Mutagenetix > Incidental Mutation

Incidental Mutation 'R4965:Cmya5'

383955

Institutional Source

Beutler Lab

Gene Symbol

Cmya5

Ensembl Gene

ENSMUSG00000047419

Gene Name

cardiomyopathy associated 5

Synonyms

Myospryn, 2310076E16Rik, 2310076E21Rik

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.303) question?

Stock #

R4965 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

93177221-93281232 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 93232295 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 931 (T931I)

Ref Sequence

ENSEMBL: ENSMUSP00000050408 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062122]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000062122
AA Change: T931I

PolyPhen 2 Score 0.838 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: T931I

Domain	Start	End	E-Value	Type
low complexity region	20	46	N/A	INTRINSIC
low complexity region	129	140	N/A	INTRINSIC
internal_repeat_1	448	535	5.09e-18	PROSPERO
internal_repeat_1	543	625	5.09e-18	PROSPERO
low complexity region	626	645	N/A	INTRINSIC
low complexity region	679	691	N/A	INTRINSIC
low complexity region	734	741	N/A	INTRINSIC
low complexity region	1001	1010	N/A	INTRINSIC
low complexity region	1166	1183	N/A	INTRINSIC
low complexity region	1259	1267	N/A	INTRINSIC
low complexity region	1440	1449	N/A	INTRINSIC
low complexity region	1876	1889	N/A	INTRINSIC
low complexity region	2632	2645	N/A	INTRINSIC
low complexity region	3048	3057	N/A	INTRINSIC
FN3	3312	3399	7.29e-4	SMART
FN3	3411	3492	1.3e0	SMART
Pfam:SPRY	3551	3668	6.7e-8	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224009

