Mutagenetix > Incidental Mutation

Incidental Mutation 'R6102:Cmya5'

485337

Institutional Source

Beutler Lab

Gene Symbol

Cmya5

Ensembl Gene

ENSMUSG00000047419

Gene Name

cardiomyopathy associated 5

Synonyms

Myospryn, 2310076E21Rik, 2310076E16Rik

MMRRC Submission

044252-MU

Accession Numbers

Essential gene?

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

Stock #

R6102 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

93040713-93144724 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 93094231 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Valine at position 1450 (M1450V)

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: M1450V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: M1450V

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: 98.4%
20x: 95.6%

Validation Efficiency

97% (65/67)

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Alox12e	A	G	11: 70,320,023 (GRCm38)	I290T	possibly damaging	Het
Apeh	T	A	9: 108,086,439 (GRCm38)	D559V	probably damaging	Het
Aspm	T	A	1: 139,477,459 (GRCm38)	Y1361*	probably null	Het
Atad5	G	T	11: 80,111,572 (GRCm38)		probably null	Het
Ccr4	C	T	9: 114,496,493 (GRCm38)		probably null	Het
Clasrp	G	A	7: 19,586,468 (GRCm38)		probably benign	Het
Cldn23	A	G	8: 35,825,551 (GRCm38)	M261T	probably benign	Het
Cyp4v3	T	A	8: 45,320,160 (GRCm38)	E202V	probably damaging	Het
Dnah7a	A	T	1: 53,559,140 (GRCm38)	V1412E	probably benign	Het
Dnah9	A	G	11: 65,990,516 (GRCm38)	S2578P	probably damaging	Het
Dsc2	T	A	18: 20,047,108 (GRCm38)	Y196F	probably benign	Het
Exoc1	T	C	5: 76,537,779 (GRCm38)	S113P	probably damaging	Het
Fbxo6	A	T	4: 148,149,522 (GRCm38)	I39N	probably damaging	Het
Frs3	C	T	17: 47,702,671 (GRCm38)	H173Y	probably damaging	Het
Ginm1	G	T	10: 7,768,496 (GRCm38)	T323K	probably benign	Het
Golgb1	T	C	16: 36,912,865 (GRCm38)	S825P	probably damaging	Het
Hs3st3b1	A	T	11: 63,921,855 (GRCm38)	C11*	probably null	Het
Ighv3-3	G	C	12: 114,196,460 (GRCm38)	A110G	possibly damaging	Het
Igkv6-20	G	A	6: 70,335,869 (GRCm38)	H107Y	probably benign	Het
Kcnj16	A	G	11: 111,025,577 (GRCm38)	E355G	probably benign	Het
Lig4	C	T	8: 9,972,872 (GRCm38)	G303S	probably damaging	Het
Map1b	A	C	13: 99,425,873 (GRCm38)	V2443G	unknown	Het
Map3k6	T	C	4: 133,247,131 (GRCm38)		probably null	Het
Mmp13	A	G	9: 7,276,688 (GRCm38)	Q261R	probably benign	Het
Mphosph9	T	A	5: 124,297,709 (GRCm38)	I554F	possibly damaging	Het
Mrgpra3	A	T	7: 47,590,149 (GRCm38)	F10I	possibly damaging	Het
Ms4a18	G	A	19: 11,013,523 (GRCm38)	T69I	probably benign	Het
Mtmr3	T	C	11: 4,487,673 (GRCm38)	N927S	probably damaging	Het
Necab1	T	A	4: 14,989,211 (GRCm38)	Q188L	probably benign	Het
Nfatc2	A	G	2: 168,519,507 (GRCm38)		probably benign	Het
Olfr152	T	C	2: 87,782,848 (GRCm38)	F103L	probably damaging	Het
Olfr495	T	C	7: 108,395,284 (GRCm38)	S55P	probably damaging	Het
Olfr854	T	C	9: 19,567,022 (GRCm38)	M121V	possibly damaging	Het
Paip2b	A	C	6: 83,808,846 (GRCm38)	V134G	possibly damaging	Het
Pax3	T	C	1: 78,132,347 (GRCm38)	T225A	probably damaging	Het
Pbx1	C	A	1: 168,183,565 (GRCm38)	A298S	probably benign	Het
Pcdhac2	A	T	18: 37,146,282 (GRCm38)	K772*	probably null	Het
Pcsk4	A	T	10: 80,325,817 (GRCm38)	Y163*	probably null	Het
Plcd3	A	G	11: 103,080,644 (GRCm38)	V58A	probably damaging	Het
Plek2	T	A	12: 78,900,093 (GRCm38)	T57S	possibly damaging	Het
Plscr2	C	T	9: 92,287,668 (GRCm38)	T57I	probably benign	Het
Ppp2r5b	A	G	19: 6,234,738 (GRCm38)	S32P	probably benign	Het
Ppp3r2	C	T	4: 49,682,022 (GRCm38)		probably benign	Het
Psme4	T	A	11: 30,865,567 (GRCm38)	L1693H	probably damaging	Het
Rrbp1	T	A	2: 143,988,393 (GRCm38)	Q618L	probably damaging	Het
Rsf1	ATGGCG	ATGGCGACGGTGGCG	7: 97,579,904 (GRCm38)		probably benign	Het
Rsrc1	C	T	3: 66,994,649 (GRCm38)	P44L	unknown	Het
Serpina3b	A	T	12: 104,134,169 (GRCm38)	T337S	probably benign	Het
Slc18a2	T	C	19: 59,293,878 (GRCm38)	Y506H	probably benign	Het
Slc9a9	A	G	9: 94,936,429 (GRCm38)	Y292C	probably benign	Het
Spta1	T	C	1: 174,224,520 (GRCm38)	V1840A	probably benign	Het
Ssb	T	C	2: 69,871,208 (GRCm38)	*416Q	probably null	Het
Strada	A	G	11: 106,168,436 (GRCm38)	V209A	probably benign	Het
Tbc1d31	A	T	15: 57,936,093 (GRCm38)	D225V	probably damaging	Het
Tgm4	T	C	9: 123,056,535 (GRCm38)	F381L	probably benign	Het
Tmem120b	T	A	5: 123,115,144 (GRCm38)	Y203N	probably damaging	Het
Tmem176b	A	G	6: 48,835,934 (GRCm38)	V109A	probably benign	Het
Tnfrsf11a	C	A	1: 105,819,946 (GRCm38)	L201M	possibly damaging	Het
Ttn	C	A	2: 76,974,350 (GRCm38)		probably null	Het
Tubb2a	T	C	13: 34,075,343 (GRCm38)	I155V	probably benign	Het
Vmn1r5	A	G	6: 56,986,114 (GRCm38)	D258G	probably damaging	Het
Vmn2r121	T	C	X: 124,133,575 (GRCm38)	T120A	probably benign	Het
Vmn2r19	A	T	6: 123,329,948 (GRCm38)	I472F	probably damaging	Het
Vwa3a	A	G	7: 120,776,138 (GRCm38)		probably null	Het
Zfp273	A	G	13: 67,822,347 (GRCm38)	Y5C	probably damaging	Het
Zfp647	G	A	15: 76,912,085 (GRCm38)	P125L	probably damaging	Het
Zfp825	A	G	13: 74,480,653 (GRCm38)	L248P	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
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
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'- TAGACATGCTGGGCAAAGGC -3'
(R):5'- TGTTGTCAAAGAATGAGCCTGAAG -3'

Sequencing Primer
(F):5'- CTGGGCAAAGGCAAACCACTG -3'
(R):5'- TCTGCAGTGAAAACGGAA -3'

Posted On

2017-08-16