Incidental Mutation 'R9564:Myh8'
ID 721378
Institutional Source Beutler Lab
Gene Symbol Myh8
Ensembl Gene ENSMUSG00000055775
Gene Name myosin, heavy polypeptide 8, skeletal muscle, perinatal
Synonyms Myhsp, MyHC-pn, Myhs-p, 4832426G23Rik
MMRRC Submission
Accession Numbers
Essential gene? Probably essential (E-score: 0.826) question?
Stock # R9564 (G1)
Quality Score 225.009
Status Not validated
Chromosome 11
Chromosomal Location 67167950-67199460 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 67177215 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 427 (V427A)
Ref Sequence ENSEMBL: ENSMUSP00000019625 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000019625] [ENSMUST00000108685]
AlphaFold P13542
Predicted Effect probably benign
Transcript: ENSMUST00000019625
AA Change: V427A

PolyPhen 2 Score 0.398 (Sensitivity: 0.89; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000019625
Gene: ENSMUSG00000055775
AA Change: V427A

DomainStartEndE-ValueType
Pfam:Myosin_N 37 76 2.1e-13 PFAM
MYSc 82 782 N/A SMART
IQ 783 805 5.44e-3 SMART
Pfam:Myosin_tail_1 846 1927 2.4e-164 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000108685
SMART Domains Protein: ENSMUSP00000104325
Gene: ENSMUSG00000055775