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 95.7%
20x: 90.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 117 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	A	G	3: 137,775,433 (GRCm39)	T1541A	probably benign	Het
9530002B09Rik	T	C	4: 122,594,285 (GRCm39)	M59T	probably benign	Het
Adam18	C	T	8: 25,131,827 (GRCm39)	C428Y	probably damaging	Het
Adcy5	A	G	16: 35,098,872 (GRCm39)	E700G	possibly damaging	Het
Adprh	G	T	16: 38,266,142 (GRCm39)	Y333*	probably null	Het
Agfg2	C	A	5: 137,665,439 (GRCm39)		probably null	Het
Akip1	A	T	7: 109,310,961 (GRCm39)	E167V	probably damaging	Het
Akr1c21	A	T	13: 4,630,304 (GRCm39)	Q199L	probably damaging	Het
Aldh9a1	C	A	1: 167,193,358 (GRCm39)	A455E	probably damaging	Het
Amph	G	A	13: 19,321,869 (GRCm39)	S520N	probably benign	Het
Ankrd52	A	G	10: 128,226,376 (GRCm39)	D1006G	probably benign	Het
Ap5z1	A	C	5: 142,453,431 (GRCm39)	Q133P	probably damaging	Het
Babam1	C	T	8: 71,857,032 (GRCm39)	A331V	possibly damaging	Het
Btc	T	C	5: 91,510,160 (GRCm39)		probably null	Het
Cacna2d3	A	G	14: 28,704,289 (GRCm39)	F831L	probably benign	Het
Cadm3	G	A	1: 173,164,664 (GRCm39)	P372L	probably damaging	Het
Capn5	A	T	7: 97,775,624 (GRCm39)	M439K	probably damaging	Het
Carf	T	C	1: 60,189,796 (GRCm39)	S639P	probably damaging	Het
Casp12	C	T	9: 5,352,250 (GRCm39)	R81C	probably benign	Het
Ces2e	G	T	8: 105,660,330 (GRCm39)	R555M	probably benign	Het
Cfap54	T	A	10: 92,902,661 (GRCm39)	I164F	probably benign	Het
Cltc	C	T	11: 86,598,327 (GRCm39)	V1012I	probably damaging	Het
Cntn6	A	G	6: 104,751,435 (GRCm39)	I364V	probably damaging	Het
Cntnap1	A	T	11: 101,068,251 (GRCm39)	I59F	possibly damaging	Het
Cop1	T	C	1: 159,067,167 (GRCm39)	M80T	probably damaging	Het
Cplx2	A	G	13: 54,527,460 (GRCm39)	S115G	possibly damaging	Het
Crtac1	A	G	19: 42,307,179 (GRCm39)	Y195H	probably damaging	Het
Csn1s2a	A	C	5: 87,929,697 (GRCm39)	S99R	possibly damaging	Het
Csn1s2b	T	A	5: 87,961,820 (GRCm39)	D41E	possibly damaging	Het
Cul9	C	T	17: 46,849,451 (GRCm39)	D565N	probably damaging	Het
Cux1	A	T	5: 136,340,410 (GRCm39)	N625K	possibly damaging	Het
Cyp2c37	A	T	19: 40,000,206 (GRCm39)	M443L	possibly damaging	Het
Cyp2s1	G	A	7: 25,508,710 (GRCm39)	T244I	possibly damaging	Het
Dgkh	C	T	14: 78,861,861 (GRCm39)	V135M	probably damaging	Het
Dtl	T	C	1: 191,278,677 (GRCm39)	E395G	possibly damaging	Het
Dyrk1a	G	T	16: 94,492,854 (GRCm39)	G658*	probably null	Het
Erlin2	T	C	8: 27,519,623 (GRCm39)	F117S	probably damaging	Het
Fkbp8	A	G	8: 70,984,173 (GRCm39)		probably null	Het
Fras1	T	C	5: 96,874,439 (GRCm39)	F2288S	possibly damaging	Het
Frmd3	A	G	4: 74,071,837 (GRCm39)	T240A	probably damaging	Het
H2-D1	A	G	17: 35,482,881 (GRCm39)	Y137C	probably damaging	Het
Helz2	A	G	2: 180,882,709 (GRCm39)	V28A	possibly damaging	Het
Hydin	A	G	8: 111,124,727 (GRCm39)	I579V	probably benign	Het
Il6	A	T	5: 30,218,491 (GRCm39)	Y29F	possibly damaging	Het
Ildr2	A	G	1: 166,135,409 (GRCm39)	D368G	probably damaging	Het
Junb	T	A	8: 85,704,788 (GRCm39)	I91F	probably damaging	Het
Kat2a	C	A	11: 100,603,029 (GRCm39)		probably benign	Het
Kat2a	A	T	11: 100,603,030 (GRCm39)		probably benign	Het
Kcnh5	T	A	12: 75,011,925 (GRCm39)	T665S	probably benign	Het
Kdm1b	A	T	13: 47,227,843 (GRCm39)	D608V	probably damaging	Het
Krcc1	A	G	6: 71,261,621 (GRCm39)	K218E	probably damaging	Het
Krt8	C	T	15: 101,905,386 (GRCm39)	V488M	probably benign	Het
Lzts1	C	T	8: 69,591,414 (GRCm39)	A245T	probably benign	Het
Mcm6	T	A	1: 128,287,223 (GRCm39)	Q27L	probably damaging	Het
Mfsd4b3-ps	G	T	10: 39,823,686 (GRCm39)	Y191*	probably null	Het
Mgme1	T	C	2: 144,121,540 (GRCm39)	L332P	probably benign	Het
Mgme1	C	T	2: 144,118,324 (GRCm39)	Q199*	probably null	Het
