Mutagenetix > Incidental Mutation

Incidental Mutation 'R6801:Mylk4'

533351

Institutional Source

Beutler Lab

Gene Symbol

Mylk4

Ensembl Gene

ENSMUSG00000044951

Gene Name

myosin light chain kinase family, member 4

Synonyms

EG238564

MMRRC Submission

044914-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6801 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

32884810-32967937 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 32912393 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Asparagine at position 189 (S189N)

Ref Sequence

ENSEMBL: ENSMUSP00000155702 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057428] [ENSMUST00000230119]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000057428

SMART Domains

Protein: ENSMUSP00000060149
Gene: ENSMUSG00000044951

Domain	Start	End	E-Value	Type
S_TKc	107	362	4.2e-90	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000230119
AA Change: S189N

PolyPhen 2 Score 0.074 (Sensitivity: 0.93; Specificity: 0.85)

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.7%
20x: 96.8%

Validation Efficiency

100% (49/49)

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam3	T	A	8: 25,174,680 (GRCm39)	Y695F	possibly damaging	Het
Arhgap20	A	G	9: 51,759,892 (GRCm39)	D545G	probably damaging	Het
Arhgef11	A	G	3: 87,643,159 (GRCm39)	E1457G	possibly damaging	Het
Atp2b4	T	A	1: 133,655,524 (GRCm39)	I747F	probably damaging	Het
Bche	T	A	3: 73,609,133 (GRCm39)	I98L	probably benign	Het
C2cd6	TC	T	1: 59,133,742 (GRCm39)		probably null	Het
Ccdc90b	A	G	7: 92,216,943 (GRCm39)	T72A	probably benign	Het
Chrd	A	G	16: 20,554,497 (GRCm39)	E352G	possibly damaging	Het
Csmd2	A	G	4: 128,277,743 (GRCm39)	E953G	probably benign	Het
Dchs2	T	A	3: 83,035,841 (GRCm39)	M196K	probably benign	Het
Ddx10	G	A	9: 53,159,207 (GRCm39)	Q33*	probably null	Het
Dennd4b	T	A	3: 90,176,086 (GRCm39)	V201E	probably damaging	Het
Fbn2	T	A	18: 58,246,420 (GRCm39)	H494L	probably benign	Het
Fbxw13	G	A	9: 109,023,795 (GRCm39)	A83V	probably null	Het
Fxr1	A	G	3: 34,108,452 (GRCm39)	D321G	possibly damaging	Het
Galm	A	G	17: 80,489,053 (GRCm39)	H233R	probably benign	Het
Gm7298	A	G	6: 121,752,768 (GRCm39)	T837A	probably benign	Het
Gmppa	C	G	1: 75,418,391 (GRCm39)	S258C	possibly damaging	Het
Hk1	T	G	10: 62,116,910 (GRCm39)	E645A	probably damaging	Het
Igkv1-132	A	G	6: 67,737,324 (GRCm39)	T97A	probably damaging	Het
Kcnc1	T	C	7: 46,084,716 (GRCm39)	F547L	probably damaging	Het
Lama5	G	A	2: 179,833,455 (GRCm39)	P1519L	probably damaging	Het
Lingo2	T	A	4: 35,709,566 (GRCm39)	E138V	probably damaging	Het
Myb	T	C	10: 21,020,865 (GRCm39)		probably null	Het
Mybl1	A	G	1: 9,753,353 (GRCm39)	V243A	probably benign	Het
Or13c7	T	A	4: 43,855,206 (GRCm39)	L299*	probably null	Het
Or2y16	A	G	11: 49,335,169 (GRCm39)	M164V	probably benign	Het
Or4k77	A	T	2: 111,199,394 (GRCm39)	Q139L	probably benign	Het
Or4x12-ps1	A	T	2: 89,915,953 (GRCm39)	I284N	probably damaging	Het
Or5w1b	A	G	2: 87,475,667 (GRCm39)	Y267H	probably benign	Het
Or8g19	A	T	9: 39,055,506 (GRCm39)	I37F	probably benign	Het
Oxld1	A	T	11: 120,347,650 (GRCm39)	D182E	probably damaging	Het
Phf13	A	T	4: 152,076,017 (GRCm39)	L295Q	probably damaging	Het
Prrc2c	TTGCTGCTGCTGCTGCTGCTGCTGCTGC	TTGCTGCTGCTGCTGCTGCTGCTGC	1: 162,536,630 (GRCm39)		probably benign	Het
Prss33	A	G	17: 24,053,813 (GRCm39)	L88P	possibly damaging	Het
Ralgds	A	G	2: 28,438,448 (GRCm39)	Y596C	probably damaging	Het
Rftn2	A	G	1: 55,233,418 (GRCm39)	I379T	possibly damaging	Het
Rnf214	C	T	9: 45,807,403 (GRCm39)	E267K	probably damaging	Het
Rpp14	T	C	14: 8,083,717 (GRCm38)		probably benign	Het
Rpusd2	A	G	2: 118,865,876 (GRCm39)	Y191C	probably damaging	Het
Serpinb9c	T	A	13: 33,341,807 (GRCm39)	M1L	probably benign	Het
Shroom3	A	G	5: 93,088,795 (GRCm39)	D434G	probably damaging	Het
Smc5	G	A	19: 23,192,010 (GRCm39)	S888L	probably benign	Het
Suv39h2	C	T	2: 3,465,458 (GRCm39)	R299K	probably benign	Het
Trappc4	A	T	9: 44,315,685 (GRCm39)	I176N	probably damaging	Het
Trim12c	A	T	7: 103,997,337 (GRCm39)	V73E	probably damaging	Het
Vmn2r111	T	C	17: 22,778,032 (GRCm39)	N549S	possibly damaging	Het

