Mutagenetix > Incidental Mutation

Incidental Mutation 'R0449:Myo15'

39537

Institutional Source

Beutler Lab

Gene Symbol

Myo15

Ensembl Gene

ENSMUSG00000042678

Gene Name

myosin XV

Synonyms

sh2; sh-2; Myo15a

MMRRC Submission

038649-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0449 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

60469339-60528369 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 60509596 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Threonine at position 2932 (A2932T)

Ref Sequence

ENSEMBL: ENSMUSP00000071777 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000071880
AA Change: A2932T

PolyPhen 2 Score 0.919 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000071777
Gene: ENSMUSG00000042678
AA Change: A2932T

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

possibly damaging
Transcript: ENSMUST00000081823
AA Change: A1727T

PolyPhen 2 Score 0.901 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000080507
Gene: ENSMUSG00000042678
AA Change: A1727T

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

possibly damaging
Transcript: ENSMUST00000094135
AA Change: A2914T

PolyPhen 2 Score 0.901 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000091686
Gene: ENSMUSG00000042678
AA Change: A2914T

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: A1745T

SMART Domains

Protein: ENSMUSP00000120839
Gene: ENSMUSG00000042678
AA Change: A1745T

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: 99.3%
3x: 98.6%
10x: 97.0%
20x: 94.7%