Morc3	G	T	16: 93,657,475 (GRCm39)	E25*	probably null	Het
Mroh7	G	A	4: 106,548,184 (GRCm39)	A1098V	possibly damaging	Het
Mtrf1	G	A	14: 79,644,027 (GRCm39)	R174H	probably benign	Het
Mybpc3	G	A	2: 90,949,592 (GRCm39)	G45D	possibly damaging	Het
Mycbpap	A	T	11: 94,395,764 (GRCm39)	N733K	probably damaging	Het
N4bp1	T	C	8: 87,578,314 (GRCm39)	I684V	possibly damaging	Het
Nav2	A	T	7: 49,202,625 (GRCm39)	R1470*	probably null	Het
Ndufa9	A	T	6: 126,799,026 (GRCm39)	S364T	probably benign	Het
Nipal4	C	A	11: 46,052,837 (GRCm39)	A43S	possibly damaging	Het
Nlrp1a	T	A	11: 70,983,141 (GRCm39)	Y1275F	possibly damaging	Het
Nova1	A	T	12: 46,767,618 (GRCm39)	L8*	probably null	Het
Odam	G	T	5: 88,037,967 (GRCm39)	G181*	probably null	Het
Optn	T	A	2: 5,026,190 (GRCm39)	Q576L	probably benign	Het
Or2c1	T	C	16: 3,657,434 (GRCm39)	L199P	probably damaging	Het
Or4k47	T	C	2: 111,451,879 (GRCm39)	D180G	probably damaging	Het
Or4l1	C	T	14: 50,166,354 (GRCm39)	V216I	probably benign	Het
Or51a39	A	T	7: 102,362,702 (GRCm39)	I306N	probably damaging	Het
Or5as1	T	A	2: 86,981,003 (GRCm39)	M1L	possibly damaging	Het
Or5h18	A	T	16: 58,847,696 (GRCm39)	D191E	probably damaging	Het
Or8s2	T	C	15: 98,277,030 (GRCm39)		probably benign	Het
Patl2	G	T	2: 121,959,329 (GRCm39)	S45*	probably null	Het
Pde2a	G	A	7: 101,152,140 (GRCm39)	G349E	probably benign	Het
Pdlim2	T	A	14: 70,405,464 (GRCm39)		probably benign	Het
Per1	T	C	11: 68,995,227 (GRCm39)	V653A	probably benign	Het
Phlda2	A	G	7: 143,056,005 (GRCm39)	S75P	probably damaging	Het
Poldip3	A	T	15: 83,021,706 (GRCm39)	M167K	possibly damaging	Het
Potegl	C	A	2: 23,135,127 (GRCm39)	T312K	probably benign	Het
Prpf38a	T	C	4: 108,436,278 (GRCm39)	I12V	probably benign	Het
Prrc1	G	A	18: 57,507,622 (GRCm39)	V259I	possibly damaging	Het
Ptges3l	A	T	11: 101,315,448 (GRCm39)	M1K	probably null	Het
Rdh5	A	G	10: 128,749,653 (GRCm39)	Y296H	probably damaging	Het
Resf1	G	T	6: 149,229,896 (GRCm39)	G981*	probably null	Het
Rnf2	T	A	1: 151,348,968 (GRCm39)	K51*	probably null	Het
Rpusd3	C	A	6: 113,393,809 (GRCm39)	R215L	probably benign	Het
Rsph4a	A	T	10: 33,785,236 (GRCm39)	E382D	probably damaging	Het
S1pr2	G	A	9: 20,879,745 (GRCm39)	Q28*	probably null	Het
Sesn1	A	T	10: 41,771,005 (GRCm39)	I179F	probably damaging	Het
Setd3	T	A	12: 108,079,630 (GRCm39)	E291V	probably benign	Het
Shc1	G	T	3: 89,334,303 (GRCm39)	R323L	probably damaging	Het
Slc22a5	T	C	11: 53,782,352 (GRCm39)	D5G	possibly damaging	Het
Slc6a19	T	C	13: 73,848,677 (GRCm39)	K26E	probably benign	Het
Slc9a3	A	G	13: 74,312,412 (GRCm39)	N670D	possibly damaging	Het
Spata19	A	T	9: 27,311,761 (GRCm39)	I127L	probably benign	Het
Speg	G	T	1: 75,404,347 (GRCm39)	V2751L	probably damaging	Het
Sptbn2	A	G	19: 4,779,337 (GRCm39)	D298G	probably benign	Het
Srm	T	C	4: 148,678,640 (GRCm39)	V289A	possibly damaging	Het
Stip1	C	T	19: 7,012,938 (GRCm39)	A49T	probably benign	Het
Tas2r118	C	A	6: 23,969,627 (GRCm39)	V145F	probably benign	Het
Tbc1d12	A	T	19: 38,854,169 (GRCm39)	K284*	probably null	Het
Tfcp2	T	C	15: 100,423,531 (GRCm39)	H125R	probably damaging	Het
Tfdp1	T	C	8: 13,423,073 (GRCm39)	V206A	probably damaging	Het
Tgtp2	A	G	11: 48,950,237 (GRCm39)	W112R	probably damaging	Het
Tmem71	T	G	15: 66,410,710 (GRCm39)	M221L	probably benign	Het
Tpcn1	T	C	5: 120,685,552 (GRCm39)	N436S	possibly damaging	Het
Usp4	C	T	9: 108,239,819 (GRCm39)	L183F	probably damaging	Het
Vmn2r55	A	T	7: 12,404,478 (GRCm39)	N308K	possibly damaging	Het
Zfp106	T	A	2: 120,364,400 (GRCm39)	D669V	probably damaging	Het
Zfp108	A	T	7: 23,959,573 (GRCm39)	I55L	probably benign	Het
Zfp512b	A	T	2: 181,228,131 (GRCm39)	S8R	probably damaging	Het
Zfp827	T	C	8: 79,787,910 (GRCm39)	S359P	probably benign	Het

