Incidental Mutation 'R4612:Kif21a'
ID 344876
Institutional Source Beutler Lab
Gene Symbol Kif21a
Ensembl Gene ENSMUSG00000022629
Gene Name kinesin family member 21A
Synonyms N-5 kinesin
MMRRC Submission 041823-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R4612 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 90817479-90934151 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 90852426 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000155710 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067205] [ENSMUST00000088614] [ENSMUST00000100304] [ENSMUST00000109287] [ENSMUST00000109288] [ENSMUST00000229801]
AlphaFold Q9QXL2
Predicted Effect probably null
Transcript: ENSMUST00000067205
SMART Domains Protein: ENSMUSP00000066911
Gene: ENSMUSG00000022629

DomainStartEndE-ValueType
KISc 7 379 8.97e-163 SMART
Blast:KISc 469 513 9e-9 BLAST
low complexity region 514 525 N/A INTRINSIC
low complexity region 542 557 N/A INTRINSIC
low complexity region 571 585 N/A INTRINSIC
low complexity region 589 628 N/A INTRINSIC
low complexity region 700 713 N/A INTRINSIC
coiled coil region 924 1008 N/A INTRINSIC
coiled coil region 1043 1066 N/A INTRINSIC
low complexity region 1101 1112 N/A INTRINSIC
low complexity region 1222 1234 N/A INTRINSIC
low complexity region 1251 1271 N/A INTRINSIC
WD40 1290 1327 1.21e-7 SMART
WD40 1330 1368 7.28e-2 SMART
WD40 1394 1432 3.33e-1 SMART
WD40 1435 1477 7e-4 SMART
WD40 1485 1523 2.4e-1 SMART
WD40 1527 1566 1.48e-2 SMART
WD40 1569 1606 2.07e-6 SMART
Predicted Effect probably null
Transcript: ENSMUST00000088614
SMART Domains Protein: ENSMUSP00000085985
Gene: ENSMUSG00000022629

DomainStartEndE-ValueType
KISc 7 379 8.97e-163 SMART
Blast:KISc 469 513 1e-8 BLAST
low complexity region 514 525 N/A INTRINSIC
low complexity region 542 564 N/A INTRINSIC
low complexity region 584 598 N/A INTRINSIC
low complexity region 602 641 N/A INTRINSIC
low complexity region 713 726 N/A INTRINSIC
coiled coil region 937 1021 N/A INTRINSIC
coiled coil region 1056 1079 N/A INTRINSIC
low complexity region 1114 1125 N/A INTRINSIC
low complexity region 1271 1283 N/A INTRINSIC
low complexity region 1300 1316 N/A INTRINSIC
WD40 1334 1371 1.21e-7 SMART
WD40 1374 1412 7.28e-2 SMART
WD40 1438 1476 3.33e-1 SMART
WD40 1479 1521 7e-4 SMART
WD40 1529 1567 2.4e-1 SMART
WD40 1571 1610 1.48e-2 SMART
WD40 1613 1650 2.07e-6 SMART
Predicted Effect probably null
Transcript: ENSMUST00000100304
SMART Domains Protein: ENSMUSP00000097877
Gene: ENSMUSG00000022629

DomainStartEndE-ValueType
KISc 7 379 8.97e-163 SMART
Blast:KISc 469 513 1e-8 BLAST
low complexity region 514 525 N/A INTRINSIC
low complexity region 542 564 N/A INTRINSIC
low complexity region 584 598 N/A INTRINSIC
low complexity region 602 641 N/A INTRINSIC
low complexity region 713 726 N/A INTRINSIC
coiled coil region 937 1021 N/A INTRINSIC
coiled coil region 1056 1079 N/A INTRINSIC
low complexity region 1271 1283 N/A INTRINSIC
low complexity region 1300 1316 N/A INTRINSIC
WD40 1334 1371 1.21e-7 SMART
WD40 1374 1412 7.28e-2 SMART
WD40 1438 1476 3.33e-1 SMART
