Mutagenetix > Incidental Mutation

Incidental Mutation 'R4967:Cmya5'

384142

Institutional Source

Beutler Lab

Gene Symbol

Cmya5

Ensembl Gene

ENSMUSG00000047419

Gene Name

cardiomyopathy associated 5

Synonyms

Myospryn, 2310076E21Rik, 2310076E16Rik

MMRRC Submission

042563-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.252) question?

Stock #

R4967 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

93040713-93144724 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 93090585 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 2665 (E2665G)

Ref Sequence

ENSEMBL: ENSMUSP00000050408 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000062122
AA Change: E2665G

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: E2665G

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

Meta Mutation Damage Score

0.1469

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.7%
20x: 93.7%

Validation Efficiency

100% (102/102)

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930447C04Rik	A	T	12: 72,909,728 (GRCm38)	Y199*	probably null	Het
Adhfe1	A	T	1: 9,566,804 (GRCm38)	I394F	probably benign	Het
Arhgap26	G	T	18: 39,246,840 (GRCm38)	R485L	probably damaging	Het
Atat1	T	A	17: 35,901,575 (GRCm38)	N231I	probably damaging	Het
B4galnt2	T	C	11: 95,869,274 (GRCm38)	N309S	probably benign	Het
Bank1	A	T	3: 136,066,373 (GRCm38)	F499I	probably damaging	Het
Bcl9l	A	G	9: 44,505,068 (GRCm38)	D146G	possibly damaging	Het
Bglap3	A	T	3: 88,376,364 (GRCm38)		probably benign	Het
Bscl2	C	A	19: 8,847,980 (GRCm38)	T376K	probably benign	Het
C87499	T	C	4: 88,629,195 (GRCm38)	T80A	probably damaging	Het
Cercam	A	T	2: 29,871,021 (GRCm38)		probably null	Het
Clec4f	C	T	6: 83,656,030 (GRCm38)	M1I	probably null	Het
Clec4n	A	T	6: 123,232,107 (GRCm38)	I14F	probably benign	Het
Cog4	T	A	8: 110,852,283 (GRCm38)		probably null	Het
Cubn	A	G	2: 13,348,045 (GRCm38)	F1961L	probably benign	Het
Cyp4a29	A	T	4: 115,246,999 (GRCm38)	H88L	probably benign	Het
Dhdh	A	G	7: 45,479,106 (GRCm38)	L216P	probably damaging	Het
Dpp6	T	C	5: 27,666,511 (GRCm38)	F544S	probably damaging	Het
Dthd1	C	T	5: 62,888,206 (GRCm38)	T771I	probably benign	Het
Dusp27	A	T	1: 166,127,106 (GRCm38)	V25E	probably damaging	Het
