Mutagenetix > Incidental Mutation

Incidental Mutation 'R5872:Cmya5'

455268

Institutional Source

Beutler Lab

Gene Symbol

Cmya5

Ensembl Gene

ENSMUSG00000047419

Gene Name

cardiomyopathy associated 5

Synonyms

Myospryn, 2310076E21Rik, 2310076E16Rik

MMRRC Submission

044079-MU

Accession Numbers

Essential gene?

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

Stock #

R5872 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

93040713-93144724 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 93097435 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Valine at position 382 (M382V)

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: M382V

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)

SMART Domains

Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: M382V

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: 99.9%
3x: 99.6%
10x: 97.8%
20x: 93.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	A	G	14: 32,660,352 (GRCm38)	S1219P	possibly damaging	Het
A2ml1	A	G	6: 128,561,526 (GRCm38)	Y644H	probably damaging	Het
Abca9	T	G	11: 110,117,076 (GRCm38)	R1232S	possibly damaging	Het
Acsf2	C	T	11: 94,573,149 (GRCm38)	V70M	probably benign	Het
Ampd1	A	G	3: 103,079,130 (GRCm38)	I42V	probably benign	Het
Arhgap10	A	G	8: 77,344,638 (GRCm38)		probably null	Het
Atp1a4	A	T	1: 172,244,408 (GRCm38)	L432Q	probably damaging	Het
Bbs12	T	A	3: 37,320,449 (GRCm38)	C349S	possibly damaging	Het
Bnc2	A	G	4: 84,292,770 (GRCm38)	V479A	possibly damaging	Het
C130060K24Rik	A	G	6: 65,441,385 (GRCm38)		probably benign	Het
Cald1	A	T	6: 34,771,108 (GRCm38)	K761*	probably null	Het
Cd177	C	T	7: 24,752,263 (GRCm38)	G443R	probably null	Het
Cdc42bpb	T	C	12: 111,325,976 (GRCm38)	D375G	probably damaging	Het
Chsy3	T	C	18: 59,176,196 (GRCm38)	Y174H	probably damaging	Het
Col1a2	G	A	6: 4,531,926 (GRCm38)	S782N	unknown	Het
Crtac1	C	T	19: 42,309,190 (GRCm38)		probably null	Het
Csmd3	T	A	15: 47,582,527 (GRCm38)	D3683V	probably damaging	Het
Ctrc	A	G	4: 141,845,043 (GRCm38)	L62P	probably damaging	Het
Cyp3a57	A	T	5: 145,371,057 (GRCm38)	K208*	probably null	Het
Dnaaf2	A	T	12: 69,197,348 (GRCm38)	L313Q	probably damaging	Het
Dtl	A	G	1: 191,546,568 (GRCm38)	L394P	probably benign	Het
Ehhadh	T	C	16: 21,766,555 (GRCm38)	E192G	probably benign	Het
Fads2	T	C	19: 10,082,633 (GRCm38)	I226V	probably benign	Het
Fat2	T	C	11: 55,270,382 (GRCm38)	E3174G	probably damaging	Het
Galnt14	C	T	17: 73,574,831 (GRCm38)	R91Q	probably damaging	Het
Hdhd5	G	T	6: 120,510,291 (GRCm38)	D368E	probably benign	Het
Hk3	T	A	13: 55,010,804 (GRCm38)	I528F	probably damaging	Het
Hrasls	T	A	16: 29,220,437 (GRCm38)	Y90N	probably benign	Het
Il10ra	A	C	9: 45,255,653 (GRCm38)	S533R	possibly damaging	Het