WD40 1479 1521 7e-4 SMART
WD40 1529 1567 2.4e-1 SMART
WD40 1571 1610 1.48e-2 SMART
WD40 1613 1650 2.07e-6 SMART
Predicted Effect probably null
Transcript: ENSMUST00000109287
SMART Domains Protein: ENSMUSP00000104910
Gene: ENSMUSG00000022629

DomainStartEndE-ValueType
KISc 7 379 8.97e-163 SMART
Blast:KISc 469 513 9e-9 BLAST
low complexity region 514 525 N/A INTRINSIC
low complexity region 542 557 N/A INTRINSIC
low complexity region 571 585 N/A INTRINSIC
low complexity region 589 628 N/A INTRINSIC
low complexity region 700 713 N/A INTRINSIC
coiled coil region 924 1008 N/A INTRINSIC
coiled coil region 1043 1066 N/A INTRINSIC
low complexity region 1101 1112 N/A INTRINSIC
WD40 1229 1266 1.21e-7 SMART
WD40 1269 1307 7.28e-2 SMART
WD40 1333 1371 3.33e-1 SMART
WD40 1374 1416 7e-4 SMART
WD40 1424 1462 2.4e-1 SMART
WD40 1466 1505 1.48e-2 SMART
WD40 1508 1545 2.07e-6 SMART
Predicted Effect probably null
Transcript: ENSMUST00000109288
SMART Domains Protein: ENSMUSP00000104911
Gene: ENSMUSG00000022629

DomainStartEndE-ValueType
KISc 7 379 8.97e-163 SMART
Blast:KISc 469 513 9e-9 BLAST
low complexity region 514 525 N/A INTRINSIC
low complexity region 542 557 N/A INTRINSIC
low complexity region 571 585 N/A INTRINSIC
low complexity region 589 628 N/A INTRINSIC
low complexity region 700 713 N/A INTRINSIC
coiled coil region 924 1008 N/A INTRINSIC
coiled coil region 1043 1066 N/A INTRINSIC
low complexity region 1205 1216 N/A INTRINSIC
WD40 1235 1272 1.21e-7 SMART
WD40 1275 1313 7.28e-2 SMART
WD40 1339 1377 3.33e-1 SMART
WD40 1380 1422 7e-4 SMART
WD40 1430 1468 2.4e-1 SMART
WD40 1472 1511 1.48e-2 SMART
WD40 1514 1551 2.07e-6 SMART
Predicted Effect probably null
Transcript: ENSMUST00000229801
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
Allele List at MGI
Other mutations in this stock
Total: 109 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700019D03Rik T C 1: 52,964,635 (GRCm39) D31G probably benign Het
5730455P16Rik A T 11: 80,268,806 (GRCm39) M1K probably null Het
Abca15 A G 7: 119,934,384 (GRCm39) D120G probably benign Het
Adam26a A T 8: 44,021,830 (GRCm39) N553K probably damaging Het
Adam32 A T 8: 25,362,752 (GRCm39) C558S probably damaging Het
Adam34l A T 8: 44,079,587 (GRCm39) F212L probably benign Het
Adam39 A T 8: 41,278,958 (GRCm39) S450C probably damaging Het
Agap2 A T 10: 126,915,965 (GRCm39) T159S unknown Het
Ahnak G A 19: 8,981,088 (GRCm39) V791I probably benign Het
Ak7 T G 12: 105,727,772 (GRCm39) L468R probably damaging Het
Akap12 A G 10: 4,304,456 (GRCm39) D422G probably damaging Het
Antxr1 T A 6: 87,265,155 (GRCm39) I129F probably damaging Het
Arhgap32 G A 9: 32,170,775 (GRCm39) G1185D probably damaging Het
Atf7ip2 A T 16: 10,059,427 (GRCm39) E322D probably benign Het
Atg4b T C 1: 93,714,263 (GRCm39) F349L probably damaging Het
Atp6v1c1 A G 15: 38,677,856 (GRCm39) K127R probably damaging Het
Atxn1l C T 8: 110,458,736 (GRCm39) V509M possibly damaging Het
B3glct T A 5: 149,663,022 (GRCm39) I260N probably damaging Het
Bcl2l12 G A 7: 44,646,009 (GRCm39) P70L probably damaging Het
Bok T A 1: 93,621,900 (GRCm39) F157L probably damaging Het
