Incidental Mutation 'IGL00565:Dnai3'
ID 332628
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dnai3
Ensembl Gene ENSMUSG00000043020
Gene Name dynein axonemal intermediate chain 3
Synonyms 4931433A13Rik, Wdr63, Ida7, IC140
Accession Numbers
Essential gene? Probably non essential (E-score: 0.115) question?
Stock # IGL00565
Quality Score
Status
Chromosome 3
Chromosomal Location 145746281-145813855 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 145750674 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000124475 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000160285]
AlphaFold B2RY71
Predicted Effect probably benign
Transcript: ENSMUST00000160285
SMART Domains Protein: ENSMUSP00000124475
Gene: ENSMUSG00000043020

DomainStartEndE-ValueType
low complexity region 3 22 N/A INTRINSIC
low complexity region 26 35 N/A INTRINSIC
low complexity region 133 150 N/A INTRINSIC
low complexity region 165 180 N/A INTRINSIC
Blast:WD40 321 367 6e-19 BLAST
low complexity region 375 383 N/A INTRINSIC
WD40 390 429 6.34e-2 SMART
WD40 470 527 1.15e-4 SMART
low complexity region 536 553 N/A INTRINSIC
WD40 693 732 1.07e1 SMART
WD40 737 776 1.1e2 SMART
coiled coil region 867 902 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161104
Predicted Effect noncoding transcript
Transcript: ENSMUST00000162572
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610021A01Rik C A 7: 41,274,996 (GRCm39) T233K possibly damaging Het
Adamts9 A T 6: 92,836,883 (GRCm39) M623K possibly damaging Het
Arid1a T G 4: 133,412,793 (GRCm39) D1467A unknown Het
Cdhr2 A G 13: 54,866,112 (GRCm39) D304G probably damaging Het
Cenpj C T 14: 56,790,487 (GRCm39) V521I probably benign Het
Ciao2a A T 9: 66,039,898 (GRCm39) I72L probably benign Het
Csf2rb G T 15: 78,232,714 (GRCm39) E674* probably null Het
Edaradd C T 13: 12,498,480 (GRCm39) probably null Het
Emilin2 A G 17: 71,559,854 (GRCm39) V1041A possibly damaging Het
Fam135b A G 15: 71,343,361 (GRCm39) V418A probably benign Het
Gnas T A 2: 174,183,504 (GRCm39) probably benign Het
Grxcr1 A T 5: 68,189,540 (GRCm39) N104Y possibly damaging Het
Gtf2a1l T A 17: 89,001,723 (GRCm39) L146Q probably damaging Het
Hectd1 T A 12: 51,837,181 (GRCm39) E791D probably damaging Het
Ifi203 A G 1: 173,765,306 (GRCm39) probably null Het
Klk1b11 A G 7: 43,649,243 (GRCm39) N260S probably damaging Het
LTO1 G T 7: 144,470,220 (GRCm39) V50F probably damaging Het
Map4 A T 9: 109,901,672 (GRCm39) probably benign Het
Marveld2 C T 13: 100,737,401 (GRCm39) V163M possibly damaging Het
Med14 T C X: 12,613,003 (GRCm39) probably benign Het
Mex3b A T 7: 82,518,116 (GRCm39) I144F probably damaging Het
Pde2a T A 7: 101,133,796 (GRCm39) C92* probably null Het
Phf6 T A X: 52,020,516 (GRCm39) Y103N probably damaging Het
Ptprt A G 2: 161,402,111 (GRCm39) I1039T probably damaging Het
Rftn2 C A 1: 55,243,444 (GRCm39) V275F probably damaging Het
Skap1 C A 11: 96,621,971 (GRCm39) Q296K probably damaging Het
Skap1 T A 11: 96,622,016 (GRCm39) F311I probably damaging Het
Tas2r115 A G 6: 132,714,741 (GRCm39) I70T probably benign Het
Vav2 T C 2: 27,167,250 (GRCm39) D613G probably benign Het
Zranb3 T C 1: 127,943,877 (GRCm39) E290G probably benign Het
Other mutations in Dnai3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00093:Dnai3 APN 3 145,788,759 (GRCm39) missense probably benign
IGL01339:Dnai3 APN 3 145,748,591 (GRCm39) missense probably benign 0.14
