Mutagenetix > Incidental Mutation

Incidental Mutation 'R7126:Cmya5'

552345

Institutional Source

Beutler Lab

Gene Symbol

Cmya5

Ensembl Gene

ENSMUSG00000047419

Gene Name

cardiomyopathy associated 5

Synonyms

Myospryn, 2310076E16Rik, 2310076E21Rik

MMRRC Submission

045213-MU

Accession Numbers

Essential gene?

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

Stock #

R7126 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

93177221-93281232 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 93226448 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Leucine at position 2880 (P2880L)

Ref Sequence

ENSEMBL: ENSMUSP00000050408 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000062122
AA Change: P2880L

PolyPhen 2 Score 0.415 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: P2880L

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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

97% (73/75)

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810062G17Rik	T	C	3: 36,535,988 (GRCm39)	C85R	unknown	Het
3110082I17Rik	G	T	5: 139,347,005 (GRCm39)	H153Q	unknown	Het
Acadsb	T	C	7: 131,039,177 (GRCm39)	I316T	probably benign	Het
Acsbg2	A	T	17: 57,153,633 (GRCm39)	N523K	probably damaging	Het
Ahnak	C	T	19: 8,979,723 (GRCm39)	P336S	possibly damaging	Het
Ankdd1b	A	G	13: 96,566,370 (GRCm39)	V277A	possibly damaging	Het
Aspm	A	G	1: 139,408,541 (GRCm39)	Y2476C	probably benign	Het
Atg13	G	A	2: 91,510,765 (GRCm39)	R321W	probably damaging	Het
B4galt2	A	G	4: 117,734,735 (GRCm39)	F211S	probably damaging	Het
Baiap3	T	A	17: 25,464,119 (GRCm39)	T913S	possibly damaging	Het
Btbd18	A	T	2: 84,496,546 (GRCm39)	E61D	possibly damaging	Het
Btnl9	G	T	11: 49,060,082 (GRCm39)	S555R	probably damaging	Het
Cbs	T	A	17: 31,838,113 (GRCm39)	M379L	probably benign	Het
Chd9	G	A	8: 91,741,853 (GRCm39)	G1614D	unknown	Het
Cnnm1	T	C	19: 43,473,292 (GRCm39)	S729P	probably damaging	Het
Cox16	T	A	12: 81,518,940 (GRCm39)	E70D	probably benign	Het
Cp	A	G	3: 20,034,788 (GRCm39)	H699R	probably damaging	Het
Cyp2d26	T	C	15: 82,678,209 (GRCm39)	N56D	probably benign	Het
Dennd4c	A	G	4: 86,725,667 (GRCm39)	Y707C	probably damaging	Het
Dnah5	A	T	15: 28,349,983 (GRCm39)	E2555D	probably benign	Het
Ess2	T	C	16: 17,729,154 (GRCm39)	T6A	unknown	Het
Filip1	A	G	9: 79,805,577 (GRCm39)	L59P	possibly damaging	Het
Fsip2	A	G	2: 82,813,485 (GRCm39)	N3268S	possibly damaging	Het
Gja10	A	T	4: 32,601,014 (GRCm39)	C457S	probably benign	Het
Gm4779	TCGGGGCCGGGGCCGGGGCCG	TCGGGGCCGGGGCCGGGGCCGGGGCCG	X: 100,837,777 (GRCm39)		probably benign	Het
Gm47959	G	A	1: 82,978,503 (GRCm39)	G57S	unknown	Het
Grep1	C	T	17: 23,939,538 (GRCm39)	V8I	probably benign	Het
Grid2	T	A	6: 64,053,794 (GRCm39)	V331E	probably damaging	Het
Inpp4a	C	A	1: 37,413,353 (GRCm39)	H123Q	probably benign	Het
Ireb2	T	A	9: 54,793,851 (GRCm39)	Y260*	probably null	Het
Itpr2	G	A	6: 146,259,294 (GRCm39)	Q628*	probably null	Het