Other mutations in Mylk4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00970:Mylk4	APN	13	32,899,905 (GRCm39)	missense	probably damaging	1.00
IGL01799:Mylk4	APN	13	32,965,674 (GRCm39)	missense	probably benign	0.00
IGL01985:Mylk4	APN	13	32,901,564 (GRCm39)	missense	possibly damaging	0.81
IGL02105:Mylk4	APN	13	32,904,545 (GRCm39)	missense	probably benign	0.17
IGL02270:Mylk4	APN	13	32,913,049 (GRCm39)	splice site	probably benign
IGL02377:Mylk4	APN	13	32,906,130 (GRCm39)	missense	possibly damaging	0.69
IGL03142:Mylk4	APN	13	32,904,582 (GRCm39)	missense	probably damaging	1.00
R0550:Mylk4	UTSW	13	32,900,649 (GRCm39)	missense	probably benign	0.00
R0599:Mylk4	UTSW	13	32,896,737 (GRCm39)	splice site	probably null
R1070:Mylk4	UTSW	13	32,908,801 (GRCm39)	missense	probably benign	0.05
R1520:Mylk4	UTSW	13	32,896,821 (GRCm39)	splice site	probably null
R1658:Mylk4	UTSW	13	32,896,772 (GRCm39)	missense	possibly damaging	0.77
R1917:Mylk4	UTSW	13	32,908,836 (GRCm39)	missense	probably benign	0.00
R1918:Mylk4	UTSW	13	32,908,836 (GRCm39)	missense	probably benign	0.00
R1919:Mylk4	UTSW	13	32,908,836 (GRCm39)	missense	probably benign	0.00
R2187:Mylk4	UTSW	13	32,905,996 (GRCm39)	missense	probably damaging	0.97
R2568:Mylk4	UTSW	13	32,906,001 (GRCm39)	missense	probably null	0.97
R4832:Mylk4	UTSW	13	32,905,960 (GRCm39)	missense	probably benign	0.04
R5268:Mylk4	UTSW	13	32,892,864 (GRCm39)	splice site	probably null
R6894:Mylk4	UTSW	13	32,905,998 (GRCm39)	missense	probably damaging	1.00
R7302:Mylk4	UTSW	13	32,904,548 (GRCm39)	missense	probably benign	0.39
R7329:Mylk4	UTSW	13	32,900,766 (GRCm39)	missense	probably damaging	1.00
R7634:Mylk4	UTSW	13	32,892,891 (GRCm39)	missense	possibly damaging	0.88
R7702:Mylk4	UTSW	13	32,904,585 (GRCm39)	critical splice acceptor site	probably null
R7944:Mylk4	UTSW	13	32,911,096 (GRCm39)	missense	probably benign	0.02
R8256:Mylk4	UTSW	13	32,904,522 (GRCm39)	missense	probably damaging	1.00
R8777:Mylk4	UTSW	13	32,913,089 (GRCm39)	missense	probably benign	0.00
R8777-TAIL:Mylk4	UTSW	13	32,913,089 (GRCm39)	missense	probably benign	0.00
R9367:Mylk4	UTSW	13	32,960,236 (GRCm39)	missense	possibly damaging	0.66
R9509:Mylk4	UTSW	13	32,904,543 (GRCm39)	missense	probably benign	0.07
R9794:Mylk4	UTSW	13	32,899,950 (GRCm39)	missense	probably damaging	1.00
R9796:Mylk4	UTSW	13	32,900,643 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGAGAGCAGGTTCTAAACATTGC -3'
(R):5'- GTTCAGAGGAATTCCACAGAGC -3'

Sequencing Primer
(F):5'- AACATTGCCGTTAAAACTGTCTCC -3'
(R):5'- TTCCACAGAGCTAAGAGAGAATGC -3'

Posted On

2018-09-12