Incidental Mutation 'R5872:Cmya5'
ID 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 13
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

DomainStartEndE-ValueType
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
GeneRefVarChr/LocMutationPredicted EffectZygosity
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
AlleleSourceChrCoordTypePredicted EffectPPH 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