Incidental Mutation 'R7524:Dnah17'
ID 582871
Institutional Source Beutler Lab
Gene Symbol Dnah17
Ensembl Gene ENSMUSG00000033987
Gene Name dynein, axonemal, heavy chain 17
Synonyms LOC382552, Dnahcl1, 2810003K23Rik, Dnahc17
MMRRC Submission 045596-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7524 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 118021723-118130634 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 118121481 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 485 (D485G)
Ref Sequence ENSEMBL: ENSMUSP00000101915 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084803] [ENSMUST00000106308] [ENSMUST00000132685]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000084803
AA Change: D485G

PolyPhen 2 Score 0.085 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000081864
Gene: ENSMUSG00000033987
AA Change: D485G

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: D485G

PolyPhen 2 Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000101915
Gene: ENSMUSG00000033987
AA Change: D485G

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
SMART Domains Protein: ENSMUSP00000120542
Gene: ENSMUSG00000033987
AA Change: D485G

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
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 100% (79/79)
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: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam29 C T 8: 55,872,360 (GRCm38) C353Y probably damaging Het
Afap1l2 T A 19: 56,918,111 (GRCm38) E452V probably damaging Het
AI464131 C A 4: 41,498,779 (GRCm38) V284L probably benign Het
Ak6 A G 13: 100,663,907 (GRCm38) D45G probably benign Het
Arhgap17 G A 7: 123,306,420 (GRCm38) P334L probably damaging Het
Asns G T 6: 7,677,259 (GRCm38) probably null Het
Bend7 A G 2: 4,799,980 (GRCm38) T424A probably benign Het
Btbd2 C T 10: 80,646,444 (GRCm38) E241K probably damaging Het
Commd2 A C 3: 57,650,148 (GRCm38) L99W probably damaging Het
Cpne9 A T 6: 113,302,064 (GRCm38) D473V probably damaging Het
Cuzd1 A T 7: 131,311,618 (GRCm38) F423L probably damaging Het
Cyp2d9 T C 15: 82,455,945 (GRCm38) F390L probably damaging Het
Dcaf5 T A 12: 80,376,696 (GRCm38) Q234L probably benign Het
Dennd3 T G 15: 73,524,246 (GRCm38) Y201* probably null Het
Dnah5 A T 15: 28,297,066 (GRCm38) T1469S possibly damaging Het
Dnah6 T C 6: 73,118,099 (GRCm38) D2167G probably damaging Het
Dst T C 1: 34,291,893 (GRCm38) V4921A possibly damaging Het
Ephb2 A G 4: 136,659,709 (GRCm38) Y736H probably damaging Het
Eri2 C G 7: 119,785,749 (GRCm38) V510L probably benign Het
Eya2 G A 2: 165,769,326 (GRCm38) probably null Het
Fam208a T A 14: 27,466,203 (GRCm38) C869S probably damaging Het
Fastkd5 G T 2: 130,616,128 (GRCm38) Q181K probably benign Het
Fcgbp T C 7: 28,102,966 (GRCm38) S1440P probably damaging Het
Fkbp9 G A 6: 56,868,740 (GRCm38) V354M probably damaging Het
Frmpd1 T A 4: 45,271,181 (GRCm38) S304T probably benign Het
Gtf2a2 T A 9: 70,015,347 (GRCm38) Y3* probably null Het
Hagh G A 17: 24,861,340 (GRCm38) V226I probably benign Het
Hemk1 T A 9: 107,328,285 (GRCm38) I293F probably benign Het
