Incidental Mutation 'R1886:Dnah17'
ID 209573
Institutional Source Beutler Lab
Gene Symbol Dnah17
Ensembl Gene ENSMUSG00000033987
Gene Name dynein, axonemal, heavy chain 17
Synonyms Dnahcl1, LOC382552, 2810003K23Rik, Dnahc17
MMRRC Submission 039907-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1886 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 117912549-118021460 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 117998987 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 929 (I929F)
Ref Sequence ENSEMBL: ENSMUSP00000081864 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084803] [ENSMUST00000106308] [ENSMUST00000132685]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000084803
AA Change: I929F

PolyPhen 2 Score 0.622 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000081864
Gene: ENSMUSG00000033987
AA Change: I929F

DomainStartEndE-ValueType
Pfam:DHC_N1 183 766 8.5e-142 PFAM
low complexity region 1015 1028 N/A INTRINSIC
Pfam:DHC_N2 1260 1673 5.8e-135 PFAM
Pfam:AAA_6 1793 2023 6e-161 PFAM
low complexity region 2092 2104 N/A INTRINSIC
Pfam:AAA_5 2107 2243 7.8e-13 PFAM
Pfam:AAA_7 2400 2671 1.1e-171 PFAM
Pfam:AAA_8 2748 3015 4.9e-166 PFAM
Pfam:MT 3027 3370 3.4e-214 PFAM
Pfam:AAA_9 3388 3615 2.4e-144 PFAM
Pfam:Dynein_heavy 3742 4452 N/A PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000106308
AA Change: I929F

PolyPhen 2 Score 0.441 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000101915
Gene: ENSMUSG00000033987
AA Change: I929F

DomainStartEndE-ValueType
Pfam:DHC_N1 184 764 1.7e-152 PFAM
low complexity region 1015 1028 N/A INTRINSIC
Pfam:DHC_N2 1262 1671 4.1e-132 PFAM
Pfam:AAA_6 1793 2023 7e-149 PFAM
low complexity region 2092 2104 N/A INTRINSIC
Pfam:AAA_5 2107 2243 2.5e-11 PFAM
Pfam:AAA_7 2400 2671 4.4e-169 PFAM
Pfam:AAA_8 2748 3015 7.1e-163 PFAM
Pfam:MT 3027 3370 1.1e-210 PFAM
Pfam:AAA_9 3392 3614 1e-84 PFAM
Pfam:Dynein_heavy 3748 4479 3.5e-230 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000132685
AA Change: I929F

PolyPhen 2 Score 0.169 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000120542
Gene: ENSMUSG00000033987
AA Change: I929F

DomainStartEndE-ValueType
Pfam:DHC_N2 279 688 3.1e-132 PFAM
Pfam:AAA_6 811 1041 5.3e-149 PFAM
low complexity region 1110 1122 N/A INTRINSIC
Blast:AAA 1123 1354 1e-104 BLAST
Pfam:AAA_7 1452 1671 8.9e-134 PFAM
Pfam:AAA_8 1763 2030 5.4e-163 PFAM
Pfam:MT 2042 2168 6.8e-52 PFAM
Pfam:MT 2163 2412 8.2e-149 PFAM
Pfam:AAA_9 2434 2656 7.9e-85 PFAM
Pfam:Dynein_heavy 2790 3457 2.6e-209 PFAM
Pfam:Dynein_heavy 3460 3569 4.6e-17 PFAM
Coding Region Coverage
  • 1x: 97.2%
  • 3x: 96.2%
  • 10x: 93.1%
  • 20x: 85.9%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. DNAH17 is a heavy chain associated with axonemal dynein (Milisav and Affara, 1998 [PubMed 9545504]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 87 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700102P08Rik T A 9: 108,270,809 (GRCm39) D124E possibly damaging Het
Aarsd1 T C 11: 101,302,227 (GRCm39) T278A probably benign Het
Acacb T A 5: 114,357,020 (GRCm39) L1317Q probably damaging Het
Acsf3 T C 8: 123,510,741 (GRCm39) V293A probably damaging Het
Adora3 A C 3: 105,812,152 (GRCm39) N13H possibly damaging Het
Aen A T 7: 78,557,073 (GRCm39) D307V probably damaging Het
Ahnak G A 19: 8,993,343 (GRCm39) D4876N probably damaging Het
