Mutagenetix > Incidental Mutation

Incidental Mutation 'R1180:Kif6'

101522

Institutional Source

Beutler Lab

Gene Symbol

Kif6

Ensembl Gene

ENSMUSG00000023999

Gene Name

kinesin family member 6

Synonyms

D130084M03Rik, D130004B10Rik

MMRRC Submission

039252-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.135) question?

Stock #

R1180 (G1)

Quality Score

153

Status

Validated

Chromosome

Chromosomal Location

49922164-50216875 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to A at 50139284 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000124674 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000162854]

AlphaFold

E9PX57

Predicted Effect

probably benign
Transcript: ENSMUST00000162854

SMART Domains

Protein: ENSMUSP00000124674
Gene: ENSMUSG00000023999

Domain	Start	End	E-Value	Type
KISc	3	353	1.67e-121	SMART
coiled coil region	358	385	N/A	INTRINSIC
Blast:KISc	400	606	1e-85	BLAST

Coding Region Coverage

1x: 98.8%
3x: 97.8%
10x: 94.5%
20x: 87.5%

Validation Efficiency

98% (55/56)

MGI Phenotype

PHENOTYPE: Mice homozgyos for an ENU-induced allele exhibit normal exercise capacity and cardiac function. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610021A01Rik	T	A	7: 41,275,141 (GRCm39)	D281E	probably benign	Het
Adam24	T	G	8: 41,134,467 (GRCm39)	V645G	probably damaging	Het
Apcdd1	A	T	18: 63,070,168 (GRCm39)	Y145F	probably damaging	Het
Cadps	A	G	14: 12,457,836 (GRCm38)		probably benign	Het
Camk1d	A	T	2: 5,366,836 (GRCm39)	Y126*	probably null	Het
Chd8	A	C	14: 52,458,565 (GRCm39)	S848A	probably damaging	Het
Col6a3	T	C	1: 90,709,577 (GRCm39)	K1873R	unknown	Het
Cpd	T	C	11: 76,692,579 (GRCm39)	T753A	possibly damaging	Het
Cxcr2	A	T	1: 74,197,527 (GRCm39)	D7V	probably benign	Het
Dock4	A	G	12: 40,690,413 (GRCm39)	E173G	possibly damaging	Het
EU599041	G	A	7: 42,875,731 (GRCm39)		noncoding transcript	Het
Fer1l6	G	A	15: 58,474,160 (GRCm39)		probably benign	Het
Flt3	T	C	5: 147,278,048 (GRCm39)	D842G	probably damaging	Het
Foxp4	G	C	17: 48,191,278 (GRCm39)		probably benign	Het
Fsip2	T	C	2: 82,805,570 (GRCm39)	Y630H	probably damaging	Het
Gprin3	C	A	6: 59,331,921 (GRCm39)	V129F	possibly damaging	Het
Gstm1	A	G	3: 107,922,127 (GRCm39)	F170S	probably damaging	Het
Hoxa3	A	C	6: 52,147,382 (GRCm39)	Y290*	probably null	Het
Htra4	G	T	8: 25,523,735 (GRCm39)	L277I	probably damaging	Het
Jak2	A	G	19: 29,259,899 (GRCm39)	Y266C	probably damaging	Het
Kiz	C	T	2: 146,811,927 (GRCm39)	R679C	unknown	Het
Kyat3	A	C	3: 142,443,531 (GRCm39)		probably null	Het
Mipep	G	A	14: 61,071,505 (GRCm39)	V537I	probably damaging	Het
Mrpl44	T	A	1: 79,755,677 (GRCm39)	N94K	probably damaging	Het
Mstn	A	T	1: 53,103,167 (GRCm39)	T168S	possibly damaging	Het
Mx2	G	A	16: 97,357,209 (GRCm39)	R434H	probably damaging	Het
Myh6	A	G	14: 55,181,925 (GRCm39)	I1792T	possibly damaging	Het
Myo16	T	C	8: 10,446,908 (GRCm39)	S450P	probably damaging	Het
Nherf4	T	A	9: 44,160,543 (GRCm39)	D284V	probably benign	Het
Nrbp1	T	A	5: 31,403,157 (GRCm39)	I210N	probably damaging	Het
Or3a1b	A	G	11: 74,012,406 (GRCm39)	Y97C	probably benign	Het
Or5d16	G	A	2: 87,773,490 (GRCm39)	L161F	probably benign	Het
Pirb	A	T	7: 3,720,637 (GRCm39)	L287Q	probably benign	Het
Pkhd1	C	T	1: 20,655,381 (GRCm39)		probably null	Het
Psmd8	A	T	7: 28,874,825 (GRCm39)	V248E	probably benign	Het
Ranbp2	A	G	10: 58,301,285 (GRCm39)	Y646C	probably damaging	Het
Samsn1	C	T	16: 75,670,536 (GRCm39)	G189E	probably damaging	Het
Sec61g	A	C	11: 16,454,722 (GRCm39)		probably benign	Het
Sfmbt2	C	T	2: 10,406,877 (GRCm39)	H59Y	probably damaging	Het
Shb	T	C	4: 45,423,996 (GRCm39)	I486V	possibly damaging	Het
Shf	G	A	2: 122,199,163 (GRCm39)	P51S	probably damaging	Het
Spag16	G	A	1: 69,962,817 (GRCm39)		probably benign	Het
Spink13	A	G	18: 62,741,241 (GRCm39)		probably benign	Het
Tenm2	C	T	11: 35,954,004 (GRCm39)	G1236R	possibly damaging	Het
Tk1	A	G	11: 117,712,921 (GRCm39)		probably null	Het
Tnni3k	A	T	3: 154,581,150 (GRCm39)	H600Q	probably damaging	Het
Ttn	A	T	2: 76,800,047 (GRCm39)	I387N	probably damaging	Het
Ube2q2	T	C	9: 55,102,700 (GRCm39)		probably benign	Het
Utp14b	C	A	1: 78,643,162 (GRCm39)	N353K	probably damaging	Het
Zfp474	C	T	18: 52,771,814 (GRCm39)	Q156*	probably null	Het