Other mutations in Cmya5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00489:Cmya5	APN	13	93,229,628 (GRCm39)	missense	probably benign	0.13
IGL00516:Cmya5	APN	13	93,234,675 (GRCm39)	missense	possibly damaging	0.73
IGL00654:Cmya5	APN	13	93,230,669 (GRCm39)	missense	probably benign	0.00
IGL00948:Cmya5	APN	13	93,227,544 (GRCm39)	missense	probably benign
IGL00966:Cmya5	APN	13	93,234,414 (GRCm39)	missense	probably benign	0.33
IGL00988:Cmya5	APN	13	93,234,441 (GRCm39)	missense	possibly damaging	0.96
IGL01106:Cmya5	APN	13	93,221,120 (GRCm39)	missense	probably damaging	1.00
IGL01331:Cmya5	APN	13	93,233,454 (GRCm39)	missense	possibly damaging	0.53
IGL01392:Cmya5	APN	13	93,225,714 (GRCm39)	missense	probably damaging	0.99
IGL01508:Cmya5	APN	13	93,230,535 (GRCm39)	missense	probably benign
IGL01679:Cmya5	APN	13	93,201,828 (GRCm39)	missense	probably damaging	1.00
IGL01749:Cmya5	APN	13	93,225,807 (GRCm39)	missense	probably benign	0.00
IGL01861:Cmya5	APN	13	93,226,256 (GRCm39)	missense	probably damaging	1.00
IGL02021:Cmya5	APN	13	93,231,057 (GRCm39)	missense	probably benign	0.00
IGL02034:Cmya5	APN	13	93,221,043 (GRCm39)	splice site	probably benign
IGL02103:Cmya5	APN	13	93,228,635 (GRCm39)	missense	probably benign	0.05
IGL02174:Cmya5	APN	13	93,185,415 (GRCm39)	missense	possibly damaging	0.76
IGL02176:Cmya5	APN	13	93,226,658 (GRCm39)	missense	probably damaging	1.00
IGL02210:Cmya5	APN	13	93,229,242 (GRCm39)	missense	probably benign	0.14
IGL02229:Cmya5	APN	13	93,229,194 (GRCm39)	missense	possibly damaging	0.54
IGL02306:Cmya5	APN	13	93,234,527 (GRCm39)	missense	probably damaging	1.00
IGL02311:Cmya5	APN	13	93,227,163 (GRCm39)	missense	probably benign	0.40
IGL02409:Cmya5	APN	13	93,226,706 (GRCm39)	missense	probably damaging	0.96
IGL02561:Cmya5	APN	13	93,228,366 (GRCm39)	missense	probably benign	0.00
IGL02676:Cmya5	APN	13	93,229,361 (GRCm39)	missense	probably damaging	1.00
IGL02683:Cmya5	APN	13	93,227,505 (GRCm39)	nonsense	probably null
IGL02685:Cmya5	APN	13	93,227,505 (GRCm39)	nonsense	probably null
IGL02686:Cmya5	APN	13	93,227,505 (GRCm39)	nonsense	probably null
IGL02724:Cmya5	APN	13	93,233,163 (GRCm39)	missense	probably benign
IGL02727:Cmya5	APN	13	93,234,753 (GRCm39)	missense	possibly damaging	0.73
IGL02965:Cmya5	APN	13	93,229,065 (GRCm39)	missense	probably benign	0.41
IGL03079:Cmya5	APN	13	93,234,209 (GRCm39)	missense	possibly damaging	0.85
IGL03144:Cmya5	APN	13	93,227,376 (GRCm39)	missense	probably damaging	1.00
IGL03253:Cmya5	APN	13	93,227,778 (GRCm39)	nonsense	probably null
IGL03336:Cmya5	APN	13	93,230,013 (GRCm39)	missense	possibly damaging	0.84
IGL03138:Cmya5	UTSW	13	93,201,850 (GRCm39)	missense	probably damaging	1.00
P0023:Cmya5	UTSW	13	93,225,854 (GRCm39)	missense	probably benign	0.22
P4748:Cmya5	UTSW	13	93,210,983 (GRCm39)	splice site	probably benign