IGL01952:Dnai3 APN 3 145,802,918 (GRCm39) missense probably damaging 0.96
IGL02663:Dnai3 APN 3 145,760,312 (GRCm39) missense possibly damaging 0.53
IGL02710:Dnai3 APN 3 145,753,903 (GRCm39) missense possibly damaging 0.96
P0041:Dnai3 UTSW 3 145,786,997 (GRCm39) missense possibly damaging 0.96
R0014:Dnai3 UTSW 3 145,787,178 (GRCm39) splice site probably null
R0014:Dnai3 UTSW 3 145,787,178 (GRCm39) splice site probably null
R0498:Dnai3 UTSW 3 145,787,119 (GRCm39) missense possibly damaging 0.54
R0589:Dnai3 UTSW 3 145,768,086 (GRCm39) missense probably benign 0.01
R1484:Dnai3 UTSW 3 145,802,996 (GRCm39) missense probably benign 0.02
R1537:Dnai3 UTSW 3 145,748,504 (GRCm39) missense probably damaging 0.98
R1611:Dnai3 UTSW 3 145,801,113 (GRCm39) missense probably damaging 1.00
R1743:Dnai3 UTSW 3 145,803,017 (GRCm39) missense possibly damaging 0.81
R1861:Dnai3 UTSW 3 145,788,801 (GRCm39) missense probably damaging 1.00
R1991:Dnai3 UTSW 3 145,769,235 (GRCm39) missense possibly damaging 0.82
R2185:Dnai3 UTSW 3 145,772,619 (GRCm39) missense possibly damaging 0.76
R4299:Dnai3 UTSW 3 145,774,561 (GRCm39) missense probably damaging 1.00
R4620:Dnai3 UTSW 3 145,748,564 (GRCm39) missense probably damaging 1.00
R4649:Dnai3 UTSW 3 145,753,922 (GRCm39) missense probably damaging 1.00
R4914:Dnai3 UTSW 3 145,772,582 (GRCm39) missense probably damaging 0.98
R4948:Dnai3 UTSW 3 145,788,820 (GRCm39) nonsense probably null
R5578:Dnai3 UTSW 3 145,802,983 (GRCm39) nonsense probably null
R6130:Dnai3 UTSW 3 145,748,559 (GRCm39) missense probably benign 0.25
R6162:Dnai3 UTSW 3 145,750,617 (GRCm39) missense probably damaging 1.00
R6291:Dnai3 UTSW 3 145,772,648 (GRCm39) missense probably benign 0.00
R6390:Dnai3 UTSW 3 145,801,143 (GRCm39) missense probably damaging 1.00
R6560:Dnai3 UTSW 3 145,801,161 (GRCm39) missense possibly damaging 0.79
R6893:Dnai3 UTSW 3 145,786,184 (GRCm39) missense probably damaging 1.00
R7090:Dnai3 UTSW 3 145,746,582 (GRCm39) missense possibly damaging 0.80
R7102:Dnai3 UTSW 3 145,761,459 (GRCm39) missense possibly damaging 0.49
R7111:Dnai3 UTSW 3 145,803,028 (GRCm39) missense probably damaging 0.99
R7260:Dnai3 UTSW 3 145,752,295 (GRCm39) missense probably benign 0.01
R7288:Dnai3 UTSW 3 145,787,007 (GRCm39) missense probably damaging 0.97
R7411:Dnai3 UTSW 3 145,802,900 (GRCm39) missense probably damaging 0.98
R7417:Dnai3 UTSW 3 145,798,835 (GRCm39) splice site probably null
R7466:Dnai3 UTSW 3 145,761,373 (GRCm39) missense probably benign 0.01
R7860:Dnai3 UTSW 3 145,772,675 (GRCm39) missense probably damaging 0.99
R7964:Dnai3 UTSW 3 145,774,531 (GRCm39) missense probably benign 0.09
R8013:Dnai3 UTSW 3 145,787,040 (GRCm39) missense probably damaging 1.00
R8059:Dnai3 UTSW 3 145,752,428 (GRCm39) missense possibly damaging 0.75
R8191:Dnai3 UTSW 3 145,800,066 (GRCm39) missense probably damaging 1.00
R8354:Dnai3 UTSW 3 145,802,982 (GRCm39) missense probably damaging 1.00
R8454:Dnai3 UTSW 3 145,802,982 (GRCm39) missense probably damaging 1.00
R8770:Dnai3 UTSW 3 145,752,298 (GRCm39) missense probably benign 0.01
R8967:Dnai3 UTSW 3 145,761,395 (GRCm39) missense possibly damaging 0.95
R9135:Dnai3 UTSW 3 145,772,589 (GRCm39) missense probably benign 0.39
R9310:Dnai3 UTSW 3 145,802,895 (GRCm39) critical splice donor site probably null
R9664:Dnai3 UTSW 3 145,748,594 (GRCm39) missense probably benign 0.01
Posted On 2015-08-05