Mutagenetix > Incidental Mutation

Incidental Mutation 'R2207:Myo15a'

239155

Institutional Source

Beutler Lab

Gene Symbol

Myo15a

Ensembl Gene

ENSMUSG00000042678

Gene Name

myosin XVA

Synonyms

Myo15

MMRRC Submission

040209-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2207 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

60360165-60419195 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 60396860 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 2643 (N2643S)

Ref Sequence

ENSEMBL: ENSMUSP00000091686 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000071880] [ENSMUST00000081823] [ENSMUST00000094135]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000071880
AA Change: N2661S

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000071777
Gene: ENSMUSG00000042678
AA Change: N2661S

Domain	Start	End	E-Value	Type
low complexity region	4	24	N/A	INTRINSIC
low complexity region	87	100	N/A	INTRINSIC
low complexity region	107	120	N/A	INTRINSIC
low complexity region	269	292	N/A	INTRINSIC
low complexity region	295	306	N/A	INTRINSIC
low complexity region	311	325	N/A	INTRINSIC
low complexity region	349	384	N/A	INTRINSIC
low complexity region	425	435	N/A	INTRINSIC
low complexity region	487	498	N/A	INTRINSIC
low complexity region	502	509	N/A	INTRINSIC
low complexity region	653	681	N/A	INTRINSIC
low complexity region	692	705	N/A	INTRINSIC
low complexity region	737	747	N/A	INTRINSIC
low complexity region	758	775	N/A	INTRINSIC
low complexity region	781	792	N/A	INTRINSIC
low complexity region	796	809	N/A	INTRINSIC
low complexity region	825	849	N/A	INTRINSIC
low complexity region	883	897	N/A	INTRINSIC
low complexity region	1067	1082	N/A	INTRINSIC
low complexity region	1115	1130	N/A	INTRINSIC
MYSc	1200	1884	N/A	SMART
IQ	1885	1907	1.63e-1	SMART
IQ	1908	1930	1.77e-2	SMART
IQ	1931	1953	2.97e2	SMART
low complexity region	1955	1974	N/A	INTRINSIC
low complexity region	1992	2006	N/A	INTRINSIC
MyTH4	2049	2195	1.8e-42	SMART
low complexity region	2396	2405	N/A	INTRINSIC
low complexity region	2451	2461	N/A	INTRINSIC
Blast:MYSc	2665	2848	2e-14	BLAST
SH3	2851	2933	1.55e-4	SMART
low complexity region	2949	2962	N/A	INTRINSIC
MyTH4	3031	3185	5.59e-48	SMART
B41	3188	3400	6.94e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000081823
AA Change: N1456S

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000080507
Gene: ENSMUSG00000042678
AA Change: N1456S

Domain	Start	End	E-Value	Type
MYSc	13	697	N/A	SMART
IQ	698	720	1.63e-1	SMART
IQ	721	743	1.77e-2	SMART
IQ	744	766	2.97e2	SMART
low complexity region	787	801	N/A	INTRINSIC
MyTH4	844	990	1.8e-42	SMART
low complexity region	1191	1200	N/A	INTRINSIC
low complexity region	1246	1256	N/A	INTRINSIC
Blast:MYSc	1460	1643	7e-15	BLAST
SH3	1646	1728	1.55e-4	SMART
low complexity region	1744	1757	N/A	INTRINSIC
MyTH4	1826	1980	5.59e-48	SMART
B41	1983	2195	6.94e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000094135
AA Change: N2643S

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000091686
Gene: ENSMUSG00000042678
AA Change: N2643S