Ap2b1 T A 11: 83,281,561 (GRCm39) N822K probably damaging Het
Arhgdia T C 11: 120,470,244 (GRCm39) D143G probably benign Het
Bcl9 G T 3: 97,122,713 (GRCm39) R29S probably benign Het
Bhmt2 T A 13: 93,798,998 (GRCm39) K274N probably benign Het
Brip1 C A 11: 86,029,641 (GRCm39) G631V probably damaging Het
Cacna1i A G 15: 80,243,145 (GRCm39) E434G probably damaging Het
Ccdc81 T C 7: 89,515,819 (GRCm39) E620G possibly damaging Het
Cdhr18 A C 14: 13,828,607 (GRCm38) Y718D probably damaging Het
Cfap299 A G 5: 98,949,690 (GRCm39) N208S probably benign Het
Cit A G 5: 116,071,545 (GRCm39) Y584C probably damaging Het
Crebl2 T C 6: 134,828,059 (GRCm39) M77T probably benign Het
Dach2 G A X: 112,208,305 (GRCm39) G61D probably benign Het
Ddx4 A T 13: 112,759,199 (GRCm39) D237E probably damaging Het
Dgcr8 A G 16: 18,096,218 (GRCm39) I490T possibly damaging Het
Dmxl1 G A 18: 49,992,202 (GRCm39) R316H probably benign Het
Eif3f A G 7: 108,539,958 (GRCm39) T289A probably benign Het
Ercc5 A T 1: 44,215,136 (GRCm39) K890* probably null Het
Esrp2 A T 8: 106,860,489 (GRCm39) V247E probably damaging Het
Evpl C T 11: 116,118,402 (GRCm39) G735E probably damaging Het
Ezhip GTCATCATCATCATC GTCATCATCATCATCATC X: 5,994,645 (GRCm39) probably benign Het
Fbxl21 A G 13: 56,674,906 (GRCm39) I60V probably benign Het
Frem3 A G 8: 81,340,514 (GRCm39) I936V probably benign Het
Fsd1l T C 4: 53,696,984 (GRCm39) probably null Het
Gad1-ps T C 10: 99,281,444 (GRCm39) noncoding transcript Het
Gbp2b A G 3: 142,314,063 (GRCm39) T448A probably benign Het
Gfus G T 15: 75,798,838 (GRCm39) T123N possibly damaging Het
Gmppa T C 1: 75,419,152 (GRCm39) V353A probably damaging Het
Hmcn1 T C 1: 150,453,046 (GRCm39) E5423G probably benign Het
Hmgxb3 A G 18: 61,270,473 (GRCm39) probably null Het
Krt12 T C 11: 99,309,402 (GRCm39) D286G probably damaging Het
Krt75 A T 15: 101,479,532 (GRCm39) M266K probably damaging Het
Ksr1 C A 11: 78,911,204 (GRCm39) V11F probably null Het
Lag3 T C 6: 124,886,402 (GRCm39) N184D probably damaging Het
Lsm10 C G 4: 125,991,741 (GRCm39) D32E probably benign Het
Mettl5 A G 2: 69,711,149 (GRCm39) V123A probably damaging Het
Mfrp A G 9: 44,014,785 (GRCm39) D274G possibly damaging Het
Mgat3 A G 15: 80,095,820 (GRCm39) I216V probably benign Het
Mkrn3 G A 7: 62,068,486 (GRCm39) A435V probably benign Het
Mob3a G A 10: 80,527,068 (GRCm39) Q86* probably null Het
Mplkipl1 A G 19: 61,164,136 (GRCm39) F100L probably damaging Het
Mttp A T 3: 137,798,376 (GRCm39) V840D probably damaging Het
Nadk2 A C 15: 9,103,446 (GRCm39) N308H possibly damaging Het
Ncoa7 T C 10: 30,524,448 (GRCm39) N823S possibly damaging Het
Nlk T A 11: 78,477,754 (GRCm39) I330F probably damaging Het
Ofcc1 T C 13: 40,360,100 (GRCm39) S310G possibly damaging Het
Or5p57 T C 7: 107,665,985 (GRCm39) N7D probably benign Het
Or5p73 A T 7: 108,064,947 (GRCm39) M139L probably benign Het
Orc2 T C 1: 58,510,247 (GRCm39) probably null Het
Orc3 A G 4: 34,584,829 (GRCm39) Y459H probably damaging Het
Pah T A 10: 87,364,190 (GRCm39) N30K possibly damaging Het
Pcsk4 T C 10: 80,164,794 (GRCm39) K74E probably benign Het
Pdlim7 C T 13: 55,653,981 (GRCm39) G212D probably benign Het
Pfkm A G 15: 98,025,627 (GRCm39) N547S probably damaging Het
Por A G 5: 135,763,128 (GRCm39) E546G probably damaging Het
Ppp1r13l T C 7: 19,111,496 (GRCm39) S774P probably damaging Het
