Incidental Mutation 'R1264:Kif13b'
ID 151124
Institutional Source Beutler Lab
Gene Symbol Kif13b
Ensembl Gene ENSMUSG00000060012
Gene Name kinesin family member 13B
Synonyms C130021D12Rik, 5330429L19Rik, N-3 kinesin, GAKIN
MMRRC Submission 039331-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1264 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 64889633-65047067 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 65013681 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000153168 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100473] [ENSMUST00000224503]
AlphaFold A0A286YCV9
Predicted Effect probably benign
Transcript: ENSMUST00000100473
SMART Domains Protein: ENSMUSP00000098041
Gene: ENSMUSG00000060012

DomainStartEndE-ValueType
KISc 3 361 1.4e-182 SMART
FHA 470 520 6.86e-1 SMART
low complexity region 546 560 N/A INTRINSIC
coiled coil region 617 646 N/A INTRINSIC
coiled coil region 669 701 N/A INTRINSIC
Pfam:KIF1B 756 802 4.1e-20 PFAM
Pfam:DUF3694 1003 1279 1.4e-37 PFAM
low complexity region 1514 1526 N/A INTRINSIC
low complexity region 1532 1548 N/A INTRINSIC
low complexity region 1574 1589 N/A INTRINSIC
low complexity region 1617 1630 N/A INTRINSIC
CAP_GLY 1719 1784 1.54e-29 SMART
low complexity region 1814 1826 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000224503
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.1%
Validation Efficiency 100% (35/35)
MGI Phenotype PHENOTYPE: Mice homozygous for a null allele exhibit increased circulating cholesterol and factor VIII levels. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc9 T C 6: 142,592,103 (GRCm39) probably benign Het
Acadl A T 1: 66,896,712 (GRCm39) C27S probably benign Het
Adgrb3 C T 1: 25,598,931 (GRCm39) G258E probably damaging Het
Akna T C 4: 63,299,962 (GRCm39) probably null Het
Angpt2 T C 8: 18,791,233 (GRCm39) N21S probably benign Het
Ano6 A G 15: 95,847,447 (GRCm39) Y585C probably damaging Het
Ascc3 A T 10: 50,518,615 (GRCm39) probably benign Het
Clec10a T A 11: 70,060,567 (GRCm39) S103T possibly damaging Het
Clstn2 T C 9: 97,339,662 (GRCm39) R770G probably benign Het
Cndp2 C A 18: 84,696,916 (GRCm39) C95F possibly damaging Het
Col12a1 A G 9: 79,527,371 (GRCm39) V2653A probably benign Het
Col4a3 A T 1: 82,621,022 (GRCm39) probably benign Het
Daam1 A G 12: 72,022,085 (GRCm39) probably benign Het
H2-M9 A G 17: 36,953,484 (GRCm39) V18A probably benign Het
Heatr1 T A 13: 12,439,491 (GRCm39) probably benign Het
Impg1 T C 9: 80,221,675 (GRCm39) D715G probably benign Het
Incenp T C 19: 9,861,379 (GRCm39) K425E unknown Het
Msh2 T A 17: 88,014,607 (GRCm39) probably null Het
Myh2 A G 11: 67,071,604 (GRCm39) N474D probably damaging Het
Myo18b T C 5: 112,978,185 (GRCm39) T1246A probably benign Het
Nob1 T C 8: 108,148,136 (GRCm39) H102R probably damaging Het
Or4z4 G T 19: 12,076,198 (GRCm39) D268E probably benign Het
Pard3b A T 1: 62,203,316 (GRCm39) I415F probably damaging Het
Pfkl T G 10: 77,829,250 (GRCm39) K386T possibly damaging Het
Plekhs1 T C 19: 56,474,195 (GRCm39) V447A probably benign Het
Poli C T 18: 70,650,574 (GRCm39) V266I probably benign Het
