Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02814:Myh15'

360750

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Myh15

Ensembl Gene

ENSMUSG00000092009

Gene Name

myosin, heavy chain 15

Synonyms

EG667772

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.156) question?

Stock #

IGL02814

Quality Score

Status

Chromosome

Chromosomal Location

49057486-49199104 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 49145438 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000127539 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000168680]

AlphaFold

E9Q264

Predicted Effect

probably benign
Transcript: ENSMUST00000168680

SMART Domains

Protein: ENSMUSP00000127539
Gene: ENSMUSG00000092009

Domain	Start	End	E-Value	Type
Pfam:Myosin_N	30	70	5.2e-12	PFAM
MYSc	76	770	N/A	SMART
Pfam:Myosin_tail_1	836	1915	9.5e-118	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700081O15Rik	C	A	19: 7,420,422 (GRCm38)	N111K	possibly damaging	Het
Abca9	A	T	11: 110,154,467 (GRCm38)	F347I	possibly damaging	Het
Adcy5	A	G	16: 35,303,649 (GRCm38)	T1233A	probably benign	Het
Blnk	C	T	19: 40,962,429 (GRCm38)	D93N	probably damaging	Het
Cadps2	T	C	6: 23,321,707 (GRCm38)	E1083G	probably damaging	Het
Capn8	C	A	1: 182,598,771 (GRCm38)	L224M	probably damaging	Het
Cdh4	A	T	2: 179,780,474 (GRCm38)	E130D	probably benign	Het
Cgn	G	A	3: 94,774,240 (GRCm38)	T515M	probably benign	Het
Chrna10	C	T	7: 102,112,262 (GRCm38)	G374D	probably benign	Het
Chrnb1	T	A	11: 69,795,680 (GRCm38)	Y38F	probably damaging	Het
Cyld	A	G	8: 88,744,897 (GRCm38)	D621G	probably benign	Het
Cyp4f37	T	C	17: 32,634,671 (GRCm38)	F443S	probably benign	Het
Dctn1	C	A	6: 83,189,914 (GRCm38)	A152E	probably damaging	Het
Eml4	T	A	17: 83,441,362 (GRCm38)	Y228*	probably null	Het
Fbln2	T	A	6: 91,265,857 (GRCm38)	C846*	probably null	Het
Fut2	C	T	7: 45,650,769 (GRCm38)	G193E	possibly damaging	Het
Gart	T	C	16: 91,623,457 (GRCm38)	S833G	possibly damaging	Het
Gda	T	C	19: 21,428,475 (GRCm38)		probably null	Het
Gjb5	C	T	4: 127,355,562 (GRCm38)	R263Q	probably benign	Het
Gtf2i	T	C	5: 134,286,704 (GRCm38)	K193E	probably damaging	Het
Hist2h4	C	A	3: 96,263,287 (GRCm38)	K6N	probably benign	Het
Ints1	C	T	5: 139,772,391 (GRCm38)	E244K	possibly damaging	Het
Kat14	G	A	2: 144,402,463 (GRCm38)	S412N	probably benign	Het
