Incidental Mutation 'IGL02174:Kif20b'
ID 283050
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Kif20b
Ensembl Gene ENSMUSG00000024795
Gene Name kinesin family member 20B
Synonyms C330014J10Rik, magoo, Kif20b, N-6 kinesin, Mphosph1, 33cex
Accession Numbers
Essential gene? Probably essential (E-score: 0.904) question?
Stock # IGL02174
Quality Score
Status
Chromosome 19
Chromosomal Location 34899761-34953145 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 34911858 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000153592 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087341] [ENSMUST00000223776] [ENSMUST00000223907] [ENSMUST00000225408]
AlphaFold Q80WE4
Predicted Effect probably benign
Transcript: ENSMUST00000087341
SMART Domains Protein: ENSMUSP00000084599
Gene: ENSMUSG00000024795

DomainStartEndE-ValueType
Blast:KISc 2 46 5e-15 BLAST
KISc 56 483 1.19e-103 SMART
low complexity region 521 551 N/A INTRINSIC
coiled coil region 565 602 N/A INTRINSIC
coiled coil region 705 746 N/A INTRINSIC
coiled coil region 823 947 N/A INTRINSIC
coiled coil region 1020 1325 N/A INTRINSIC
coiled coil region 1348 1510 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000223776
Predicted Effect probably benign
Transcript: ENSMUST00000223907
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224603
Predicted Effect probably benign
Transcript: ENSMUST00000224728
Predicted Effect probably benign
Transcript: ENSMUST00000225408
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for ENU induced mutations display craniofacial and nervous system abnormalities including exencephaly, microcephaly, decreased forebrain size and impaired neuronal progenitor proliferation. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc4 T C 14: 118,738,154 (GRCm39) I1199V probably damaging Het
Adgrv1 G A 13: 81,575,783 (GRCm39) T4861I probably benign Het
Ampd2 T C 3: 107,987,601 (GRCm39) D108G probably damaging Het
Azin1 A G 15: 38,493,730 (GRCm39) F298L probably benign Het
Bag1 T A 4: 40,941,555 (GRCm39) E123D possibly damaging Het
Cabs1 A G 5: 88,128,339 (GRCm39) E330G probably benign Het
Ccdc33 T C 9: 57,940,938 (GRCm39) K435E probably benign Het
Clip2 T G 5: 134,523,118 (GRCm39) K943T probably damaging Het
Cmya5 T C 13: 93,185,415 (GRCm39) I3527V possibly damaging Het
Cyp2w1 C T 5: 139,341,384 (GRCm39) R244C probably benign Het
Dcaf13 C A 15: 39,001,544 (GRCm39) A284E probably damaging Het
Ddx31 T A 2: 28,749,041 (GRCm39) L279Q probably damaging Het
Dgki A G 6: 37,009,856 (GRCm39) L497P probably damaging Het
Dnah12 A T 14: 26,428,072 (GRCm39) I233F probably benign Het
Dpp6 G T 5: 27,926,085 (GRCm39) G720* probably null Het
Emc1 T C 4: 139,098,979 (GRCm39) Y821H possibly damaging Het
Esr1 C T 10: 4,948,003 (GRCm39) R519W probably damaging Het
Gamt A T 10: 80,094,230 (GRCm39) V227E possibly damaging Het
Habp2 A G 19: 56,300,169 (GRCm39) Q206R probably damaging Het
Ihh A G 1: 74,990,105 (GRCm39) I90T probably damaging Het
Lcp2 T C 11: 34,000,966 (GRCm39) probably benign Het
Lyrm2 A G 4: 32,800,649 (GRCm39) I29V probably benign Het
Macf1 T C 4: 123,385,587 (GRCm39) D1168G probably damaging Het
Mocos T C 18: 24,828,953 (GRCm39) S753P probably benign Het
Myo3a A G 2: 22,337,204 (GRCm39) E367G probably benign Het
Ndor1 G A 2: 25,139,206 (GRCm39) A255V possibly damaging Het