Kcna3 A G 3: 107,037,207 (GRCm38) E262G probably damaging Het
Kcnt2 A T 1: 140,584,055 (GRCm38) T983S probably damaging Het
Klhdc3 A T 17: 46,678,414 (GRCm38) H7Q probably damaging Het
Knl1 A T 2: 119,065,979 (GRCm38) Q94L probably damaging Het
Krt12 T C 11: 99,419,659 (GRCm38) D224G probably damaging Het
Lats1 T A 10: 7,701,978 (GRCm38) S289T possibly damaging Het
Man2a2 G C 7: 80,368,865 (GRCm38) A82G probably benign Het
Map1a G A 2: 121,289,812 (GRCm38) V60M probably damaging Het
Mms22l T A 4: 24,536,138 (GRCm38) F536I possibly damaging Het
Ms4a14 T C 19: 11,303,836 (GRCm38) T453A unknown Het
Muc3a A C 5: 137,210,563 (GRCm38) I151S probably benign Het
Oaf G A 9: 43,222,780 (GRCm38) R215C probably damaging Het
Olfr1019 T A 2: 85,841,357 (GRCm38) M145L probably benign Het
Olfr1217 T A 2: 89,023,971 (GRCm38) I11L probably benign Het
Olfr1233 A G 2: 89,339,877 (GRCm38) C142R probably benign Het
Olfr1507 T C 14: 52,490,293 (GRCm38) I224V probably damaging Het
Olfr5 T C 7: 6,480,587 (GRCm38) N190D probably benign Het
Olfr8 T A 10: 78,955,491 (GRCm38) Y95* probably null Het
Pcdhgb4 A T 18: 37,721,608 (GRCm38) D352V probably benign Het
Pced1a A G 2: 130,422,028 (GRCm38) F235L probably benign Het
Pclo A G 5: 14,678,303 (GRCm38) I2392V unknown Het
Pld1 A T 3: 28,024,321 (GRCm38) D43V possibly damaging Het
Ppp1r1b C A 11: 98,350,894 (GRCm38) A51D possibly damaging Het
Prr23a1 T A 9: 98,842,864 (GRCm38) L93H probably damaging Het
Psg20 T C 7: 18,684,659 (GRCm38) D61G probably benign Het
Rab40b T A 11: 121,388,052 (GRCm38) I31F probably damaging Het
Rasd2 T C 8: 75,222,081 (GRCm38) F212L probably benign Het
Rbl2 A G 8: 91,115,193 (GRCm38) I1006V probably benign Het
Sema6c A G 3: 95,167,060 (GRCm38) E59G probably benign Het
Slc22a2 G T 17: 12,606,057 (GRCm38) V269L possibly damaging Het
Slc2a1 C T 4: 119,132,612 (GRCm38) P149S probably damaging Het
Smad4 T G 18: 73,675,871 (GRCm38) E108D probably damaging Het
Sorbs2 T A 8: 45,795,656 (GRCm38) I648K probably benign Het
Suclg1 A T 6: 73,263,841 (GRCm38) I118F probably damaging Het
Tet2 A G 3: 133,480,229 (GRCm38) I1149T probably benign Het
Tfr2 G T 5: 137,583,489 (GRCm38) V613L probably benign Het
Tfr2 T A 5: 137,571,489 (GRCm38) Y82* probably null Het
Tg A T 15: 66,696,161 (GRCm38) M1305L probably benign Het
Tmem176a A T 6: 48,844,105 (GRCm38) M170L probably benign Het
Trim71 T C 9: 114,513,162 (GRCm38) N684S probably benign Het
Tspan9 A G 6: 127,965,251 (GRCm38) I212T probably benign Het
Ttn A G 2: 76,942,975 (GRCm38) V2361A possibly damaging Het
Uqcrc1 C T 9: 108,936,759 (GRCm38) T14M possibly damaging Het
Vmn2r11 T C 5: 109,053,982 (GRCm38) I219V probably benign Het
Vmn2r76 C T 7: 86,230,166 (GRCm38) G309R probably benign Het
Vmn2r76 T C 7: 86,225,369 (GRCm38) H800R probably benign Het
Xpc A T 6: 91,499,531 (GRCm38) C529S probably benign Het
Zfp455 T A 13: 67,207,624 (GRCm38) S254T possibly damaging Het
Zfp746 T C 6: 48,064,889 (GRCm38) H301R possibly damaging Het
Zyg11a A T 4: 108,192,074 (GRCm38) I490N probably damaging Het
