Incidental Mutation 'IGL02663:Dnai3'
ID 302622
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 # IGL02663
Quality Score
Status
Chromosome 3
Chromosomal Location 145746281-145813855 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 145760312 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 692 (M692K)
Ref Sequence ENSEMBL: ENSMUSP00000124475 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000160285]
AlphaFold B2RY71
Predicted Effect possibly damaging
Transcript: ENSMUST00000160285
AA Change: M692K

PolyPhen 2 Score 0.529 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000124475
Gene: ENSMUSG00000043020
AA Change: M692K

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
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bcl9 A C 3: 97,112,648 (GRCm39) F1269C probably damaging Het
Cdc20b T A 13: 113,192,665 (GRCm39) probably null Het
Chrna1 A G 2: 73,404,660 (GRCm39) probably benign Het
Creb5 A G 6: 53,657,946 (GRCm39) H236R probably damaging Het
Cyp17a1 A G 19: 46,661,005 (GRCm39) F93S probably damaging Het
Cyp4a32 T A 4: 115,467,787 (GRCm39) L257H probably damaging Het
Fahd1 C T 17: 25,068,478 (GRCm39) G200R probably damaging Het
Ifit1 A G 19: 34,618,380 (GRCm39) probably benign Het
Mfhas1 G T 8: 36,057,060 (GRCm39) V512L probably damaging Het
Myh13 C T 11: 67,245,753 (GRCm39) Q1095* probably null Het
Nfia A G 4: 97,929,856 (GRCm39) T339A probably benign Het
Npas3 T C 12: 54,115,691 (GRCm39) L840P probably damaging Het
Nsf T C 11: 103,821,641 (GRCm39) T2A probably benign Het
Or11g7 A G 14: 50,691,309 (GRCm39) T267A probably benign Het
Or14j10 A T 17: 37,934,935 (GRCm39) I197K probably benign Het
Or5b111 A G 19: 13,290,743 (GRCm39) V302A probably benign Het
P2rx2 C T 5: 110,488,115 (GRCm39) E480K possibly damaging Het
P2rx2 G T 5: 110,488,052 (GRCm39) probably null Het
Ppp1r8 G A 4: 132,560,419 (GRCm39) T94I probably damaging Het
S100a11 A T 3: 93,431,464 (GRCm39) E33D probably damaging Het
Sec31b C A 19: 44,522,717 (GRCm39) A92S probably damaging Het
Serpina3g C T 12: 104,205,399 (GRCm39) T46I possibly damaging Het
Sgo2b A T 8: 64,396,148 (GRCm39) I36N probably damaging Het
Slc35e1 A G 8: 73,242,053 (GRCm39) L223P probably damaging Het
St14 T C 9: 31,011,678 (GRCm39) probably null Het
Sult2a8 A G 7: 14,159,368 (GRCm39) Y84H possibly damaging Het
Tas1r2 T C 4: 139,387,593 (GRCm39) Y322H probably benign Het
Tmem59 T C 4: 107,054,738 (GRCm39) L181P probably damaging Het
Trp73 A G 4: 154,146,963 (GRCm39) probably null Het
Ube2h A G 6: 30,241,412 (GRCm39) V86A probably damaging Het
Vmn2r22 A T 6: 123,626,117 (GRCm39) H106Q probably benign Het
Xirp2 T C 2: 67,339,802 (GRCm39) V681A possibly damaging Het
Other mutations in Dnai3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00093:Dnai3 APN 3 145,788,759 (GRCm39) missense probably benign
IGL00565:Dnai3 APN 3 145,750,674 (GRCm39) splice site 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
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 2015-04-16