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: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb4	A	T	5: 8,939,885 (GRCm38)	R813*	probably null	Het
Accsl	T	A	2: 93,866,074 (GRCm38)	I60F	probably benign	Het
Adam29	C	T	8: 55,872,681 (GRCm38)	G246D	probably benign	Het
Ankrd13c	A	G	3: 157,991,714 (GRCm38)	I319V	probably benign	Het
B020004J07Rik	T	C	4: 101,836,961 (GRCm38)	S242G	probably benign	Het
Bag6	T	G	17: 35,141,466 (GRCm38)	V327G	probably damaging	Het
Barhl1	C	T	2: 28,915,292 (GRCm38)	A130T	probably benign	Het
Bend4	T	C	5: 67,398,240 (GRCm38)	D541G	probably damaging	Het
Birc6	A	C	17: 74,692,295 (GRCm38)	T4673P	probably damaging	Het
Ccdc81	T	C	7: 89,890,471 (GRCm38)	R186G	probably damaging	Het
Cdyl2	A	G	8: 116,583,192 (GRCm38)	F342L	probably damaging	Het
Chd3	C	A	11: 69,357,541 (GRCm38)	V748L	probably damaging	Het
CN725425	G	T	15: 91,238,944 (GRCm38)	R72I	possibly damaging	Het
Col22a1	A	G	15: 71,962,671 (GRCm38)		probably null	Het
Cops3	A	G	11: 59,818,417 (GRCm38)		probably null	Het
Ctnnd1	G	T	2: 84,603,262 (GRCm38)	Q940K	possibly damaging	Het
Dtnb	C	T	12: 3,591,971 (GRCm38)	Q45*	probably null	Het
Efr3a	T	A	15: 65,842,704 (GRCm38)	I280K	probably damaging	Het
Eml6	A	C	11: 29,893,213 (GRCm38)	V167G	probably benign	Het
Fam83c	T	A	2: 155,830,295 (GRCm38)	M407L	probably benign	Het
Fasn	T	C	11: 120,811,068 (GRCm38)	T1862A	probably benign	Het
Fbxl6	A	G	15: 76,535,955 (GRCm38)	I486T	probably damaging	Het
Gpr182	A	G	10: 127,750,696 (GRCm38)	Y129H	probably damaging	Het
Gpr75	A	G	11: 30,892,456 (GRCm38)	S454G	probably damaging	Het
Hectd4	G	A	5: 121,364,590 (GRCm38)		probably null	Het
Hsf4	A	G	8: 105,275,590 (GRCm38)	T411A	probably benign	Het
Hsh2d	G	A	8: 72,200,460 (GRCm38)	D229N	probably benign	Het
Il4	A	T	11: 53,618,605 (GRCm38)	M1K	probably null	Het
Ints11	G	T	4: 155,887,948 (GRCm38)	R463L	probably benign	Het
Ints4	G	A	7: 97,529,223 (GRCm38)	E677K	probably damaging	Het
Klk1b11	G	A	7: 43,997,792 (GRCm38)	C50Y	probably damaging	Het
Krt14	C	A	11: 100,207,395 (GRCm38)	G21C	unknown	Het
Krt81	C	A	15: 101,463,627 (GRCm38)	R24L	possibly damaging	Het
L3mbtl2	C	T	15: 81,668,741 (GRCm38)	A125V	probably damaging	Het
Lama3	A	G	18: 12,500,512 (GRCm38)		probably null	Het
Lrrk2	T	C	15: 91,750,275 (GRCm38)	L1414P	probably damaging	Het
Matn2	T	C	15: 34,428,541 (GRCm38)	S684P	probably damaging	Het
Mga	T	A	2: 119,941,381 (GRCm38)	V1574D	probably damaging	Het
Mia2	T	C	12: 59,172,594 (GRCm38)		probably null	Het
Mrpl21	T	A	19: 3,292,459 (GRCm38)		probably benign	Het
Msh5	T	A	17: 35,041,482 (GRCm38)	Q266L	probably benign	Het
Mybpc1	C	A	10: 88,540,960 (GRCm38)	C758F	probably damaging	Het
Nbas	T	A	12: 13,519,108 (GRCm38)	I2021K	probably benign	Het
Neurl4	T	C	11: 69,905,567 (GRCm38)	S424P	probably damaging	Het
Olfr16	T	A	1: 172,957,398 (GRCm38)	V201E	probably damaging	Het
Olfr322	A	C	11: 58,665,963 (GRCm38)	I135L	probably benign	Het
Olfr782	A	G	10: 129,351,234 (GRCm38)	M224V	probably benign	Het
Olfr829	T	C	9: 18,856,649 (GRCm38)	M8T	probably benign	Het
Olfr850	T	A	9: 19,478,092 (GRCm38)	I53F	possibly damaging	Het
Phlpp1	C	T	1: 106,350,578 (GRCm38)	R907W	probably damaging	Het
Pigg	T	C	5: 108,336,411 (GRCm38)	V508A	probably benign	Het
Pkhd1l1	T	G	15: 44,501,519 (GRCm38)	Y685D	probably damaging	Het
Polr3a	A	T	14: 24,484,466 (GRCm38)	I34N	probably damaging	Het
Prex1	A	G	2: 166,569,377 (GRCm38)	V1434A	probably benign	Het
Ptprh	T	A	7: 4,598,006 (GRCm38)	D124V	probably damaging	Het
Rad54b	T	A	4: 11,606,131 (GRCm38)	I513N	probably benign	Het
Rbm12b1	A	G	4: 12,145,507 (GRCm38)	N493S	probably benign	Het
Rfx7	A	T	9: 72,610,304 (GRCm38)		probably null	Het
Serpini1	A	G	3: 75,613,341 (GRCm38)	K82E	probably benign	Het
Slc27a6	T	G	18: 58,609,165 (GRCm38)		probably null	Het
Slc35f2	G	T	9: 53,816,917 (GRCm38)	L358F	probably damaging	Het
Slc45a1	A	C	4: 150,643,305 (GRCm38)	I158M	probably damaging	Het
Slurp2	G	A	15: 74,743,106 (GRCm38)	P62L	probably damaging	Het
Sspo	C	T	6: 48,466,740 (GRCm38)	H1949Y	probably damaging	Het
Tiam1	A	T	16: 89,837,827 (GRCm38)	V865E	possibly damaging	Het
Tlr4	A	C	4: 66,839,620 (GRCm38)	I217L	probably damaging	Het
Top1	C	T	2: 160,712,708 (GRCm38)	R460*	probably null	Het
Trpm3	T	A	19: 22,988,054 (GRCm38)	S1638T	probably benign	Het
Tubgcp5	C	T	7: 55,823,567 (GRCm38)	R798C	probably benign	Het
Vars	T	G	17: 35,012,727 (GRCm38)		probably null	Het
Xylt2	A	G	11: 94,666,333 (GRCm38)	Y111H	probably benign	Het
Zbed5	G	A	5: 129,901,726 (GRCm38)	G172D	probably damaging	Het
Zfp53	C	T	17: 21,508,833 (GRCm38)	T376I	probably benign	Het
Zfp937	G	T	2: 150,239,546 (GRCm38)	V499L	probably benign	Het
Zyx	T	A	6: 42,351,313 (GRCm38)	L152Q	probably damaging	Het