Other mutations in Dnah17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00231:Dnah17 APN 11 118,088,214 (GRCm38) missense possibly damaging 0.81
IGL00531:Dnah17 APN 11 118,043,173 (GRCm38) missense probably damaging 0.97
IGL00764:Dnah17 APN 11 118,096,485 (GRCm38) missense probably damaging 0.99
IGL00795:Dnah17 APN 11 118,093,634 (GRCm38) missense probably benign 0.35
IGL00823:Dnah17 APN 11 118,047,161 (GRCm38) missense probably benign 0.22
IGL01145:Dnah17 APN 11 118,047,173 (GRCm38) missense possibly damaging 0.63
IGL01433:Dnah17 APN 11 118,049,934 (GRCm38) missense probably damaging 1.00
IGL01454:Dnah17 APN 11 118,058,397 (GRCm38) missense probably damaging 1.00
IGL01545:Dnah17 APN 11 118,119,568 (GRCm38) missense probably damaging 1.00
IGL01548:Dnah17 APN 11 118,098,612 (GRCm38) missense probably benign 0.21
IGL01557:Dnah17 APN 11 118,073,686 (GRCm38) missense probably damaging 0.98
IGL01632:Dnah17 APN 11 118,033,881 (GRCm38) missense probably damaging 1.00
IGL01636:Dnah17 APN 11 118,041,056 (GRCm38) missense probably benign 0.03
IGL01672:Dnah17 APN 11 118,042,160 (GRCm38) missense probably damaging 0.97
IGL01822:Dnah17 APN 11 118,081,993 (GRCm38) missense probably damaging 1.00
IGL01869:Dnah17 APN 11 118,052,676 (GRCm38) missense probably benign 0.09
IGL01916:Dnah17 APN 11 118,125,288 (GRCm38) missense probably benign 0.00
IGL02131:Dnah17 APN 11 118,072,908 (GRCm38) missense probably damaging 1.00
IGL02154:Dnah17 APN 11 118,124,261 (GRCm38) missense probably benign 0.01
IGL02220:Dnah17 APN 11 118,072,967 (GRCm38) nonsense probably null
IGL02454:Dnah17 APN 11 118,080,767 (GRCm38) missense probably damaging 0.98
IGL02458:Dnah17 APN 11 118,036,350 (GRCm38) missense probably damaging 1.00
IGL02588:Dnah17 APN 11 118,025,653 (GRCm38) missense possibly damaging 0.95
IGL02865:Dnah17 APN 11 118,073,548 (GRCm38) missense probably damaging 1.00
IGL02881:Dnah17 APN 11 118,042,118 (GRCm38) missense probably damaging 1.00
IGL02952:Dnah17 APN 11 118,088,268 (GRCm38) missense probably benign 0.03
IGL03382:Dnah17 APN 11 118,081,943 (GRCm38) missense probably damaging 1.00
IGL03389:Dnah17 APN 11 118,094,979 (GRCm38) missense probably damaging 1.00
ergos UTSW 11 118,041,158 (GRCm38) splice site probably benign
watt UTSW 11 118,080,766 (GRCm38) missense probably damaging 0.96
PIT4280001:Dnah17 UTSW 11 118,098,582 (GRCm38) missense possibly damaging 0.85
R0004:Dnah17 UTSW 11 118,060,092 (GRCm38) missense possibly damaging 0.90
R0112:Dnah17 UTSW 11 118,074,434 (GRCm38) missense possibly damaging 0.82
R0116:Dnah17 UTSW 11 118,058,306 (GRCm38) missense probably benign 0.01
R0157:Dnah17 UTSW 11 118,127,171 (GRCm38) missense probably benign
R0320:Dnah17 UTSW 11 118,052,674 (GRCm38) missense possibly damaging 0.56
R0362:Dnah17 UTSW 11 118,098,539 (GRCm38) missense probably benign 0.10
R0382:Dnah17 UTSW 11 118,128,996 (GRCm38) missense probably damaging 1.00
R0383:Dnah17 UTSW 11 118,067,547 (GRCm38) missense probably benign
R0400:Dnah17 UTSW 11 118,082,078 (GRCm38) missense probably damaging 1.00
R0420:Dnah17 UTSW 11 118,039,939 (GRCm38) missense probably damaging 1.00
R0483:Dnah17 UTSW 11 118,047,124 (GRCm38) missense probably benign