Prdm1 T A 10: 44,315,754 (GRCm39) D794V probably damaging Het
Prdx5 A G 19: 6,885,558 (GRCm39) I32T probably benign Het
Prlhr G T 19: 60,455,932 (GRCm39) C211* probably null Het
Ripk3 C T 14: 56,025,694 (GRCm39) probably null Het
Rmnd5b G A 11: 51,518,465 (GRCm39) A137V probably damaging Het
Rwdd2b A T 16: 87,234,013 (GRCm39) F72I probably benign Het
Scml4 A G 10: 42,788,223 (GRCm39) Y51C probably damaging Het
Septin1 A G 7: 126,813,937 (GRCm39) probably benign Het
Serpinb9h C T 13: 33,588,203 (GRCm39) R263C possibly damaging Het
Slc30a10 T A 1: 185,195,061 (GRCm39) I291N probably damaging Het
Slc7a9 T G 7: 35,152,827 (GRCm39) C20W possibly damaging Het
Slc7a9 G C 7: 35,152,828 (GRCm39) A21P probably damaging Het
Slco1b2 A T 6: 141,628,951 (GRCm39) Y551F probably damaging Het
Sra1 T C 18: 36,801,830 (GRCm39) M87V probably benign Het
Syvn1 T C 19: 6,099,257 (GRCm39) S169P possibly damaging Het
Tmc7 A T 7: 118,160,310 (GRCm39) F176I possibly damaging Het
Tmem62 A T 2: 120,817,151 (GRCm39) I236F probably damaging Het
Trip4 T A 9: 65,782,163 (GRCm39) I190F probably null Het
Trpa1 T C 1: 14,959,649 (GRCm39) D679G probably benign Het
Ttc22 T A 4: 106,494,063 (GRCm39) probably null Het
Ttn A T 2: 76,641,587 (GRCm39) L5176Q possibly damaging Het
Tyrp1 T A 4: 80,759,043 (GRCm39) probably null Het
Ubap2 C T 4: 41,199,872 (GRCm39) A752T probably benign Het
Usp36 A T 11: 118,163,784 (GRCm39) Y255N probably damaging Het
Zfp944 A T 17: 22,558,960 (GRCm39) Y96N probably benign Het
Other mutations in Dnah17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00231:Dnah17 APN 11 117,979,040 (GRCm39) missense possibly damaging 0.81
IGL00531:Dnah17 APN 11 117,933,999 (GRCm39) missense probably damaging 0.97
IGL00764:Dnah17 APN 11 117,987,311 (GRCm39) missense probably damaging 0.99
IGL00795:Dnah17 APN 11 117,984,460 (GRCm39) missense probably benign 0.35
IGL00823:Dnah17 APN 11 117,937,987 (GRCm39) missense probably benign 0.22
IGL01145:Dnah17 APN 11 117,937,999 (GRCm39) missense possibly damaging 0.63
IGL01433:Dnah17 APN 11 117,940,760 (GRCm39) missense probably damaging 1.00
IGL01454:Dnah17 APN 11 117,949,223 (GRCm39) missense probably damaging 1.00
IGL01545:Dnah17 APN 11 118,010,394 (GRCm39) missense probably damaging 1.00
IGL01548:Dnah17 APN 11 117,989,438 (GRCm39) missense probably benign 0.21
IGL01557:Dnah17 APN 11 117,964,512 (GRCm39) missense probably damaging 0.98
IGL01632:Dnah17 APN 11 117,924,707 (GRCm39) missense probably damaging 1.00
IGL01636:Dnah17 APN 11 117,931,882 (GRCm39) missense probably benign 0.03
IGL01672:Dnah17 APN 11 117,932,986 (GRCm39) missense probably damaging 0.97
IGL01822:Dnah17 APN 11 117,972,819 (GRCm39) missense probably damaging 1.00
IGL01869:Dnah17 APN 11 117,943,502 (GRCm39) missense probably benign 0.09
IGL01916:Dnah17 APN 11 118,016,114 (GRCm39) missense probably benign 0.00
IGL02131:Dnah17 APN 11 117,963,734 (GRCm39) missense probably damaging 1.00
IGL02154:Dnah17 APN 11 118,015,087 (GRCm39) missense probably benign 0.01
IGL02220:Dnah17 APN 11 117,963,793 (GRCm39) nonsense probably null
IGL02454:Dnah17 APN 11 117,971,593 (GRCm39) missense probably damaging 0.98
IGL02458:Dnah17 APN 11 117,927,176 (GRCm39) missense probably damaging 1.00
IGL02588:Dnah17 APN 11 117,916,479 (GRCm39) missense possibly damaging 0.95
IGL02865:Dnah17 APN 11 117,964,374 (GRCm39) missense probably damaging 1.00
