Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03031:Myh1'

408434

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Myh1

Ensembl Gene

ENSMUSG00000056328

Gene Name

myosin, heavy polypeptide 1, skeletal muscle, adult

Synonyms

A530084A17Rik, Myhsf2, Myhs-f2, Myhs-f, IId/x, IId, myosin heavy chain 2X, MYHC-IIX, MyHC-IId/x

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL03031

Quality Score

Status

Chromosome

Chromosomal Location

67200052-67224575 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 67206387 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Leucine at position 422 (Q422L)

Ref Sequence

ENSEMBL: ENSMUSP00000117569 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000018637] [ENSMUST00000075734] [ENSMUST00000124516] [ENSMUST00000129018]

AlphaFold

Q5SX40

Predicted Effect

possibly damaging
Transcript: ENSMUST00000018637
AA Change: Q422L

PolyPhen 2 Score 0.472 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000018637
Gene: ENSMUSG00000056328
AA Change: Q422L

Domain	Start	End	E-Value	Type
Pfam:Myosin_N	35	76	1.8e-15	PFAM
MYSc	80	786	N/A	SMART
IQ	787	809	1.18e-3	SMART
low complexity region	860	883	N/A	INTRINSIC
low complexity region	931	945	N/A	INTRINSIC
Pfam:Myosin_tail_1	1075	1933	N/A	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000075734
AA Change: Q422L

PolyPhen 2 Score 0.472 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000075147
Gene: ENSMUSG00000056328
AA Change: Q422L

Domain	Start	End	E-Value	Type
Pfam:Myosin_N	35	74	7.2e-14	PFAM
MYSc	80	786	N/A	SMART
IQ	787	809	1.18e-3	SMART
Pfam:Myosin_tail_1	850	1931	1.9e-165	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000124516
AA Change: Q422L

PolyPhen 2 Score 0.472 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000117569
Gene: ENSMUSG00000056328
AA Change: Q422L

Domain	Start	End	E-Value	Type
Pfam:Myosin_N	35	76	1.8e-15	PFAM
MYSc	80	786	N/A	SMART
IQ	787	809	1.18e-3	SMART
low complexity region	860	883	N/A	INTRINSIC
low complexity region	931	945	N/A	INTRINSIC
Pfam:Myosin_tail_1	1075	1933	N/A	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000129018

SMART Domains

Protein: ENSMUSP00000115583
Gene: ENSMUSG00000056328

Domain	Start	End	E-Value	Type
Pfam:Myosin_N	35	76	1.7e-17	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145021