Domain	Start	End	E-Value	Type
low complexity region	4	24	N/A	INTRINSIC
low complexity region	87	100	N/A	INTRINSIC
low complexity region	107	120	N/A	INTRINSIC
low complexity region	269	292	N/A	INTRINSIC
low complexity region	295	306	N/A	INTRINSIC
low complexity region	311	325	N/A	INTRINSIC
low complexity region	349	384	N/A	INTRINSIC
low complexity region	425	435	N/A	INTRINSIC
low complexity region	487	498	N/A	INTRINSIC
low complexity region	502	509	N/A	INTRINSIC
low complexity region	653	681	N/A	INTRINSIC
low complexity region	692	705	N/A	INTRINSIC
low complexity region	737	747	N/A	INTRINSIC
low complexity region	758	775	N/A	INTRINSIC
low complexity region	781	792	N/A	INTRINSIC
low complexity region	796	809	N/A	INTRINSIC
low complexity region	825	849	N/A	INTRINSIC
low complexity region	883	897	N/A	INTRINSIC
low complexity region	1067	1082	N/A	INTRINSIC
low complexity region	1115	1130	N/A	INTRINSIC
MYSc	1200	1884	N/A	SMART
IQ	1885	1907	1.63e-1	SMART
IQ	1908	1930	1.77e-2	SMART
IQ	1931	1953	2.97e2	SMART
low complexity region	1974	1988	N/A	INTRINSIC
MyTH4	2031	2177	1.8e-42	SMART
low complexity region	2378	2387	N/A	INTRINSIC
low complexity region	2433	2443	N/A	INTRINSIC
Blast:MYSc	2647	2830	2e-14	BLAST
SH3	2833	2915	1.55e-4	SMART
low complexity region	2931	2944	N/A	INTRINSIC
MyTH4	3013	3167	5.59e-48	SMART
B41	3170	3382	6.94e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000122825