Bves G A 10: 45,215,373 (GRCm39) G16D probably benign Het
Cacna1b T A 2: 24,516,864 (GRCm39) K65* probably null Het
Casc3 A G 11: 98,713,784 (GRCm39) T339A probably benign Het
Ccdc18 C T 5: 108,283,307 (GRCm39) S6L probably benign Het
Cd86 A G 16: 36,435,692 (GRCm39) Y242H probably benign Het
Chd3 A C 11: 69,244,035 (GRCm39) Y1249* probably null Het
Chrne T C 11: 70,507,848 (GRCm39) T284A probably damaging Het
Col12a1 T C 9: 79,523,339 (GRCm39) D2746G probably damaging Het
Cryaa T A 17: 31,897,448 (GRCm39) M72K probably benign Het
Csmd1 G T 8: 15,971,908 (GRCm39) probably null Het
Det1 A T 7: 78,493,454 (GRCm39) N183K probably damaging Het
Dis3 C A 14: 99,328,871 (GRCm39) V294L probably benign Het
Dnah2 G A 11: 69,374,193 (GRCm39) L1493F possibly damaging Het
Dsc2 A T 18: 20,174,876 (GRCm39) D466E probably damaging Het
Dsg4 T A 18: 20,595,470 (GRCm39) S558T probably benign Het
Dzip3 A T 16: 48,772,403 (GRCm39) L422* probably null Het
Elp6 T C 9: 110,143,087 (GRCm39) F100S probably damaging Het
Epg5 C T 18: 78,025,629 (GRCm39) T1224I possibly damaging Het
Exoc1l A T 5: 76,664,345 (GRCm39) N145Y probably damaging Het
F830016B08Rik T A 18: 60,434,087 (GRCm39) I390N probably benign Het
Fam110c A G 12: 31,124,655 (GRCm39) T206A unknown Het
Fam187b G A 7: 30,676,518 (GRCm39) G9D possibly damaging Het
Fat1 A G 8: 45,478,184 (GRCm39) D2410G probably damaging Het
Fbln1 T A 15: 85,122,760 (GRCm39) F390Y probably benign Het
Fgg A G 3: 82,917,397 (GRCm39) N142S probably damaging Het
Fhip1a G A 3: 85,637,679 (GRCm39) R207* probably null Het
Flcn T C 11: 59,683,513 (GRCm39) T555A probably damaging Het
Foxq1 G T 13: 31,742,808 (GRCm39) probably benign Het
Gm3233 A T 10: 77,595,498 (GRCm39) probably benign Het
Gprc5a G A 6: 135,055,927 (GRCm39) V125I probably damaging Het
Gria2 T C 3: 80,639,358 (GRCm39) D218G probably damaging Het
Gtf3c5 C T 2: 28,469,596 (GRCm39) A103T probably benign Het
Hspg2 C T 4: 137,246,251 (GRCm39) R1010C probably damaging Het
Hspg2 A G 4: 137,266,886 (GRCm39) T1964A possibly damaging Het
Htatip2 G T 7: 49,422,345 (GRCm39) E188* probably null Het
Ifna13 T G 4: 88,562,113 (GRCm39) E170D probably damaging Het
Il4ra A G 7: 125,175,255 (GRCm39) T488A probably benign Het
Jup G T 11: 100,272,660 (GRCm39) H251N probably damaging Het
Klhl28 T A 12: 65,004,034 (GRCm39) I160L probably damaging Het
Klk1b5 A T 7: 43,494,696 (GRCm39) T60S possibly damaging Het
Kntc1 A G 5: 123,950,706 (GRCm39) R1995G probably damaging Het
Lrig2 A C 3: 104,370,099 (GRCm39) I844M probably damaging Het
Lrp2 C T 2: 69,288,771 (GRCm39) W3698* probably null Het
Lyar T A 5: 38,382,053 (GRCm39) S12T possibly damaging Het
Map3k19 T C 1: 127,743,037 (GRCm39) K1507E probably benign Het
Mre11a G A 9: 14,714,199 (GRCm39) G267R probably damaging Het
Mthfd1l A G 10: 3,980,717 (GRCm39) Q473R probably damaging Het
Ncald T A 15: 37,397,593 (GRCm39) E29V probably benign Het
Neb T C 2: 52,177,255 (GRCm39) D1362G probably damaging Het
Nme2 T C 11: 93,846,428 (GRCm39) T7A possibly damaging Het
