Mutagenetix > Incidental Mutation

Incidental Mutation 'R7088:Cmya5'

550040

Institutional Source

Beutler Lab

Gene Symbol

Cmya5

Ensembl Gene

ENSMUSG00000047419

Gene Name

cardiomyopathy associated 5

Synonyms

Myospryn, 2310076E16Rik, 2310076E21Rik

MMRRC Submission

045182-MU

Accession Numbers

Essential gene?

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

Stock #

R7088 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

93177221-93281232 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 93228372 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 2239 (S2239T)

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: S2239T

PolyPhen 2 Score 0.954 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: S2239T

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: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

99% (77/78)

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700020L24Rik	G	T	11: 83,331,232 (GRCm39)	E48*	probably null	Het
Acaca	T	C	11: 84,169,783 (GRCm39)		probably null	Het
Albfm1	T	A	5: 90,720,609 (GRCm39)	L260*	probably null	Het
Alkbh3	A	G	2: 93,835,097 (GRCm39)	S83P	possibly damaging	Het
Ammecr1l	T	C	18: 31,904,872 (GRCm39)	S38P	probably benign	Het
Armc10	T	C	5: 21,858,390 (GRCm39)	V145A	probably damaging	Het
BC048671	A	G	6: 90,280,222 (GRCm39)	K46R	probably null	Het
C2cd3	A	G	7: 100,065,388 (GRCm39)	T347A		Het
C8b	G	T	4: 104,650,540 (GRCm39)	E449D	probably benign	Het
Camk4	T	C	18: 33,072,584 (GRCm39)	S46P	probably benign	Het
Ccdc113	G	A	8: 96,264,733 (GRCm39)	R81H	probably benign	Het
Cd177	A	T	7: 24,444,558 (GRCm39)	C674*	probably null	Het
Cdc6	T	A	11: 98,810,065 (GRCm39)	V458D	probably damaging	Het
Cenpo	C	T	12: 4,265,307 (GRCm39)	E238K	probably benign	Het
Ckap2	G	T	8: 22,659,882 (GRCm39)	P533Q	possibly damaging	Het
Cma1	T	A	14: 56,181,273 (GRCm39)	H44L	probably damaging	Het
Cntnap5b	T	A	1: 100,087,802 (GRCm39)	I141N	probably damaging	Het
Col6a4	T	A	9: 105,877,885 (GRCm39)	T2031S	possibly damaging	Het
Cplane1	C	T	15: 8,248,431 (GRCm39)	T1660M	probably benign	Het
Cxcr5	T	A	9: 44,424,683 (GRCm39)	T325S	possibly damaging	Het
Dhx32	A	T	7: 133,344,417 (GRCm39)	L204Q	probably damaging	Het
Dse	A	G	10: 34,029,885 (GRCm39)	Y402H	probably damaging	Het
Ecpas	A	T	4: 58,849,766 (GRCm39)	L458I	possibly damaging	Het
Exoc6	G	T	19: 37,565,458 (GRCm39)	C178F	probably damaging	Het
Fam149a	A	G	8: 45,803,582 (GRCm39)	V384A	probably benign	Het
Fcrl5	T	C	3: 87,365,141 (GRCm39)	*597Q	probably null	Het
Fer1l6	A	G	15: 58,435,899 (GRCm39)	K431E	possibly damaging	Het
Fmo3	T	A	1: 162,796,434 (GRCm39)	H46L	probably benign	Het
Gcm2	T	C	13: 41,256,840 (GRCm39)	D303G	probably damaging	Het
Gk2	T	C	5: 97,603,534 (GRCm39)	M435V	probably damaging	Het
Gli1	C	A	10: 127,171,868 (GRCm39)	M295I	probably damaging	Het
Gm11444	G	T	11: 85,737,862 (GRCm39)	H109Q		Het
Gtpbp1	T	A	15: 79,603,483 (GRCm39)	D182E		Het
Hnf4g	A	T	3: 3,713,185 (GRCm39)		probably null	Het
Hsf2	G	A	10: 57,388,188 (GRCm39)	R483H	probably damaging	Het