Kcnn3	A	T	3: 89,521,175 (GRCm38)	H236L	possibly damaging	Het
Kif15	T	A	9: 123,003,640 (GRCm38)	I1005K	possibly damaging	Het
Klrc1	T	C	6: 129,678,892 (GRCm38)	T7A	possibly damaging	Het
Lcp2	T	C	11: 34,071,033 (GRCm38)	S130P	probably damaging	Het
Ldha	T	A	7: 46,850,891 (GRCm38)	Y133*	probably null	Het
Lrp2	A	G	2: 69,506,736 (GRCm38)	C1231R	probably damaging	Het
Lrrn1	T	A	6: 107,567,352 (GRCm38)	V37D	probably damaging	Het
Mep1a	T	A	17: 43,477,221 (GRCm38)	H648L	probably benign	Het
Mmp25	C	T	17: 23,639,762 (GRCm38)	G272R	probably damaging	Het
Myl3	G	T	9: 110,767,991 (GRCm38)	E140*	probably null	Het
Nlrp4f	A	G	13: 65,185,042 (GRCm38)	S809P	probably damaging	Het
Nrde2	T	C	12: 100,144,135 (GRCm38)	I207M	probably null	Het
Olfr1373	C	T	11: 52,144,810 (GRCm38)	C240Y	probably damaging	Het
Olfr474	T	C	7: 107,954,770 (GRCm38)	I43T	probably benign	Het
Olfr541	T	C	7: 140,705,133 (GRCm38)	L294P	probably damaging	Het
Paics	T	G	5: 76,962,473 (GRCm38)	V245G	probably damaging	Het
Pank1	A	G	19: 34,840,855 (GRCm38)	F95L	probably damaging	Het
Pde4dip	A	C	3: 97,767,100 (GRCm38)	C167G	probably damaging	Het
Picalm	C	A	7: 90,191,749 (GRCm38)	T542K	possibly damaging	Het
Piezo1	A	G	8: 122,498,215 (GRCm38)	Y651H	probably damaging	Het
Pikfyve	T	A	1: 65,250,194 (GRCm38)	C1208*	probably null	Het
Pkd1l1	T	A	11: 8,902,582 (GRCm38)	T634S	probably benign	Het
Rab32	T	C	10: 10,546,427 (GRCm38)	T183A	probably benign	Het
Rad18	T	C	6: 112,644,622 (GRCm38)	I206V	possibly damaging	Het
Rbm15b	T	C	9: 106,885,776 (GRCm38)	I398V	probably benign	Het
Rbm28	T	C	6: 29,159,726 (GRCm38)	E101G	probably benign	Het
Rsf1	T	C	7: 97,661,227 (GRCm38)	L388P	probably damaging	Het
Scnn1g	A	G	7: 121,740,365 (GRCm38)	Y129C	probably damaging	Het
Slc7a13	G	A	4: 19,839,387 (GRCm38)	C330Y	probably benign	Het
Spock1	A	T	13: 57,587,673 (GRCm38)	V101E	probably damaging	Het
Sympk	T	A	7: 19,053,273 (GRCm38)	W1029R	probably damaging	Het
Syne2	T	A	12: 75,945,376 (GRCm38)	H2008Q	possibly damaging	Het
Tgs1	T	A	4: 3,585,719 (GRCm38)	Y199N	probably damaging	Het
Trim10	T	A	17: 36,877,336 (GRCm38)	C481*	probably null	Het
Vmn2r102	A	G	17: 19,677,908 (GRCm38)	E395G	probably damaging	Het
Wfs1	A	C	5: 36,967,669 (GRCm38)	V626G	possibly damaging	Het
Zfp689	A	G	7: 127,445,021 (GRCm38)	S146P	possibly damaging	Het
Zfp786	T	C	6: 47,819,841 (GRCm38)	H721R	probably damaging	Het