Predicted Effect

unknown
Transcript: ENSMUST00000126522
AA Change: N1474S

SMART Domains

Protein: ENSMUSP00000120839
Gene: ENSMUSG00000042678
AA Change: N1474S

Domain	Start	End	E-Value	Type
MYSc	34	716	N/A	SMART
IQ	717	739	1.63e-1	SMART
IQ	740	762	1.77e-2	SMART
IQ	763	785	2.97e2	SMART
low complexity region	806	820	N/A	INTRINSIC
MyTH4	863	1009	1.8e-42	SMART
low complexity region	1210	1219	N/A	INTRINSIC
low complexity region	1265	1275	N/A	INTRINSIC
Blast:MYSc	1479	1662	5e-15	BLAST
SH3	1665	1747	1.55e-4	SMART
low complexity region	1763	1776	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.5%
20x: 95.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an unconventional myosin. This protein differs from other myosins in that it has a long N-terminal extension preceding the conserved motor domain. Studies in mice suggest that this protein is necessary for actin organization in the hair cells of the cochlea. Mutations in this gene have been associated with profound, congenital, neurosensory, nonsyndromal deafness. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Read-through transcripts containing an upstream gene and this gene have been identified, but they are not thought to encode a fusion protein. Several alternatively spliced transcript variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mutations in this gene result in profound deafness and neurological behavior. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 99 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410137M14Rik	A	G	17: 37,288,965 (GRCm39)		probably benign	Het
Abcb1b	C	T	5: 8,874,803 (GRCm39)	R488C	probably benign	Het
Adam34	T	C	8: 44,105,274 (GRCm39)	I124V	probably benign	Het
Aicda	T	A	6: 122,538,244 (GRCm39)	V134D	possibly damaging	Het
Akt2	T	A	7: 27,336,625 (GRCm39)		probably null	Het
Aldh1a3	T	C	7: 66,055,769 (GRCm39)	R341G	probably damaging	Het
Ankrd12	G	T	17: 66,338,569 (GRCm39)		probably null	Het
Anxa11	A	G	14: 25,874,721 (GRCm39)	Y244C	probably damaging	Het
Atp2c2	G	A	8: 120,475,048 (GRCm39)	R551Q	probably damaging	Het
B4galt3	C	A	1: 171,101,613 (GRCm39)	H196N	probably damaging	Het
Bcl11a	G	T	11: 24,113,343 (GRCm39)	G229W	probably damaging	Het
Brip1	A	G	11: 85,952,703 (GRCm39)	V1026A	probably benign	Het
Cacna1h	A	T	17: 25,603,987 (GRCm39)	S1282T	probably benign	Het
Calcr	T	C	6: 3,717,133 (GRCm39)	Y109C	probably damaging	Het
Ccdc39	T	C	3: 33,890,882 (GRCm39)	I241V	probably damaging	Het
Ccdc9	A	G	7: 16,018,194 (GRCm39)		probably benign	Het
Cdk17	G	A	10: 93,064,624 (GRCm39)	D298N	probably damaging	Het
Cdkl3	A	G	11: 51,918,020 (GRCm39)	*354W	probably null	Het
Celf6	A	T	9: 59,511,610 (GRCm39)	Y401F	possibly damaging	Het
Clec4a4	C	T	6: 122,990,766 (GRCm39)	L169F	probably damaging	Het
Col14a1	T	C	15: 55,327,082 (GRCm39)	F1411L	unknown	Het
Col4a2	G	T	8: 11,493,352 (GRCm39)	G1354W	probably damaging	Het
Crygs	C	T	16: 22,624,301 (GRCm39)	G102D	possibly damaging	Het
Cst13	A	T	2: 148,665,202 (GRCm39)	R66W	probably damaging	Het
Depp1	G	A	6: 116,628,683 (GRCm39)	V9M	possibly damaging	Het
Dhx8	A	G	11: 101,641,797 (GRCm39)	T632A	probably benign	Het
Disp1	A	G	1: 182,869,906 (GRCm39)	F838S	possibly damaging	Het
Dlg1	A	G	16: 31,672,664 (GRCm39)	H599R	probably benign	Het
Dnah12	T	A	14: 26,503,744 (GRCm39)	V1654E	probably damaging	Het
Dnah5	C	T	15: 28,343,817 (GRCm39)	L2406F	probably benign	Het
Fam98b	C	G	2: 117,098,300 (GRCm39)	R257G	probably damaging	Het
Fbn2	A	T	18: 58,214,471 (GRCm39)	C900*	probably null	Het
Fgf1	A	G	18: 38,980,138 (GRCm39)	Y79H	possibly damaging	Het
Foxn1	C	A	11: 78,249,630 (GRCm39)	A632S	probably benign	Het
Fsip2	T	G	2: 82,807,823 (GRCm39)	S1381A	probably benign	Het
Gtf2b	G	A	3: 142,484,081 (GRCm39)	G85D	probably benign	Het
Gyg1	C	A	3: 20,204,703 (GRCm39)	G161C	probably damaging	Het