Rapgef4 A T 2: 71,861,449 (GRCm39) K46N possibly damaging Het
Shisa6 T C 11: 66,265,975 (GRCm39) probably benign Het
Six3 T A 17: 85,929,285 (GRCm39) D206E probably damaging Het
Slc12a1 A T 2: 125,060,158 (GRCm39) E944D possibly damaging Het
Sptb A G 12: 76,659,381 (GRCm39) F1173S probably damaging Het
Tfdp1 C A 8: 13,423,837 (GRCm39) probably benign Het
Trrap A G 5: 144,726,409 (GRCm39) probably benign Het
Wbp11 A G 6: 136,791,513 (GRCm39) probably benign Het
Other mutations in Kif13b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Kif13b APN 14 64,907,142 (GRCm39) missense possibly damaging 0.81
IGL00485:Kif13b APN 14 65,002,522 (GRCm39) missense possibly damaging 0.88
IGL00495:Kif13b APN 14 64,951,562 (GRCm39) missense probably benign 0.07
IGL00556:Kif13b APN 14 64,982,337 (GRCm39) missense probably damaging 1.00
IGL00571:Kif13b APN 14 64,983,866 (GRCm39) missense probably damaging 0.99
IGL00590:Kif13b APN 14 65,016,911 (GRCm39) missense probably damaging 1.00
IGL01650:Kif13b APN 14 65,002,594 (GRCm39) missense probably benign 0.00
IGL01730:Kif13b APN 14 64,987,810 (GRCm39) critical splice donor site probably null
IGL01908:Kif13b APN 14 64,995,007 (GRCm39) missense probably damaging 1.00
IGL02388:Kif13b APN 14 65,037,807 (GRCm39) missense probably damaging 1.00
IGL02573:Kif13b APN 14 65,040,880 (GRCm39) missense probably damaging 1.00
IGL02661:Kif13b APN 14 65,005,140 (GRCm39) missense probably benign 0.06
IGL02794:Kif13b APN 14 65,040,889 (GRCm39) missense probably benign 0.00
IGL02959:Kif13b APN 14 65,005,166 (GRCm39) missense probably damaging 1.00
IGL02979:Kif13b APN 14 65,027,146 (GRCm39) missense probably damaging 0.96
IGL03114:Kif13b APN 14 65,025,897 (GRCm39) missense probably benign 0.00
R0024:Kif13b UTSW 14 64,987,722 (GRCm39) missense probably benign 0.30
R0330:Kif13b UTSW 14 65,040,669 (GRCm39) missense probably benign
R0376:Kif13b UTSW 14 64,994,853 (GRCm39) splice site probably benign
R0571:Kif13b UTSW 14 64,988,977 (GRCm39) missense probably damaging 1.00
R0718:Kif13b UTSW 14 64,989,111 (GRCm39) splice site probably benign
R1144:Kif13b UTSW 14 64,951,566 (GRCm39) missense probably benign 0.01
R1183:Kif13b UTSW 14 65,019,826 (GRCm39) missense probably benign 0.00
R1497:Kif13b UTSW 14 64,973,715 (GRCm39) missense probably damaging 0.99
R1579:Kif13b UTSW 14 65,019,790 (GRCm39) critical splice acceptor site probably null
R1624:Kif13b UTSW 14 64,976,068 (GRCm39) missense probably damaging 0.99
R1706:Kif13b UTSW 14 64,998,115 (GRCm39) splice site probably benign
R2176:Kif13b UTSW 14 64,907,120 (GRCm39) missense probably benign 0.01
R3727:Kif13b UTSW 14 65,003,197 (GRCm39) splice site probably benign
R3785:Kif13b UTSW 14 65,037,849 (GRCm39) missense probably benign 0.00
R3786:Kif13b UTSW 14 65,037,849 (GRCm39) missense probably benign 0.00
R4088:Kif13b UTSW 14 65,004,904 (GRCm39) critical splice donor site probably null
R4279:Kif13b UTSW 14 65,016,805 (GRCm39) missense probably damaging 1.00
R4559:Kif13b UTSW 14 65,043,581 (GRCm39) missense probably damaging 0.98
R4689:Kif13b UTSW 14 65,010,513 (GRCm39) missense probably damaging 1.00