R0533:Dnah17 UTSW 11 118,110,537 (GRCm38) missense possibly damaging 0.50
R0562:Dnah17 UTSW 11 118,072,900 (GRCm38) missense probably damaging 1.00
R0564:Dnah17 UTSW 11 118,082,981 (GRCm38) missense probably damaging 1.00
R0604:Dnah17 UTSW 11 118,121,471 (GRCm38) missense probably benign 0.00
R0608:Dnah17 UTSW 11 118,090,749 (GRCm38) nonsense probably null
R0614:Dnah17 UTSW 11 118,070,568 (GRCm38) splice site probably benign
R0632:Dnah17 UTSW 11 118,067,682 (GRCm38) splice site probably benign
R0831:Dnah17 UTSW 11 118,060,271 (GRCm38) missense probably damaging 0.99
R0838:Dnah17 UTSW 11 118,060,104 (GRCm38) missense probably damaging 1.00
R0879:Dnah17 UTSW 11 118,056,835 (GRCm38) splice site probably benign
R1061:Dnah17 UTSW 11 118,052,688 (GRCm38) missense possibly damaging 0.51
R1190:Dnah17 UTSW 11 118,042,175 (GRCm38) missense probably damaging 1.00
R1293:Dnah17 UTSW 11 118,127,137 (GRCm38) critical splice donor site probably null
R1297:Dnah17 UTSW 11 118,121,366 (GRCm38) splice site probably benign
R1332:Dnah17 UTSW 11 118,043,215 (GRCm38) missense possibly damaging 0.70
R1336:Dnah17 UTSW 11 118,043,215 (GRCm38) missense possibly damaging 0.70
R1364:Dnah17 UTSW 11 118,125,606 (GRCm38) splice site probably benign
R1418:Dnah17 UTSW 11 118,074,023 (GRCm38) missense probably damaging 0.98
R1432:Dnah17 UTSW 11 118,023,327 (GRCm38) missense probably damaging 1.00
R1497:Dnah17 UTSW 11 118,114,233 (GRCm38) missense probably damaging 1.00
R1500:Dnah17 UTSW 11 118,101,053 (GRCm38) missense probably benign
R1506:Dnah17 UTSW 11 118,125,387 (GRCm38) missense possibly damaging 0.53
R1512:Dnah17 UTSW 11 118,095,015 (GRCm38) missense probably benign
R1567:Dnah17 UTSW 11 118,125,985 (GRCm38) missense probably damaging 1.00
R1597:Dnah17 UTSW 11 118,103,498 (GRCm38) splice site probably benign
R1665:Dnah17 UTSW 11 118,121,495 (GRCm38) splice site probably benign
R1703:Dnah17 UTSW 11 118,026,749 (GRCm38) missense probably damaging 1.00
R1716:Dnah17 UTSW 11 118,032,598 (GRCm38) missense probably benign 0.00
R1727:Dnah17 UTSW 11 118,096,536 (GRCm38) nonsense probably null
R1727:Dnah17 UTSW 11 118,070,489 (GRCm38) missense probably damaging 0.98
R1728:Dnah17 UTSW 11 118,069,519 (GRCm38) missense possibly damaging 0.76
R1784:Dnah17 UTSW 11 118,069,519 (GRCm38) missense possibly damaging 0.76
R1852:Dnah17 UTSW 11 118,121,916 (GRCm38) missense probably damaging 0.97
R1869:Dnah17 UTSW 11 118,047,189 (GRCm38) nonsense probably null
R1886:Dnah17 UTSW 11 118,108,161 (GRCm38) missense possibly damaging 0.62
R1893:Dnah17 UTSW 11 118,066,968 (GRCm38) missense probably benign 0.00
R1954:Dnah17 UTSW 11 118,024,731 (GRCm38) missense probably damaging 1.00
R1969:Dnah17 UTSW 11 118,104,535 (GRCm38) missense probably benign 0.00
R1971:Dnah17 UTSW 11 118,104,535 (GRCm38) missense probably benign 0.00
R1975:Dnah17 UTSW 11 118,096,536 (GRCm38) nonsense probably null
R1977:Dnah17 UTSW 11 118,112,591 (GRCm38) missense possibly damaging 0.52
R2055:Dnah17 UTSW 11 118,067,531 (GRCm38) missense probably benign 0.00