IGL02881:Dnah17 APN 11 117,932,944 (GRCm39) missense probably damaging 1.00
IGL02952:Dnah17 APN 11 117,979,094 (GRCm39) missense probably benign 0.03
IGL03382:Dnah17 APN 11 117,972,769 (GRCm39) missense probably damaging 1.00
IGL03389:Dnah17 APN 11 117,985,805 (GRCm39) missense probably damaging 1.00
ergos UTSW 11 117,931,984 (GRCm39) splice site probably benign
watt UTSW 11 117,971,592 (GRCm39) missense probably damaging 0.96
PIT4280001:Dnah17 UTSW 11 117,989,408 (GRCm39) missense possibly damaging 0.85
R0004:Dnah17 UTSW 11 117,950,918 (GRCm39) missense possibly damaging 0.90
R0112:Dnah17 UTSW 11 117,965,260 (GRCm39) missense possibly damaging 0.82
R0116:Dnah17 UTSW 11 117,949,132 (GRCm39) missense probably benign 0.01
R0157:Dnah17 UTSW 11 118,017,997 (GRCm39) missense probably benign
R0320:Dnah17 UTSW 11 117,943,500 (GRCm39) missense possibly damaging 0.56
R0362:Dnah17 UTSW 11 117,989,365 (GRCm39) missense probably benign 0.10
R0382:Dnah17 UTSW 11 118,019,822 (GRCm39) missense probably damaging 1.00
R0383:Dnah17 UTSW 11 117,958,373 (GRCm39) missense probably benign
R0400:Dnah17 UTSW 11 117,972,904 (GRCm39) missense probably damaging 1.00
R0420:Dnah17 UTSW 11 117,930,765 (GRCm39) missense probably damaging 1.00
R0483:Dnah17 UTSW 11 117,937,950 (GRCm39) missense probably benign
R0533:Dnah17 UTSW 11 118,001,363 (GRCm39) missense possibly damaging 0.50
R0562:Dnah17 UTSW 11 117,963,726 (GRCm39) missense probably damaging 1.00
R0564:Dnah17 UTSW 11 117,973,807 (GRCm39) missense probably damaging 1.00
R0604:Dnah17 UTSW 11 118,012,297 (GRCm39) missense probably benign 0.00
R0608:Dnah17 UTSW 11 117,981,575 (GRCm39) nonsense probably null
R0614:Dnah17 UTSW 11 117,961,394 (GRCm39) splice site probably benign
R0632:Dnah17 UTSW 11 117,958,508 (GRCm39) splice site probably benign
R0831:Dnah17 UTSW 11 117,951,097 (GRCm39) missense probably damaging 0.99
R0838:Dnah17 UTSW 11 117,950,930 (GRCm39) missense probably damaging 1.00
R0879:Dnah17 UTSW 11 117,947,661 (GRCm39) splice site probably benign
R1061:Dnah17 UTSW 11 117,943,514 (GRCm39) missense possibly damaging 0.51
R1190:Dnah17 UTSW 11 117,933,001 (GRCm39) missense probably damaging 1.00
R1293:Dnah17 UTSW 11 118,017,963 (GRCm39) critical splice donor site probably null
R1297:Dnah17 UTSW 11 118,012,192 (GRCm39) splice site probably benign
R1332:Dnah17 UTSW 11 117,934,041 (GRCm39) missense possibly damaging 0.70
R1336:Dnah17 UTSW 11 117,934,041 (GRCm39) missense possibly damaging 0.70
R1364:Dnah17 UTSW 11 118,016,432 (GRCm39) splice site probably benign
R1418:Dnah17 UTSW 11 117,964,849 (GRCm39) missense probably damaging 0.98
R1432:Dnah17 UTSW 11 117,914,153 (GRCm39) missense probably damaging 1.00
R1497:Dnah17 UTSW 11 118,005,059 (GRCm39) missense probably damaging 1.00
R1500:Dnah17 UTSW 11 117,991,879 (GRCm39) missense probably benign
R1506:Dnah17 UTSW 11 118,016,213 (GRCm39) missense possibly damaging 0.53
R1512:Dnah17 UTSW 11 117,985,841 (GRCm39) missense probably benign
R1567:Dnah17 UTSW 11 118,016,811 (GRCm39) missense probably damaging 1.00
R1597:Dnah17 UTSW 11 117,994,324 (GRCm39) splice site probably benign
R1665:Dnah17 UTSW 11 118,012,321 (GRCm39) splice site probably benign
R1703:Dnah17 UTSW 11 117,917,575 (GRCm39) missense probably damaging 1.00
R1716:Dnah17 UTSW 11 117,923,424 (GRCm39) missense probably benign 0.00