Other mutations in Myo15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00845:Myo15	APN	11	60,477,779 (GRCm38)	missense	probably damaging	1.00
IGL01011:Myo15	APN	11	60,476,992 (GRCm38)	missense	probably benign	0.33
IGL01100:Myo15	APN	11	60,511,158 (GRCm38)	missense	probably damaging	1.00
IGL01357:Myo15	APN	11	60,502,289 (GRCm38)	splice site	probably benign
IGL01634:Myo15	APN	11	60,495,472 (GRCm38)	missense	probably damaging	1.00
IGL01763:Myo15	APN	11	60,521,738 (GRCm38)	missense	probably benign	0.07
IGL01901:Myo15	APN	11	60,527,434 (GRCm38)	utr 3 prime	probably benign
IGL01931:Myo15	APN	11	60,496,138 (GRCm38)	missense	probably damaging	1.00
IGL02006:Myo15	APN	11	60,511,128 (GRCm38)	missense	probably damaging	1.00
IGL02041:Myo15	APN	11	60,506,863 (GRCm38)	missense	probably damaging	0.99
IGL02094:Myo15	APN	11	60,510,647 (GRCm38)	unclassified	probably benign
IGL02122:Myo15	APN	11	60,483,466 (GRCm38)	missense	probably benign	0.23
IGL02153:Myo15	APN	11	60,498,397 (GRCm38)	missense	probably damaging	1.00
IGL02328:Myo15	APN	11	60,526,607 (GRCm38)	missense	probably benign	0.13
IGL02330:Myo15	APN	11	60,477,161 (GRCm38)	missense	possibly damaging	0.94
IGL02431:Myo15	APN	11	60,510,639 (GRCm38)	missense	possibly damaging	0.73
IGL02639:Myo15	APN	11	60,478,621 (GRCm38)	missense	probably benign
IGL02659:Myo15	APN	11	60,491,783 (GRCm38)	splice site	probably benign
IGL02800:Myo15	APN	11	60,502,369 (GRCm38)	missense	probably damaging	1.00
IGL02812:Myo15	APN	11	60,477,179 (GRCm38)	missense	probably benign	0.15
IGL02863:Myo15	APN	11	60,478,127 (GRCm38)	missense	probably damaging	1.00
IGL02873:Myo15	APN	11	60,483,482 (GRCm38)	missense	probably damaging	1.00
IGL02990:Myo15	APN	11	60,479,440 (GRCm38)	missense	probably benign	0.02
IGL03011:Myo15	APN	11	60,509,531 (GRCm38)	splice site	probably benign
IGL03243:Myo15	APN	11	60,496,518 (GRCm38)	missense	probably damaging	1.00
IGL03297:Myo15	APN	11	60,479,141 (GRCm38)	missense	probably damaging	1.00
novichok	UTSW	11	60,481,740 (GRCm38)	critical splice donor site	probably null
parker	UTSW	11	60,520,914 (GRCm38)	critical splice donor site	probably null
Typhoon	UTSW	11	60,487,425 (GRCm38)	critical splice donor site	probably null
PIT4131001:Myo15	UTSW	11	60,495,454 (GRCm38)	missense	probably damaging	1.00
PIT4131001:Myo15	UTSW	11	60,483,127 (GRCm38)	missense	probably damaging	1.00
R0133:Myo15	UTSW	11	60,477,850 (GRCm38)	missense	possibly damaging	0.94
R0265:Myo15	UTSW	11	60,514,897 (GRCm38)	critical splice acceptor site	probably null
R0389:Myo15	UTSW	11	60,478,538 (GRCm38)	missense	probably benign
R0416:Myo15	UTSW	11	60,511,174 (GRCm38)	missense	probably damaging	1.00
R0477:Myo15	UTSW	11	60,520,914 (GRCm38)	critical splice donor site	probably null
R0543:Myo15	UTSW	11	60,479,051 (GRCm38)	missense	probably benign
R0546:Myo15	UTSW	11	60,506,313 (GRCm38)	missense	probably damaging	1.00
R0555:Myo15	UTSW	11	60,521,638 (GRCm38)	missense	probably damaging	1.00
R0639:Myo15	UTSW	11	60,479,336 (GRCm38)	missense	probably benign	0.12
R0723:Myo15	UTSW	11	60,478,977 (GRCm38)	missense	possibly damaging	0.94
