Incidental Mutation 'R4957:Dnah17'
ID 381663
Institutional Source Beutler Lab
Gene Symbol Dnah17
Ensembl Gene ENSMUSG00000033987
Gene Name dynein, axonemal, heavy chain 17
Synonyms LOC382552, Dnahcl1, 2810003K23Rik, Dnahc17
MMRRC Submission 042554-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4957 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 118021723-118130634 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 118074298 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 2306 (I2306N)
Ref Sequence ENSEMBL: ENSMUSP00000081864 (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: I2306N

PolyPhen 2 Score 0.441 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000081864
Gene: ENSMUSG00000033987
AA Change: I2306N

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: I2306N

PolyPhen 2 Score 0.120 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000101915
Gene: ENSMUSG00000033987
AA Change: I2306N

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: I2319N

PolyPhen 2 Score 0.041 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000120542
Gene: ENSMUSG00000033987
AA Change: I2319N

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 0.1585 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.3%
  • 20x: 92.5%
Validation Efficiency 99% (80/81)
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: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3110009E18Rik G C 1: 120,169,110 (GRCm38) probably benign Het
3110009E18Rik G T 1: 120,169,119 (GRCm38) probably benign Het
3110009E18Rik C T 1: 120,169,120 (GRCm38) probably benign Het
6820408C15Rik T A 2: 152,444,093 (GRCm38) V342D probably damaging Het
Arhgap33 C T 7: 30,532,361 (GRCm38) G101R probably damaging Het
Atf7ip C T 6: 136,606,810 (GRCm38) R1280C probably damaging Het
Cacnb4 T C 2: 52,558,291 (GRCm38) H8R probably damaging Het
Ccdc150 T A 1: 54,364,868 (GRCm38) probably benign Het
Cd163l1 T C 7: 140,228,522 (GRCm38) V782A probably damaging Het
Cd74 A G 18: 60,809,037 (GRCm38) N113D probably benign Het
Cdc25b T C 2: 131,193,605 (GRCm38) V341A possibly damaging Het
Clptm1l T C 13: 73,612,428 (GRCm38) I310T probably damaging Het
Clptm1l T A 13: 73,611,196 (GRCm38) I245N possibly damaging Het
Creb5 A T 6: 53,693,922 (GRCm38) probably null Het
Crebbp T C 16: 4,117,367 (GRCm38) Q460R probably benign Het
Dync1h1 C A 12: 110,658,126 (GRCm38) T3700N probably damaging Het
Elovl1 A T 4: 118,431,923 (GRCm38) H215L probably damaging Het
Enkd1 A G 8: 105,704,489 (GRCm38) I202T probably benign Het
Epha7 C T 4: 28,871,892 (GRCm38) A407V probably damaging Het
Ercc3 G T 18: 32,243,117 (GRCm38) G130W probably damaging Het
Fbxl8 A G 8: 105,268,195 (GRCm38) E113G probably damaging Het
Frmpd1 T G 4: 45,273,099 (GRCm38) N339K probably damaging Het
Frrs1 G A 3: 116,885,248 (GRCm38) D240N probably benign Het
Gemin2 A G 12: 59,017,168 (GRCm38) S105G probably benign Het
Glra1 T A 11: 55,527,398 (GRCm38) I257F probably damaging Het
Gmcl1 G A 6: 86,710,521 (GRCm38) P354S probably damaging Het
Gpr15 G T 16: 58,718,174 (GRCm38) A184E probably damaging Het
Grm7 G A 6: 111,358,863 (GRCm38) G745E probably damaging Het
H2-T10 T A 17: 36,117,416 (GRCm38) probably benign Het