Kbtbd11	G	A	8: 15,078,759 (GRCm39)	A453T	probably damaging	Het
Kcnj2	A	G	11: 110,963,648 (GRCm39)	T347A	probably damaging	Het
Kif19b	A	T	5: 140,477,073 (GRCm39)	D874V	probably benign	Het
Klhl12	A	G	1: 134,395,521 (GRCm39)	H161R	probably damaging	Het
Krt78	T	C	15: 101,856,871 (GRCm39)	E412G	probably damaging	Het
Lzic	A	G	4: 149,573,132 (GRCm39)	I95V	probably damaging	Het
Mme	C	T	3: 63,276,322 (GRCm39)	P700S	probably damaging	Het
Mroh2a	G	T	1: 88,182,657 (GRCm39)	R1195L	possibly damaging	Het
Mthfd2	A	G	6: 83,290,472 (GRCm39)	V53A	probably benign	Het
Mtus1	A	G	8: 41,468,439 (GRCm39)	L210P	probably damaging	Het
Muc16	T	C	9: 18,552,512 (GRCm39)	T4594A	probably benign	Het
Niban1	T	A	1: 151,590,318 (GRCm39)	C537*	probably null	Het
Olfm5	A	T	7: 103,809,187 (GRCm39)	C208S	probably damaging	Het
Or10q1	T	A	19: 13,726,887 (GRCm39)	I139N	possibly damaging	Het
Or2ad1	A	T	13: 21,326,888 (GRCm39)	L113H	probably damaging	Het
Or7a39	T	C	10: 78,715,411 (GRCm39)	V135A	possibly damaging	Het
Parp12	T	C	6: 39,088,670 (GRCm39)	I189V	probably benign	Het
Plin1	T	C	7: 79,376,412 (GRCm39)		probably null	Het
Prl7a1	C	T	13: 27,826,402 (GRCm39)		probably null	Het
Ptpn23	T	C	9: 110,217,812 (GRCm39)	D711G	probably benign	Het
Rgs22	A	T	15: 36,103,954 (GRCm39)	I169N	probably damaging	Het
Scn7a	G	T	2: 66,587,630 (GRCm39)	H24Q	possibly damaging	Het
Scrt2	C	T	2: 151,935,006 (GRCm39)	P53L	probably damaging	Het
Sh3rf1	A	T	8: 61,802,458 (GRCm39)	I264L	probably benign	Het
Smarcd1	A	T	15: 99,607,206 (GRCm39)	D393V	probably damaging	Het
Spag17	T	G	3: 100,008,751 (GRCm39)	N1960K	probably benign	Het
Ssb	A	G	2: 69,696,845 (GRCm39)	T62A	possibly damaging	Het
Taar7b	T	A	10: 23,875,960 (GRCm39)	Y42N	possibly damaging	Het
Terf1	A	T	1: 15,883,363 (GRCm39)	I159L	probably benign	Het
Tff3	T	G	17: 31,346,410 (GRCm39)	N54T	probably benign	Het
Top2a	A	G	11: 98,905,818 (GRCm39)	L285P	probably benign	Het
Trim24	A	G	6: 37,896,392 (GRCm39)	Y283C	probably damaging	Het
Trim58	T	C	11: 58,531,405 (GRCm39)	C38R	probably damaging	Het
Trpa1	T	A	1: 14,960,648 (GRCm39)	T647S	probably benign	Het
Trpm4	A	T	7: 44,960,133 (GRCm39)		probably null	Het
Trpm6	C	T	19: 18,831,397 (GRCm39)	Q1421*	probably null	Het
Ubr2	A	T	17: 47,284,982 (GRCm39)		probably null	Het
Vmn1r46	T	G	6: 89,953,976 (GRCm39)	I275S	possibly damaging	Het
Vmn2r54	A	G	7: 12,366,088 (GRCm39)	F282S	possibly damaging	Het
Vmn2r57	A	G	7: 41,049,218 (GRCm39)	S844P	possibly damaging	Het
Vps13a	A	C	19: 16,688,243 (GRCm39)	C855G	probably benign	Het
Wdr31	T	A	4: 62,381,666 (GRCm39)	Q55L	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
R4965:Cmya5	UTSW	13	93,232,295 (GRCm39)	missense	possibly damaging	0.84
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
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'- TGCATAGCTCATCTTCTGGG -3'
(R):5'- TGAAGGCGAAACAGCTTCAG -3'

Sequencing Primer
(F):5'- CATAGCTCATCTTCTGGGTGACTG -3'
(R):5'- CTTCAGAAGGTGACAGTGTGGACTC -3'

Posted On

2019-05-15