R0123:Cmya5	UTSW	13	93,232,412 (GRCm39)	missense	possibly damaging	0.84
R0206:Cmya5	UTSW	13	93,232,065 (GRCm39)	missense	probably damaging	0.98
R0206:Cmya5	UTSW	13	93,232,065 (GRCm39)	missense	probably damaging	0.98
R0242:Cmya5	UTSW	13	93,232,108 (GRCm39)	missense	probably benign
R0242:Cmya5	UTSW	13	93,232,108 (GRCm39)	missense	probably benign
R0331:Cmya5	UTSW	13	93,280,911 (GRCm39)	missense	possibly damaging	0.53
R0363:Cmya5	UTSW	13	93,231,377 (GRCm39)	missense	possibly damaging	0.77
R0382:Cmya5	UTSW	13	93,229,256 (GRCm39)	missense	probably benign	0.06
R0416:Cmya5	UTSW	13	93,226,364 (GRCm39)	missense	probably benign	0.05
R0446:Cmya5	UTSW	13	93,230,164 (GRCm39)	missense	probably benign
R0457:Cmya5	UTSW	13	93,232,095 (GRCm39)	missense	possibly damaging	0.84
R0673:Cmya5	UTSW	13	93,226,505 (GRCm39)	missense	probably damaging	1.00
R0674:Cmya5	UTSW	13	93,229,299 (GRCm39)	missense	probably damaging	1.00
R0692:Cmya5	UTSW	13	93,230,357 (GRCm39)	nonsense	probably null
R0698:Cmya5	UTSW	13	93,232,065 (GRCm39)	missense	probably damaging	0.98
R1227:Cmya5	UTSW	13	93,230,954 (GRCm39)	missense	probably damaging	0.99
R1272:Cmya5	UTSW	13	93,231,620 (GRCm39)	missense	possibly damaging	0.79
R1335:Cmya5	UTSW	13	93,178,043 (GRCm39)	missense	possibly damaging	0.65
R1353:Cmya5	UTSW	13	93,178,033 (GRCm39)	missense	probably damaging	1.00
R1354:Cmya5	UTSW	13	93,228,566 (GRCm39)	missense	possibly damaging	0.46
R1458:Cmya5	UTSW	13	93,201,835 (GRCm39)	missense	probably benign	0.44
R1572:Cmya5	UTSW	13	93,230,777 (GRCm39)	missense	possibly damaging	0.61
R1698:Cmya5	UTSW	13	93,200,027 (GRCm39)	missense	probably benign	0.27
R1735:Cmya5	UTSW	13	93,226,297 (GRCm39)	missense	probably benign	0.11
R1743:Cmya5	UTSW	13	93,233,825 (GRCm39)	missense	probably benign	0.33
R1750:Cmya5	UTSW	13	93,232,171 (GRCm39)	missense	probably benign
R1827:Cmya5	UTSW	13	93,210,956 (GRCm39)	missense	possibly damaging	0.80
R2068:Cmya5	UTSW	13	93,227,032 (GRCm39)	missense	possibly damaging	0.93
R2088:Cmya5	UTSW	13	93,229,320 (GRCm39)	missense	probably damaging	1.00
R2132:Cmya5	UTSW	13	93,205,891 (GRCm39)	missense	probably damaging	1.00
R2216:Cmya5	UTSW	13	93,230,003 (GRCm39)	missense	probably damaging	1.00
R2363:Cmya5	UTSW	13	93,230,210 (GRCm39)	missense	probably benign	0.15
R2497:Cmya5	UTSW	13	93,234,513 (GRCm39)	missense	possibly damaging	0.53
R2509:Cmya5	UTSW	13	93,230,066 (GRCm39)	missense	probably benign	0.41
R2917:Cmya5	UTSW	13	93,227,572 (GRCm39)	nonsense	probably null
R2944:Cmya5	UTSW	13	93,229,350 (GRCm39)	nonsense	probably null
R3039:Cmya5	UTSW	13	93,228,758 (GRCm39)	missense	probably benign	0.12
R3078:Cmya5	UTSW	13	93,185,435 (GRCm39)	missense	probably damaging	0.99
R3708:Cmya5	UTSW	13	93,231,874 (GRCm39)	nonsense	probably null
R3717:Cmya5	UTSW	13	93,228,995 (GRCm39)	missense	probably benign	0.12
R3768:Cmya5	UTSW	13	93,233,201 (GRCm39)	missense	possibly damaging	0.73