Emc10	A	G	7: 44,493,188 (GRCm38)		probably null	Het
Fam198a	C	T	9: 121,965,718 (GRCm38)	R313W	probably damaging	Het
Fgg	A	T	3: 83,012,765 (GRCm38)	T284S	probably benign	Het
Gm3002	T	A	14: 3,824,737 (GRCm38)	N24K	probably damaging	Het
Gm8674	G	A	13: 49,901,998 (GRCm38)		noncoding transcript	Het
Gpr63	G	A	4: 25,008,368 (GRCm38)	W364*	probably null	Het
Hcn4	C	G	9: 58,859,828 (GRCm38)	P891A	unknown	Het
Hcrtr1	A	T	4: 130,130,999 (GRCm38)	F365I	possibly damaging	Het
Hmcn2	A	G	2: 31,354,164 (GRCm38)		probably null	Het
Hoxc5	T	A	15: 103,015,354 (GRCm38)	L194H	probably damaging	Het
Ifna11	A	G	4: 88,820,050 (GRCm38)	N31S	probably null	Het
Ikbke	GCC	G	1: 131,275,267 (GRCm38)		probably null	Het
Iqgap2	A	T	13: 95,630,006 (GRCm38)	D1496E	probably benign	Het
Kif28	G	T	1: 179,708,442 (GRCm38)	Q556K	probably damaging	Het
Klhl42	C	T	6: 147,108,004 (GRCm38)	T447I	possibly damaging	Het
Lrp1b	A	C	2: 41,788,974 (GRCm38)	D35E	probably damaging	Het
Lsm14b	A	G	2: 180,033,899 (GRCm38)		probably benign	Het
Map3k1	T	C	13: 111,772,738 (GRCm38)	E226G	probably damaging	Het
Map3k14	T	A	11: 103,239,531 (GRCm38)	N187Y	probably benign	Het
Mcm6	A	T	1: 128,335,849 (GRCm38)	V645E	probably damaging	Het
Mdh1b	G	T	1: 63,719,863 (GRCm38)	P190Q	probably damaging	Het
Meiob	T	G	17: 24,818,379 (GRCm38)	L77R	probably damaging	Het
Mkl1	C	A	15: 81,045,275 (GRCm38)		probably benign	Het
Mrgpra3	A	T	7: 47,589,519 (GRCm38)	F220I	probably benign	Het
Mtor	T	A	4: 148,491,360 (GRCm38)	S1324T	possibly damaging	Het
Myot	T	A	18: 44,354,928 (GRCm38)	D437E	possibly damaging	Het
Ncoa6	G	T	2: 155,421,332 (GRCm38)	T394K	possibly damaging	Het
Nf1	T	A	11: 79,565,553 (GRCm38)		probably null	Het
Nup210	T	A	6: 91,036,469 (GRCm38)	T1190S	possibly damaging	Het
Odf1	T	A	15: 38,226,408 (GRCm38)	I184N	probably damaging	Het
Olfr178	G	T	16: 58,889,594 (GRCm38)	Q209K	possibly damaging	Het
Olfr270	T	C	4: 52,970,960 (GRCm38)	V113A	possibly damaging	Het
Olfr353	A	G	2: 36,890,707 (GRCm38)	I47T	probably damaging	Het
Olfr959	C	T	9: 39,572,758 (GRCm38)	C167Y	probably damaging	Het
Padi1	A	G	4: 140,845,590 (GRCm38)	V21A	probably benign	Het
Pdzrn3	C	T	6: 101,151,590 (GRCm38)	R705H	probably damaging	Het
Pik3cb	T	C	9: 99,105,632 (GRCm38)	I18V	probably benign	Het