R2115:Dnah17 UTSW 11 118,119,802 (GRCm38) missense probably benign 0.00
R2132:Dnah17 UTSW 11 118,033,747 (GRCm38) missense probably damaging 0.98
R2200:Dnah17 UTSW 11 118,102,409 (GRCm38) splice site probably benign
R2277:Dnah17 UTSW 11 118,096,561 (GRCm38) missense possibly damaging 0.81
R2279:Dnah17 UTSW 11 118,096,561 (GRCm38) missense possibly damaging 0.81
R2400:Dnah17 UTSW 11 118,126,384 (GRCm38) critical splice acceptor site probably null
R2402:Dnah17 UTSW 11 118,125,974 (GRCm38) missense probably benign 0.10
R2497:Dnah17 UTSW 11 118,087,024 (GRCm38) splice site probably null
R2923:Dnah17 UTSW 11 118,093,547 (GRCm38) missense probably damaging 1.00
R3121:Dnah17 UTSW 11 118,041,086 (GRCm38) missense probably damaging 1.00
R3236:Dnah17 UTSW 11 118,094,854 (GRCm38) missense probably benign 0.08
R3237:Dnah17 UTSW 11 118,094,854 (GRCm38) missense probably benign 0.08
R3498:Dnah17 UTSW 11 118,080,849 (GRCm38) splice site probably benign
R3499:Dnah17 UTSW 11 118,080,849 (GRCm38) splice site probably benign
R3746:Dnah17 UTSW 11 118,082,916 (GRCm38) missense probably benign 0.00
R3749:Dnah17 UTSW 11 118,082,916 (GRCm38) missense probably benign 0.00
R3762:Dnah17 UTSW 11 118,104,526 (GRCm38) missense probably benign 0.00
R3826:Dnah17 UTSW 11 118,041,158 (GRCm38) splice site probably benign
R3828:Dnah17 UTSW 11 118,041,158 (GRCm38) splice site probably benign
R3829:Dnah17 UTSW 11 118,041,158 (GRCm38) splice site probably benign
R3877:Dnah17 UTSW 11 118,024,707 (GRCm38) missense probably damaging 1.00
R3899:Dnah17 UTSW 11 118,094,808 (GRCm38) missense possibly damaging 0.78
R3900:Dnah17 UTSW 11 118,094,808 (GRCm38) missense possibly damaging 0.78
R3911:Dnah17 UTSW 11 118,080,849 (GRCm38) splice site probably benign
R3913:Dnah17 UTSW 11 118,080,849 (GRCm38) splice site probably benign
R3930:Dnah17 UTSW 11 118,080,849 (GRCm38) splice site probably benign
R3931:Dnah17 UTSW 11 118,080,849 (GRCm38) splice site probably benign
R3969:Dnah17 UTSW 11 118,041,158 (GRCm38) splice site probably benign
R3970:Dnah17 UTSW 11 118,041,158 (GRCm38) splice site probably benign
R4056:Dnah17 UTSW 11 118,070,538 (GRCm38) missense probably benign 0.05
R4113:Dnah17 UTSW 11 118,112,594 (GRCm38) missense possibly damaging 0.50
R4295:Dnah17 UTSW 11 118,118,772 (GRCm38) missense probably damaging 1.00
R4324:Dnah17 UTSW 11 118,094,213 (GRCm38) missense probably benign 0.01
R4412:Dnah17 UTSW 11 118,073,683 (GRCm38) missense probably damaging 1.00
R4413:Dnah17 UTSW 11 118,025,168 (GRCm38) missense probably benign 0.00
R4422:Dnah17 UTSW 11 118,081,973 (GRCm38) missense possibly damaging 0.91
R4552:Dnah17 UTSW 11 118,052,943 (GRCm38) missense possibly damaging 0.79
R4669:Dnah17 UTSW 11 118,074,293 (GRCm38) missense probably benign 0.02
R4677:Dnah17 UTSW 11 118,119,814 (GRCm38) missense probably damaging 1.00
R4716:Dnah17 UTSW 11 118,073,648 (GRCm38) missense probably benign 0.02
R4832:Dnah17 UTSW 11 118,026,780 (GRCm38) missense probably damaging 1.00
R4868:Dnah17 UTSW 11 118,108,212 (GRCm38) missense probably benign 0.03
R4897:Dnah17 UTSW 11 118,078,593 (GRCm38) missense probably damaging 1.00