R3769:Cmya5	UTSW	13	93,233,201 (GRCm39)	missense	possibly damaging	0.73
R3840:Cmya5	UTSW	13	93,231,140 (GRCm39)	missense	probably damaging	0.96
R3841:Cmya5	UTSW	13	93,231,140 (GRCm39)	missense	probably damaging	0.96
R3882:Cmya5	UTSW	13	93,227,727 (GRCm39)	missense	probably benign	0.07
R3888:Cmya5	UTSW	13	93,230,164 (GRCm39)	missense	probably benign
R3897:Cmya5	UTSW	13	93,233,189 (GRCm39)	missense	possibly damaging	0.72
R3952:Cmya5	UTSW	13	93,225,707 (GRCm39)	missense	possibly damaging	0.89
R4366:Cmya5	UTSW	13	93,228,464 (GRCm39)	missense	probably benign	0.36
R4471:Cmya5	UTSW	13	93,228,833 (GRCm39)	missense	probably benign	0.01
R4493:Cmya5	UTSW	13	93,230,573 (GRCm39)	missense	probably benign
R4495:Cmya5	UTSW	13	93,230,573 (GRCm39)	missense	probably benign
R4544:Cmya5	UTSW	13	93,228,426 (GRCm39)	nonsense	probably null
R4545:Cmya5	UTSW	13	93,228,426 (GRCm39)	nonsense	probably null
R4624:Cmya5	UTSW	13	93,200,059 (GRCm39)	missense	probably damaging	1.00
R4648:Cmya5	UTSW	13	93,230,336 (GRCm39)	missense	possibly damaging	0.84
R4824:Cmya5	UTSW	13	93,230,082 (GRCm39)	missense	probably benign	0.04
R4967:Cmya5	UTSW	13	93,227,093 (GRCm39)	missense	probably damaging	1.00
R5101:Cmya5	UTSW	13	93,228,111 (GRCm39)	missense	possibly damaging	0.61
R5133:Cmya5	UTSW	13	93,229,880 (GRCm39)	missense	possibly damaging	0.79
R5139:Cmya5	UTSW	13	93,232,569 (GRCm39)	missense	probably benign	0.00
R5220:Cmya5	UTSW	13	93,228,804 (GRCm39)	missense	probably damaging	0.99
R5332:Cmya5	UTSW	13	93,232,703 (GRCm39)	missense	probably damaging	0.96
R5337:Cmya5	UTSW	13	93,219,781 (GRCm39)	missense	probably benign	0.28
R5356:Cmya5	UTSW	13	93,199,993 (GRCm39)	missense	probably damaging	1.00
R5401:Cmya5	UTSW	13	93,228,476 (GRCm39)	missense	probably damaging	1.00
R5438:Cmya5	UTSW	13	93,231,707 (GRCm39)	missense	possibly damaging	0.89
R5604:Cmya5	UTSW	13	93,229,271 (GRCm39)	missense	probably benign	0.15
R5628:Cmya5	UTSW	13	93,226,218 (GRCm39)	missense	probably damaging	1.00
R5666:Cmya5	UTSW	13	93,182,457 (GRCm39)	missense	possibly damaging	0.75
R5687:Cmya5	UTSW	13	93,234,684 (GRCm39)	missense	possibly damaging	0.53
R5695:Cmya5	UTSW	13	93,182,374 (GRCm39)	critical splice donor site	probably null
R5806:Cmya5	UTSW	13	93,230,445 (GRCm39)	missense	possibly damaging	0.84
R5820:Cmya5	UTSW	13	93,229,288 (GRCm39)	missense	probably benign	0.04
R5872:Cmya5	UTSW	13	93,233,943 (GRCm39)	missense	probably benign	0.01
R5875:Cmya5	UTSW	13	93,231,692 (GRCm39)	missense	probably benign	0.13
R5896:Cmya5	UTSW	13	93,182,373 (GRCm39)	critical splice donor site	probably null
R5910:Cmya5	UTSW	13	93,229,151 (GRCm39)	missense	probably damaging	0.98
R5969:Cmya5	UTSW	13	93,226,052 (GRCm39)	missense	possibly damaging	0.78
R6064:Cmya5	UTSW	13	93,226,157 (GRCm39)	missense	probably damaging	1.00
R6081:Cmya5	UTSW	13	93,281,021 (GRCm39)	unclassified	probably benign