Kcnq4	C	T	4: 120,561,596 (GRCm39)	R491H	probably damaging	Het
Lama3	T	C	18: 12,715,602 (GRCm39)	V1686A	possibly damaging	Het
Larp6	A	G	9: 60,631,638 (GRCm39)	K137E	probably damaging	Het
Mboat1	T	G	13: 30,379,772 (GRCm39)		probably null	Het
Mdh1	T	C	11: 21,508,484 (GRCm39)	Y286C	probably damaging	Het
Mga	G	T	2: 119,792,417 (GRCm39)	K2607N	probably damaging	Het
Morf4l1	C	A	9: 89,979,433 (GRCm39)	V183F	possibly damaging	Het
Mroh4	G	A	15: 74,497,993 (GRCm39)	R196W	probably benign	Het
Muc16	C	A	9: 18,503,976 (GRCm39)	M6438I	probably damaging	Het
Myom3	A	G	4: 135,530,589 (GRCm39)	Y1167C	probably damaging	Het
Neurl3	T	C	1: 36,308,302 (GRCm39)	E170G	possibly damaging	Het
Nsd3	T	C	8: 26,156,050 (GRCm39)	I539T	probably benign	Het
Nup155	T	C	15: 8,186,177 (GRCm39)	F1313S	probably benign	Het
Nxn	A	T	11: 76,153,974 (GRCm39)	V287E	possibly damaging	Het
Or4a80	G	A	2: 89,582,443 (GRCm39)	T243I	probably benign	Het
Or7a38	A	C	10: 78,753,593 (GRCm39)	L306F	probably benign	Het
Or8c13	C	A	9: 38,091,748 (GRCm39)	V124F	probably damaging	Het
Pax6	A	G	2: 105,526,753 (GRCm39)	N220D	probably benign	Het
Pcdha11	G	A	18: 37,138,470 (GRCm39)	R33H	probably benign	Het
Pdzd8	A	G	19: 59,333,389 (GRCm39)	F211L	probably damaging	Het
Pear1	C	A	3: 87,661,945 (GRCm39)	V477F	possibly damaging	Het
Pex19	GTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTC	GTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTC	1: 171,956,150 (GRCm39)		probably null	Het
Pidd1	A	T	7: 141,020,400 (GRCm39)	V539E	probably damaging	Het
Ptprg	A	T	14: 12,207,365 (GRCm38)	I878F	probably damaging	Het
Rabepk	T	C	2: 34,675,711 (GRCm39)	T140A	probably benign	Het
Ranbp2	G	T	10: 58,299,728 (GRCm39)	R454L	probably damaging	Het
Rnf123	C	T	9: 107,935,735 (GRCm39)	R943Q	probably null	Het
Sash1	G	A	10: 8,605,481 (GRCm39)	R970*	probably null	Het
Serpinb2	C	A	1: 107,452,422 (GRCm39)	F333L	probably damaging	Het
Shank3	T	A	15: 89,387,728 (GRCm39)		probably null	Het
Slc9a2	A	C	1: 40,765,539 (GRCm39)	I310L	probably damaging	Het
Strip2	T	A	6: 29,920,532 (GRCm39)		probably null	Het
Thoc3	T	C	13: 54,611,565 (GRCm39)	T241A	probably damaging	Het
Tmem139	T	A	6: 42,240,199 (GRCm39)	V2E	probably damaging	Het
Usp24	G	T	4: 106,244,743 (GRCm39)	V1233F	probably damaging	Het
Vnn1	A	G	10: 23,776,645 (GRCm39)	Q332R	probably benign	Het
Wac	T	A	18: 7,921,455 (GRCm39)	H530Q	probably damaging	Het
Wdr35	T	A	12: 9,028,659 (GRCm39)	N92K	probably benign	Het
Zbtb18	T	G	1: 177,274,820 (GRCm39)	L60R	probably damaging	Het
Zfp184	T	A	13: 22,144,162 (GRCm39)	C623S	probably damaging	Het
Zfp292	A	G	4: 34,806,796 (GRCm39)	Y2088H	probably damaging	Het
Zfp975	G	T	7: 42,312,096 (GRCm39)	S172R	probably benign	Het
Zswim2	G	A	2: 83,746,071 (GRCm39)	Q456*	probably null	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
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'- TGTGGTTGAGCCTTATCCAAAG -3'
(R):5'- GCCAAAACCCACTTCTTTGG -3'

Sequencing Primer
(F):5'- TGGTTGAGCCTTATCCAAAGAAACAG -3'
(R):5'- CCCACTTCTTTGGAACATTGTGAAG -3'

Posted On

2019-05-15