R4928:Dnah17 UTSW 11 118,027,433 (GRCm38) missense probably damaging 1.00
R4937:Dnah17 UTSW 11 118,042,154 (GRCm38) missense probably damaging 1.00
R4957:Dnah17 UTSW 11 118,074,298 (GRCm38) missense probably benign 0.44
R5008:Dnah17 UTSW 11 118,110,577 (GRCm38) missense probably benign 0.01
R5016:Dnah17 UTSW 11 118,080,766 (GRCm38) missense probably damaging 0.96
R5027:Dnah17 UTSW 11 118,102,539 (GRCm38) missense probably benign 0.01
R5133:Dnah17 UTSW 11 118,117,113 (GRCm38) missense probably benign 0.00
R5140:Dnah17 UTSW 11 118,086,945 (GRCm38) missense probably damaging 1.00
R5146:Dnah17 UTSW 11 118,114,179 (GRCm38) missense probably damaging 0.99
R5151:Dnah17 UTSW 11 118,027,467 (GRCm38) missense probably damaging 1.00
R5153:Dnah17 UTSW 11 118,082,974 (GRCm38) nonsense probably null
R5192:Dnah17 UTSW 11 118,034,359 (GRCm38) missense possibly damaging 0.96
R5315:Dnah17 UTSW 11 118,127,283 (GRCm38) missense possibly damaging 0.79
R5317:Dnah17 UTSW 11 118,127,283 (GRCm38) missense possibly damaging 0.79
R5335:Dnah17 UTSW 11 118,112,514 (GRCm38) missense probably damaging 1.00
R5379:Dnah17 UTSW 11 118,117,203 (GRCm38) intron probably benign
R5396:Dnah17 UTSW 11 118,127,282 (GRCm38) missense probably benign
R5418:Dnah17 UTSW 11 118,094,984 (GRCm38) missense probably benign 0.04
R5534:Dnah17 UTSW 11 118,052,770 (GRCm38) missense possibly damaging 0.83
R5539:Dnah17 UTSW 11 118,073,660 (GRCm38) missense probably benign 0.03
R5594:Dnah17 UTSW 11 118,043,229 (GRCm38) splice site probably null
R5634:Dnah17 UTSW 11 118,052,926 (GRCm38) splice site probably null
R5696:Dnah17 UTSW 11 118,101,056 (GRCm38) missense probably benign 0.44
R5802:Dnah17 UTSW 11 118,036,446 (GRCm38) missense possibly damaging 0.79
R5826:Dnah17 UTSW 11 118,034,367 (GRCm38) missense probably damaging 1.00
R5873:Dnah17 UTSW 11 118,056,897 (GRCm38) missense probably benign 0.01
R5898:Dnah17 UTSW 11 118,114,213 (GRCm38) missense probably benign 0.00
R5934:Dnah17 UTSW 11 118,041,102 (GRCm38) missense probably benign
R6030:Dnah17 UTSW 11 118,025,549 (GRCm38) missense probably benign 0.32
R6030:Dnah17 UTSW 11 118,025,549 (GRCm38) missense probably benign 0.32
R6038:Dnah17 UTSW 11 118,055,889 (GRCm38) missense probably benign 0.00
R6038:Dnah17 UTSW 11 118,055,889 (GRCm38) missense probably benign 0.00
R6113:Dnah17 UTSW 11 118,126,275 (GRCm38) missense probably damaging 1.00
R6117:Dnah17 UTSW 11 118,119,571 (GRCm38) missense probably benign 0.00
R6137:Dnah17 UTSW 11 118,025,654 (GRCm38) missense probably damaging 1.00
R6173:Dnah17 UTSW 11 118,039,946 (GRCm38) missense probably damaging 1.00
R6258:Dnah17 UTSW 11 118,126,324 (GRCm38) missense probably damaging 1.00
R6258:Dnah17 UTSW 11 118,126,322 (GRCm38) missense probably damaging 1.00
R6258:Dnah17 UTSW 11 118,126,323 (GRCm38) nonsense probably null
R6260:Dnah17 UTSW 11 118,126,323 (GRCm38) nonsense probably null
R6260:Dnah17 UTSW 11 118,126,324 (GRCm38) missense probably damaging 1.00
R6260:Dnah17 UTSW 11 118,126,322 (GRCm38) missense probably damaging 1.00
R6278:Dnah17 UTSW 11 118,126,290 (GRCm38) missense probably damaging 0.99