R6102:Cmya5	UTSW	13	93,230,739 (GRCm39)	missense	probably benign
R6117:Cmya5	UTSW	13	93,231,674 (GRCm39)	missense	probably damaging	0.98
R6188:Cmya5	UTSW	13	93,233,784 (GRCm39)	missense	possibly damaging	0.73
R6188:Cmya5	UTSW	13	93,229,952 (GRCm39)	missense	possibly damaging	0.61
R6219:Cmya5	UTSW	13	93,230,951 (GRCm39)	missense	probably damaging	1.00
R6229:Cmya5	UTSW	13	93,229,814 (GRCm39)	missense	probably benign	0.41
R6346:Cmya5	UTSW	13	93,228,698 (GRCm39)	missense	probably damaging	1.00
R6431:Cmya5	UTSW	13	93,210,972 (GRCm39)	missense	possibly damaging	0.60
R6436:Cmya5	UTSW	13	93,225,723 (GRCm39)	missense	probably damaging	0.98
R6598:Cmya5	UTSW	13	93,226,316 (GRCm39)	missense	probably benign	0.05
R6649:Cmya5	UTSW	13	93,234,533 (GRCm39)	missense	possibly damaging	0.91
R6652:Cmya5	UTSW	13	93,229,547 (GRCm39)	missense	probably damaging	0.99
R6652:Cmya5	UTSW	13	93,229,403 (GRCm39)	missense	probably benign	0.04
R6669:Cmya5	UTSW	13	93,229,767 (GRCm39)	missense	probably benign	0.03
R6881:Cmya5	UTSW	13	93,226,800 (GRCm39)	missense	probably damaging	1.00
R6909:Cmya5	UTSW	13	93,227,760 (GRCm39)	missense	probably benign	0.04
R6933:Cmya5	UTSW	13	93,231,644 (GRCm39)	missense	probably benign	0.03
R7021:Cmya5	UTSW	13	93,230,063 (GRCm39)	missense	possibly damaging	0.62
R7022:Cmya5	UTSW	13	93,205,786 (GRCm39)	critical splice donor site	probably null
R7068:Cmya5	UTSW	13	93,229,205 (GRCm39)	missense	possibly damaging	0.59
R7087:Cmya5	UTSW	13	93,227,483 (GRCm39)	missense	probably benign	0.00
R7088:Cmya5	UTSW	13	93,228,372 (GRCm39)	missense	possibly damaging	0.95
R7126:Cmya5	UTSW	13	93,226,448 (GRCm39)	missense	probably benign	0.41
R7177:Cmya5	UTSW	13	93,231,836 (GRCm39)	missense	probably benign	0.00
R7188:Cmya5	UTSW	13	93,182,546 (GRCm39)	missense	probably damaging	1.00
R7217:Cmya5	UTSW	13	93,226,938 (GRCm39)	missense	probably damaging	1.00
R7278:Cmya5	UTSW	13	93,232,208 (GRCm39)	missense	probably damaging	0.96
R7293:Cmya5	UTSW	13	93,229,305 (GRCm39)	missense	possibly damaging	0.90
R7332:Cmya5	UTSW	13	93,229,061 (GRCm39)	missense	possibly damaging	0.60
R7375:Cmya5	UTSW	13	93,228,169 (GRCm39)	missense	probably damaging	0.97
R7386:Cmya5	UTSW	13	93,205,831 (GRCm39)	missense	probably damaging	1.00
R7489:Cmya5	UTSW	13	93,228,346 (GRCm39)	missense	possibly damaging	0.87
R7529:Cmya5	UTSW	13	93,233,942 (GRCm39)	missense	probably benign	0.02
R7552:Cmya5	UTSW	13	93,205,820 (GRCm39)	missense	probably benign	0.41
R7624:Cmya5	UTSW	13	93,226,865 (GRCm39)	missense	possibly damaging	0.79
R7637:Cmya5	UTSW	13	93,219,720 (GRCm39)	missense	possibly damaging	0.87
R7673:Cmya5	UTSW	13	93,230,629 (GRCm39)	missense	probably benign	0.13
R7753:Cmya5	UTSW	13	93,234,680 (GRCm39)	missense	probably benign	0.18
R7757:Cmya5	UTSW	13	93,234,780 (GRCm39)	missense	possibly damaging	0.53