Other mutations in Myh15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00943:Myh15	APN	16	49,165,813 (GRCm38)	missense	probably damaging	0.98
IGL01095:Myh15	APN	16	49,132,015 (GRCm38)	missense	probably damaging	1.00
IGL01343:Myh15	APN	16	49,155,677 (GRCm38)	missense	probably benign	0.09
IGL01474:Myh15	APN	16	49,132,098 (GRCm38)	missense	probably damaging	1.00
IGL01572:Myh15	APN	16	49,100,222 (GRCm38)	missense	possibly damaging	0.55
IGL01595:Myh15	APN	16	49,172,949 (GRCm38)	missense	probably damaging	1.00
IGL01632:Myh15	APN	16	49,061,511 (GRCm38)	missense	probably benign	0.00
IGL01638:Myh15	APN	16	49,069,480 (GRCm38)	missense	probably damaging	1.00
IGL01667:Myh15	APN	16	49,195,579 (GRCm38)	missense	probably benign	0.20
IGL01715:Myh15	APN	16	49,057,484 (GRCm38)	unclassified	probably benign
IGL01833:Myh15	APN	16	49,114,058 (GRCm38)	missense	probably damaging	1.00
IGL02004:Myh15	APN	16	49,110,529 (GRCm38)	splice site	probably benign
IGL02033:Myh15	APN	16	49,145,344 (GRCm38)	missense	probably benign	0.05
IGL02148:Myh15	APN	16	49,116,315 (GRCm38)	missense	probably damaging	1.00
IGL02225:Myh15	APN	16	49,091,163 (GRCm38)	missense	probably benign	0.14
IGL02249:Myh15	APN	16	49,110,484 (GRCm38)	missense	probably damaging	0.99
IGL02505:Myh15	APN	16	49,117,263 (GRCm38)	missense	possibly damaging	0.90
IGL02622:Myh15	APN	16	49,176,954 (GRCm38)	missense	probably benign	0.02
IGL02869:Myh15	APN	16	49,145,404 (GRCm38)	missense	probably benign
IGL02879:Myh15	APN	16	49,173,059 (GRCm38)	missense	possibly damaging	0.68
IGL02881:Myh15	APN	16	49,117,265 (GRCm38)	missense	possibly damaging	0.51
IGL03077:Myh15	APN	16	49,096,538 (GRCm38)	missense	probably benign	0.10
IGL03354:Myh15	APN	16	49,172,010 (GRCm38)	missense	probably benign	0.01
IGL03411:Myh15	APN	16	49,159,967 (GRCm38)	missense	possibly damaging	0.58
ANU74:Myh15	UTSW	16	49,172,932 (GRCm38)	missense	possibly damaging	0.58
P0027:Myh15	UTSW	16	49,081,208 (GRCm38)	missense	possibly damaging	0.77
PIT1430001:Myh15	UTSW	16	49,196,891 (GRCm38)	critical splice donor site	probably null
R0017:Myh15	UTSW	16	49,163,060 (GRCm38)	missense	probably damaging	0.97
R0038:Myh15	UTSW	16	49,071,141 (GRCm38)	splice site	probably benign
R0149:Myh15	UTSW	16	49,114,005 (GRCm38)	missense	probably benign	0.01
R0361:Myh15	UTSW	16	49,114,005 (GRCm38)	missense	probably benign	0.01
R0373:Myh15	UTSW	16	49,182,959 (GRCm38)	missense	possibly damaging	0.86
R0433:Myh15	UTSW	16	49,145,236 (GRCm38)	missense	probably damaging	1.00
R0525:Myh15	UTSW	16	49,132,051 (GRCm38)	missense	probably benign	0.03
R0586:Myh15	UTSW	16	49,171,887 (GRCm38)	splice site	probably benign
R0601:Myh15	UTSW	16	49,061,581 (GRCm38)	missense	probably damaging	1.00
R0717:Myh15	UTSW	16	49,142,993 (GRCm38)	missense	probably benign	0.03
R0963:Myh15	UTSW	16	49,132,149 (GRCm38)	missense	probably damaging	0.97