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. Myosin heavy chains are encoded by a multigene family. In mammals at least 10 different myosin heavy chain (MYH) isoforms have been described from striated, smooth, and nonmuscle cells. These isoforms show expression that is spatially and temporally regulated during development. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit reduced growth, muscular weakness, kyphosis, and abnormal kinetics of muscle contraction and relaxation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca12	T	C	1: 71,314,024 (GRCm38)	D753G	probably benign	Het
Adat2	T	C	10: 13,556,846 (GRCm38)		probably benign	Het
Ahsa2	A	G	11: 23,490,426 (GRCm38)	L275S	probably benign	Het
Arhgef38	C	T	3: 133,132,067 (GRCm38)	D118N	possibly damaging	Het
Bicra	A	T	7: 15,975,801 (GRCm38)	H1097Q	probably benign	Het
C4b	T	C	17: 34,731,130 (GRCm38)	T1389A	possibly damaging	Het
Cd180	A	G	13: 102,705,027 (GRCm38)	S194G	probably benign	Het
Chgb	C	A	2: 132,793,514 (GRCm38)	Q459K	probably benign	Het
Clvs1	G	T	4: 9,449,385 (GRCm38)		probably benign	Het
Cpox	G	A	16: 58,672,560 (GRCm38)	G186R	probably damaging	Het
Cul5	A	G	9: 53,642,675 (GRCm38)		probably benign	Het
Epsti1	G	A	14: 77,974,581 (GRCm38)	R249K	probably benign	Het
Gabrg1	A	T	5: 70,794,682 (GRCm38)	Y90*	probably null	Het
Gabrp	T	C	11: 33,554,980 (GRCm38)	R274G	probably damaging	Het
Gm597	A	G	1: 28,778,583 (GRCm38)	F123L	probably benign	Het
Gm6401	C	T	14: 41,966,894 (GRCm38)	E73K	possibly damaging	Het
Gm9825	T	C	6: 7,982,857 (GRCm38)		noncoding transcript	Het
Hectd4	C	T	5: 121,348,794 (GRCm38)	T3284M	possibly damaging	Het
Hoxc9	T	C	15: 102,984,090 (GRCm38)	M245T	probably damaging	Het
Lpar6	T	C	14: 73,239,442 (GRCm38)	V281A	possibly damaging	Het
Med18	G	T	4: 132,459,613 (GRCm38)	Q192K	possibly damaging	Het
Mis18bp1	A	G	12: 65,161,930 (GRCm38)	V3A	probably benign	Het
Mpped2	G	T	2: 106,783,623 (GRCm38)		probably benign	Het
Ms4a10	A	G	19: 10,968,671 (GRCm38)	V32A	probably benign	Het
Mthfd1l	T	A	10: 4,018,601 (GRCm38)		probably null	Het
Myo3b	A	T	2: 70,255,377 (GRCm38)	Q819L	possibly damaging	Het
Ncoa1	G	A	12: 4,274,818 (GRCm38)	T921I	possibly damaging	Het
Olfr807	A	G	10: 129,755,369 (GRCm38)	L27P	possibly damaging	Het
Olfr894	A	C	9: 38,219,065 (GRCm38)	T81P	probably damaging	Het
Olfr960	A	G	9: 39,623,398 (GRCm38)	I92V	probably damaging	Het
Phf3	A	G	1: 30,804,653 (GRCm38)	S1742P	probably benign	Het
Plxdc2	G	A	2: 16,650,232 (GRCm38)		probably null	Het
Poc5	A	G	13: 96,401,615 (GRCm38)	T263A	probably benign	Het
Prss41	T	A	17: 23,842,422 (GRCm38)	I132F	probably damaging	Het
Pxylp1	A	G	9: 96,825,142 (GRCm38)	I329T	probably benign	Het
Rbm27	T	C	18: 42,333,399 (GRCm38)		probably null	Het
Rpgrip1l	A	T	8: 91,260,783 (GRCm38)	V882E	probably damaging	Het
Sec16b	T	C	1: 157,560,799 (GRCm38)	S579P	probably benign	Het
Senp7	A	G	16: 56,175,886 (GRCm38)	E776G	probably damaging	Het
Smc2	A	G	4: 52,449,638 (GRCm38)	I207V	probably benign	Het
Spats2	A	G	15: 99,180,688 (GRCm38)	T211A	probably benign	Het
Sphkap	A	T	1: 83,276,831 (GRCm38)	S779T	probably damaging	Het
Syt11	A	T	3: 88,748,841 (GRCm38)	M1K	probably null	Het
Tacc2	A	G	7: 130,623,855 (GRCm38)	T757A	possibly damaging	Het
Tecta	A	C	9: 42,345,493 (GRCm38)	M1629R	probably benign	Het
Ufsp2	T	A	8: 45,984,100 (GRCm38)	I101N	probably damaging	Het
Unc13b	T	A	4: 43,235,368 (GRCm38)	C892S	probably damaging	Het
Ush1c	A	G	7: 46,224,937 (GRCm38)		probably benign	Het
Vwde	A	T	6: 13,208,382 (GRCm38)	V167E	probably benign	Het
Wdfy4	A	G	14: 33,140,651 (GRCm38)	L588P	probably damaging	Het
Zfyve1	T	C	12: 83,574,821 (GRCm38)	T267A	probably damaging	Het