R0837:Myo15	UTSW	11	60,487,251 (GRCm38)	missense	probably damaging	0.98
R0865:Myo15	UTSW	11	60,491,688 (GRCm38)	missense	probably damaging	1.00
R0899:Myo15	UTSW	11	60,477,185 (GRCm38)	missense	possibly damaging	0.87
R1022:Myo15	UTSW	11	60,479,616 (GRCm38)	missense	probably benign	0.00
R1024:Myo15	UTSW	11	60,479,616 (GRCm38)	missense	probably benign	0.00
R1035:Myo15	UTSW	11	60,510,558 (GRCm38)	unclassified	probably benign
R1109:Myo15	UTSW	11	60,493,066 (GRCm38)	missense	probably damaging	1.00
R1170:Myo15	UTSW	11	60,479,407 (GRCm38)	missense	probably benign	0.04
R1241:Myo15	UTSW	11	60,499,430 (GRCm38)	missense	possibly damaging	0.58
R1392:Myo15	UTSW	11	60,477,974 (GRCm38)	missense	possibly damaging	0.95
R1392:Myo15	UTSW	11	60,477,974 (GRCm38)	missense	possibly damaging	0.95
R1434:Myo15	UTSW	11	60,504,331 (GRCm38)	missense	probably benign	0.00
R1450:Myo15	UTSW	11	60,495,482 (GRCm38)	missense	probably damaging	1.00
R1456:Myo15	UTSW	11	60,508,202 (GRCm38)	missense	probably damaging	1.00
R1468:Myo15	UTSW	11	60,506,006 (GRCm38)	missense	probably damaging	1.00
R1468:Myo15	UTSW	11	60,506,006 (GRCm38)	missense	probably damaging	1.00
R1548:Myo15	UTSW	11	60,488,238 (GRCm38)	missense	probably damaging	1.00
R1551:Myo15	UTSW	11	60,492,965 (GRCm38)	missense	possibly damaging	0.70
R1571:Myo15	UTSW	11	60,518,464 (GRCm38)	missense	probably damaging	1.00
R1662:Myo15	UTSW	11	60,501,701 (GRCm38)	missense	probably damaging	1.00
R1777:Myo15	UTSW	11	60,514,936 (GRCm38)	missense	probably benign
R1778:Myo15	UTSW	11	60,478,412 (GRCm38)	missense	possibly damaging	0.57
R1847:Myo15	UTSW	11	60,499,495 (GRCm38)	nonsense	probably null
R1875:Myo15	UTSW	11	60,507,528 (GRCm38)	missense	probably damaging	0.99
R1944:Myo15	UTSW	11	60,502,083 (GRCm38)	missense	probably damaging	0.99
R1945:Myo15	UTSW	11	60,502,083 (GRCm38)	missense	probably damaging	0.99
R2013:Myo15	UTSW	11	60,494,231 (GRCm38)	missense	probably damaging	1.00
R2107:Myo15	UTSW	11	60,491,810 (GRCm38)	missense	probably damaging	1.00
R2108:Myo15	UTSW	11	60,491,810 (GRCm38)	missense	probably damaging	1.00
R2112:Myo15	UTSW	11	60,494,168 (GRCm38)	missense	probably damaging	0.99
R2147:Myo15	UTSW	11	60,510,229 (GRCm38)	missense	possibly damaging	0.66
R2196:Myo15	UTSW	11	60,510,021 (GRCm38)	nonsense	probably null
R2207:Myo15	UTSW	11	60,506,034 (GRCm38)	missense	probably benign	0.01
R2245:Myo15	UTSW	11	60,509,099 (GRCm38)	missense	probably damaging	1.00
R2367:Myo15	UTSW	11	60,517,238 (GRCm38)	missense	probably damaging	0.99
R2374:Myo15	UTSW	11	60,478,843 (GRCm38)	missense	possibly damaging	0.88
R2438:Myo15	UTSW	11	60,483,052 (GRCm38)	missense	probably damaging	1.00
R3154:Myo15	UTSW	11	60,479,360 (GRCm38)	splice site	probably null
R3423:Myo15	UTSW	11	60,510,300 (GRCm38)	critical splice donor site	probably null
R3551:Myo15	UTSW	11	60,509,663 (GRCm38)	missense	possibly damaging	0.93
R3552:Myo15	UTSW	11	60,509,663 (GRCm38)	missense	possibly damaging	0.93
R3612:Myo15	UTSW	11	60,477,679 (GRCm38)	missense	probably damaging	1.00
R3620:Myo15	UTSW	11	60,478,642 (GRCm38)	missense	possibly damaging	0.63