Nod2 T A 8: 89,391,664 (GRCm39) L657Q possibly damaging Het
Nrm T A 17: 36,174,421 (GRCm39) V75E probably benign Het
Ogfod1 A C 8: 94,763,975 (GRCm39) K20T possibly damaging Het
Omp T C 7: 97,794,348 (GRCm39) N93S probably damaging Het
Or10h28 T A 17: 33,488,454 (GRCm39) V252E probably benign Het
Or14a256 T A 7: 86,264,944 (GRCm39) Q303L probably benign Het
Or5h27 T C 16: 59,006,674 (GRCm39) I57M probably damaging Het
Pcdhb15 A C 18: 37,608,648 (GRCm39) T627P probably damaging Het
Pld1 A G 3: 28,185,882 (GRCm39) T1036A possibly damaging Het
Pogk C A 1: 166,226,334 (GRCm39) E606* probably null Het
Ppp1r10 T A 17: 36,238,823 (GRCm39) L292Q probably damaging Het
Prpf6 T C 2: 181,273,872 (GRCm39) C339R possibly damaging Het
Psd T A 19: 46,301,778 (GRCm39) D937V probably benign Het
Rbak T C 5: 143,160,222 (GRCm39) Q277R probably benign Het
Sbno1 T A 5: 124,542,087 (GRCm39) Y355F probably damaging Het
Sec23ip C T 7: 128,352,226 (GRCm39) Q201* probably null Het
Serpinb3a T C 1: 106,975,337 (GRCm39) K157E probably damaging Het
Slc22a28 A T 19: 8,078,770 (GRCm39) N306K probably damaging Het
Smarca2 C A 19: 26,753,625 (GRCm39) D1584E possibly damaging Het
Snx29 C A 16: 11,265,359 (GRCm39) Q530K probably damaging Het
Stard10 C A 7: 100,994,877 (GRCm39) Q278K possibly damaging Het
Tgm2 C T 2: 157,966,124 (GRCm39) C510Y probably benign Het
Tlr9 C T 9: 106,101,006 (GRCm39) P99L probably damaging Het
Tmco4 T C 4: 138,717,871 (GRCm39) W4R probably benign Het
Tmem151a T A 19: 5,121,862 (GRCm39) probably benign Het
Tmem255b T C 8: 13,504,228 (GRCm39) V140A probably benign Het
Trbj1-2 C T 6: 41,510,950 (GRCm39) probably benign Het
Trpm2 T C 10: 77,781,750 (GRCm39) T290A probably damaging Het
Tsc22d1 G A 14: 76,656,445 (GRCm39) E120K possibly damaging Het
Ttc29 A G 8: 79,052,175 (GRCm39) D352G probably benign Het
Usp25 A T 16: 76,830,833 (GRCm39) I30F possibly damaging Het
Usp34 A C 11: 23,382,268 (GRCm39) N1993T probably damaging Het
Vmn2r124 A C 17: 18,283,284 (GRCm39) H326P probably benign Het
Vmn2r92 C A 17: 18,387,132 (GRCm39) T157K probably benign Het
Vstm5 A T 9: 15,168,789 (GRCm39) I118F probably benign Het
Vwa7 T C 17: 35,242,426 (GRCm39) V510A probably damaging Het
Zfhx4 G A 3: 5,462,123 (GRCm39) S1266N probably damaging Het
Zfp763 T A 17: 33,237,922 (GRCm39) N408Y probably benign Het
Zswim5 C T 4: 116,843,901 (GRCm39) H980Y probably damaging Het
Other mutations in Kif21a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00539:Kif21a APN 15 90,821,504 (GRCm39) missense probably damaging 1.00
IGL01476:Kif21a APN 15 90,828,067 (GRCm39) missense possibly damaging 0.66
IGL01617:Kif21a APN 15 90,879,840 (GRCm39) splice site probably benign
IGL01736:Kif21a APN 15 90,843,948 (GRCm39) missense possibly damaging 0.59
IGL01923:Kif21a APN 15 90,840,633 (GRCm39) missense probably damaging 0.96
IGL01985:Kif21a APN 15 90,875,970 (GRCm39) missense probably damaging 1.00
IGL02304:Kif21a APN 15 90,849,738 (GRCm39) missense probably damaging 1.00
IGL02589:Kif21a APN 15 90,869,489 (GRCm39) missense probably damaging 1.00
IGL03115:Kif21a APN 15 90,869,598 (GRCm39) missense probably damaging 0.99