R7806:Cmya5	UTSW	13	93,230,770 (GRCm39)	missense	probably benign	0.00
R7825:Cmya5	UTSW	13	93,234,136 (GRCm39)	missense	possibly damaging	0.53
R7878:Cmya5	UTSW	13	93,226,265 (GRCm39)	missense	probably damaging	0.98
R7892:Cmya5	UTSW	13	93,232,865 (GRCm39)	missense	probably damaging	0.96
R7952:Cmya5	UTSW	13	93,233,512 (GRCm39)	small deletion	probably benign
R8127:Cmya5	UTSW	13	93,231,122 (GRCm39)	missense	probably damaging	0.99
R8256:Cmya5	UTSW	13	93,229,986 (GRCm39)	missense	possibly damaging	0.62
R8339:Cmya5	UTSW	13	93,228,142 (GRCm39)	nonsense	probably null
R8446:Cmya5	UTSW	13	93,230,336 (GRCm39)	missense	possibly damaging	0.84
R8553:Cmya5	UTSW	13	93,230,304 (GRCm39)	missense	probably benign	0.00
R8686:Cmya5	UTSW	13	93,231,888 (GRCm39)	missense	possibly damaging	0.91
R8748:Cmya5	UTSW	13	93,226,229 (GRCm39)	missense	probably damaging	1.00
R8783:Cmya5	UTSW	13	93,225,888 (GRCm39)	missense	possibly damaging	0.58
R8803:Cmya5	UTSW	13	93,177,991 (GRCm39)	missense	probably damaging	1.00
R8810:Cmya5	UTSW	13	93,200,048 (GRCm39)	missense	possibly damaging	0.47
R8937:Cmya5	UTSW	13	93,232,840 (GRCm39)	missense	probably benign	0.01
R8985:Cmya5	UTSW	13	93,233,664 (GRCm39)	missense	possibly damaging	0.73
R9017:Cmya5	UTSW	13	93,228,572 (GRCm39)	missense	probably benign	0.03
R9087:Cmya5	UTSW	13	93,233,711 (GRCm39)	missense	possibly damaging	0.72
R9133:Cmya5	UTSW	13	93,234,108 (GRCm39)	missense	possibly damaging	0.73
R9156:Cmya5	UTSW	13	93,233,878 (GRCm39)	missense	unknown
R9209:Cmya5	UTSW	13	93,226,866 (GRCm39)	missense	probably benign	0.45
R9222:Cmya5	UTSW	13	93,230,579 (GRCm39)	missense	probably benign	0.00
R9229:Cmya5	UTSW	13	93,232,176 (GRCm39)	missense	possibly damaging	0.92
R9382:Cmya5	UTSW	13	93,229,884 (GRCm39)	missense	probably benign
R9385:Cmya5	UTSW	13	93,230,880 (GRCm39)	missense	probably damaging	0.99
R9418:Cmya5	UTSW	13	93,226,209 (GRCm39)	missense	probably benign	0.22
R9452:Cmya5	UTSW	13	93,232,394 (GRCm39)	missense	probably benign
R9492:Cmya5	UTSW	13	93,177,822 (GRCm39)	makesense	probably null
R9600:Cmya5	UTSW	13	93,226,604 (GRCm39)	missense	probably damaging	1.00
R9712:Cmya5	UTSW	13	93,201,881 (GRCm39)	critical splice acceptor site	probably null
R9742:Cmya5	UTSW	13	93,231,935 (GRCm39)	missense	possibly damaging	0.89
RF020:Cmya5	UTSW	13	93,205,799 (GRCm39)	missense	possibly damaging	0.56
X0028:Cmya5	UTSW	13	93,233,195 (GRCm39)	missense	possibly damaging	0.53
Z1088:Cmya5	UTSW	13	93,200,087 (GRCm39)	missense	probably benign
Z1176:Cmya5	UTSW	13	93,233,298 (GRCm39)	missense	unknown
Z1176:Cmya5	UTSW	13	93,200,087 (GRCm39)	missense	probably benign
Z1177:Cmya5	UTSW	13	93,200,087 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- CACTTGTTCGGATGAGATGGCC -3'
(R):5'- GTCCCAACGTGTTTCTGAGC -3'

Sequencing Primer
(F):5'- CTTTCAGAAAGCAGCTCAGTG -3'
(R):5'- TCTGAGCCCATCATTCAGGCAG -3'

Posted On

2016-04-27