Hemgn	G	T	4: 46,396,301 (GRCm39)	L312I	possibly damaging	Het
Hic2	T	C	16: 17,075,324 (GRCm39)	M51T	possibly damaging	Het
Hivep2	C	A	10: 14,004,713 (GRCm39)	T437K	probably benign	Het
Hpx	C	T	7: 105,241,633 (GRCm39)	R287H	probably damaging	Het
Igf2bp3	C	T	6: 49,065,488 (GRCm39)	G468E	possibly damaging	Het
Il5ra	C	A	6: 106,689,402 (GRCm39)	E397*	probably null	Het
Itfg1	A	T	8: 86,502,827 (GRCm39)	S246R	probably benign	Het
Kdm2a	A	T	19: 4,412,898 (GRCm39)	D29E	probably damaging	Het
Lamc2	T	G	1: 153,009,452 (GRCm39)	E784D	possibly damaging	Het
Lrp2	A	T	2: 69,297,372 (GRCm39)	N3196K	possibly damaging	Het
Lyzl1	T	A	18: 4,181,962 (GRCm39)	C96*	probably null	Het
Maf1	A	G	15: 76,236,718 (GRCm39)	T17A	probably benign	Het
Map1b	T	C	13: 99,567,591 (GRCm39)	D1710G	unknown	Het
Megf8	C	T	7: 25,049,222 (GRCm39)	T1773I	probably damaging	Het
Mei1	T	C	15: 81,987,450 (GRCm39)	M414T	probably benign	Het
Ndufa9	A	G	6: 126,821,772 (GRCm39)	Y64H	probably damaging	Het
Neb	A	T	2: 52,101,579 (GRCm39)	L4354*	probably null	Het
Nom1	T	A	5: 29,644,972 (GRCm39)	I480N	probably damaging	Het
Nrxn3	C	T	12: 89,315,082 (GRCm39)	T331M	probably damaging	Het
Or1a1	G	T	11: 74,087,150 (GRCm39)	V274L	possibly damaging	Het
Or1j16	G	T	2: 36,530,201 (GRCm39)	R50M	possibly damaging	Het
Or4f14b	A	C	2: 111,775,270 (GRCm39)	F177C	probably damaging	Het
Or51a42	A	G	7: 103,708,612 (GRCm39)	S66P	probably damaging	Het
Pcdhb15	A	T	18: 37,608,075 (GRCm39)	T436S	probably benign	Het
Pcdhb18	T	A	18: 37,624,342 (GRCm39)	N557K	probably damaging	Het
Pcdhb6	T	C	18: 37,468,633 (GRCm39)	M518T	probably benign	Het
Pgm2l1	T	A	7: 99,917,319 (GRCm39)		probably null	Het
Pih1d2	C	A	9: 50,532,379 (GRCm39)	H162N	probably benign	Het
Pitrm1	T	A	13: 6,619,327 (GRCm39)	Y721N	probably damaging	Het
Pla2r1	C	A	2: 60,288,779 (GRCm39)	V618F	probably damaging	Het
Plb1	T	C	5: 32,473,984 (GRCm39)	S599P	possibly damaging	Het
Prkg1	T	C	19: 30,556,260 (GRCm39)	D562G	probably damaging	Het
Proser1	T	G	3: 53,385,812 (GRCm39)	S565A	probably benign	Het
Prx	T	A	7: 27,216,213 (GRCm39)	V238E	probably damaging	Het
Psapl1	T	C	5: 36,362,509 (GRCm39)	I367T	probably damaging	Het
Rc3h1	T	C	1: 160,767,595 (GRCm39)	V128A	probably damaging	Het
Rrm1	T	A	7: 102,091,233 (GRCm39)	M1K	probably null	Het
Rsf1	GCG	GCGACG	7: 97,229,114 (GRCm39)		probably benign	Het
Rsl1	A	G	13: 67,330,892 (GRCm39)	T447A	probably benign	Het
Ryr2	A	G	13: 11,825,823 (GRCm39)	S552P	probably damaging	Het
Sbf1	A	G	15: 89,190,896 (GRCm39)	S225P	possibly damaging	Het
Serpina3c	T	A	12: 104,117,757 (GRCm39)	I194F	probably benign	Het
Setd3	C	T	12: 108,073,544 (GRCm39)	V578M	probably benign	Het
Setx	GTGGCT	GT	2: 29,044,073 (GRCm39)	1814	probably null	Het
Slc6a1	T	A	6: 114,285,632 (GRCm39)	V356E	probably damaging	Het
Slfn1	A	G	11: 83,011,992 (GRCm39)	E36G	possibly damaging	Het
Sorcs1	T	C	19: 50,218,655 (GRCm39)	H609R	possibly damaging	Het
Spag16	A	G	1: 70,764,043 (GRCm39)	H621R	probably benign	Het
Spata31d1e	A	G	13: 59,890,920 (GRCm39)	V300A	probably benign	Het
Tg	G	A	15: 66,553,788 (GRCm39)	G401D	probably benign	Het
Tnxb	A	C	17: 34,928,391 (GRCm39)	T2602P	possibly damaging	Het
Trip11	T	C	12: 101,839,701 (GRCm39)	N1643S	probably benign	Het
Ttn	G	A	2: 76,709,687 (GRCm39)	R1581*	probably null	Het
Ttn	A	T	2: 76,796,155 (GRCm39)	I590K	probably benign	Het
Vmn1r225	A	G	17: 20,722,611 (GRCm39)	I17M	possibly damaging	Het
Vmn1r232	A	G	17: 21,134,465 (GRCm39)	L45P	probably benign	Het
Wdr7	T	A	18: 63,910,678 (GRCm39)	V690E	possibly damaging	Het
Xaf1	A	T	11: 72,194,228 (GRCm39)	E36D	possibly damaging	Het
Zfp131	A	T	13: 120,237,348 (GRCm39)	F303I	probably damaging	Het
Zfp513	T	G	5: 31,357,767 (GRCm39)	K202T	probably damaging	Het
Zfp788	A	T	7: 41,299,064 (GRCm39)	I567F	probably damaging	Het
Zfyve26	A	G	12: 79,292,861 (GRCm39)	V2096A	probably damaging	Het