Itpr3	G	T	17: 27,086,976 (GRCm38)	K169N	probably benign	Het
Lrrc17	A	G	5: 21,575,266 (GRCm38)	T413A	probably benign	Het
Mcm2	C	T	6: 88,884,071 (GRCm38)	D882N	probably benign	Het
Met	T	C	6: 17,562,198 (GRCm38)	V1186A	probably damaging	Het
Msh5	C	T	17: 35,029,652 (GRCm38)		probably null	Het
Nav3	T	C	10: 109,764,787 (GRCm38)	I1326M	probably damaging	Het
Nek10	A	G	14: 14,850,896 (GRCm38)	I314V	probably benign	Het
Olfr1510	A	C	14: 52,410,768 (GRCm38)	F35V	probably damaging	Het
Olfr920	T	A	9: 38,756,116 (GRCm38)	Y143N	probably benign	Het
Pim1	A	G	17: 29,493,746 (GRCm38)	E211G	probably damaging	Het
Ppp1r12b	A	T	1: 134,776,406 (GRCm38)	D903E	probably benign	Het
Ptpn14	T	C	1: 189,851,032 (GRCm38)	L692P	probably benign	Het
Ptprt	A	G	2: 162,135,218 (GRCm38)	C387R	probably damaging	Het
Scarb1	A	G	5: 125,304,277 (GRCm38)	Y68H	possibly damaging	Het
Shisa6	T	A	11: 66,217,974 (GRCm38)	D359V	probably damaging	Het
Shprh	T	C	10: 11,188,073 (GRCm38)	S1297P	probably damaging	Het
Sik1	T	C	17: 31,850,151 (GRCm38)	D250G	probably damaging	Het
Slamf7	A	G	1: 171,639,067 (GRCm38)	L190S	probably damaging	Het
Slc22a3	G	A	17: 12,433,468 (GRCm38)	P423L	probably damaging	Het
Slc35e2	A	T	4: 155,612,680 (GRCm38)	E217V	probably damaging	Het
Spocd1	A	T	4: 129,956,461 (GRCm38)	N760I	probably damaging	Het
Tas2r136	G	T	6: 132,777,331 (GRCm38)	P278T	possibly damaging	Het
Tchhl1	A	T	3: 93,470,529 (GRCm38)	Q180L	probably benign	Het
Tmem151b	T	A	17: 45,547,084 (GRCm38)	T79S	probably benign	Het
Tomm70a	T	A	16: 57,144,742 (GRCm38)	C430S	probably benign	Het
Trbv16	T	A	6: 41,152,002 (GRCm38)	L40Q	probably damaging	Het
Trmt1l	T	G	1: 151,440,843 (GRCm38)	I32S	probably damaging	Het
Ubr4	A	G	4: 139,425,330 (GRCm38)	T2011A	probably damaging	Het
Urb1	C	T	16: 90,772,764 (GRCm38)	W1358*	probably null	Het
Usp31	T	G	7: 121,649,475 (GRCm38)	H915P	probably benign	Het
Vmn2r10	A	T	5: 109,003,511 (GRCm38)	M79K	possibly damaging	Het
Vmn2r14	A	G	5: 109,221,356 (GRCm38)	I117T	probably benign	Het
Vps13b	A	G	15: 35,869,351 (GRCm38)	H2667R	possibly damaging	Het
Vwa5b1	G	A	4: 138,578,651 (GRCm38)	T912M	possibly damaging	Het
Zfp709	G	A	8: 71,889,519 (GRCm38)	C264Y	probably benign	Het
Zkscan5	A	G	5: 145,220,088 (GRCm38)	I467V	probably benign	Het
Zxdc	A	T	6: 90,370,299 (GRCm38)	D214V	probably damaging	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
R4967:Cmya5	UTSW	13	93,090,585 (GRCm38)	missense	probably damaging	1.00
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
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'- GCTCAAACTTTTCTTGGATGGC -3'
(R):5'- GCAAAAGAAAACGTATGCCGATTC -3'

Sequencing Primer
(F):5'- CTTGGTGGTCCTGTCTCTAAAG -3'
(R):5'- GCCGATTCCAATTTAAATGTTCC -3'

Posted On

2017-02-10