R4692:Kif13b UTSW 14 65,041,024 (GRCm39) missense probably benign 0.05
R4878:Kif13b UTSW 14 65,043,603 (GRCm39) missense probably benign 0.00
R4971:Kif13b UTSW 14 64,995,011 (GRCm39) missense possibly damaging 0.90
R5037:Kif13b UTSW 14 64,996,038 (GRCm39) nonsense probably null
R5119:Kif13b UTSW 14 64,994,902 (GRCm39) missense probably benign 0.01
R5167:Kif13b UTSW 14 65,010,384 (GRCm39) missense probably damaging 1.00
R5408:Kif13b UTSW 14 65,017,138 (GRCm39) critical splice acceptor site probably null
R5437:Kif13b UTSW 14 65,043,563 (GRCm39) missense probably damaging 0.99
R5756:Kif13b UTSW 14 64,973,754 (GRCm39) missense probably damaging 1.00
R5838:Kif13b UTSW 14 64,975,004 (GRCm39) missense probably damaging 1.00
R5891:Kif13b UTSW 14 65,025,854 (GRCm39) splice site probably null
R6120:Kif13b UTSW 14 64,989,007 (GRCm39) missense probably damaging 1.00
R6150:Kif13b UTSW 14 64,989,088 (GRCm39) missense probably damaging 0.99
R6165:Kif13b UTSW 14 64,979,760 (GRCm39) missense probably damaging 1.00
R6187:Kif13b UTSW 14 64,973,664 (GRCm39) missense probably damaging 1.00
R6229:Kif13b UTSW 14 64,976,016 (GRCm39) missense probably damaging 1.00
R6267:Kif13b UTSW 14 64,976,083 (GRCm39) missense probably damaging 1.00
R6347:Kif13b UTSW 14 65,005,068 (GRCm39) missense probably benign 0.26
R6479:Kif13b UTSW 14 64,988,974 (GRCm39) missense probably benign 0.08
R6512:Kif13b UTSW 14 64,982,323 (GRCm39) critical splice acceptor site probably null
R6851:Kif13b UTSW 14 65,010,514 (GRCm39) missense probably damaging 1.00
R7131:Kif13b UTSW 14 65,010,517 (GRCm39) missense probably damaging 1.00
R7217:Kif13b UTSW 14 65,010,517 (GRCm39) missense probably damaging 1.00
R7398:Kif13b UTSW 14 64,994,972 (GRCm39) missense probably null 0.02
R7427:Kif13b UTSW 14 65,025,909 (GRCm39) missense probably benign
R7428:Kif13b UTSW 14 65,025,909 (GRCm39) missense probably benign
R7573:Kif13b UTSW 14 65,041,107 (GRCm39) missense probably benign 0.00
R7629:Kif13b UTSW 14 65,016,784 (GRCm39) nonsense probably null
R7683:Kif13b UTSW 14 64,994,956 (GRCm39) missense probably benign 0.24
R7835:Kif13b UTSW 14 65,004,901 (GRCm39) missense probably benign 0.00
R7895:Kif13b UTSW 14 64,973,598 (GRCm39) missense probably damaging 1.00
R8285:Kif13b UTSW 14 65,019,825 (GRCm39) missense probably benign 0.03
R8374:Kif13b UTSW 14 65,025,884 (GRCm39) missense probably damaging 0.97
R8467:Kif13b UTSW 14 64,996,154 (GRCm39) missense probably damaging 0.96
R8804:Kif13b UTSW 14 64,987,791 (GRCm39) missense probably damaging 0.99
R8859:Kif13b UTSW 14 64,979,882 (GRCm39) missense probably benign 0.04
R8891:Kif13b UTSW 14 64,982,326 (GRCm39) missense probably damaging 1.00
R9236:Kif13b UTSW 14 64,982,383 (GRCm39) missense probably benign 0.22
R9446:Kif13b UTSW 14 64,984,470 (GRCm39) missense probably damaging 1.00
R9589:Kif13b UTSW 14 65,013,759 (GRCm39) missense possibly damaging 0.82
Z1176:Kif13b UTSW 14 65,040,793 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- AAGCGTCACCAGTCCTTGCTTCCA -3'
(R):5'- AGCATCCCCAGCCCGTTTCATTGA -3'

Sequencing Primer
(F):5'- GGCACATTATAGGTCCCAGTC -3'
(R):5'- CAGCCCGTTTCATTGACTATG -3'
Posted On 2014-01-29