Other mutations in Myo15a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00845:Myo15a	APN	11	60,368,605 (GRCm39)	missense	probably damaging	1.00
IGL01011:Myo15a	APN	11	60,367,818 (GRCm39)	missense	probably benign	0.33
IGL01100:Myo15a	APN	11	60,401,984 (GRCm39)	missense	probably damaging	1.00
IGL01357:Myo15a	APN	11	60,393,115 (GRCm39)	splice site	probably benign
IGL01634:Myo15a	APN	11	60,386,298 (GRCm39)	missense	probably damaging	1.00
IGL01763:Myo15a	APN	11	60,412,564 (GRCm39)	missense	probably benign	0.07
IGL01901:Myo15a	APN	11	60,418,260 (GRCm39)	utr 3 prime	probably benign
IGL01931:Myo15a	APN	11	60,386,964 (GRCm39)	missense	probably damaging	1.00
IGL02006:Myo15a	APN	11	60,401,954 (GRCm39)	missense	probably damaging	1.00
IGL02041:Myo15a	APN	11	60,397,689 (GRCm39)	missense	probably damaging	0.99
IGL02094:Myo15a	APN	11	60,401,473 (GRCm39)	unclassified	probably benign
IGL02122:Myo15a	APN	11	60,374,292 (GRCm39)	missense	probably benign	0.23
IGL02153:Myo15a	APN	11	60,389,223 (GRCm39)	missense	probably damaging	1.00
IGL02328:Myo15a	APN	11	60,417,433 (GRCm39)	missense	probably benign	0.13
IGL02330:Myo15a	APN	11	60,367,987 (GRCm39)	missense	possibly damaging	0.94
IGL02431:Myo15a	APN	11	60,401,465 (GRCm39)	missense	possibly damaging	0.73
IGL02639:Myo15a	APN	11	60,369,447 (GRCm39)	missense	probably benign
IGL02659:Myo15a	APN	11	60,382,609 (GRCm39)	splice site	probably benign
IGL02800:Myo15a	APN	11	60,393,195 (GRCm39)	missense	probably damaging	1.00
IGL02812:Myo15a	APN	11	60,368,005 (GRCm39)	missense	probably benign	0.15
IGL02863:Myo15a	APN	11	60,368,953 (GRCm39)	missense	probably damaging	1.00
IGL02873:Myo15a	APN	11	60,374,308 (GRCm39)	missense	probably damaging	1.00
IGL02990:Myo15a	APN	11	60,370,266 (GRCm39)	missense	probably benign	0.02
IGL03011:Myo15a	APN	11	60,400,357 (GRCm39)	splice site	probably benign
IGL03243:Myo15a	APN	11	60,387,344 (GRCm39)	missense	probably damaging	1.00
IGL03297:Myo15a	APN	11	60,369,967 (GRCm39)	missense	probably damaging	1.00
novichok	UTSW	11	60,372,566 (GRCm39)	critical splice donor site	probably null
parker	UTSW	11	60,411,740 (GRCm39)	critical splice donor site	probably null
Typhoon	UTSW	11	60,378,251 (GRCm39)	critical splice donor site	probably null
PIT4131001:Myo15a	UTSW	11	60,386,280 (GRCm39)	missense	probably damaging	1.00
PIT4131001:Myo15a	UTSW	11	60,373,953 (GRCm39)	missense	probably damaging	1.00
R0133:Myo15a	UTSW	11	60,368,676 (GRCm39)	missense	possibly damaging	0.94
R0265:Myo15a	UTSW	11	60,405,723 (GRCm39)	critical splice acceptor site	probably null
R0389:Myo15a	UTSW	11	60,369,364 (GRCm39)	missense	probably benign
R0416:Myo15a	UTSW	11	60,402,000 (GRCm39)	missense	probably damaging	1.00
R0449:Myo15a	UTSW	11	60,400,422 (GRCm39)	missense	possibly damaging	0.92
R0477:Myo15a	UTSW	11	60,411,740 (GRCm39)	critical splice donor site	probably null
R0543:Myo15a	UTSW	11	60,369,877 (GRCm39)	missense	probably benign
R0546:Myo15a	UTSW	11	60,397,139 (GRCm39)	missense	probably damaging	1.00
R0555:Myo15a	UTSW	11	60,412,464 (GRCm39)	missense	probably damaging	1.00
R0639:Myo15a	UTSW	11	60,370,162 (GRCm39)	missense	probably benign	0.12