R1727:Dnah17 UTSW 11 117,987,362 (GRCm39) nonsense probably null
R1727:Dnah17 UTSW 11 117,961,315 (GRCm39) missense probably damaging 0.98
R1728:Dnah17 UTSW 11 117,960,345 (GRCm39) missense possibly damaging 0.76
R1784:Dnah17 UTSW 11 117,960,345 (GRCm39) missense possibly damaging 0.76
R1852:Dnah17 UTSW 11 118,012,742 (GRCm39) missense probably damaging 0.97
R1869:Dnah17 UTSW 11 117,938,015 (GRCm39) nonsense probably null
R1893:Dnah17 UTSW 11 117,957,794 (GRCm39) missense probably benign 0.00
R1954:Dnah17 UTSW 11 117,915,557 (GRCm39) missense probably damaging 1.00
R1969:Dnah17 UTSW 11 117,995,361 (GRCm39) missense probably benign 0.00
R1971:Dnah17 UTSW 11 117,995,361 (GRCm39) missense probably benign 0.00
R1975:Dnah17 UTSW 11 117,987,362 (GRCm39) nonsense probably null
R1977:Dnah17 UTSW 11 118,003,417 (GRCm39) missense possibly damaging 0.52
R2055:Dnah17 UTSW 11 117,958,357 (GRCm39) missense probably benign 0.00
R2115:Dnah17 UTSW 11 118,010,628 (GRCm39) missense probably benign 0.00
R2132:Dnah17 UTSW 11 117,924,573 (GRCm39) missense probably damaging 0.98
R2200:Dnah17 UTSW 11 117,993,235 (GRCm39) splice site probably benign
R2277:Dnah17 UTSW 11 117,987,387 (GRCm39) missense possibly damaging 0.81
R2279:Dnah17 UTSW 11 117,987,387 (GRCm39) missense possibly damaging 0.81
R2400:Dnah17 UTSW 11 118,017,210 (GRCm39) critical splice acceptor site probably null
R2402:Dnah17 UTSW 11 118,016,800 (GRCm39) missense probably benign 0.10
R2497:Dnah17 UTSW 11 117,977,850 (GRCm39) splice site probably null
R2923:Dnah17 UTSW 11 117,984,373 (GRCm39) missense probably damaging 1.00
R3121:Dnah17 UTSW 11 117,931,912 (GRCm39) missense probably damaging 1.00
R3236:Dnah17 UTSW 11 117,985,680 (GRCm39) missense probably benign 0.08
R3237:Dnah17 UTSW 11 117,985,680 (GRCm39) missense probably benign 0.08
R3498:Dnah17 UTSW 11 117,971,675 (GRCm39) splice site probably benign
R3499:Dnah17 UTSW 11 117,971,675 (GRCm39) splice site probably benign
R3746:Dnah17 UTSW 11 117,973,742 (GRCm39) missense probably benign 0.00
R3749:Dnah17 UTSW 11 117,973,742 (GRCm39) missense probably benign 0.00
R3762:Dnah17 UTSW 11 117,995,352 (GRCm39) missense probably benign 0.00
R3826:Dnah17 UTSW 11 117,931,984 (GRCm39) splice site probably benign
R3828:Dnah17 UTSW 11 117,931,984 (GRCm39) splice site probably benign
R3829:Dnah17 UTSW 11 117,931,984 (GRCm39) splice site probably benign
R3877:Dnah17 UTSW 11 117,915,533 (GRCm39) missense probably damaging 1.00
R3899:Dnah17 UTSW 11 117,985,634 (GRCm39) missense possibly damaging 0.78
R3900:Dnah17 UTSW 11 117,985,634 (GRCm39) missense possibly damaging 0.78
R3911:Dnah17 UTSW 11 117,971,675 (GRCm39) splice site probably benign
R3913:Dnah17 UTSW 11 117,971,675 (GRCm39) splice site probably benign
R3930:Dnah17 UTSW 11 117,971,675 (GRCm39) splice site probably benign
R3931:Dnah17 UTSW 11 117,971,675 (GRCm39) splice site probably benign
R3969:Dnah17 UTSW 11 117,931,984 (GRCm39) splice site probably benign
R3970:Dnah17 UTSW 11 117,931,984 (GRCm39) splice site probably benign
R4056:Dnah17 UTSW 11 117,961,364 (GRCm39) missense probably benign 0.05
R4113:Dnah17 UTSW 11 118,003,420 (GRCm39) missense possibly damaging 0.50
R4295:Dnah17 UTSW 11 118,009,598 (GRCm39) missense probably damaging 1.00
R4324:Dnah17 UTSW 11 117,985,039 (GRCm39) missense probably benign 0.01
