Mutagenetix > Incidental Mutation

Incidental Mutation 'R9031:Kif15'

713535

Institutional Source

Beutler Lab

Gene Symbol

Kif15

Ensembl Gene

ENSMUSG00000036768

Gene Name

kinesin family member 15

Synonyms

N-10 kinesin, 3930402I10Rik, 3110023M17Rik, HKLP2, Knsl7

MMRRC Submission

068860-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9031 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

122780146-122847798 bp(+) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

A to T at 122846492 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000149776 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040717] [ENSMUST00000084733] [ENSMUST00000213514] [ENSMUST00000214785] [ENSMUST00000216048] [ENSMUST00000216062]

AlphaFold

Q6P9L6

Predicted Effect

probably benign
Transcript: ENSMUST00000040717

SMART Domains

Protein: ENSMUSP00000035490
Gene: ENSMUSG00000036768

Domain	Start	End	E-Value	Type
KISc	24	371	2.86e-179	SMART
Pfam:Kinesin-relat_1	463	551	6.6e-26	PFAM
coiled coil region	579	643	N/A	INTRINSIC
coiled coil region	706	1037	N/A	INTRINSIC
coiled coil region	1065	1133	N/A	INTRINSIC
Pfam:HMMR_C	1265	1387	3.5e-12	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000084733

SMART Domains

Protein: ENSMUSP00000081784
Gene: ENSMUSG00000066233

Domain	Start	End	E-Value	Type
transmembrane domain	37	59	N/A	INTRINSIC
transmembrane domain	66	88	N/A	INTRINSIC
transmembrane domain	98	120	N/A	INTRINSIC
transmembrane domain	127	144	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000213514

Predicted Effect

probably benign
Transcript: ENSMUST00000214785

Predicted Effect

probably benign
Transcript: ENSMUST00000216048

Predicted Effect

probably benign
Transcript: ENSMUST00000216062

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.2%

Validation Efficiency

100% (81/81)