Hdac5 C A 11: 102,205,256 (GRCm38) probably benign Het
Ift22 G A 5: 136,908,216 (GRCm38) probably benign Het
Ighg3 T C 12: 113,361,130 (GRCm38) E34G unknown Het
Itga11 A T 9: 62,767,648 (GRCm38) T821S probably benign Het
Lmod2 T C 6: 24,603,872 (GRCm38) V282A possibly damaging Het
Maml2 A G 9: 13,620,276 (GRCm38) K262R probably damaging Het
Mme T A 3: 63,343,489 (GRCm38) probably benign Het
Mnat1 A G 12: 73,123,878 (GRCm38) Y14C probably damaging Het
Mtdh A T 15: 34,083,135 (GRCm38) T34S possibly damaging Het
Ncaph T C 2: 127,121,257 (GRCm38) D352G possibly damaging Het
Olfr1014 T C 2: 85,777,115 (GRCm38) F177S probably damaging Het
Olfr1036 T A 2: 86,075,510 (GRCm38) Y257N probably damaging Het
Olfr1293-ps C A 2: 111,528,224 (GRCm38) N321K probably benign Het
Olfr224 A G 11: 58,566,518 (GRCm38) Y276H probably damaging Het
Pcdhb13 T A 18: 37,444,784 (GRCm38) D738E possibly damaging Het
Pla2g4f C T 2: 120,300,499 (GRCm38) R825Q probably benign Het
Pnliprp2 C T 19: 58,775,145 (GRCm38) L409F possibly damaging Het
Prlr G T 15: 10,319,195 (GRCm38) C70F probably damaging Het
Ptpn14 C T 1: 189,851,272 (GRCm38) T772I probably benign Het
Ryr2 T C 13: 11,785,080 (GRCm38) Q927R probably damaging Het
Scarf1 A G 11: 75,525,634 (GRCm38) E634G probably benign Het
Slc39a14 A T 14: 70,315,811 (GRCm38) S158R probably damaging Het
Slc9c1 A T 16: 45,544,831 (GRCm38) T176S probably benign Het
Srsf10 T C 4: 135,856,230 (GRCm38) S2P probably damaging Het
Tcam1 T A 11: 106,282,879 (GRCm38) C50S probably damaging Het
Tcf7l2 A G 19: 55,931,432 (GRCm38) probably null Het
Tdrd3 T A 14: 87,505,787 (GRCm38) H390Q probably benign Het
Tlk2 T C 11: 105,253,359 (GRCm38) probably null Het
Tnc G C 4: 63,976,556 (GRCm38) P1531R probably damaging Het
Tnfrsf1b T G 4: 145,246,758 (GRCm38) Q15P possibly damaging Het
Tnfrsf1b C A 4: 145,246,757 (GRCm38) Q15H probably damaging Het
Tssk4 A T 14: 55,651,809 (GRCm38) E264V probably damaging Het
Ttc37 T G 13: 76,185,113 (GRCm38) probably null Het
Ugt3a2 G A 15: 9,365,188 (GRCm38) V296I probably benign Het
Usp5 C G 6: 124,822,630 (GRCm38) K318N possibly damaging Het
Vmn2r8 T G 5: 108,799,263 (GRCm38) E541A probably benign Het
Ybx1 A T 4: 119,278,938 (GRCm38) probably benign Het
Zfp39 T A 11: 58,891,231 (GRCm38) Y235F possibly damaging Het
Zfp422 T A 6: 116,626,943 (GRCm38) K32* probably null Het
Zpbp2 T A 11: 98,551,324 (GRCm38) probably null 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
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 11 118,126,323 (GRCm38) nonsense probably null
R6258:Dnah17 UTSW 11 118,126,322 (GRCm38) missense probably damaging 1.00
R6258:Dnah17 UTSW 11 118,126,324 (GRCm38) missense probably damaging 1.00
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
R6260:Dnah17 UTSW 11 118,126,323 (GRCm38) nonsense probably null
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
R7524:Dnah17 UTSW 11 118,121,481 (GRCm38) missense probably benign 0.03
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'- CACTTGCTGAACTCCACTCG -3'
(R):5'- GACTGACCGTCGGCCATC -3'

Sequencing Primer
(F):5'- TCCACTCGATAATCAATGAGCTG -3'
(R):5'- GGCCATCCCTCCCTCCAG -3'
Posted On 2016-04-27