Other mutations in Myh1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00427:Myh1	APN	11	67,220,865 (GRCm38)	missense	probably damaging	0.99
IGL00514:Myh1	APN	11	67,219,784 (GRCm38)	missense	probably damaging	1.00
IGL00851:Myh1	APN	11	67,217,910 (GRCm38)	missense	probably damaging	0.96
IGL01061:Myh1	APN	11	67,217,862 (GRCm38)	missense	probably benign	0.05
IGL01113:Myh1	APN	11	67,202,180 (GRCm38)	missense	probably benign	0.00
IGL01125:Myh1	APN	11	67,220,660 (GRCm38)	missense	probably benign
IGL01391:Myh1	APN	11	67,217,863 (GRCm38)	missense	probably benign	0.00
IGL01392:Myh1	APN	11	67,221,301 (GRCm38)	missense	probably benign	0.20
IGL01404:Myh1	APN	11	67,222,151 (GRCm38)	missense	possibly damaging	0.83
IGL01700:Myh1	APN	11	67,211,412 (GRCm38)	missense	probably damaging	1.00
IGL01739:Myh1	APN	11	67,214,528 (GRCm38)	missense	probably damaging	0.99
IGL01759:Myh1	APN	11	67,219,906 (GRCm38)	missense	probably damaging	1.00
IGL01922:Myh1	APN	11	67,210,466 (GRCm38)	critical splice donor site	probably null
IGL01952:Myh1	APN	11	67,220,392 (GRCm38)	splice site	probably null
IGL02007:Myh1	APN	11	67,220,556 (GRCm38)	missense	probably benign	0.03
IGL02028:Myh1	APN	11	67,210,615 (GRCm38)	missense	probably damaging	1.00
IGL02245:Myh1	APN	11	67,211,487 (GRCm38)	missense	possibly damaging	0.58
IGL02628:Myh1	APN	11	67,206,262 (GRCm38)	unclassified	probably benign
IGL02942:Myh1	APN	11	67,202,482 (GRCm38)	missense	probably damaging	1.00
IGL02967:Myh1	APN	11	67,209,070 (GRCm38)	missense	possibly damaging	0.76
IGL03187:Myh1	APN	11	67,206,525 (GRCm38)	missense	possibly damaging	0.56
IGL03302:Myh1	APN	11	67,211,502 (GRCm38)	missense	probably benign	0.01
compelling	UTSW	11	67,219,805 (GRCm38)	critical splice donor site	probably null
convincing	UTSW	11	67,202,539 (GRCm38)	missense	probably damaging	1.00
muscle	UTSW	11	67,206,048 (GRCm38)	nonsense	probably null
Persuasive	UTSW	11	67,209,064 (GRCm38)	missense	possibly damaging	0.90
G1patch:Myh1	UTSW	11	67,201,893 (GRCm38)	missense	probably damaging	1.00
R0041:Myh1	UTSW	11	67,209,078 (GRCm38)	missense	possibly damaging	0.88
R0079:Myh1	UTSW	11	67,213,411 (GRCm38)	missense	probably damaging	1.00
R0081:Myh1	UTSW	11	67,215,857 (GRCm38)	missense	probably benign
R0317:Myh1	UTSW	11	67,217,512 (GRCm38)	missense	probably damaging	1.00
R0465:Myh1	UTSW	11	67,210,417 (GRCm38)	missense	possibly damaging	0.50
R0528:Myh1	UTSW	11	67,220,619 (GRCm38)	missense	probably damaging	1.00
R0731:Myh1	UTSW	11	67,202,533 (GRCm38)	missense	probably damaging	0.98
R0964:Myh1	UTSW	11	67,221,604 (GRCm38)	missense	probably damaging	1.00
R0964:Myh1	UTSW	11	67,205,925 (GRCm38)	missense	probably benign
R1427:Myh1	UTSW	11	67,219,747 (GRCm38)	missense	probably damaging	0.99
R1429:Myh1	UTSW	11	67,217,910 (GRCm38)	missense	possibly damaging	0.78
R1481:Myh1	UTSW	11	67,205,499 (GRCm38)	unclassified	probably benign
R1562:Myh1	UTSW	11	67,211,370 (GRCm38)	missense	probably benign	0.04
R1727:Myh1	UTSW	11	67,210,466 (GRCm38)	critical splice donor site	probably benign
R1796:Myh1	UTSW	11	67,224,357 (GRCm38)	missense	probably benign	0.00
R1808:Myh1	UTSW	11	67,211,474 (GRCm38)	nonsense	probably null
R1836:Myh1	UTSW	11	67,204,822 (GRCm38)	missense	probably damaging	0.98
R1848:Myh1	UTSW	11	67,213,630 (GRCm38)	missense	probably benign	0.10