R0723:Myo15a	UTSW	11	60,369,803 (GRCm39)	missense	possibly damaging	0.94
R0837:Myo15a	UTSW	11	60,378,077 (GRCm39)	missense	probably damaging	0.98
R0865:Myo15a	UTSW	11	60,382,514 (GRCm39)	missense	probably damaging	1.00
R0899:Myo15a	UTSW	11	60,368,011 (GRCm39)	missense	possibly damaging	0.87
R1022:Myo15a	UTSW	11	60,370,442 (GRCm39)	missense	probably benign	0.00
R1024:Myo15a	UTSW	11	60,370,442 (GRCm39)	missense	probably benign	0.00
R1035:Myo15a	UTSW	11	60,401,384 (GRCm39)	unclassified	probably benign
R1109:Myo15a	UTSW	11	60,383,892 (GRCm39)	missense	probably damaging	1.00
R1170:Myo15a	UTSW	11	60,370,233 (GRCm39)	missense	probably benign	0.04
R1241:Myo15a	UTSW	11	60,390,256 (GRCm39)	missense	possibly damaging	0.58
R1392:Myo15a	UTSW	11	60,368,800 (GRCm39)	missense	possibly damaging	0.95
R1392:Myo15a	UTSW	11	60,368,800 (GRCm39)	missense	possibly damaging	0.95
R1434:Myo15a	UTSW	11	60,395,157 (GRCm39)	missense	probably benign	0.00
R1450:Myo15a	UTSW	11	60,386,308 (GRCm39)	missense	probably damaging	1.00
R1456:Myo15a	UTSW	11	60,399,028 (GRCm39)	missense	probably damaging	1.00
R1468:Myo15a	UTSW	11	60,396,832 (GRCm39)	missense	probably damaging	1.00
R1468:Myo15a	UTSW	11	60,396,832 (GRCm39)	missense	probably damaging	1.00
R1548:Myo15a	UTSW	11	60,379,064 (GRCm39)	missense	probably damaging	1.00
R1551:Myo15a	UTSW	11	60,383,791 (GRCm39)	missense	possibly damaging	0.70
R1571:Myo15a	UTSW	11	60,409,290 (GRCm39)	missense	probably damaging	1.00
R1662:Myo15a	UTSW	11	60,392,527 (GRCm39)	missense	probably damaging	1.00
R1777:Myo15a	UTSW	11	60,405,762 (GRCm39)	missense	probably benign
R1778:Myo15a	UTSW	11	60,369,238 (GRCm39)	missense	possibly damaging	0.57
R1847:Myo15a	UTSW	11	60,390,321 (GRCm39)	nonsense	probably null
R1875:Myo15a	UTSW	11	60,398,354 (GRCm39)	missense	probably damaging	0.99
R1944:Myo15a	UTSW	11	60,392,909 (GRCm39)	missense	probably damaging	0.99
R1945:Myo15a	UTSW	11	60,392,909 (GRCm39)	missense	probably damaging	0.99
R2013:Myo15a	UTSW	11	60,385,057 (GRCm39)	missense	probably damaging	1.00
R2107:Myo15a	UTSW	11	60,382,636 (GRCm39)	missense	probably damaging	1.00
R2108:Myo15a	UTSW	11	60,382,636 (GRCm39)	missense	probably damaging	1.00
R2112:Myo15a	UTSW	11	60,384,994 (GRCm39)	missense	probably damaging	0.99
R2147:Myo15a	UTSW	11	60,401,055 (GRCm39)	missense	possibly damaging	0.66
R2196:Myo15a	UTSW	11	60,400,847 (GRCm39)	nonsense	probably null
R2245:Myo15a	UTSW	11	60,399,925 (GRCm39)	missense	probably damaging	1.00
R2367:Myo15a	UTSW	11	60,408,064 (GRCm39)	missense	probably damaging	0.99
R2374:Myo15a	UTSW	11	60,369,669 (GRCm39)	missense	possibly damaging	0.88
R2438:Myo15a	UTSW	11	60,373,878 (GRCm39)	missense	probably damaging	1.00
R3154:Myo15a	UTSW	11	60,370,186 (GRCm39)	splice site	probably null
R3423:Myo15a	UTSW	11	60,401,126 (GRCm39)	critical splice donor site	probably null
R3551:Myo15a	UTSW	11	60,400,489 (GRCm39)	missense	possibly damaging	0.93
R3552:Myo15a	UTSW	11	60,400,489 (GRCm39)	missense	possibly damaging	0.93
R3612:Myo15a	UTSW	11	60,368,505 (GRCm39)	missense	probably damaging	1.00
R3620:Myo15a	UTSW	11	60,369,468 (GRCm39)	missense	possibly damaging	0.63