R4412:Dnah17 UTSW 11 117,964,509 (GRCm39) missense probably damaging 1.00
R4413:Dnah17 UTSW 11 117,915,994 (GRCm39) missense probably benign 0.00
R4422:Dnah17 UTSW 11 117,972,799 (GRCm39) missense possibly damaging 0.91
R4552:Dnah17 UTSW 11 117,943,769 (GRCm39) missense possibly damaging 0.79
R4669:Dnah17 UTSW 11 117,965,119 (GRCm39) missense probably benign 0.02
R4677:Dnah17 UTSW 11 118,010,640 (GRCm39) missense probably damaging 1.00
R4716:Dnah17 UTSW 11 117,964,474 (GRCm39) missense probably benign 0.02
R4832:Dnah17 UTSW 11 117,917,606 (GRCm39) missense probably damaging 1.00
R4868:Dnah17 UTSW 11 117,999,038 (GRCm39) missense probably benign 0.03
R4897:Dnah17 UTSW 11 117,969,419 (GRCm39) missense probably damaging 1.00
R4928:Dnah17 UTSW 11 117,918,259 (GRCm39) missense probably damaging 1.00
R4937:Dnah17 UTSW 11 117,932,980 (GRCm39) missense probably damaging 1.00
R4957:Dnah17 UTSW 11 117,965,124 (GRCm39) missense probably benign 0.44
R5008:Dnah17 UTSW 11 118,001,403 (GRCm39) missense probably benign 0.01
R5016:Dnah17 UTSW 11 117,971,592 (GRCm39) missense probably damaging 0.96
R5027:Dnah17 UTSW 11 117,993,365 (GRCm39) missense probably benign 0.01
R5133:Dnah17 UTSW 11 118,007,939 (GRCm39) missense probably benign 0.00
R5140:Dnah17 UTSW 11 117,977,771 (GRCm39) missense probably damaging 1.00
R5146:Dnah17 UTSW 11 118,005,005 (GRCm39) missense probably damaging 0.99
R5151:Dnah17 UTSW 11 117,918,293 (GRCm39) missense probably damaging 1.00
R5153:Dnah17 UTSW 11 117,973,800 (GRCm39) nonsense probably null
R5192:Dnah17 UTSW 11 117,925,185 (GRCm39) missense possibly damaging 0.96
R5315:Dnah17 UTSW 11 118,018,109 (GRCm39) missense possibly damaging 0.79
R5317:Dnah17 UTSW 11 118,018,109 (GRCm39) missense possibly damaging 0.79
R5335:Dnah17 UTSW 11 118,003,340 (GRCm39) missense probably damaging 1.00
R5379:Dnah17 UTSW 11 118,008,029 (GRCm39) intron probably benign
R5396:Dnah17 UTSW 11 118,018,108 (GRCm39) missense probably benign
R5418:Dnah17 UTSW 11 117,985,810 (GRCm39) missense probably benign 0.04
R5534:Dnah17 UTSW 11 117,943,596 (GRCm39) missense possibly damaging 0.83
R5539:Dnah17 UTSW 11 117,964,486 (GRCm39) missense probably benign 0.03
R5594:Dnah17 UTSW 11 117,934,055 (GRCm39) splice site probably null
R5634:Dnah17 UTSW 11 117,943,752 (GRCm39) splice site probably null
R5696:Dnah17 UTSW 11 117,991,882 (GRCm39) missense probably benign 0.44
R5802:Dnah17 UTSW 11 117,927,272 (GRCm39) missense possibly damaging 0.79
R5826:Dnah17 UTSW 11 117,925,193 (GRCm39) missense probably damaging 1.00
R5873:Dnah17 UTSW 11 117,947,723 (GRCm39) missense probably benign 0.01
R5898:Dnah17 UTSW 11 118,005,039 (GRCm39) missense probably benign 0.00
R5934:Dnah17 UTSW 11 117,931,928 (GRCm39) missense probably benign
R6030:Dnah17 UTSW 11 117,916,375 (GRCm39) missense probably benign 0.32
R6030:Dnah17 UTSW 11 117,916,375 (GRCm39) missense probably benign 0.32
R6038:Dnah17 UTSW 11 117,946,715 (GRCm39) missense probably benign 0.00
R6038:Dnah17 UTSW 11 117,946,715 (GRCm39) missense probably benign 0.00
R6113:Dnah17 UTSW 11 118,017,101 (GRCm39) missense probably damaging 1.00
R6117:Dnah17 UTSW 11 118,010,397 (GRCm39) missense probably benign 0.00
R6137:Dnah17 UTSW 11 117,916,480 (GRCm39) missense probably damaging 1.00
R6173:Dnah17 UTSW 11 117,930,772 (GRCm39) missense probably damaging 1.00