Nfat5 C T 8: 108,065,683 (GRCm39) P148S probably damaging Het
Or4c121 A T 2: 89,023,712 (GRCm39) F222Y probably benign Het
Or5al7 T A 2: 85,992,442 (GRCm39) M284L possibly damaging Het
Or6z7 T C 7: 6,483,438 (GRCm39) Y239C probably benign Het
Or8b41 A T 9: 38,055,081 (GRCm39) T217S possibly damaging Het
Pappa2 C T 1: 158,589,188 (GRCm39) C1679Y probably damaging Het
Pcdhb2 T A 18: 37,429,551 (GRCm39) I508N probably damaging Het
Pkd2l1 G A 19: 44,145,707 (GRCm39) T172I probably benign Het
Pld5 A G 1: 176,102,310 (GRCm39) V44A possibly damaging Het
Prss44 T C 9: 110,646,199 (GRCm39) W309R probably damaging Het
Rc3h2 A T 2: 37,301,237 (GRCm39) N88K probably benign Het
Rspry1 A G 8: 95,359,768 (GRCm39) I102M possibly damaging Het
Stab2 A G 10: 86,695,606 (GRCm39) probably null Het
Tbx3 C A 5: 119,813,649 (GRCm39) Y228* probably null Het
Tcf15 G T 2: 151,986,065 (GRCm39) probably benign Het
Tmem41b A G 7: 109,578,003 (GRCm39) S94P possibly damaging Het
Trmt10b A T 4: 45,308,508 (GRCm39) I223F possibly damaging Het
Tyrp1 G T 4: 80,763,063 (GRCm39) G317* probably null Het
Urod T A 4: 116,847,479 (GRCm39) probably benign Het
Vwf G T 6: 125,532,358 (GRCm39) R52L probably damaging Het
Wnk2 C A 13: 49,210,643 (GRCm39) Q232H probably damaging Het
Zbtb10 C A 3: 9,316,872 (GRCm39) P228Q probably damaging Het
Zfp764l1 G A 7: 126,991,525 (GRCm39) T154I possibly damaging Het
Other mutations in Kif20b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00513:Kif20b APN 19 34,925,060 (GRCm39) missense possibly damaging 0.77
IGL01021:Kif20b APN 19 34,915,660 (GRCm39) missense possibly damaging 0.89
IGL01590:Kif20b APN 19 34,932,126 (GRCm39) missense possibly damaging 0.87
IGL01691:Kif20b APN 19 34,913,143 (GRCm39) splice site probably benign
IGL01730:Kif20b APN 19 34,927,923 (GRCm39) nonsense probably null
IGL02078:Kif20b APN 19 34,913,044 (GRCm39) missense probably damaging 1.00
IGL02536:Kif20b APN 19 34,951,959 (GRCm39) missense probably benign 0.42
IGL03029:Kif20b APN 19 34,928,313 (GRCm39) missense probably benign
IGL03186:Kif20b APN 19 34,912,344 (GRCm39) missense probably benign 0.45
IGL03205:Kif20b APN 19 34,936,863 (GRCm39) missense probably damaging 1.00
IGL03493:Kif20b APN 19 34,936,950 (GRCm39) nonsense probably null
R0319:Kif20b UTSW 19 34,925,132 (GRCm39) splice site probably benign
R1069:Kif20b UTSW 19 34,928,251 (GRCm39) missense probably damaging 1.00
R1137:Kif20b UTSW 19 34,914,486 (GRCm39) critical splice donor site probably null
R1255:Kif20b UTSW 19 34,927,506 (GRCm39) missense probably benign 0.08
R1352:Kif20b UTSW 19 34,902,035 (GRCm39) missense probably benign
R1466:Kif20b UTSW 19 34,927,999 (GRCm39) missense probably benign 0.00
R1466:Kif20b UTSW 19 34,927,999 (GRCm39) missense probably benign 0.00
R1473:Kif20b UTSW 19 34,951,896 (GRCm39) missense possibly damaging 0.93
R1545:Kif20b UTSW 19 34,906,318 (GRCm39) missense probably damaging 1.00
R1647:Kif20b UTSW 19 34,914,190 (GRCm39) missense possibly damaging 0.65
R1648:Kif20b UTSW 19 34,914,190 (GRCm39) missense possibly damaging 0.65
R1752:Kif20b UTSW 19 34,915,736 (GRCm39) missense probably benign 0.13
R1835:Kif20b UTSW 19 34,933,438 (GRCm39) missense probably damaging 1.00
R1889:Kif20b UTSW 19 34,918,608 (GRCm39) unclassified probably benign
R1937:Kif20b UTSW 19 34,930,278 (GRCm39) missense possibly damaging 0.73