IGL03211:Kif21a APN 15 90,882,166 (GRCm39) missense possibly damaging 0.73
IGL03372:Kif21a APN 15 90,840,579 (GRCm39) missense probably benign 0.38
reflex UTSW 15 90,852,561 (GRCm39) missense probably null 1.00
R0052:Kif21a UTSW 15 90,855,060 (GRCm39) missense probably damaging 0.98
R0052:Kif21a UTSW 15 90,855,060 (GRCm39) missense probably damaging 0.98
R0304:Kif21a UTSW 15 90,860,724 (GRCm39) splice site probably null
R0378:Kif21a UTSW 15 90,853,977 (GRCm39) splice site probably null
R0420:Kif21a UTSW 15 90,852,257 (GRCm39) unclassified probably benign
R0536:Kif21a UTSW 15 90,843,886 (GRCm39) splice site probably benign
R0826:Kif21a UTSW 15 90,881,744 (GRCm39) critical splice donor site probably null
R0971:Kif21a UTSW 15 90,824,784 (GRCm39) missense possibly damaging 0.46
R1052:Kif21a UTSW 15 90,819,853 (GRCm39) missense probably benign 0.17
R1168:Kif21a UTSW 15 90,877,956 (GRCm39) missense probably damaging 1.00
R1324:Kif21a UTSW 15 90,832,525 (GRCm39) critical splice donor site probably null
R1471:Kif21a UTSW 15 90,840,622 (GRCm39) missense probably benign 0.04
R1625:Kif21a UTSW 15 90,826,378 (GRCm39) missense probably damaging 1.00
R1636:Kif21a UTSW 15 90,869,008 (GRCm39) splice site probably benign
R1647:Kif21a UTSW 15 90,878,570 (GRCm39) missense probably damaging 1.00
R1648:Kif21a UTSW 15 90,878,570 (GRCm39) missense probably damaging 1.00
R1699:Kif21a UTSW 15 90,843,946 (GRCm39) missense probably damaging 0.99
R1703:Kif21a UTSW 15 90,833,250 (GRCm39) splice site probably null
R1795:Kif21a UTSW 15 90,856,930 (GRCm39) splice site probably null
R1812:Kif21a UTSW 15 90,855,969 (GRCm39) missense possibly damaging 0.63
R1959:Kif21a UTSW 15 90,855,051 (GRCm39) missense probably damaging 0.99
R1960:Kif21a UTSW 15 90,855,051 (GRCm39) missense probably damaging 0.99
R1961:Kif21a UTSW 15 90,855,051 (GRCm39) missense probably damaging 0.99
R1996:Kif21a UTSW 15 90,878,574 (GRCm39) nonsense probably null
R2230:Kif21a UTSW 15 90,869,565 (GRCm39) nonsense probably null
R2231:Kif21a UTSW 15 90,869,565 (GRCm39) nonsense probably null
R2232:Kif21a UTSW 15 90,869,565 (GRCm39) nonsense probably null
R2424:Kif21a UTSW 15 90,855,399 (GRCm39) missense probably damaging 1.00
R2429:Kif21a UTSW 15 90,882,208 (GRCm39) missense probably damaging 1.00
R2513:Kif21a UTSW 15 90,878,594 (GRCm39) missense possibly damaging 0.96
R2846:Kif21a UTSW 15 90,818,667 (GRCm39) missense probably benign
R3027:Kif21a UTSW 15 90,856,845 (GRCm39) missense probably damaging 0.99
R3624:Kif21a UTSW 15 90,849,798 (GRCm39) missense probably damaging 0.99
R3820:Kif21a UTSW 15 90,852,277 (GRCm39) missense probably benign 0.17
R3923:Kif21a UTSW 15 90,821,497 (GRCm39) missense possibly damaging 0.46
R3962:Kif21a UTSW 15 90,869,612 (GRCm39) missense probably damaging 1.00
R4355:Kif21a UTSW 15 90,855,036 (GRCm39) missense probably benign 0.17
R4516:Kif21a UTSW 15 90,855,345 (GRCm39) missense probably benign 0.38
R4530:Kif21a UTSW 15 90,852,292 (GRCm39) splice site probably null
R4674:Kif21a UTSW 15 90,824,748 (GRCm39) missense possibly damaging 0.66