R3713:Myo15a	UTSW	11	60,370,057 (GRCm39)	missense	possibly damaging	0.55
R3714:Myo15a	UTSW	11	60,370,057 (GRCm39)	missense	possibly damaging	0.55
R3715:Myo15a	UTSW	11	60,370,057 (GRCm39)	missense	possibly damaging	0.55
R3783:Myo15a	UTSW	11	60,368,398 (GRCm39)	missense	probably damaging	0.97
R3784:Myo15a	UTSW	11	60,368,398 (GRCm39)	missense	probably damaging	0.97
R3785:Myo15a	UTSW	11	60,368,398 (GRCm39)	missense	probably damaging	0.97
R3786:Myo15a	UTSW	11	60,368,398 (GRCm39)	missense	probably damaging	0.97
R3787:Myo15a	UTSW	11	60,368,398 (GRCm39)	missense	probably damaging	0.97
R3894:Myo15a	UTSW	11	60,395,145 (GRCm39)	missense	probably benign	0.00
R3962:Myo15a	UTSW	11	60,370,654 (GRCm39)	missense	probably benign	0.00
R4082:Myo15a	UTSW	11	60,378,022 (GRCm39)	missense	possibly damaging	0.92
R4555:Myo15a	UTSW	11	60,387,763 (GRCm39)	missense	probably damaging	1.00
R4641:Myo15a	UTSW	11	60,393,867 (GRCm39)	missense	probably damaging	1.00
R4665:Myo15a	UTSW	11	60,395,705 (GRCm39)	critical splice acceptor site	probably null
R4713:Myo15a	UTSW	11	60,370,756 (GRCm39)	missense	probably benign	0.21
R4820:Myo15a	UTSW	11	60,367,741 (GRCm39)	missense	probably damaging	0.98
R5013:Myo15a	UTSW	11	60,382,493 (GRCm39)	missense	probably damaging	1.00
R5051:Myo15a	UTSW	11	60,378,251 (GRCm39)	critical splice donor site	probably null
R5187:Myo15a	UTSW	11	60,394,440 (GRCm39)	missense	probably damaging	1.00
R5230:Myo15a	UTSW	11	60,393,674 (GRCm39)	missense	possibly damaging	0.68
R5277:Myo15a	UTSW	11	60,367,940 (GRCm39)	nonsense	probably null
R5345:Myo15a	UTSW	11	60,388,364 (GRCm39)	missense	probably damaging	0.99
R5349:Myo15a	UTSW	11	60,384,409 (GRCm39)	missense	probably damaging	1.00
R5356:Myo15a	UTSW	11	60,389,192 (GRCm39)	missense	probably damaging	1.00
R5445:Myo15a	UTSW	11	60,411,603 (GRCm39)	nonsense	probably null
R5477:Myo15a	UTSW	11	60,368,503 (GRCm39)	missense	probably damaging	1.00
R5629:Myo15a	UTSW	11	60,370,578 (GRCm39)	missense	probably benign
R5728:Myo15a	UTSW	11	60,379,722 (GRCm39)	missense	probably damaging	1.00
R5818:Myo15a	UTSW	11	60,388,777 (GRCm39)	missense	probably benign	0.06
R5952:Myo15a	UTSW	11	60,370,246 (GRCm39)	missense	possibly damaging	0.50
R6338:Myo15a	UTSW	11	60,368,959 (GRCm39)	missense	probably damaging	0.99
R6467:Myo15a	UTSW	11	60,417,487 (GRCm39)	critical splice donor site	probably null
R6488:Myo15a	UTSW	11	60,369,313 (GRCm39)	missense	possibly damaging	0.86
R6521:Myo15a	UTSW	11	60,393,195 (GRCm39)	missense	probably damaging	1.00
R6645:Myo15a	UTSW	11	60,368,118 (GRCm39)	missense	probably benign	0.00
R6702:Myo15a	UTSW	11	60,383,818 (GRCm39)	missense	probably benign	0.16
R6703:Myo15a	UTSW	11	60,383,818 (GRCm39)	missense	probably benign	0.16
R6821:Myo15a	UTSW	11	60,415,301 (GRCm39)	missense	probably damaging	1.00
R6882:Myo15a	UTSW	11	60,414,832 (GRCm39)	missense	probably damaging	1.00
R6908:Myo15a	UTSW	11	60,396,832 (GRCm39)	missense	probably damaging	1.00
R6932:Myo15a	UTSW	11	60,390,320 (GRCm39)	missense	probably damaging	1.00
R6958:Myo15a	UTSW	11	60,394,451 (GRCm39)	missense	probably benign	0.07