Pmpca	T	C	2: 26,390,308 (GRCm38)	S117P	probably damaging	Het
Poteg	T	A	8: 27,494,981 (GRCm38)		probably benign	Het
Rab30	G	A	7: 92,829,563 (GRCm38)	R72H	probably damaging	Het
Ramp2	T	A	11: 101,247,557 (GRCm38)		probably null	Het
Rbks	G	A	5: 31,624,532 (GRCm38)	T308I	probably damaging	Het
Rnf112	A	G	11: 61,452,926 (GRCm38)		probably benign	Het
Rnf38	G	A	4: 44,152,460 (GRCm38)	P3S	probably damaging	Het
Sec16a	A	G	2: 26,412,871 (GRCm38)	S2344P	probably benign	Het
Slc16a8	C	T	15: 79,252,884 (GRCm38)	V109M	possibly damaging	Het
Slc28a1	A	T	7: 81,142,009 (GRCm38)	T308S	possibly damaging	Het
Slc39a3	T	C	10: 81,031,619 (GRCm38)	T98A	possibly damaging	Het
Smarcc2	T	C	10: 128,483,180 (GRCm38)	F731L	probably damaging	Het
Smc4	A	G	3: 69,018,239 (GRCm38)		probably benign	Het
Sparcl1	T	G	5: 104,092,910 (GRCm38)	D216A	probably damaging	Het
Speg	G	A	1: 75,387,869 (GRCm38)	R192H	probably damaging	Het
Sspo	T	C	6: 48,464,605 (GRCm38)	L1892P	probably damaging	Het
Tacc2	A	G	7: 130,623,948 (GRCm38)	N807D	probably damaging	Het
Teddm1a	A	T	1: 153,892,233 (GRCm38)	K148*	probably null	Het
Tex15	T	A	8: 33,574,470 (GRCm38)	D1309E	probably benign	Het
Thbs1	A	T	2: 118,114,778 (GRCm38)	E277D	probably benign	Het
Ticrr	G	A	7: 79,660,410 (GRCm38)	R24Q	probably damaging	Het
Tigd4	A	G	3: 84,595,153 (GRCm38)	E459G	probably benign	Het
Tln2	C	A	9: 67,355,125 (GRCm38)	A615S	probably damaging	Het
Tmprss5	T	C	9: 49,115,517 (GRCm38)	V410A	probably damaging	Het
Tnrc6a	G	T	7: 123,189,872 (GRCm38)	W1638L	probably damaging	Het
Tpr	A	G	1: 150,410,059 (GRCm38)	D424G	probably damaging	Het
Trim34a	A	T	7: 104,261,064 (GRCm38)	K358*	probably null	Het
Tssk5	T	A	15: 76,374,656 (GRCm38)	D10V	possibly damaging	Het
Usp35	A	C	7: 97,313,575 (GRCm38)	L470R	probably damaging	Het
Usp42	T	C	5: 143,715,364 (GRCm38)	D968G	possibly damaging	Het
Utrn	A	G	10: 12,455,420 (GRCm38)	V2924A	probably damaging	Het
Wdtc1	C	A	4: 133,294,343 (GRCm38)	A627S	probably damaging	Het
Xrra1	A	G	7: 99,906,523 (GRCm38)	T366A	probably damaging	Het
Zfp712	T	A	13: 67,040,709 (GRCm38)	K585*	probably null	Het
Zfp97	T	A	17: 17,145,131 (GRCm38)	N297K	probably damaging	Het
Zfp97	G	T	17: 17,144,676 (GRCm38)	E146*	probably null	Het