R3713:Myo15	UTSW	11	60,479,231 (GRCm38)	missense	possibly damaging	0.55
R3714:Myo15	UTSW	11	60,479,231 (GRCm38)	missense	possibly damaging	0.55
R3715:Myo15	UTSW	11	60,479,231 (GRCm38)	missense	possibly damaging	0.55
R3783:Myo15	UTSW	11	60,477,572 (GRCm38)	missense	probably damaging	0.97
R3784:Myo15	UTSW	11	60,477,572 (GRCm38)	missense	probably damaging	0.97
R3785:Myo15	UTSW	11	60,477,572 (GRCm38)	missense	probably damaging	0.97
R3786:Myo15	UTSW	11	60,477,572 (GRCm38)	missense	probably damaging	0.97
R3787:Myo15	UTSW	11	60,477,572 (GRCm38)	missense	probably damaging	0.97
R3894:Myo15	UTSW	11	60,504,319 (GRCm38)	missense	probably benign	0.00
R3962:Myo15	UTSW	11	60,479,828 (GRCm38)	missense	probably benign	0.00
R4082:Myo15	UTSW	11	60,487,196 (GRCm38)	missense	possibly damaging	0.92
R4555:Myo15	UTSW	11	60,496,937 (GRCm38)	missense	probably damaging	1.00
R4641:Myo15	UTSW	11	60,503,041 (GRCm38)	missense	probably damaging	1.00
R4665:Myo15	UTSW	11	60,504,879 (GRCm38)	critical splice acceptor site	probably null
R4713:Myo15	UTSW	11	60,479,930 (GRCm38)	missense	probably benign	0.21
R4820:Myo15	UTSW	11	60,476,915 (GRCm38)	missense	probably damaging	0.98
R5013:Myo15	UTSW	11	60,491,667 (GRCm38)	missense	probably damaging	1.00
R5051:Myo15	UTSW	11	60,487,425 (GRCm38)	critical splice donor site	probably null
R5187:Myo15	UTSW	11	60,503,614 (GRCm38)	missense	probably damaging	1.00
R5230:Myo15	UTSW	11	60,502,848 (GRCm38)	missense	possibly damaging	0.68
R5277:Myo15	UTSW	11	60,477,114 (GRCm38)	nonsense	probably null
R5345:Myo15	UTSW	11	60,497,538 (GRCm38)	missense	probably damaging	0.99
R5349:Myo15	UTSW	11	60,493,583 (GRCm38)	missense	probably damaging	1.00
R5356:Myo15	UTSW	11	60,498,366 (GRCm38)	missense	probably damaging	1.00
R5445:Myo15	UTSW	11	60,520,777 (GRCm38)	nonsense	probably null
R5477:Myo15	UTSW	11	60,477,677 (GRCm38)	missense	probably damaging	1.00
R5629:Myo15	UTSW	11	60,479,752 (GRCm38)	missense	probably benign
R5728:Myo15	UTSW	11	60,488,896 (GRCm38)	missense	probably damaging	1.00
R5818:Myo15	UTSW	11	60,497,951 (GRCm38)	missense	probably benign	0.06
R5952:Myo15	UTSW	11	60,479,420 (GRCm38)	missense	possibly damaging	0.50
R6338:Myo15	UTSW	11	60,478,133 (GRCm38)	missense	probably damaging	0.99
R6467:Myo15	UTSW	11	60,526,661 (GRCm38)	critical splice donor site	probably null
R6488:Myo15	UTSW	11	60,478,487 (GRCm38)	missense	possibly damaging	0.86
R6521:Myo15	UTSW	11	60,502,369 (GRCm38)	missense	probably damaging	1.00
R6645:Myo15	UTSW	11	60,477,292 (GRCm38)	missense	probably benign	0.00
R6702:Myo15	UTSW	11	60,492,992 (GRCm38)	missense	probably benign	0.16
R6703:Myo15	UTSW	11	60,492,992 (GRCm38)	missense	probably benign	0.16
R6821:Myo15	UTSW	11	60,524,475 (GRCm38)	missense	probably damaging	1.00
R6882:Myo15	UTSW	11	60,524,006 (GRCm38)	missense	probably damaging	1.00
R6908:Myo15	UTSW	11	60,506,006 (GRCm38)	missense	probably damaging	1.00
R6932:Myo15	UTSW	11	60,499,494 (GRCm38)	missense	probably damaging	1.00
R6958:Myo15	UTSW	11	60,503,625 (GRCm38)	missense	probably benign	0.07