R6258:Dnah17 UTSW 11 118,017,149 (GRCm39) nonsense probably null
R6258:Dnah17 UTSW 11 118,017,148 (GRCm39) missense probably damaging 1.00
R6258:Dnah17 UTSW 11 118,017,150 (GRCm39) missense probably damaging 1.00
R6260:Dnah17 UTSW 11 118,017,150 (GRCm39) missense probably damaging 1.00
R6260:Dnah17 UTSW 11 118,017,148 (GRCm39) missense probably damaging 1.00
R6260:Dnah17 UTSW 11 118,017,149 (GRCm39) nonsense probably null
R6278:Dnah17 UTSW 11 118,017,116 (GRCm39) missense probably damaging 0.99
R6298:Dnah17 UTSW 11 117,998,987 (GRCm39) missense probably benign 0.00
R6300:Dnah17 UTSW 11 117,925,136 (GRCm39) missense probably damaging 1.00
R6302:Dnah17 UTSW 11 118,019,981 (GRCm39) missense probably benign 0.09
R6363:Dnah17 UTSW 11 118,001,331 (GRCm39) missense probably benign
R6381:Dnah17 UTSW 11 118,020,011 (GRCm39) missense probably benign 0.08
R6418:Dnah17 UTSW 11 118,020,023 (GRCm39) missense probably damaging 0.99
R6660:Dnah17 UTSW 11 117,991,014 (GRCm39) missense probably benign
R6803:Dnah17 UTSW 11 118,016,198 (GRCm39) missense probably benign 0.00
R6820:Dnah17 UTSW 11 117,959,826 (GRCm39) missense probably damaging 0.99
R6885:Dnah17 UTSW 11 117,981,598 (GRCm39) missense possibly damaging 0.47
R6921:Dnah17 UTSW 11 117,932,310 (GRCm39) missense probably damaging 0.98
R6932:Dnah17 UTSW 11 117,950,905 (GRCm39) missense possibly damaging 0.95
R6954:Dnah17 UTSW 11 117,957,258 (GRCm39) missense probably damaging 1.00
R7000:Dnah17 UTSW 11 117,916,528 (GRCm39) critical splice acceptor site probably null
R7007:Dnah17 UTSW 11 118,009,697 (GRCm39) missense possibly damaging 0.92
R7048:Dnah17 UTSW 11 117,936,944 (GRCm39) missense possibly damaging 0.80
R7056:Dnah17 UTSW 11 118,016,212 (GRCm39) missense probably benign
R7131:Dnah17 UTSW 11 117,970,484 (GRCm39) missense probably benign 0.14
R7143:Dnah17 UTSW 11 117,976,956 (GRCm39) missense probably damaging 1.00
R7146:Dnah17 UTSW 11 117,972,936 (GRCm39) missense probably damaging 0.98
R7147:Dnah17 UTSW 11 117,985,755 (GRCm39) missense probably benign 0.31
R7172:Dnah17 UTSW 11 117,931,957 (GRCm39) nonsense probably null
R7183:Dnah17 UTSW 11 118,020,014 (GRCm39) missense probably benign
R7297:Dnah17 UTSW 11 117,994,182 (GRCm39) missense probably damaging 0.98
R7297:Dnah17 UTSW 11 117,946,556 (GRCm39) critical splice donor site probably null
R7367:Dnah17 UTSW 11 118,006,022 (GRCm39) missense probably benign
R7398:Dnah17 UTSW 11 117,971,550 (GRCm39) missense probably damaging 0.96
R7426:Dnah17 UTSW 11 117,981,543 (GRCm39) missense probably null 0.79
R7524:Dnah17 UTSW 11 118,012,307 (GRCm39) missense probably benign 0.03
R7529:Dnah17 UTSW 11 117,940,692 (GRCm39) critical splice donor site probably null
R7615:Dnah17 UTSW 11 118,001,373 (GRCm39) nonsense probably null
R7681:Dnah17 UTSW 11 117,916,012 (GRCm39) missense probably damaging 1.00
R7702:Dnah17 UTSW 11 118,012,304 (GRCm39) missense possibly damaging 0.64
R7702:Dnah17 UTSW 11 117,916,466 (GRCm39) missense probably benign 0.00
R7713:Dnah17 UTSW 11 117,915,997 (GRCm39) missense probably benign 0.02
R7809:Dnah17 UTSW 11 117,995,462 (GRCm39) missense probably benign 0.09
R7842:Dnah17 UTSW 11 117,970,508 (GRCm39) critical splice acceptor site probably null
R7935:Dnah17 UTSW 11 118,018,048 (GRCm39) missense probably benign 0.20
R7951:Dnah17 UTSW 11 118,009,592 (GRCm39) missense possibly damaging 0.64