R2112:Kif20b UTSW 19 34,909,132 (GRCm39) missense probably benign 0.04
R2315:Kif20b UTSW 19 34,908,999 (GRCm39) missense probably damaging 1.00
R2385:Kif20b UTSW 19 34,936,819 (GRCm39) missense probably damaging 0.98
R2867:Kif20b UTSW 19 34,917,528 (GRCm39) missense probably damaging 1.00
R2867:Kif20b UTSW 19 34,917,528 (GRCm39) missense probably damaging 1.00
R3086:Kif20b UTSW 19 34,907,115 (GRCm39) missense probably damaging 1.00
R3116:Kif20b UTSW 19 34,947,480 (GRCm39) missense probably benign 0.38
R3407:Kif20b UTSW 19 34,927,900 (GRCm39) missense probably damaging 1.00
R3834:Kif20b UTSW 19 34,912,428 (GRCm39) missense probably damaging 1.00
R3882:Kif20b UTSW 19 34,927,480 (GRCm39) missense probably damaging 1.00
R4698:Kif20b UTSW 19 34,928,944 (GRCm39) missense probably damaging 1.00
R4721:Kif20b UTSW 19 34,915,773 (GRCm39) missense probably benign 0.41
R4883:Kif20b UTSW 19 34,943,522 (GRCm39) missense probably benign 0.00
R4901:Kif20b UTSW 19 34,911,836 (GRCm39) missense probably benign 0.00
R4923:Kif20b UTSW 19 34,918,611 (GRCm39) critical splice acceptor site probably null
R5538:Kif20b UTSW 19 34,930,364 (GRCm39) nonsense probably null
R5540:Kif20b UTSW 19 34,915,860 (GRCm39) missense probably benign 0.01
R5558:Kif20b UTSW 19 34,928,949 (GRCm39) missense probably damaging 1.00
R5580:Kif20b UTSW 19 34,927,128 (GRCm39) splice site probably null
R5934:Kif20b UTSW 19 34,918,721 (GRCm39) missense probably benign 0.02
R6019:Kif20b UTSW 19 34,927,864 (GRCm39) missense probably benign 0.00
R6464:Kif20b UTSW 19 34,911,841 (GRCm39) missense probably benign
R6613:Kif20b UTSW 19 34,914,384 (GRCm39) nonsense probably null
R6745:Kif20b UTSW 19 34,906,276 (GRCm39) missense possibly damaging 0.94
R7097:Kif20b UTSW 19 34,951,892 (GRCm39) missense probably damaging 0.98
R7237:Kif20b UTSW 19 34,928,005 (GRCm39) missense probably damaging 1.00
R7260:Kif20b UTSW 19 34,927,610 (GRCm39) missense probably damaging 1.00
R7373:Kif20b UTSW 19 34,913,071 (GRCm39) missense probably damaging 1.00
R7418:Kif20b UTSW 19 34,907,087 (GRCm39) missense probably damaging 0.99
R7814:Kif20b UTSW 19 34,928,355 (GRCm39) missense possibly damaging 0.63
R7861:Kif20b UTSW 19 34,917,322 (GRCm39) missense probably damaging 1.00
R8017:Kif20b UTSW 19 34,917,279 (GRCm39) missense probably damaging 1.00
R8696:Kif20b UTSW 19 34,914,752 (GRCm39) missense probably benign 0.02
R8724:Kif20b UTSW 19 34,916,146 (GRCm39) unclassified probably benign
R8849:Kif20b UTSW 19 34,915,716 (GRCm39) nonsense probably null
R8947:Kif20b UTSW 19 34,918,629 (GRCm39) missense possibly damaging 0.46
R8998:Kif20b UTSW 19 34,914,253 (GRCm39) splice site probably benign
R9017:Kif20b UTSW 19 34,927,203 (GRCm39) missense probably benign 0.00
R9245:Kif20b UTSW 19 34,915,725 (GRCm39) missense probably benign 0.02
R9613:Kif20b UTSW 19 34,919,934 (GRCm39) missense possibly damaging 0.80
R9619:Kif20b UTSW 19 34,933,429 (GRCm39) missense probably damaging 1.00
R9732:Kif20b UTSW 19 34,930,353 (GRCm39) missense probably benign 0.18
R9746:Kif20b UTSW 19 34,928,149 (GRCm39) nonsense probably null
Z1088:Kif20b UTSW 19 34,927,851 (GRCm39) missense probably damaging 0.99
Z1176:Kif20b UTSW 19 34,930,275 (GRCm39) missense probably benign 0.11
Z1177:Kif20b UTSW 19 34,927,866 (GRCm39) nonsense probably null
Posted On 2015-04-16