R1851:Myh1	UTSW	11	67,204,398 (GRCm38)	missense	probably damaging	1.00
R1925:Myh1	UTSW	11	67,211,170 (GRCm38)	missense	probably benign	0.01
R1967:Myh1	UTSW	11	67,213,447 (GRCm38)	missense	probably benign	0.08
R1999:Myh1	UTSW	11	67,222,408 (GRCm38)	missense	probably benign	0.04
R2067:Myh1	UTSW	11	67,214,620 (GRCm38)	missense	possibly damaging	0.83
R2111:Myh1	UTSW	11	67,214,620 (GRCm38)	missense	possibly damaging	0.83
R2150:Myh1	UTSW	11	67,222,408 (GRCm38)	missense	probably benign	0.04
R2189:Myh1	UTSW	11	67,221,604 (GRCm38)	missense	probably damaging	1.00
R2352:Myh1	UTSW	11	67,220,537 (GRCm38)	missense	probably benign	0.00
R2436:Myh1	UTSW	11	67,213,271 (GRCm38)	missense	probably benign	0.04
R2483:Myh1	UTSW	11	67,211,226 (GRCm38)	missense	probably benign
R2508:Myh1	UTSW	11	67,213,598 (GRCm38)	missense	possibly damaging	0.61
R2509:Myh1	UTSW	11	67,205,597 (GRCm38)	missense	probably benign	0.01
R2511:Myh1	UTSW	11	67,205,597 (GRCm38)	missense	probably benign	0.01
R2908:Myh1	UTSW	11	67,220,696 (GRCm38)	nonsense	probably null
R2966:Myh1	UTSW	11	67,214,584 (GRCm38)	missense	probably damaging	1.00
R3829:Myh1	UTSW	11	67,205,597 (GRCm38)	missense	probably benign	0.01
R4106:Myh1	UTSW	11	67,211,577 (GRCm38)	missense	probably benign	0.33
R4108:Myh1	UTSW	11	67,211,577 (GRCm38)	missense	probably benign	0.33
R4457:Myh1	UTSW	11	67,220,615 (GRCm38)	missense	probably benign	0.42
R4629:Myh1	UTSW	11	67,209,293 (GRCm38)	missense	probably benign	0.01
R4981:Myh1	UTSW	11	67,224,474 (GRCm38)	utr 3 prime	probably benign
R5032:Myh1	UTSW	11	67,206,048 (GRCm38)	nonsense	probably null
R5239:Myh1	UTSW	11	67,215,225 (GRCm38)	missense	probably benign	0.19
R5241:Myh1	UTSW	11	67,204,449 (GRCm38)	missense	probably benign
R5303:Myh1	UTSW	11	67,202,017 (GRCm38)	missense	probably benign	0.09
R5666:Myh1	UTSW	11	67,221,352 (GRCm38)	missense	probably benign	0.30
R5717:Myh1	UTSW	11	67,208,956 (GRCm38)	missense	probably benign
R5761:Myh1	UTSW	11	67,219,252 (GRCm38)	missense	probably damaging	0.98
R5870:Myh1	UTSW	11	67,201,979 (GRCm38)	missense	possibly damaging	0.70
R6077:Myh1	UTSW	11	67,211,447 (GRCm38)	missense	probably damaging	1.00
R6089:Myh1	UTSW	11	67,220,787 (GRCm38)	splice site	probably null
R6089:Myh1	UTSW	11	67,202,167 (GRCm38)	splice site	probably null
R6197:Myh1	UTSW	11	67,220,967 (GRCm38)	missense	probably benign	0.01
R6460:Myh1	UTSW	11	67,221,376 (GRCm38)	missense	probably benign
R6627:Myh1	UTSW	11	67,215,009 (GRCm38)	missense	probably damaging	1.00
R6634:Myh1	UTSW	11	67,209,064 (GRCm38)	missense	possibly damaging	0.90
R6725:Myh1	UTSW	11	67,201,893 (GRCm38)	missense	probably damaging	1.00
R6784:Myh1	UTSW	11	67,214,570 (GRCm38)	missense	probably damaging	0.99
R6813:Myh1	UTSW	11	67,220,460 (GRCm38)	missense	probably benign	0.34
R6866:Myh1	UTSW	11	67,224,393 (GRCm38)	missense	probably damaging	0.99
R6997:Myh1	UTSW	11	67,220,637 (GRCm38)	missense	possibly damaging	0.94
R7028:Myh1	UTSW	11	67,220,421 (GRCm38)	missense	possibly damaging	0.64
R7133:Myh1	UTSW	11	67,202,586 (GRCm38)	missense	probably benign
R7185:Myh1	UTSW	11	67,207,459 (GRCm38)	missense	probably damaging	1.00
R7194:Myh1	UTSW	11	67,211,357 (GRCm38)	missense	probably benign
R7283:Myh1	UTSW	11	67,201,844 (GRCm38)	critical splice acceptor site	probably null