R8070:Dnah17 UTSW 11 117,915,497 (GRCm39) missense probably damaging 0.97
R8098:Dnah17 UTSW 11 117,941,193 (GRCm39) missense probably damaging 1.00
R8101:Dnah17 UTSW 11 118,016,744 (GRCm39) missense probably benign
R8177:Dnah17 UTSW 11 118,019,753 (GRCm39) missense possibly damaging 0.60
R8343:Dnah17 UTSW 11 118,005,021 (GRCm39) missense probably benign
R8350:Dnah17 UTSW 11 117,977,873 (GRCm39) missense probably damaging 0.98
R8393:Dnah17 UTSW 11 117,947,855 (GRCm39) missense probably damaging 1.00
R8401:Dnah17 UTSW 11 117,915,485 (GRCm39) missense probably damaging 0.96
R8418:Dnah17 UTSW 11 117,994,284 (GRCm39) missense probably benign 0.01
R8450:Dnah17 UTSW 11 117,977,873 (GRCm39) missense probably damaging 0.98
R8546:Dnah17 UTSW 11 118,015,101 (GRCm39) missense probably benign 0.00
R8697:Dnah17 UTSW 11 117,976,985 (GRCm39) missense possibly damaging 0.96
R8710:Dnah17 UTSW 11 117,932,973 (GRCm39) missense probably damaging 1.00
R8713:Dnah17 UTSW 11 117,979,028 (GRCm39) missense probably damaging 1.00
R8722:Dnah17 UTSW 11 117,961,283 (GRCm39) nonsense probably null
R8797:Dnah17 UTSW 11 117,992,201 (GRCm39) missense probably benign 0.00
R8953:Dnah17 UTSW 11 118,016,238 (GRCm39) splice site probably benign
R8965:Dnah17 UTSW 11 117,915,492 (GRCm39) missense probably damaging 1.00
R8976:Dnah17 UTSW 11 117,917,666 (GRCm39) missense probably damaging 1.00
R9090:Dnah17 UTSW 11 117,931,870 (GRCm39) missense probably damaging 1.00
R9128:Dnah17 UTSW 11 117,937,004 (GRCm39) missense possibly damaging 0.76
R9134:Dnah17 UTSW 11 117,978,972 (GRCm39) missense probably damaging 1.00
R9245:Dnah17 UTSW 11 118,016,503 (GRCm39) missense probably benign 0.02
R9251:Dnah17 UTSW 11 118,012,618 (GRCm39) missense probably benign 0.03
R9271:Dnah17 UTSW 11 117,931,870 (GRCm39) missense probably damaging 1.00
R9367:Dnah17 UTSW 11 118,012,212 (GRCm39) missense possibly damaging 0.93
R9367:Dnah17 UTSW 11 117,987,464 (GRCm39) missense possibly damaging 0.95
R9381:Dnah17 UTSW 11 117,914,219 (GRCm39) missense probably benign
R9405:Dnah17 UTSW 11 118,009,737 (GRCm39) missense probably benign
R9449:Dnah17 UTSW 11 117,987,452 (GRCm39) missense probably benign 0.07
R9517:Dnah17 UTSW 11 117,915,440 (GRCm39) missense possibly damaging 0.76
R9588:Dnah17 UTSW 11 118,012,783 (GRCm39) missense probably benign 0.00
R9629:Dnah17 UTSW 11 117,979,804 (GRCm39) missense probably damaging 1.00
R9654:Dnah17 UTSW 11 117,927,156 (GRCm39) critical splice donor site probably null
R9655:Dnah17 UTSW 11 117,971,649 (GRCm39) missense possibly damaging 0.94
R9662:Dnah17 UTSW 11 117,925,166 (GRCm39) missense probably damaging 0.97
R9686:Dnah17 UTSW 11 117,979,048 (GRCm39) missense possibly damaging 0.46
R9689:Dnah17 UTSW 11 117,963,731 (GRCm39) missense probably damaging 1.00
R9706:Dnah17 UTSW 11 118,017,026 (GRCm39) missense probably damaging 1.00
X0058:Dnah17 UTSW 11 117,973,751 (GRCm39) missense probably damaging 1.00
Z1176:Dnah17 UTSW 11 118,017,992 (GRCm39) missense probably benign 0.01
Z1177:Dnah17 UTSW 11 117,977,786 (GRCm39) missense probably damaging 1.00
Z1177:Dnah17 UTSW 11 117,969,389 (GRCm39) missense possibly damaging 0.91
Z1177:Dnah17 UTSW 11 118,017,968 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- ACCACAGACTGTCACATTCTG -3'
(R):5'- GCTGAAGTGGTCTGAACTGC -3'

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