Other mutations in Cmya5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00489:Cmya5	APN	13	93,093,120 (GRCm38)	missense	probably benign	0.13
IGL00516:Cmya5	APN	13	93,098,167 (GRCm38)	missense	possibly damaging	0.73
IGL00654:Cmya5	APN	13	93,094,161 (GRCm38)	missense	probably benign	0.00
IGL00948:Cmya5	APN	13	93,091,036 (GRCm38)	missense	probably benign
IGL00966:Cmya5	APN	13	93,097,906 (GRCm38)	missense	probably benign	0.33
IGL00988:Cmya5	APN	13	93,097,933 (GRCm38)	missense	possibly damaging	0.96
IGL01106:Cmya5	APN	13	93,084,612 (GRCm38)	missense	probably damaging	1.00
IGL01331:Cmya5	APN	13	93,096,946 (GRCm38)	missense	possibly damaging	0.53
IGL01392:Cmya5	APN	13	93,089,206 (GRCm38)	missense	probably damaging	0.99
IGL01508:Cmya5	APN	13	93,094,027 (GRCm38)	missense	probably benign
IGL01679:Cmya5	APN	13	93,065,320 (GRCm38)	missense	probably damaging	1.00
IGL01749:Cmya5	APN	13	93,089,299 (GRCm38)	missense	probably benign	0.00
IGL01861:Cmya5	APN	13	93,089,748 (GRCm38)	missense	probably damaging	1.00
IGL02021:Cmya5	APN	13	93,094,549 (GRCm38)	missense	probably benign	0.00
IGL02034:Cmya5	APN	13	93,084,535 (GRCm38)	splice site	probably benign
IGL02103:Cmya5	APN	13	93,092,127 (GRCm38)	missense	probably benign	0.05
IGL02174:Cmya5	APN	13	93,048,907 (GRCm38)	missense	possibly damaging	0.76
IGL02176:Cmya5	APN	13	93,090,150 (GRCm38)	missense	probably damaging	1.00
IGL02210:Cmya5	APN	13	93,092,734 (GRCm38)	missense	probably benign	0.14
IGL02229:Cmya5	APN	13	93,092,686 (GRCm38)	missense	possibly damaging	0.54
IGL02306:Cmya5	APN	13	93,098,019 (GRCm38)	missense	probably damaging	1.00
IGL02311:Cmya5	APN	13	93,090,655 (GRCm38)	missense	probably benign	0.40
IGL02409:Cmya5	APN	13	93,090,198 (GRCm38)	missense	probably damaging	0.96
IGL02561:Cmya5	APN	13	93,091,858 (GRCm38)	missense	probably benign	0.00
IGL02676:Cmya5	APN	13	93,092,853 (GRCm38)	missense	probably damaging	1.00
IGL02683:Cmya5	APN	13	93,090,997 (GRCm38)	nonsense	probably null
IGL02685:Cmya5	APN	13	93,090,997 (GRCm38)	nonsense	probably null
IGL02686:Cmya5	APN	13	93,090,997 (GRCm38)	nonsense	probably null
IGL02724:Cmya5	APN	13	93,096,655 (GRCm38)	missense	probably benign
IGL02727:Cmya5	APN	13	93,098,245 (GRCm38)	missense	possibly damaging	0.73
IGL02965:Cmya5	APN	13	93,092,557 (GRCm38)	missense	probably benign	0.41
IGL03079:Cmya5	APN	13	93,097,701 (GRCm38)	missense	possibly damaging	0.85
IGL03144:Cmya5	APN	13	93,090,868 (GRCm38)	missense	probably damaging	1.00
IGL03253:Cmya5	APN	13	93,091,270 (GRCm38)	nonsense	probably null
IGL03336:Cmya5	APN	13	93,093,505 (GRCm38)	missense	possibly damaging	0.84
IGL03138:Cmya5	UTSW	13	93,065,342 (GRCm38)	missense	probably damaging	1.00
P0023:Cmya5	UTSW	13	93,089,346 (GRCm38)	missense	probably benign	0.22
P4748:Cmya5	UTSW	13	93,074,475 (GRCm38)	splice site	probably benign