R1075:Myh15	UTSW	16	49,120,054 (GRCm38)	missense	possibly damaging	0.63
R1143:Myh15	UTSW	16	49,065,086 (GRCm38)	missense	probably benign	0.02
R1200:Myh15	UTSW	16	49,096,519 (GRCm38)	missense	probably damaging	1.00
R1644:Myh15	UTSW	16	49,132,203 (GRCm38)	missense	probably benign	0.12
R1646:Myh15	UTSW	16	49,195,568 (GRCm38)	missense	probably damaging	1.00
R1720:Myh15	UTSW	16	49,092,782 (GRCm38)	missense	probably damaging	1.00
R1768:Myh15	UTSW	16	49,163,135 (GRCm38)	missense	probably benign	0.27
R1881:Myh15	UTSW	16	49,071,083 (GRCm38)	missense	probably damaging	0.98
R2048:Myh15	UTSW	16	49,155,565 (GRCm38)	missense	probably damaging	0.99
R2064:Myh15	UTSW	16	49,155,621 (GRCm38)	missense	possibly damaging	0.50
R2184:Myh15	UTSW	16	49,137,511 (GRCm38)	missense	probably damaging	0.99
R2212:Myh15	UTSW	16	49,138,732 (GRCm38)	missense	probably benign	0.02
R2216:Myh15	UTSW	16	49,165,838 (GRCm38)	nonsense	probably null
R2321:Myh15	UTSW	16	49,113,073 (GRCm38)	missense	possibly damaging	0.93
R2327:Myh15	UTSW	16	49,142,950 (GRCm38)	missense	probably benign	0.01
R2395:Myh15	UTSW	16	49,069,514 (GRCm38)	missense	probably benign	0.04
R2399:Myh15	UTSW	16	49,137,589 (GRCm38)	missense	probably damaging	0.97
R3413:Myh15	UTSW	16	49,138,732 (GRCm38)	missense	probably benign	0.02
R4234:Myh15	UTSW	16	49,163,042 (GRCm38)	missense	probably benign	0.04
R4382:Myh15	UTSW	16	49,142,943 (GRCm38)	missense	probably benign	0.03
R4421:Myh15	UTSW	16	49,109,344 (GRCm38)	missense	probably damaging	0.99
R4580:Myh15	UTSW	16	49,065,025 (GRCm38)	missense	possibly damaging	0.93
R4657:Myh15	UTSW	16	49,172,058 (GRCm38)	nonsense	probably null
R4780:Myh15	UTSW	16	49,120,057 (GRCm38)	missense	probably benign	0.13
R5004:Myh15	UTSW	16	49,132,048 (GRCm38)	missense	probably damaging	0.99
R5175:Myh15	UTSW	16	49,069,426 (GRCm38)	missense	possibly damaging	0.85
R5189:Myh15	UTSW	16	49,101,507 (GRCm38)	missense	probably benign	0.20
R5311:Myh15	UTSW	16	49,165,841 (GRCm38)	missense	possibly damaging	0.94
R5318:Myh15	UTSW	16	49,110,471 (GRCm38)	missense	probably damaging	0.99
R5404:Myh15	UTSW	16	49,159,978 (GRCm38)	missense	probably benign	0.15
R5415:Myh15	UTSW	16	49,117,295 (GRCm38)	missense	probably null	1.00
R5558:Myh15	UTSW	16	49,069,537 (GRCm38)	missense	probably benign	0.32
R5977:Myh15	UTSW	16	49,153,503 (GRCm38)	missense	probably damaging	1.00
R6004:Myh15	UTSW	16	49,159,699 (GRCm38)	missense	probably benign	0.00
R6275:Myh15	UTSW	16	49,145,247 (GRCm38)	missense	probably benign	0.00
R6381:Myh15	UTSW	16	49,101,481 (GRCm38)	missense	probably damaging	1.00
R6448:Myh15	UTSW	16	49,171,932 (GRCm38)	missense	probably damaging	0.99
R6516:Myh15	UTSW	16	49,137,633 (GRCm38)	missense	probably benign	0.19
R6752:Myh15	UTSW	16	49,182,927 (GRCm38)	missense	probably damaging	1.00
R6847:Myh15	UTSW	16	49,145,088 (GRCm38)	missense	possibly damaging	0.70
