 0.91
R8121:Dnah9 UTSW 11 66,017,375 (GRCm38) missense probably benign 0.02
R8232:Dnah9 UTSW 11 65,855,323 (GRCm38) missense possibly damaging 0.91
R8311:Dnah9 UTSW 11 65,989,818 (GRCm38) missense probably benign 0.00
R8326:Dnah9 UTSW 11 66,117,626 (GRCm38) missense probably benign 0.01
R8338:Dnah9 UTSW 11 65,841,241 (GRCm38) critical splice donor site probably null
R8356:Dnah9 UTSW 11 66,156,938 (GRCm38) missense probably damaging 0.99
R8456:Dnah9 UTSW 11 66,156,938 (GRCm38) missense probably damaging 0.99
R8468:Dnah9 UTSW 11 65,831,730 (GRCm38) missense probably benign 0.00
R8721:Dnah9 UTSW 11 66,095,298 (GRCm38) missense probably damaging 1.00
R8747:Dnah9 UTSW 11 65,927,990 (GRCm38) missense possibly damaging 0.69
R8798:Dnah9 UTSW 11 65,905,231 (GRCm38) missense probably damaging 0.99
R8806:Dnah9 UTSW 11 65,859,483 (GRCm38) missense probably damaging 1.00
R8826:Dnah9 UTSW 11 65,849,916 (GRCm38) missense probably benign 0.13
R8837:Dnah9 UTSW 11 65,855,234 (GRCm38) missense possibly damaging 0.72
R8886:Dnah9 UTSW 11 66,053,014 (GRCm38) missense probably damaging 1.00
R8887:Dnah9 UTSW 11 65,855,384 (GRCm38) missense probably benign 0.01
R8921:Dnah9 UTSW 11 65,911,921 (GRCm38) missense probably benign
R8933:Dnah9 UTSW 11 65,855,252 (GRCm38) missense possibly damaging 0.88
R8949:Dnah9 UTSW 11 66,168,400 (GRCm38) missense possibly damaging 0.91
R8967:Dnah9 UTSW 11 66,125,112 (GRCm38) critical splice donor site probably null
R8979:Dnah9 UTSW 11 66,005,152 (GRCm38) missense probably benign
R8991:Dnah9 UTSW 11 65,886,680 (GRCm38) missense probably damaging 0.96
R9016:Dnah9 UTSW 11 66,108,030 (GRCm38) missense probably damaging 0.99
R9025:Dnah9 UTSW 11 66,005,825 (GRCm38) missense probably damaging 1.00
R9043:Dnah9 UTSW 11 65,954,854 (GRCm38) missense
R9047:Dnah9 UTSW 11 66,072,099 (GRCm38) missense possibly damaging 0.89
R9076:Dnah9 UTSW 11 66,117,638 (GRCm38) missense probably benign 0.21
R9113:Dnah9 UTSW 11 65,989,887 (GRCm38) missense probably damaging 1.00
R9152:Dnah9 UTSW 11 66,130,631 (GRCm38) missense probably damaging 1.00
R9187:Dnah9 UTSW 11 66,005,146 (GRCm38) missense probably benign
R9198:Dnah9 UTSW 11 65,955,744 (GRCm38) missense probably benign 0.02
R9203:Dnah9 UTSW 11 65,855,287 (GRCm38) missense possibly damaging 0.58
R9234:Dnah9 UTSW 11 66,033,925 (GRCm38) missense possibly damaging 0.68
R9245:Dnah9 UTSW 11 65,895,905 (GRCm38) missense probably benign 0.30
R9265:Dnah9 UTSW 11 65,841,255 (GRCm38) missense probably benign 0.01
R9307:Dnah9 UTSW 11 66,085,474 (GRCm38) missense probably benign 0.14
R9336:Dnah9 UTSW 11 65,870,949 (GRCm38) missense probably damaging 1.00
R9386:Dnah9 UTSW 11 65,947,542 (GRCm38) missense probably damaging 1.00
R9498:Dnah9 UTSW 11 65,848,373 (GRCm38) missense probably damaging 0.99
R9508:Dnah9 UTSW 11 65,834,263 (GRCm38) missense probably damaging 1.00
R9524:Dnah9 UTSW 11 66,085,483 (GRCm38) missense possibly damaging 0.92
R9577:Dnah9 UTSW 11 65,976,521 (GRCm38) missense probably benign 0.00
R9583:Dnah9 UTSW 11 65,965,681 (GRCm38) missense probably damaging 1.00
R9587:Dnah9 UTSW 11 66,108,391 (GRCm38) missense probably null 0.92
R9612:Dnah9 UTSW 11 65,927,649 (GRCm38) missense probably benign 0.00
R9748:Dnah9 UTSW 11 66,085,464 (GRCm38) missense possibly damaging 0.51
R9749:Dnah9 UTSW 11 66,095,376 (GRCm38) missense probably damaging 1.00
R9759:Dnah9 UTSW 11 66,075,118 (GRCm38) missense probably null 0.93
R9784:Dnah9 UTSW 11 66,085,134 (GRCm38) missense probably damaging 0.99
V3553:Dnah9 UTSW 11 65,970,076 (GRCm38) missense probably damaging 1.00
X0027:Dnah9 UTSW 11 66,085,479 (GRCm38) missense probably benign 0.07
X0028:Dnah9 UTSW 11 65,990,452 (GRCm38) missense probably damaging 1.00
Z1176:Dnah9 UTSW 11 65,970,084 (GRCm38) missense probably damaging 1.00
Z1176:Dnah9 UTSW 11 65,927,853 (GRCm38) missense probably damaging 1.00
Z1176:Dnah9 UTSW 11 65,895,972 (GRCm38) missense probably damaging 1.00
Z1176:Dnah9 UTSW 11 66,072,835 (GRCm38) missense probably damaging 1.00
Z1176:Dnah9 UTSW 11 66,037,474 (GRCm38) missense probably damaging 1.00
Z1177:Dnah9 UTSW 11 66,126,650 (GRCm38) missense probably damaging 1.00
Z1186:Dnah9 UTSW 11 66,085,174 (GRCm38) missense probably benign
Z1186:Dnah9 UTSW 11 66,147,381 (GRCm38) missense probably benign
Z1187:Dnah9 UTSW 11 66,147,381 (GRCm38) missense probably benign
Z1187:Dnah9 UTSW 11 66,085,174 (GRCm38) missense probably benign
Z1188:Dnah9 UTSW 11 66,147,381 (GRCm38) missense probably benign
Z1188:Dnah9 UTSW 11 66,085,174 (GRCm38) missense probably benign
Z1189:Dnah9 UTSW 11 66,147,381 (GRCm38) missense probably benign
Z1189:Dnah9 UTSW 11 66,085,174 (GRCm38) missense probably benign
Z1190:Dnah9 UTSW 11 66,147,381 (GRCm38) missense probably benign
Z1190:Dnah9 UTSW 11 66,085,174 (GRCm38) missense probably benign
Z1191:Dnah9 UTSW 11 66,147,381 (GRCm38) missense probably benign
Z1191:Dnah9 UTSW 11 66,085,174 (GRCm38) missense probably benign
Z1192:Dnah9 UTSW 11 66,147,381 (GRCm38) missense probably benign
Z1192:Dnah9 UTSW 11 66,085,174 (GRCm38) missense probably benign
Predicted Primers PCR Primer
(F):5'- GCCATGAAGGAGACAATGACTC -3'
(R):5'- AAAAGCAGTGTTCTTCCCAGC -3'

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