R0123:Cmya5	UTSW	13	93,095,904 (GRCm38)	missense	possibly damaging	0.84
R0206:Cmya5	UTSW	13	93,095,557 (GRCm38)	missense	probably damaging	0.98
R0206:Cmya5	UTSW	13	93,095,557 (GRCm38)	missense	probably damaging	0.98
R0242:Cmya5	UTSW	13	93,095,600 (GRCm38)	missense	probably benign
R0242:Cmya5	UTSW	13	93,095,600 (GRCm38)	missense	probably benign
R0331:Cmya5	UTSW	13	93,144,403 (GRCm38)	missense	possibly damaging	0.53
R0363:Cmya5	UTSW	13	93,094,869 (GRCm38)	missense	possibly damaging	0.77
R0382:Cmya5	UTSW	13	93,092,748 (GRCm38)	missense	probably benign	0.06
R0416:Cmya5	UTSW	13	93,089,856 (GRCm38)	missense	probably benign	0.05
R0446:Cmya5	UTSW	13	93,093,656 (GRCm38)	missense	probably benign
R0457:Cmya5	UTSW	13	93,095,587 (GRCm38)	missense	possibly damaging	0.84
R0673:Cmya5	UTSW	13	93,089,997 (GRCm38)	missense	probably damaging	1.00
R0674:Cmya5	UTSW	13	93,092,791 (GRCm38)	missense	probably damaging	1.00
R0692:Cmya5	UTSW	13	93,093,849 (GRCm38)	nonsense	probably null
R0698:Cmya5	UTSW	13	93,095,557 (GRCm38)	missense	probably damaging	0.98
R1227:Cmya5	UTSW	13	93,094,446 (GRCm38)	missense	probably damaging	0.99
R1272:Cmya5	UTSW	13	93,095,112 (GRCm38)	missense	possibly damaging	0.79
R1335:Cmya5	UTSW	13	93,041,535 (GRCm38)	missense	possibly damaging	0.65
R1353:Cmya5	UTSW	13	93,041,525 (GRCm38)	missense	probably damaging	1.00
R1354:Cmya5	UTSW	13	93,092,058 (GRCm38)	missense	possibly damaging	0.46
R1458:Cmya5	UTSW	13	93,065,327 (GRCm38)	missense	probably benign	0.44
R1572:Cmya5	UTSW	13	93,094,269 (GRCm38)	missense	possibly damaging	0.61
R1698:Cmya5	UTSW	13	93,063,519 (GRCm38)	missense	probably benign	0.27
R1735:Cmya5	UTSW	13	93,089,789 (GRCm38)	missense	probably benign	0.11
R1743:Cmya5	UTSW	13	93,097,317 (GRCm38)	missense	probably benign	0.33
R1750:Cmya5	UTSW	13	93,095,663 (GRCm38)	missense	probably benign
R1827:Cmya5	UTSW	13	93,074,448 (GRCm38)	missense	possibly damaging	0.80
R2068:Cmya5	UTSW	13	93,090,524 (GRCm38)	missense	possibly damaging	0.93
R2088:Cmya5	UTSW	13	93,092,812 (GRCm38)	missense	probably damaging	1.00
R2132:Cmya5	UTSW	13	93,069,383 (GRCm38)	missense	probably damaging	1.00
R2216:Cmya5	UTSW	13	93,093,495 (GRCm38)	missense	probably damaging	1.00
R2363:Cmya5	UTSW	13	93,093,702 (GRCm38)	missense	probably benign	0.15
R2497:Cmya5	UTSW	13	93,098,005 (GRCm38)	missense	possibly damaging	0.53
R2509:Cmya5	UTSW	13	93,093,558 (GRCm38)	missense	probably benign	0.41
R2917:Cmya5	UTSW	13	93,091,064 (GRCm38)	nonsense	probably null
R2944:Cmya5	UTSW	13	93,092,842 (GRCm38)	nonsense	probably null
R3039:Cmya5	UTSW	13	93,092,250 (GRCm38)	missense	probably benign	0.12
R3078:Cmya5	UTSW	13	93,048,927 (GRCm38)	missense	probably damaging	0.99
R3708:Cmya5	UTSW	13	93,095,366 (GRCm38)	nonsense	probably null
R3717:Cmya5	UTSW	13	93,092,487 (GRCm38)	missense	probably benign	0.12
R3768:Cmya5	UTSW	13	93,096,693 (GRCm38)	missense	possibly damaging	0.73