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc2	G	A	19: 43,810,466 (GRCm39)	R921H	probably benign	Het
Adcy5	A	G	16: 35,119,859 (GRCm39)	I1123V	probably damaging	Het
Agr2	G	C	12: 36,045,565 (GRCm39)	G17A	probably benign	Het
Akap6	A	T	12: 53,188,831 (GRCm39)	T2082S	probably benign	Het
Asxl3	G	T	18: 22,657,401 (GRCm39)	V1804F	probably damaging	Het
Atat1	A	G	17: 36,220,381 (GRCm39)	V37A	probably benign	Het
Atp1a3	A	T	7: 24,689,212 (GRCm39)		probably null	Het
Bpifb1	A	G	2: 154,051,848 (GRCm39)	T218A	probably benign	Het
C030006K11Rik	T	A	15: 76,607,961 (GRCm39)	Q19L	probably benign	Het
Ccdc138	T	C	10: 58,380,893 (GRCm39)	F508S	probably damaging	Het
Ccdc81	T	A	7: 89,542,358 (GRCm39)	M173L	probably benign	Het
Cdhr1	T	C	14: 36,815,976 (GRCm39)	I141V	probably benign	Het
Chia1	T	C	3: 106,035,777 (GRCm39)	F206L	probably benign	Het
Clca3a2	C	T	3: 144,511,475 (GRCm39)	G640E	probably damaging	Het
Clcn7	T	C	17: 25,376,497 (GRCm39)	V609A	probably damaging	Het
Cmklr2	T	C	1: 63,223,145 (GRCm39)	E30G	probably benign	Het
Col22a1	C	A	15: 71,753,523 (GRCm39)	G126*	probably null	Het
Cpne7	C	T	8: 123,856,951 (GRCm39)	P402L	probably damaging	Het
Ctcfl	A	T	2: 172,959,044 (GRCm39)	D227E	probably benign	Het
Cwf19l2	A	G	9: 3,417,942 (GRCm39)	D134G	probably benign	Het
Cyp2c65	C	A	19: 39,061,663 (GRCm39)	C216*	probably null	Het
Cyp2d12	T	A	15: 82,443,423 (GRCm39)	C462S	probably null	Het
Cyp4a12a	A	C	4: 115,189,199 (GRCm39)	*509Y	probably null	Het
Cyp4a12b	A	G	4: 115,290,865 (GRCm39)	M298V	probably benign	Het
Dennd4b	T	C	3: 90,178,188 (GRCm39)	V471A	probably benign	Het
Dlc1	A	G	8: 37,405,055 (GRCm39)	S245P	possibly damaging	Het
Dnah1	C	T	14: 31,001,128 (GRCm39)	G2406S	probably benign	Het
Dnah8	A	G	17: 30,956,401 (GRCm39)	K2127R	probably damaging	Het
Dusp13b	G	A	14: 21,790,233 (GRCm39)	R38C	probably benign	Het
Ebf2	T	A	14: 67,472,594 (GRCm39)	I4N	probably benign	Het
Eef1ece2	C	T	16: 20,459,375 (GRCm39)	P570L	probably damaging	Het
Fcgbp	A	G	7: 27,790,908 (GRCm39)	N723S	possibly damaging	Het
Galnt15	T	A	14: 31,770,027 (GRCm39)	V368E	probably damaging	Het
Garem2	A	G	5: 30,313,262 (GRCm39)	E42G	possibly damaging	Het
Gcc1	C	T	6: 28,418,182 (GRCm39)	S717N	probably damaging	Het
Gfm2	T	C	13: 97,309,201 (GRCm39)		probably null	Het
Helb	T	C	10: 119,920,790 (GRCm39)	D1051G	possibly damaging	Het
Helz2	T	A	2: 180,874,261 (GRCm39)	I2078F	possibly damaging	Het
Hsph1	A	T	5: 149,553,270 (GRCm39)	V297D	probably damaging	Het
Ifnar1	A	G	16: 91,302,079 (GRCm39)	Y518C	probably benign	Het
Kcnip2	T	A	19: 45,783,210 (GRCm39)	D153V	probably damaging	Het