Other mutations in Kif6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01793:Kif6	APN	17	49,931,521 (GRCm39)	missense	probably damaging	0.99
IGL02098:Kif6	APN	17	50,177,922 (GRCm39)	missense	probably benign	0.36
IGL02259:Kif6	APN	17	50,202,919 (GRCm39)	splice site	probably benign
IGL03003:Kif6	APN	17	50,060,899 (GRCm39)	nonsense	probably null
PIT4280001:Kif6	UTSW	17	50,062,148 (GRCm39)	missense	probably benign	0.32
R0044:Kif6	UTSW	17	50,139,284 (GRCm39)	splice site	probably benign
R1432:Kif6	UTSW	17	49,927,728 (GRCm39)	missense	probably damaging	1.00
R1522:Kif6	UTSW	17	50,021,141 (GRCm39)	missense	probably damaging	0.99
R1760:Kif6	UTSW	17	49,922,311 (GRCm39)	missense	probably benign	0.00
R1770:Kif6	UTSW	17	50,210,677 (GRCm39)	missense	possibly damaging	0.92
R1809:Kif6	UTSW	17	50,208,812 (GRCm39)	missense	probably benign	0.00
R1854:Kif6	UTSW	17	50,208,799 (GRCm39)	missense	probably benign	0.25
R2176:Kif6	UTSW	17	50,062,258 (GRCm39)	missense	probably damaging	1.00
R3766:Kif6	UTSW	17	50,065,671 (GRCm39)	splice site	probably benign
R4620:Kif6	UTSW	17	50,208,324 (GRCm39)	missense	probably benign
R4661:Kif6	UTSW	17	50,060,909 (GRCm39)	missense	probably benign	0.21
R4972:Kif6	UTSW	17	50,014,647 (GRCm39)	missense	probably damaging	1.00
R5735:Kif6	UTSW	17	50,139,210 (GRCm39)	missense	probably damaging	1.00
R5950:Kif6	UTSW	17	50,022,116 (GRCm39)	missense	probably damaging	0.99
R6364:Kif6	UTSW	17	49,927,651 (GRCm39)	missense	probably benign	0.01
R7604:Kif6	UTSW	17	49,978,129 (GRCm39)	missense	probably damaging	1.00
R7879:Kif6	UTSW	17	50,139,214 (GRCm39)	missense	probably benign	0.08
R7966:Kif6	UTSW	17	49,993,453 (GRCm39)	missense	probably damaging	0.98
R8246:Kif6	UTSW	17	50,065,542 (GRCm39)	nonsense	probably null
R8487:Kif6	UTSW	17	49,978,164 (GRCm39)	missense	probably damaging	1.00
X0067:Kif6	UTSW	17	50,139,195 (GRCm39)	missense	probably benign	0.01
Z1177:Kif6	UTSW	17	50,022,128 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AAATGATGTGACTGAAGCCATCCCC -3'
(R):5'- CCCCTGGAGATTATGAAGGCACTTG -3'

Sequencing Primer
(F):5'- AAGCCATCCCCCCTGTG -3'
(R):5'- tgggaggcagaggcagg -3'

Posted On

2014-01-15