R3769:Cmya5	UTSW	13	93,096,693 (GRCm38)	missense	possibly damaging	0.73
R3840:Cmya5	UTSW	13	93,094,632 (GRCm38)	missense	probably damaging	0.96
R3841:Cmya5	UTSW	13	93,094,632 (GRCm38)	missense	probably damaging	0.96
R3882:Cmya5	UTSW	13	93,091,219 (GRCm38)	missense	probably benign	0.07
R3888:Cmya5	UTSW	13	93,093,656 (GRCm38)	missense	probably benign
R3897:Cmya5	UTSW	13	93,096,681 (GRCm38)	missense	possibly damaging	0.72
R3952:Cmya5	UTSW	13	93,089,199 (GRCm38)	missense	possibly damaging	0.89
R4366:Cmya5	UTSW	13	93,091,956 (GRCm38)	missense	probably benign	0.36
R4471:Cmya5	UTSW	13	93,092,325 (GRCm38)	missense	probably benign	0.01
R4493:Cmya5	UTSW	13	93,094,065 (GRCm38)	missense	probably benign
R4495:Cmya5	UTSW	13	93,094,065 (GRCm38)	missense	probably benign
R4544:Cmya5	UTSW	13	93,091,918 (GRCm38)	nonsense	probably null
R4545:Cmya5	UTSW	13	93,091,918 (GRCm38)	nonsense	probably null
R4624:Cmya5	UTSW	13	93,063,551 (GRCm38)	missense	probably damaging	1.00
R4648:Cmya5	UTSW	13	93,093,828 (GRCm38)	missense	possibly damaging	0.84
R4824:Cmya5	UTSW	13	93,093,574 (GRCm38)	missense	probably benign	0.04
R4965:Cmya5	UTSW	13	93,095,787 (GRCm38)	missense	possibly damaging	0.84
R5101:Cmya5	UTSW	13	93,091,603 (GRCm38)	missense	possibly damaging	0.61
R5133:Cmya5	UTSW	13	93,093,372 (GRCm38)	missense	possibly damaging	0.79
R5139:Cmya5	UTSW	13	93,096,061 (GRCm38)	missense	probably benign	0.00
R5220:Cmya5	UTSW	13	93,092,296 (GRCm38)	missense	probably damaging	0.99
R5332:Cmya5	UTSW	13	93,096,195 (GRCm38)	missense	probably damaging	0.96
R5337:Cmya5	UTSW	13	93,083,273 (GRCm38)	missense	probably benign	0.28
R5356:Cmya5	UTSW	13	93,063,485 (GRCm38)	missense	probably damaging	1.00
R5401:Cmya5	UTSW	13	93,091,968 (GRCm38)	missense	probably damaging	1.00
R5438:Cmya5	UTSW	13	93,095,199 (GRCm38)	missense	possibly damaging	0.89
R5604:Cmya5	UTSW	13	93,092,763 (GRCm38)	missense	probably benign	0.15
R5628:Cmya5	UTSW	13	93,089,710 (GRCm38)	missense	probably damaging	1.00
R5666:Cmya5	UTSW	13	93,045,949 (GRCm38)	missense	possibly damaging	0.75
R5687:Cmya5	UTSW	13	93,098,176 (GRCm38)	missense	possibly damaging	0.53
R5695:Cmya5	UTSW	13	93,045,866 (GRCm38)	critical splice donor site	probably null
R5806:Cmya5	UTSW	13	93,093,937 (GRCm38)	missense	possibly damaging	0.84
R5820:Cmya5	UTSW	13	93,092,780 (GRCm38)	missense	probably benign	0.04
R5872:Cmya5	UTSW	13	93,097,435 (GRCm38)	missense	probably benign	0.01
R5875:Cmya5	UTSW	13	93,095,184 (GRCm38)	missense	probably benign	0.13
R5896:Cmya5	UTSW	13	93,045,865 (GRCm38)	critical splice donor site	probably null
R5910:Cmya5	UTSW	13	93,092,643 (GRCm38)	missense	probably damaging	0.98
R5969:Cmya5	UTSW	13	93,089,544 (GRCm38)	missense	possibly damaging	0.78
R6064:Cmya5	UTSW	13	93,089,649 (GRCm38)	missense	probably damaging	1.00
R6081:Cmya5	UTSW	13	93,144,513 (GRCm38)	unclassified	probably benign