Kif21b	T	C	1: 136,073,042 (GRCm39)	F147L	probably damaging	Het
Klhl29	T	C	12: 5,140,537 (GRCm39)	R702G	probably damaging	Het
Lemd3	C	T	10: 120,767,878 (GRCm39)	E667K	possibly damaging	Het
Loxl3	T	C	6: 83,012,503 (GRCm39)	L14P	probably damaging	Het
Lrrd1	A	T	5: 3,900,963 (GRCm39)	K423*	probably null	Het
Mia2	A	G	12: 59,155,586 (GRCm39)	D433G	probably damaging	Het
Mpp2	G	T	11: 101,954,099 (GRCm39)	A216E	probably benign	Het
Mro	T	C	18: 74,009,911 (GRCm39)		probably null	Het
Mybpc1	T	G	10: 88,358,906 (GRCm39)	Y1081S	probably damaging	Het
Myh8	T	G	11: 67,190,141 (GRCm39)	S1260R	possibly damaging	Het
Myo3b	T	C	2: 70,082,094 (GRCm39)	V618A	probably damaging	Het
Naip2	T	G	13: 100,314,776 (GRCm39)	D334A	possibly damaging	Het
Naip5	T	A	13: 100,356,338 (GRCm39)	E1092D	probably benign	Het
Nlrp4c	T	C	7: 6,107,608 (GRCm39)	*983Q	probably null	Het
Nlrp9a	T	G	7: 26,257,698 (GRCm39)	F439V	probably damaging	Het
Nploc4	A	T	11: 120,319,368 (GRCm39)	L64H	probably damaging	Het
Ola1	T	C	2: 72,924,060 (GRCm39)	E246G	probably benign	Het
Otof	G	A	5: 30,537,532 (GRCm39)	S1259F	probably benign	Het
Pde4dip	T	C	3: 97,599,675 (GRCm39)	T2438A	probably damaging	Het
Pex1	A	G	5: 3,686,844 (GRCm39)	T1242A	probably damaging	Het
Pink1	A	T	4: 138,043,056 (GRCm39)		probably benign	Het
Prkcq	A	G	2: 11,251,819 (GRCm39)	T219A	probably damaging	Het
Ptcd3	A	T	6: 71,880,458 (GRCm39)	Y88*	probably null	Het
Ptpru	A	G	4: 131,515,691 (GRCm39)	Y888H	probably damaging	Het
Rapgef6	A	G	11: 54,578,667 (GRCm39)	N1063S	probably benign	Het
Slc1a4	G	A	11: 20,282,532 (GRCm39)		probably benign	Het
Slc4a4	T	C	5: 89,205,568 (GRCm39)		probably benign	Het
Slc6a18	A	T	13: 73,819,822 (GRCm39)	N249K	possibly damaging	Het
Slco2b1	T	G	7: 99,338,214 (GRCm39)	I104L	probably damaging	Het
Syne3	A	T	12: 104,905,871 (GRCm39)	S897R	probably benign	Het
Tlcd5	C	T	9: 43,022,664 (GRCm39)	R230Q	probably benign	Het
Tnni3k	A	G	3: 154,744,146 (GRCm39)	S69P	probably damaging	Het
Tnpo2	A	G	8: 85,780,163 (GRCm39)	K700E	probably benign	Het
Top3a	T	C	11: 60,636,695 (GRCm39)	K657E	probably damaging	Het
Trgv4	C	T	13: 19,369,169 (GRCm39)	Q7*	probably null	Het
Trim6	T	C	7: 103,875,159 (GRCm39)	L132P	probably damaging	Het
Tshz1	T	C	18: 84,032,987 (GRCm39)	T474A	probably benign	Het
Unc13d	AATGCCTCCCATGCC	AATGCCTCCCATGCCTCCCATGCC	11: 115,958,998 (GRCm39)		probably benign	Het
Vmn1r179	A	T	7: 23,628,234 (GRCm39)	I142L	probably benign	Het
Zbtb2	A	T	10: 4,319,183 (GRCm39)	F281Y	probably damaging	Het
Zfp318	T	C	17: 46,723,433 (GRCm39)	V1812A	probably benign	Het