R6868:Myh15	UTSW	16	49,069,403 (GRCm38)	missense	probably damaging	1.00
R6889:Myh15	UTSW	16	49,153,111 (GRCm38)	missense	possibly damaging	0.75
R6896:Myh15	UTSW	16	49,113,071 (GRCm38)	missense	probably benign	0.44
R6955:Myh15	UTSW	16	49,081,235 (GRCm38)	critical splice donor site	probably null
R6984:Myh15	UTSW	16	49,110,412 (GRCm38)	missense	probably damaging	1.00
R7046:Myh15	UTSW	16	49,109,299 (GRCm38)	nonsense	probably null
R7095:Myh15	UTSW	16	49,171,909 (GRCm38)	missense	possibly damaging	0.90
R7098:Myh15	UTSW	16	49,177,057 (GRCm38)	missense	possibly damaging	0.53
R7134:Myh15	UTSW	16	49,081,342 (GRCm38)	missense	possibly damaging	0.86
R7159:Myh15	UTSW	16	49,061,574 (GRCm38)	missense	probably damaging	0.97
R7244:Myh15	UTSW	16	49,196,786 (GRCm38)	missense	probably damaging	1.00
R7278:Myh15	UTSW	16	49,091,105 (GRCm38)	missense	probably damaging	0.98
R7309:Myh15	UTSW	16	49,096,465 (GRCm38)	missense	probably benign	0.34
R7327:Myh15	UTSW	16	49,173,006 (GRCm38)	missense	possibly damaging	0.88
R7418:Myh15	UTSW	16	49,155,537 (GRCm38)	missense	possibly damaging	0.69
R7937:Myh15	UTSW	16	49,155,646 (GRCm38)	missense	probably benign	0.00
R8053:Myh15	UTSW	16	49,142,939 (GRCm38)	missense	possibly damaging	0.89
R8313:Myh15	UTSW	16	49,120,018 (GRCm38)	missense	probably damaging	0.99
R8315:Myh15	UTSW	16	49,120,018 (GRCm38)	missense	probably damaging	0.99
R8316:Myh15	UTSW	16	49,120,018 (GRCm38)	missense	probably damaging	0.99
R8317:Myh15	UTSW	16	49,120,018 (GRCm38)	missense	probably damaging	0.99
R8342:Myh15	UTSW	16	49,092,757 (GRCm38)	missense	probably benign
R8379:Myh15	UTSW	16	49,081,188 (GRCm38)	missense	probably benign
R8445:Myh15	UTSW	16	49,120,018 (GRCm38)	missense	probably damaging	0.99
R8707:Myh15	UTSW	16	49,153,087 (GRCm38)	missense	probably damaging	1.00
R8729:Myh15	UTSW	16	49,061,488 (GRCm38)	missense	probably damaging	0.97
R8773:Myh15	UTSW	16	49,195,537 (GRCm38)	missense	possibly damaging	0.89
R8869:Myh15	UTSW	16	49,177,003 (GRCm38)	missense	probably benign
R8890:Myh15	UTSW	16	49,138,767 (GRCm38)	missense	probably damaging	1.00
R9026:Myh15	UTSW	16	49,187,070 (GRCm38)	missense	probably damaging	1.00
R9063:Myh15	UTSW	16	49,092,755 (GRCm38)	missense	probably benign	0.00
R9290:Myh15	UTSW	16	49,177,012 (GRCm38)	missense	probably damaging	1.00
R9630:Myh15	UTSW	16	49,159,978 (GRCm38)	missense	probably benign	0.15
R9710:Myh15	UTSW	16	49,138,681 (GRCm38)	missense	probably damaging	1.00
X0012:Myh15	UTSW	16	49,142,978 (GRCm38)	missense	probably damaging	1.00
X0020:Myh15	UTSW	16	49,165,874 (GRCm38)	missense	probably damaging	1.00
Z1176:Myh15	UTSW	16	49,096,531 (GRCm38)	missense	probably damaging	0.98
Z1177:Myh15	UTSW	16	49,159,826 (GRCm38)	missense	probably benign	0.09
Z1177:Myh15	UTSW	16	49,155,618 (GRCm38)	missense	probably damaging	0.97
Z1177:Myh15	UTSW	16	49,081,228 (GRCm38)	missense	probably benign	0.02

Posted On

2015-12-18