R6102:Cmya5	UTSW	13	93,094,231 (GRCm38)	missense	probably benign
R6117:Cmya5	UTSW	13	93,095,166 (GRCm38)	missense	probably damaging	0.98
R6188:Cmya5	UTSW	13	93,097,276 (GRCm38)	missense	possibly damaging	0.73
R6188:Cmya5	UTSW	13	93,093,444 (GRCm38)	missense	possibly damaging	0.61
R6219:Cmya5	UTSW	13	93,094,443 (GRCm38)	missense	probably damaging	1.00
R6229:Cmya5	UTSW	13	93,093,306 (GRCm38)	missense	probably benign	0.41
R6346:Cmya5	UTSW	13	93,092,190 (GRCm38)	missense	probably damaging	1.00
R6431:Cmya5	UTSW	13	93,074,464 (GRCm38)	missense	possibly damaging	0.60
R6436:Cmya5	UTSW	13	93,089,215 (GRCm38)	missense	probably damaging	0.98
R6598:Cmya5	UTSW	13	93,089,808 (GRCm38)	missense	probably benign	0.05
R6649:Cmya5	UTSW	13	93,098,025 (GRCm38)	missense	possibly damaging	0.91
R6652:Cmya5	UTSW	13	93,093,039 (GRCm38)	missense	probably damaging	0.99
R6652:Cmya5	UTSW	13	93,092,895 (GRCm38)	missense	probably benign	0.04
R6669:Cmya5	UTSW	13	93,093,259 (GRCm38)	missense	probably benign	0.03
R6881:Cmya5	UTSW	13	93,090,292 (GRCm38)	missense	probably damaging	1.00
R6909:Cmya5	UTSW	13	93,091,252 (GRCm38)	missense	probably benign	0.04
R6933:Cmya5	UTSW	13	93,095,136 (GRCm38)	missense	probably benign	0.03
R7021:Cmya5	UTSW	13	93,093,555 (GRCm38)	missense	possibly damaging	0.62
R7022:Cmya5	UTSW	13	93,069,278 (GRCm38)	critical splice donor site	probably null
R7068:Cmya5	UTSW	13	93,092,697 (GRCm38)	missense	possibly damaging	0.59
R7087:Cmya5	UTSW	13	93,090,975 (GRCm38)	missense	probably benign	0.00
R7088:Cmya5	UTSW	13	93,091,864 (GRCm38)	missense	possibly damaging	0.95
R7126:Cmya5	UTSW	13	93,089,940 (GRCm38)	missense	probably benign	0.41
R7177:Cmya5	UTSW	13	93,095,328 (GRCm38)	missense	probably benign	0.00
R7188:Cmya5	UTSW	13	93,046,038 (GRCm38)	missense	probably damaging	1.00
R7217:Cmya5	UTSW	13	93,090,430 (GRCm38)	missense	probably damaging	1.00
R7278:Cmya5	UTSW	13	93,095,700 (GRCm38)	missense	probably damaging	0.96
R7293:Cmya5	UTSW	13	93,092,797 (GRCm38)	missense	possibly damaging	0.90
R7332:Cmya5	UTSW	13	93,092,553 (GRCm38)	missense	possibly damaging	0.60
R7375:Cmya5	UTSW	13	93,091,661 (GRCm38)	missense	probably damaging	0.97
R7386:Cmya5	UTSW	13	93,069,323 (GRCm38)	missense	probably damaging	1.00
R7489:Cmya5	UTSW	13	93,091,838 (GRCm38)	missense	possibly damaging	0.87
R7529:Cmya5	UTSW	13	93,097,434 (GRCm38)	missense	probably benign	0.02
R7552:Cmya5	UTSW	13	93,069,312 (GRCm38)	missense	probably benign	0.41
R7624:Cmya5	UTSW	13	93,090,357 (GRCm38)	missense	possibly damaging	0.79
R7637:Cmya5	UTSW	13	93,083,212 (GRCm38)	missense	possibly damaging	0.87
R7673:Cmya5	UTSW	13	93,094,121 (GRCm38)	missense	probably benign	0.13
R7753:Cmya5	UTSW	13	93,098,172 (GRCm38)	missense	probably benign	0.18
R7757:Cmya5	UTSW	13	93,098,272 (GRCm38)	missense	possibly damaging	0.53