Other mutations in Kif15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01459:Kif15	APN	9	122,804,820 (GRCm39)	missense	probably damaging	1.00
IGL01577:Kif15	APN	9	122,825,399 (GRCm39)	missense	probably benign	0.06
IGL01647:Kif15	APN	9	122,792,536 (GRCm39)	intron	probably benign
IGL01921:Kif15	APN	9	122,808,569 (GRCm39)	missense	probably damaging	1.00
IGL02040:Kif15	APN	9	122,846,450 (GRCm39)	missense	probably damaging	0.99
IGL02191:Kif15	APN	9	122,804,744 (GRCm39)	missense	probably damaging	1.00
IGL02218:Kif15	APN	9	122,824,892 (GRCm39)	splice site	probably benign
IGL02537:Kif15	APN	9	122,822,914 (GRCm39)	missense	probably benign	0.08
IGL02814:Kif15	APN	9	122,832,705 (GRCm39)	missense	possibly damaging	0.83
PIT4480001:Kif15	UTSW	9	122,840,608 (GRCm39)	missense	probably benign
R0034:Kif15	UTSW	9	122,828,350 (GRCm39)	missense	possibly damaging	0.47
R0458:Kif15	UTSW	9	122,838,424 (GRCm39)	missense	probably benign
R0526:Kif15	UTSW	9	122,826,862 (GRCm39)	missense	probably damaging	0.96
R0533:Kif15	UTSW	9	122,838,498 (GRCm39)	unclassified	probably benign
R0726:Kif15	UTSW	9	122,788,993 (GRCm39)	missense	probably benign	0.21
R1580:Kif15	UTSW	9	122,789,021 (GRCm39)	missense	probably benign	0.22
R1597:Kif15	UTSW	9	122,823,074 (GRCm39)	missense	probably benign	0.22
R2096:Kif15	UTSW	9	122,815,252 (GRCm39)	missense	probably damaging	1.00
R3125:Kif15	UTSW	9	122,817,026 (GRCm39)	missense	probably damaging	0.99
R3176:Kif15	UTSW	9	122,816,905 (GRCm39)	splice site	probably benign
R4088:Kif15	UTSW	9	122,815,254 (GRCm39)	missense	probably benign	0.29
R4308:Kif15	UTSW	9	122,843,047 (GRCm39)	missense	probably benign	0.00
R4597:Kif15	UTSW	9	122,822,914 (GRCm39)	missense	probably benign	0.08
R4705:Kif15	UTSW	9	122,789,058 (GRCm39)	splice site	probably null
R4832:Kif15	UTSW	9	122,831,191 (GRCm39)	splice site	probably null
R5100:Kif15	UTSW	9	122,821,059 (GRCm39)	missense	probably damaging	0.98
R5126:Kif15	UTSW	9	122,804,823 (GRCm39)	missense	probably damaging	1.00
R5180:Kif15	UTSW	9	122,828,275 (GRCm39)	missense	probably damaging	0.99
R5247:Kif15	UTSW	9	122,815,507 (GRCm39)	missense	possibly damaging	0.65
R5376:Kif15	UTSW	9	122,823,036 (GRCm39)	missense	probably benign	0.04
R5392:Kif15	UTSW	9	122,825,360 (GRCm39)	missense	probably damaging	0.99
R5422:Kif15	UTSW	9	122,813,954 (GRCm39)	splice site	probably null
R5562:Kif15	UTSW	9	122,807,081 (GRCm39)	missense	probably damaging	1.00
R5663:Kif15	UTSW	9	122,820,916 (GRCm39)	splice site	probably null
R5767:Kif15	UTSW	9	122,843,039 (GRCm39)	missense	possibly damaging	0.78
R5927:Kif15	UTSW	9	122,846,326 (GRCm39)	missense	probably benign	0.00
R6049:Kif15	UTSW	9	122,840,687 (GRCm39)	missense	probably damaging	0.98
R6435:Kif15	UTSW	9	122,815,556 (GRCm39)	missense	probably damaging	1.00
R7040:Kif15	UTSW	9	122,840,679 (GRCm39)	missense	possibly damaging	0.67
R7158:Kif15	UTSW	9	122,828,379 (GRCm39)	missense	probably benign
R7163:Kif15	UTSW	9	122,846,722 (GRCm39)	missense	probably damaging	1.00
R7197:Kif15	UTSW	9	122,838,991 (GRCm39)	critical splice donor site	probably null
R7318:Kif15	UTSW	9	122,817,014 (GRCm39)	missense	probably damaging	1.00
R7360:Kif15	UTSW	9	122,820,202 (GRCm39)	missense	probably benign
R8039:Kif15	UTSW	9	122,836,490 (GRCm39)	missense	possibly damaging	0.82
R8228:Kif15	UTSW	9	122,821,041 (GRCm39)	missense	possibly damaging	0.82
R8549:Kif15	UTSW	9	122,815,236 (GRCm39)	missense	probably benign
R9001:Kif15	UTSW	9	122,826,855 (GRCm39)	missense	probably benign	0.00
R9044:Kif15	UTSW	9	122,840,781 (GRCm39)	missense	probably benign	0.01
R9063:Kif15	UTSW	9	122,833,706 (GRCm39)	missense	probably damaging	1.00
R9306:Kif15	UTSW	9	122,807,056 (GRCm39)	missense	probably damaging	1.00
R9490:Kif15	UTSW	9	122,788,203 (GRCm39)	missense	probably benign	0.10
R9554:Kif15	UTSW	9	122,828,585 (GRCm39)	missense	probably damaging	1.00
R9682:Kif15	UTSW	9	122,815,712 (GRCm39)	missense	probably damaging	0.98
R9752:Kif15	UTSW	9	122,824,890 (GRCm39)	critical splice donor site	probably null
Z1177:Kif15	UTSW	9	122,780,116 (GRCm39)	unclassified	probably benign

Predicted Primers

PCR Primer
(F):5'- ATGCTTATTCCAGTCTAGAAGAAGTCC -3'
(R):5'- TTCCTCAGCAAGAAATTCTAGTTGC -3'

Sequencing Primer
(F):5'- TCTAGAAGAAGTCCAGAGTGCACTTC -3'
(R):5'- CAGCAAGAAATTCTAGTTGCTTTTTC -3'

Posted On

2022-06-09