R7336:Myh1	UTSW	11	67,220,609 (GRCm38)	missense	probably benign	0.00
R7348:Myh1	UTSW	11	67,202,539 (GRCm38)	missense	probably damaging	1.00
R7369:Myh1	UTSW	11	67,220,698 (GRCm38)	missense	probably damaging	1.00
R7375:Myh1	UTSW	11	67,210,428 (GRCm38)	missense	probably damaging	1.00
R7384:Myh1	UTSW	11	67,224,375 (GRCm38)	missense	possibly damaging	0.46
R7387:Myh1	UTSW	11	67,208,889 (GRCm38)	missense	probably benign	0.14
R7424:Myh1	UTSW	11	67,213,663 (GRCm38)	missense	probably damaging	1.00
R7430:Myh1	UTSW	11	67,205,567 (GRCm38)	nonsense	probably null
R7443:Myh1	UTSW	11	67,220,505 (GRCm38)	missense	probably benign
R7447:Myh1	UTSW	11	67,219,180 (GRCm38)	missense	probably benign	0.01
R7509:Myh1	UTSW	11	67,210,461 (GRCm38)	missense	probably benign	0.40
R7583:Myh1	UTSW	11	67,220,913 (GRCm38)	missense	probably benign	0.00
R7611:Myh1	UTSW	11	67,210,417 (GRCm38)	missense	possibly damaging	0.50
R7617:Myh1	UTSW	11	67,215,875 (GRCm38)	missense	possibly damaging	0.94
R7727:Myh1	UTSW	11	67,215,922 (GRCm38)	missense	probably benign	0.00
R8029:Myh1	UTSW	11	67,211,240 (GRCm38)	critical splice donor site	probably null
R8042:Myh1	UTSW	11	67,206,603 (GRCm38)	missense	probably damaging	1.00
R8060:Myh1	UTSW	11	67,215,251 (GRCm38)	missense	probably benign
R8080:Myh1	UTSW	11	67,211,402 (GRCm38)	missense	probably benign	0.10
R8117:Myh1	UTSW	11	67,222,205 (GRCm38)	missense	probably damaging	1.00
R8171:Myh1	UTSW	11	67,202,572 (GRCm38)	missense	probably damaging	1.00
R8183:Myh1	UTSW	11	67,202,006 (GRCm38)	missense	possibly damaging	0.50
R8397:Myh1	UTSW	11	67,221,639 (GRCm38)	missense	probably damaging	0.97
R8545:Myh1	UTSW	11	67,202,201 (GRCm38)	missense	probably benign	0.00
R8807:Myh1	UTSW	11	67,220,528 (GRCm38)	missense	probably benign	0.02
R8812:Myh1	UTSW	11	67,209,141 (GRCm38)	missense	probably benign	0.00
R8855:Myh1	UTSW	11	67,211,421 (GRCm38)	missense	probably damaging	1.00
R8906:Myh1	UTSW	11	67,205,913 (GRCm38)	missense	probably benign	0.02
R8959:Myh1	UTSW	11	67,211,502 (GRCm38)	missense	probably benign
R8992:Myh1	UTSW	11	67,205,781 (GRCm38)	missense	probably benign
R9140:Myh1	UTSW	11	67,209,263 (GRCm38)	missense	probably benign	0.04
R9293:Myh1	UTSW	11	67,209,103 (GRCm38)	missense	probably benign	0.25
R9366:Myh1	UTSW	11	67,219,288 (GRCm38)	missense	probably damaging	1.00
R9371:Myh1	UTSW	11	67,219,805 (GRCm38)	critical splice donor site	probably null
R9378:Myh1	UTSW	11	67,202,433 (GRCm38)	missense	probably damaging	0.99
R9482:Myh1	UTSW	11	67,217,919 (GRCm38)	missense	probably damaging	1.00
R9507:Myh1	UTSW	11	67,211,223 (GRCm38)	missense	probably benign	0.00
R9558:Myh1	UTSW	11	67,217,792 (GRCm38)	missense	possibly damaging	0.90
R9561:Myh1	UTSW	11	67,217,792 (GRCm38)	missense	possibly damaging	0.90
R9587:Myh1	UTSW	11	67,211,370 (GRCm38)	missense	probably benign	0.03
X0062:Myh1	UTSW	11	67,207,541 (GRCm38)	missense	probably damaging	0.99
Z1177:Myh1	UTSW	11	67,206,318 (GRCm38)	missense	probably damaging	1.00
Z1187:Myh1	UTSW	11	67,204,446 (GRCm38)	missense	probably benign
Z1188:Myh1	UTSW	11	67,204,446 (GRCm38)	missense	probably benign
Z1190:Myh1	UTSW	11	67,204,446 (GRCm38)	missense	probably benign
Z1191:Myh1	UTSW	11	67,204,446 (GRCm38)	missense	probably benign

Posted On

2016-08-02