R6298:Dnah17 UTSW 11 118,108,161 (GRCm38) missense probably benign 0.00
R6300:Dnah17 UTSW 11 118,034,310 (GRCm38) missense probably damaging 1.00
R6302:Dnah17 UTSW 11 118,129,155 (GRCm38) missense probably benign 0.09
R6363:Dnah17 UTSW 11 118,110,505 (GRCm38) missense probably benign
R6381:Dnah17 UTSW 11 118,129,185 (GRCm38) missense probably benign 0.08
R6418:Dnah17 UTSW 11 118,129,197 (GRCm38) missense probably damaging 0.99
R6660:Dnah17 UTSW 11 118,100,188 (GRCm38) missense probably benign
R6803:Dnah17 UTSW 11 118,125,372 (GRCm38) missense probably benign 0.00
R6820:Dnah17 UTSW 11 118,069,000 (GRCm38) missense probably damaging 0.99
R6885:Dnah17 UTSW 11 118,090,772 (GRCm38) missense possibly damaging 0.47
R6921:Dnah17 UTSW 11 118,041,484 (GRCm38) missense probably damaging 0.98
R6932:Dnah17 UTSW 11 118,060,079 (GRCm38) missense possibly damaging 0.95
R6954:Dnah17 UTSW 11 118,066,432 (GRCm38) missense probably damaging 1.00
R7000:Dnah17 UTSW 11 118,025,702 (GRCm38) critical splice acceptor site probably null
R7007:Dnah17 UTSW 11 118,118,871 (GRCm38) missense possibly damaging 0.92
R7048:Dnah17 UTSW 11 118,046,118 (GRCm38) missense possibly damaging 0.80
R7056:Dnah17 UTSW 11 118,125,386 (GRCm38) missense probably benign
R7131:Dnah17 UTSW 11 118,079,658 (GRCm38) missense probably benign 0.14
R7143:Dnah17 UTSW 11 118,086,130 (GRCm38) missense probably damaging 1.00
R7146:Dnah17 UTSW 11 118,082,110 (GRCm38) missense probably damaging 0.98
R7147:Dnah17 UTSW 11 118,094,929 (GRCm38) missense probably benign 0.31
R7172:Dnah17 UTSW 11 118,041,131 (GRCm38) nonsense probably null
R7183:Dnah17 UTSW 11 118,129,188 (GRCm38) missense probably benign
R7297:Dnah17 UTSW 11 118,103,356 (GRCm38) missense probably damaging 0.98
R7297:Dnah17 UTSW 11 118,055,730 (GRCm38) critical splice donor site probably null
R7367:Dnah17 UTSW 11 118,115,196 (GRCm38) missense probably benign
R7398:Dnah17 UTSW 11 118,080,724 (GRCm38) missense probably damaging 0.96
R7426:Dnah17 UTSW 11 118,090,717 (GRCm38) missense probably null 0.79
R7529:Dnah17 UTSW 11 118,049,866 (GRCm38) critical splice donor site probably null
R7615:Dnah17 UTSW 11 118,110,547 (GRCm38) nonsense probably null
R7681:Dnah17 UTSW 11 118,025,186 (GRCm38) missense probably damaging 1.00
R7702:Dnah17 UTSW 11 118,121,478 (GRCm38) missense possibly damaging 0.64
R7702:Dnah17 UTSW 11 118,025,640 (GRCm38) missense probably benign 0.00
R7713:Dnah17 UTSW 11 118,025,171 (GRCm38) missense probably benign 0.02
R7809:Dnah17 UTSW 11 118,104,636 (GRCm38) missense probably benign 0.09
R7842:Dnah17 UTSW 11 118,079,682 (GRCm38) critical splice acceptor site probably null
R7935:Dnah17 UTSW 11 118,127,222 (GRCm38) missense probably benign 0.20
R7951:Dnah17 UTSW 11 118,118,766 (GRCm38) missense possibly damaging 0.64
R8070:Dnah17 UTSW 11 118,024,671 (GRCm38) missense probably damaging 0.97
R8098:Dnah17 UTSW 11 118,050,367 (GRCm38) missense probably damaging 1.00
R8101:Dnah17 UTSW 11 118,125,918 (GRCm38) missense probably benign
R8177:Dnah17 UTSW 11 118,128,927 (GRCm38) missense possibly damaging 0.60