R7041:Myo15	UTSW	11	60,506,006 (GRCm38)	missense	probably damaging	1.00
R7149:Myo15	UTSW	11	60,510,010 (GRCm38)	missense	possibly damaging	0.56
R7163:Myo15	UTSW	11	60,498,369 (GRCm38)	missense
R7229:Myo15	UTSW	11	60,496,495 (GRCm38)	missense	probably benign	0.08
R7347:Myo15	UTSW	11	60,477,961 (GRCm38)	missense	probably benign
R7368:Myo15	UTSW	11	60,490,915 (GRCm38)	splice site	probably null
R7392:Myo15	UTSW	11	60,505,976 (GRCm38)	missense
R7414:Myo15	UTSW	11	60,483,483 (GRCm38)	missense
R7461:Myo15	UTSW	11	60,505,152 (GRCm38)	missense
R7609:Myo15	UTSW	11	60,488,811 (GRCm38)	missense
R7613:Myo15	UTSW	11	60,505,152 (GRCm38)	missense
R7734:Myo15	UTSW	11	60,510,282 (GRCm38)	missense	probably benign
R7748:Myo15	UTSW	11	60,504,901 (GRCm38)	missense
R7767:Myo15	UTSW	11	60,502,096 (GRCm38)	missense
R7769:Myo15	UTSW	11	60,509,149 (GRCm38)	missense
R7894:Myo15	UTSW	11	60,491,137 (GRCm38)	missense
R7919:Myo15	UTSW	11	60,526,530 (GRCm38)	missense	probably damaging	1.00
R8100:Myo15	UTSW	11	60,517,190 (GRCm38)	missense	probably damaging	1.00
R8124:Myo15	UTSW	11	60,507,453 (GRCm38)	missense
R8129:Myo15	UTSW	11	60,508,200 (GRCm38)	missense
R8428:Myo15	UTSW	11	60,496,415 (GRCm38)	missense	probably damaging	1.00
R8706:Myo15	UTSW	11	60,479,617 (GRCm38)	missense	probably benign
R8735:Myo15	UTSW	11	60,510,853 (GRCm38)	critical splice acceptor site	probably null
R8739:Myo15	UTSW	11	60,477,262 (GRCm38)	missense	probably benign	0.06
R8790:Myo15	UTSW	11	60,487,221 (GRCm38)	missense
R8790:Myo15	UTSW	11	60,476,536 (GRCm38)	missense	possibly damaging	0.73
R8822:Myo15	UTSW	11	60,476,914 (GRCm38)	missense	probably damaging	0.99
R8907:Myo15	UTSW	11	60,526,608 (GRCm38)	missense
R8931:Myo15	UTSW	11	60,477,194 (GRCm38)	missense	probably benign
R9061:Myo15	UTSW	11	60,502,866 (GRCm38)	missense
R9124:Myo15	UTSW	11	60,479,126 (GRCm38)	missense	probably benign	0.37
R9297:Myo15	UTSW	11	60,495,073 (GRCm38)	missense	probably null
R9347:Myo15	UTSW	11	60,483,729 (GRCm38)	missense
R9417:Myo15	UTSW	11	60,487,417 (GRCm38)	missense
R9456:Myo15	UTSW	11	60,501,842 (GRCm38)	missense
R9460:Myo15	UTSW	11	60,481,740 (GRCm38)	critical splice donor site	probably null
R9615:Myo15	UTSW	11	60,483,494 (GRCm38)	missense
R9630:Myo15	UTSW	11	60,517,162 (GRCm38)	missense	probably damaging	1.00
R9746:Myo15	UTSW	11	60,487,408 (GRCm38)	nonsense	probably null
X0021:Myo15	UTSW	11	60,482,359 (GRCm38)	nonsense	probably null
X0066:Myo15	UTSW	11	60,478,220 (GRCm38)	missense	probably damaging	1.00
X0067:Myo15	UTSW	11	60,478,618 (GRCm38)	missense	possibly damaging	0.88
Z1176:Myo15	UTSW	11	60,498,403 (GRCm38)	missense
Z1176:Myo15	UTSW	11	60,488,258 (GRCm38)	missense
Z1176:Myo15	UTSW	11	60,524,441 (GRCm38)	missense	probably damaging	1.00
Z1177:Myo15	UTSW	11	60,495,475 (GRCm38)	missense
Z1177:Myo15	UTSW	11	60,488,837 (GRCm38)	missense
Z1177:Myo15	UTSW	11	60,477,523 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TATGGCCTGTTGCTCTTGGCAC -3'
(R):5'- TGCATAGGATTGGCTGCATCCAC -3'

Sequencing Primer
(F):5'- aacaaaacaaaacaaacaaaaAACCC -3'
(R):5'- CTGCATCCACGGATGGC -3'

Posted On

2013-05-23