R4675:Kif21a UTSW 15 90,824,748 (GRCm39) missense possibly damaging 0.66
R4698:Kif21a UTSW 15 90,840,508 (GRCm39) missense possibly damaging 0.85
R4712:Kif21a UTSW 15 90,868,958 (GRCm39) missense probably damaging 1.00
R4955:Kif21a UTSW 15 90,821,393 (GRCm39) missense probably damaging 1.00
R4974:Kif21a UTSW 15 90,833,213 (GRCm39) missense probably benign 0.16
R5034:Kif21a UTSW 15 90,852,561 (GRCm39) missense probably null 1.00
R5165:Kif21a UTSW 15 90,840,579 (GRCm39) missense probably benign 0.38
R5464:Kif21a UTSW 15 90,878,058 (GRCm39) missense probably damaging 1.00
R5541:Kif21a UTSW 15 90,852,316 (GRCm39) missense probably damaging 0.99
R5757:Kif21a UTSW 15 90,835,548 (GRCm39) missense probably damaging 1.00
R5936:Kif21a UTSW 15 90,819,850 (GRCm39) missense possibly damaging 0.95
R5976:Kif21a UTSW 15 90,820,015 (GRCm39) missense probably damaging 1.00
R6074:Kif21a UTSW 15 90,865,095 (GRCm39) missense probably benign
R6638:Kif21a UTSW 15 90,850,610 (GRCm39) missense probably damaging 1.00
R6723:Kif21a UTSW 15 90,824,649 (GRCm39) missense probably damaging 0.97
R6785:Kif21a UTSW 15 90,819,933 (GRCm39) missense probably damaging 1.00
R6977:Kif21a UTSW 15 90,865,040 (GRCm39) missense probably damaging 1.00
R7058:Kif21a UTSW 15 90,833,106 (GRCm39) splice site probably null
R7147:Kif21a UTSW 15 90,865,086 (GRCm39) missense probably benign 0.13
R7290:Kif21a UTSW 15 90,851,432 (GRCm39) nonsense probably null
R7438:Kif21a UTSW 15 90,877,999 (GRCm39) missense probably benign 0.37
R7593:Kif21a UTSW 15 90,828,064 (GRCm39) missense probably benign 0.03
R7661:Kif21a UTSW 15 90,865,122 (GRCm39) missense possibly damaging 0.89
R7891:Kif21a UTSW 15 90,840,517 (GRCm39) missense probably damaging 1.00
R8137:Kif21a UTSW 15 90,852,645 (GRCm39) missense probably benign
R8182:Kif21a UTSW 15 90,819,964 (GRCm39) missense possibly damaging 0.77
R8303:Kif21a UTSW 15 90,855,399 (GRCm39) missense probably damaging 0.99
R8388:Kif21a UTSW 15 90,843,327 (GRCm39) missense possibly damaging 0.60
R8867:Kif21a UTSW 15 90,852,382 (GRCm39) missense probably damaging 0.96
R8921:Kif21a UTSW 15 90,855,930 (GRCm39) missense probably benign 0.04
R8984:Kif21a UTSW 15 90,840,559 (GRCm39) missense probably benign 0.00
R9024:Kif21a UTSW 15 90,821,399 (GRCm39) nonsense probably null
R9254:Kif21a UTSW 15 90,854,030 (GRCm39) missense probably damaging 0.99
R9366:Kif21a UTSW 15 90,843,951 (GRCm39) missense probably damaging 0.99
R9379:Kif21a UTSW 15 90,854,030 (GRCm39) missense probably damaging 0.99
R9393:Kif21a UTSW 15 90,853,981 (GRCm39) missense probably benign 0.00
R9518:Kif21a UTSW 15 90,840,676 (GRCm39) missense probably damaging 1.00
R9712:Kif21a UTSW 15 90,879,715 (GRCm39) missense probably benign 0.13
R9712:Kif21a UTSW 15 90,869,528 (GRCm39) missense probably damaging 0.98
R9721:Kif21a UTSW 15 90,855,330 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- TGTCAGCTAAGGAGGCATTTAGC -3'
(R):5'- GCAGAAAATGAGGATCCCCG -3'

Sequencing Primer
(F):5'- GCATTTAGCTTCAGGGGTCCC -3'
(R):5'- GTGGCAAGAGTCCAGGCATTAC -3'
Posted On 2015-09-25