R7806:Cmya5	UTSW	13	93,094,262 (GRCm38)	missense	probably benign	0.00
R7825:Cmya5	UTSW	13	93,097,628 (GRCm38)	missense	possibly damaging	0.53
R7878:Cmya5	UTSW	13	93,089,757 (GRCm38)	missense	probably damaging	0.98
R7892:Cmya5	UTSW	13	93,096,357 (GRCm38)	missense	probably damaging	0.96
R7952:Cmya5	UTSW	13	93,097,004 (GRCm38)	small deletion	probably benign
R8127:Cmya5	UTSW	13	93,094,614 (GRCm38)	missense	probably damaging	0.99
R8256:Cmya5	UTSW	13	93,093,478 (GRCm38)	missense	possibly damaging	0.62
R8339:Cmya5	UTSW	13	93,091,634 (GRCm38)	nonsense	probably null
R8446:Cmya5	UTSW	13	93,093,828 (GRCm38)	missense	possibly damaging	0.84
R8553:Cmya5	UTSW	13	93,093,796 (GRCm38)	missense	probably benign	0.00
R8686:Cmya5	UTSW	13	93,095,380 (GRCm38)	missense	possibly damaging	0.91
R8748:Cmya5	UTSW	13	93,089,721 (GRCm38)	missense	probably damaging	1.00
R8783:Cmya5	UTSW	13	93,089,380 (GRCm38)	missense	possibly damaging	0.58
R8803:Cmya5	UTSW	13	93,041,483 (GRCm38)	missense	probably damaging	1.00
R8810:Cmya5	UTSW	13	93,063,540 (GRCm38)	missense	possibly damaging	0.47
R8937:Cmya5	UTSW	13	93,096,332 (GRCm38)	missense	probably benign	0.01
R8985:Cmya5	UTSW	13	93,097,156 (GRCm38)	missense	possibly damaging	0.73
R9017:Cmya5	UTSW	13	93,092,064 (GRCm38)	missense	probably benign	0.03
R9087:Cmya5	UTSW	13	93,097,203 (GRCm38)	missense	possibly damaging	0.72
R9133:Cmya5	UTSW	13	93,097,600 (GRCm38)	missense	possibly damaging	0.73
R9156:Cmya5	UTSW	13	93,097,370 (GRCm38)	missense	unknown
R9209:Cmya5	UTSW	13	93,090,358 (GRCm38)	missense	probably benign	0.45
R9222:Cmya5	UTSW	13	93,094,071 (GRCm38)	missense	probably benign	0.00
R9229:Cmya5	UTSW	13	93,095,668 (GRCm38)	missense	possibly damaging	0.92
R9382:Cmya5	UTSW	13	93,093,376 (GRCm38)	missense	probably benign
R9385:Cmya5	UTSW	13	93,094,372 (GRCm38)	missense	probably damaging	0.99
R9418:Cmya5	UTSW	13	93,089,701 (GRCm38)	missense	probably benign	0.22
R9452:Cmya5	UTSW	13	93,095,886 (GRCm38)	missense	probably benign
R9492:Cmya5	UTSW	13	93,041,314 (GRCm38)	makesense	probably null
R9600:Cmya5	UTSW	13	93,090,096 (GRCm38)	missense	probably damaging	1.00
R9712:Cmya5	UTSW	13	93,065,373 (GRCm38)	critical splice acceptor site	probably null
R9742:Cmya5	UTSW	13	93,095,427 (GRCm38)	missense	possibly damaging	0.89
RF020:Cmya5	UTSW	13	93,069,291 (GRCm38)	missense	possibly damaging	0.56
X0028:Cmya5	UTSW	13	93,096,687 (GRCm38)	missense	possibly damaging	0.53
Z1088:Cmya5	UTSW	13	93,063,579 (GRCm38)	missense	probably benign
Z1176:Cmya5	UTSW	13	93,096,790 (GRCm38)	missense	unknown
Z1176:Cmya5	UTSW	13	93,063,579 (GRCm38)	missense	probably benign
Z1177:Cmya5	UTSW	13	93,063,579 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- GGATAGCCAAAGACTTTTGCATC -3'
(R):5'- GCAGCTGCTTCCCATAAAAC -3'

Sequencing Primer
(F):5'- TCTGGCCCATAAAAGCTCTCG -3'
(R):5'- TGCTTCCCATAAAACGCAGAAGAG -3'

Posted On

2016-04-27