R8343:Dnah17 UTSW 11 118,114,195 (GRCm38) missense probably benign
R8350:Dnah17 UTSW 11 118,087,047 (GRCm38) missense probably damaging 0.98
R8393:Dnah17 UTSW 11 118,057,029 (GRCm38) missense probably damaging 1.00
R8401:Dnah17 UTSW 11 118,024,659 (GRCm38) missense probably damaging 0.96
R8418:Dnah17 UTSW 11 118,103,458 (GRCm38) missense probably benign 0.01
R8450:Dnah17 UTSW 11 118,087,047 (GRCm38) missense probably damaging 0.98
R8546:Dnah17 UTSW 11 118,124,275 (GRCm38) missense probably benign 0.00
R8697:Dnah17 UTSW 11 118,086,159 (GRCm38) missense possibly damaging 0.96
R8710:Dnah17 UTSW 11 118,042,147 (GRCm38) missense probably damaging 1.00
R8713:Dnah17 UTSW 11 118,088,202 (GRCm38) missense probably damaging 1.00
R8722:Dnah17 UTSW 11 118,070,457 (GRCm38) nonsense probably null
R8797:Dnah17 UTSW 11 118,101,375 (GRCm38) missense probably benign 0.00
R8953:Dnah17 UTSW 11 118,125,412 (GRCm38) splice site probably benign
R8965:Dnah17 UTSW 11 118,024,666 (GRCm38) missense probably damaging 1.00
R8976:Dnah17 UTSW 11 118,026,840 (GRCm38) missense probably damaging 1.00
R9090:Dnah17 UTSW 11 118,041,044 (GRCm38) missense probably damaging 1.00
R9128:Dnah17 UTSW 11 118,046,178 (GRCm38) missense possibly damaging 0.76
R9134:Dnah17 UTSW 11 118,088,146 (GRCm38) missense probably damaging 1.00
R9245:Dnah17 UTSW 11 118,125,677 (GRCm38) missense probably benign 0.02
R9251:Dnah17 UTSW 11 118,121,792 (GRCm38) missense probably benign 0.03
R9271:Dnah17 UTSW 11 118,041,044 (GRCm38) missense probably damaging 1.00
R9367:Dnah17 UTSW 11 118,121,386 (GRCm38) missense possibly damaging 0.93
R9367:Dnah17 UTSW 11 118,096,638 (GRCm38) missense possibly damaging 0.95
R9381:Dnah17 UTSW 11 118,023,393 (GRCm38) missense probably benign
R9405:Dnah17 UTSW 11 118,118,911 (GRCm38) missense probably benign
R9449:Dnah17 UTSW 11 118,096,626 (GRCm38) missense probably benign 0.07
R9517:Dnah17 UTSW 11 118,024,614 (GRCm38) missense possibly damaging 0.76
R9588:Dnah17 UTSW 11 118,121,957 (GRCm38) missense probably benign 0.00
R9629:Dnah17 UTSW 11 118,088,978 (GRCm38) missense probably damaging 1.00
R9654:Dnah17 UTSW 11 118,036,330 (GRCm38) critical splice donor site probably null
R9655:Dnah17 UTSW 11 118,080,823 (GRCm38) missense possibly damaging 0.94
R9662:Dnah17 UTSW 11 118,034,340 (GRCm38) missense probably damaging 0.97
R9686:Dnah17 UTSW 11 118,088,222 (GRCm38) missense possibly damaging 0.46
R9689:Dnah17 UTSW 11 118,072,905 (GRCm38) missense probably damaging 1.00
R9706:Dnah17 UTSW 11 118,126,200 (GRCm38) missense probably damaging 1.00
X0058:Dnah17 UTSW 11 118,082,925 (GRCm38) missense probably damaging 1.00
Z1176:Dnah17 UTSW 11 118,127,166 (GRCm38) missense probably benign 0.01
Z1177:Dnah17 UTSW 11 118,086,960 (GRCm38) missense probably damaging 1.00
Z1177:Dnah17 UTSW 11 118,078,563 (GRCm38) missense possibly damaging 0.91
Z1177:Dnah17 UTSW 11 118,127,142 (GRCm38) nonsense probably null
Predicted Primers PCR Primer
(F):5'- TATATGGACAGTCAGGGAGCTG -3'
(R):5'- CTGAACGTGTAGAAGCTCCAG -3'

Sequencing Primer
(F):5'- AGCTGACAGATAGGCTCGCTG -3'
(R):5'- TGTAGAAGCTCCAGGCCCTG -3'
Posted On 2019-10-17