R7041:Myo15a	UTSW	11	60,396,832 (GRCm39)	missense	probably damaging	1.00
R7149:Myo15a	UTSW	11	60,400,836 (GRCm39)	missense	possibly damaging	0.56
R7163:Myo15a	UTSW	11	60,389,195 (GRCm39)	missense
R7229:Myo15a	UTSW	11	60,387,321 (GRCm39)	missense	probably benign	0.08
R7347:Myo15a	UTSW	11	60,368,787 (GRCm39)	missense	probably benign
R7368:Myo15a	UTSW	11	60,381,741 (GRCm39)	splice site	probably null
R7392:Myo15a	UTSW	11	60,396,802 (GRCm39)	missense
R7414:Myo15a	UTSW	11	60,374,309 (GRCm39)	missense
R7461:Myo15a	UTSW	11	60,395,978 (GRCm39)	missense
R7609:Myo15a	UTSW	11	60,379,637 (GRCm39)	missense
R7613:Myo15a	UTSW	11	60,395,978 (GRCm39)	missense
R7734:Myo15a	UTSW	11	60,401,108 (GRCm39)	missense	probably benign
R7748:Myo15a	UTSW	11	60,395,727 (GRCm39)	missense
R7767:Myo15a	UTSW	11	60,392,922 (GRCm39)	missense
R7769:Myo15a	UTSW	11	60,399,975 (GRCm39)	missense
R7894:Myo15a	UTSW	11	60,381,963 (GRCm39)	missense
R7919:Myo15a	UTSW	11	60,417,356 (GRCm39)	missense	probably damaging	1.00
R8100:Myo15a	UTSW	11	60,408,016 (GRCm39)	missense	probably damaging	1.00
R8124:Myo15a	UTSW	11	60,398,279 (GRCm39)	missense
R8129:Myo15a	UTSW	11	60,399,026 (GRCm39)	missense
R8428:Myo15a	UTSW	11	60,387,241 (GRCm39)	missense	probably damaging	1.00
R8706:Myo15a	UTSW	11	60,370,443 (GRCm39)	missense	probably benign
R8735:Myo15a	UTSW	11	60,401,679 (GRCm39)	critical splice acceptor site	probably null
R8739:Myo15a	UTSW	11	60,368,088 (GRCm39)	missense	probably benign	0.06
R8790:Myo15a	UTSW	11	60,378,047 (GRCm39)	missense
R8790:Myo15a	UTSW	11	60,367,362 (GRCm39)	missense	possibly damaging	0.73
R8822:Myo15a	UTSW	11	60,367,740 (GRCm39)	missense	probably damaging	0.99
R8907:Myo15a	UTSW	11	60,417,434 (GRCm39)	missense
R8931:Myo15a	UTSW	11	60,368,020 (GRCm39)	missense	probably benign
R9061:Myo15a	UTSW	11	60,393,692 (GRCm39)	missense
R9124:Myo15a	UTSW	11	60,369,952 (GRCm39)	missense	probably benign	0.37
R9297:Myo15a	UTSW	11	60,385,899 (GRCm39)	missense	probably null
R9347:Myo15a	UTSW	11	60,374,555 (GRCm39)	missense
R9417:Myo15a	UTSW	11	60,378,243 (GRCm39)	missense
R9456:Myo15a	UTSW	11	60,392,668 (GRCm39)	missense
R9460:Myo15a	UTSW	11	60,372,566 (GRCm39)	critical splice donor site	probably null
R9615:Myo15a	UTSW	11	60,374,320 (GRCm39)	missense
R9630:Myo15a	UTSW	11	60,407,988 (GRCm39)	missense	probably damaging	1.00
R9746:Myo15a	UTSW	11	60,378,234 (GRCm39)	nonsense	probably null
X0021:Myo15a	UTSW	11	60,373,185 (GRCm39)	nonsense	probably null
X0066:Myo15a	UTSW	11	60,369,046 (GRCm39)	missense	probably damaging	1.00
X0067:Myo15a	UTSW	11	60,369,444 (GRCm39)	missense	possibly damaging	0.88
Z1176:Myo15a	UTSW	11	60,389,229 (GRCm39)	missense
Z1176:Myo15a	UTSW	11	60,379,084 (GRCm39)	missense
Z1176:Myo15a	UTSW	11	60,415,267 (GRCm39)	missense	probably damaging	1.00
Z1177:Myo15a	UTSW	11	60,386,301 (GRCm39)	missense
Z1177:Myo15a	UTSW	11	60,379,663 (GRCm39)	missense
Z1177:Myo15a	UTSW	11	60,368,349 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACCCTGCTGTACTTCCACAA -3'
(R):5'- GGGTTACCCATCCTTTTGATTG -3'

Sequencing Primer
(F):5'- GCTGTACTTCCACAATACCTCCTG -3'
(R):5'- GATTGGACCTCACCCCCAGATG -3'

Posted On

2014-10-02