DomainStartEndE-ValueType
Pfam:Myosin_N 37 78 3.8e-17 PFAM
Pfam:Myosin_head 90 172 1.7e-31 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes a myosin heavy chain. The encoded protein forms a hexamer with two heavy chains, two alkali light chains, and two regulatory light chain components. This complex functions in muscle contraction. This gene is located in a cluster of related genes on chromosome 11. [provided by RefSeq, Jun 2013]
Allele List at MGI
Other mutations in this stock
Total: 135 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700097O09Rik A T 12: 55,104,090 (GRCm39) N176K possibly damaging Het
3110009E18Rik T A 1: 120,097,006 (GRCm39) V134E Het
Abca8a T A 11: 109,965,010 (GRCm39) H429L probably benign Het
Acsf2 T A 11: 94,463,891 (GRCm39) I98F possibly damaging Het
Actr5 A G 2: 158,470,135 (GRCm39) D255G probably damaging Het
Adam21 C T 12: 81,605,833 (GRCm39) C643Y probably damaging Het
Adcy7 TGG TG 8: 89,053,053 (GRCm39) probably null Het
AI429214 A G 8: 37,461,067 (GRCm39) S72G possibly damaging Het
Akap13 T C 7: 75,259,161 (GRCm39) V595A probably benign Het
Akt3 T C 1: 176,907,769 (GRCm39) T209A possibly damaging Het
Alpk2 C T 18: 65,439,014 (GRCm39) G793D probably damaging Het
Amotl1 T C 9: 14,473,513 (GRCm39) K562R possibly damaging Het
Ankib1 T A 5: 3,805,733 (GRCm39) N178I possibly damaging Het
Arfgef1 A T 1: 10,217,758 (GRCm39) D1560E probably benign Het
Arhgap20 AAGAGAG AAGAG 9: 51,761,413 (GRCm39) probably null Het
Arpc5l A G 2: 38,905,124 (GRCm39) T152A probably benign Het
Asic3 C G 5: 24,620,875 (GRCm39) D252E possibly damaging Het
Atf7 T A 15: 102,442,712 (GRCm39) M466L probably benign Het
Bcl9l A G 9: 44,420,554 (GRCm39) D1320G probably damaging Het
Bdkrb1 G A 12: 105,571,078 (GRCm39) V215I probably benign Het
Brpf3 T G 17: 29,026,152 (GRCm39) D408E probably benign Het
Btn2a2 C A 13: 23,662,848 (GRCm39) K367N possibly damaging Het
Btnl10 T A 11: 58,813,189 (GRCm39) F273I probably benign Het
C1qtnf12 C T 4: 156,049,473 (GRCm39) T145I probably benign Het
Cacna1s T C 1: 136,046,516 (GRCm39) C1763R probably benign Het
Ccdc154 C A 17: 25,387,381 (GRCm39) Q372K possibly damaging Het
Cd300ld2 CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG 11: 114,903,257 (GRCm39) probably benign Het
Celsr2 T C 3: 108,321,834 (GRCm39) Y326C probably damaging Het
Cfap46 A T 7: 139,231,471 (GRCm39) V914E Het
Coil T A 11: 88,872,626 (GRCm39) V329E possibly damaging Het
Copb1 A G 7: 113,836,034 (GRCm39) I449T possibly damaging Het
Copg1 T G 6: 87,869,683 (GRCm39) S187R probably damaging Het
Cps1 T A 1: 67,198,048 (GRCm39) F371Y probably benign Het
Cpt1b A T 15: 89,303,472 (GRCm39) F554L probably damaging Het
Ctdsp2 A G 10: 126,832,040 (GRCm39) D216G probably damaging Het
Ctla2b A T 13: 61,043,856 (GRCm39) Y104* probably null Het
Cyp2j6 A G 4: 96,414,245 (GRCm39) I340T probably damaging Het
Ddi1 T A 9: 6,265,730 (GRCm39) D213V probably damaging Het
Degs1l G T 1: 180,882,810 (GRCm39) V191F possibly damaging Het
Dennd2b G T 7: 109,125,536 (GRCm39) D980E probably damaging Het
Dlgap1 T G 17: 70,964,458 (GRCm39) N400K probably benign Het
Dnah5 G A 15: 28,290,422 (GRCm39) V1271M probably benign Het
Dnah8 T A 17: 30,932,021 (GRCm39) V1463E probably benign Het
Dstyk G A 1: 132,362,023 (GRCm39) R151H probably damaging Het
Ehd3 T G 17: 74,137,361 (GRCm39) V510G probably benign Het
Enthd1 G T 15: 80,444,235 (GRCm39) Q107K probably damaging Het
Entpd7 A G 19: 43,705,889 (GRCm39) E237G probably benign Het
Fadd A T 7: 144,136,048 (GRCm39) C27S probably damaging Het
Fan1 A G 7: 63,999,240 (GRCm39) L874P possibly damaging Het
Fbxw17 T C 13: 50,579,605 (GRCm39) W141R probably damaging Het
Fig4 A G 10: 41,161,387 (GRCm39) V63A probably benign Het
Fmo3 T C 1: 162,786,021 (GRCm39) D323G probably damaging Het
Gas8 T A 8: 124,263,179 (GRCm39) V452E possibly damaging Het
Gdf9 T A 11: 53,327,511 (GRCm39) S156T probably damaging Het
Hlcs T C 16: 93,935,580 (GRCm39) S571G probably benign Het
Hmox2 A G 16: 4,582,870 (GRCm39) Y201C probably damaging Het
Ikzf3 T A 11: 98,358,032 (GRCm39) D435V probably damaging Het
Kank2 T C 9: 21,705,852 (GRCm39) T389A possibly damaging Het
Kank2 A G 9: 21,706,631 (GRCm39) L129P probably damaging Het
Kdr T A 5: 76,125,565 (GRCm39) K339N probably benign Het
Lmntd2 A G 7: 140,790,701 (GRCm39) S516P Het
Lrrc37 T C 11: 103,503,822 (GRCm39) I2715M unknown Het
Lrrc40 T A 3: 157,746,078 (GRCm39) V51D probably benign Het
Lrrtm1 A G 6: 77,221,536 (GRCm39) N331S probably benign Het
Lvrn T G 18: 47,017,506 (GRCm39) I612S probably damaging Het
Map3k3 T A 11: 106,041,860 (GRCm39) I413N probably damaging Het
Mcm9 C T 10: 53,506,104 (GRCm39) A57T possibly damaging Het
Met T A 6: 17,531,425 (GRCm39) F568I probably benign Het
Mkx A G 18: 7,002,457 (GRCm39) F30L probably benign Het
Mrc1 A G 2: 14,266,117 (GRCm39) N345S probably benign Het
Mstn T A 1: 53,103,367 (GRCm39) N234K probably benign Het
Mtmr3 A T 11: 4,440,992 (GRCm39) S554T possibly damaging Het
Mug1 G A 6: 121,861,587 (GRCm39) V1350I probably benign Het
Nr4a2 A T 2: 57,000,190 (GRCm39) I365N probably damaging Het
Nrxn2 A G 19: 6,559,887 (GRCm39) D1215G probably damaging Het
Or2d3c A G 7: 106,525,847 (GRCm39) M273T probably benign Het
Or6c33 T C 10: 129,853,287 (GRCm39) I19T probably benign Het
Or7g18 G A 9: 18,786,640 (GRCm39) V3I probably benign Het
Osbpl6 T A 2: 76,426,321 (GRCm39) W967R probably damaging Het
Pcdhb21 T C 18: 37,646,972 (GRCm39) S34P possibly damaging Het
Pibf1 G T 14: 99,374,610 (GRCm39) D350Y possibly damaging Het
Pira1 C T 7: 3,742,646 (GRCm39) V21M possibly damaging Het
Plekhs1 A T 19: 56,461,628 (GRCm39) I123F probably damaging Het
Pold2 C T 11: 5,824,163 (GRCm39) G214D probably benign Het
Pomc A G 12: 4,009,971 (GRCm39) T71A probably benign Het
Pot1b A G 17: 55,969,465 (GRCm39) S568P possibly damaging Het
Prkd2 C A 7: 16,591,744 (GRCm39) Q592K possibly damaging Het
Prss28 C T 17: 25,528,911 (GRCm39) A84V probably damaging Het
Prtg T A 9: 72,766,153 (GRCm39) Y649N probably damaging Het
Psip1 T C 4: 83,386,888 (GRCm39) E161G possibly damaging Het
Rab3gap2 A G 1: 185,014,691 (GRCm39) D1280G probably damaging Het
Rab3ip A T 10: 116,751,780 (GRCm39) I329N probably damaging Het
Rarres2 C T 6: 48,549,164 (GRCm39) G13D possibly damaging Het
Rbp3 A G 14: 33,677,477 (GRCm39) D475G probably damaging Het
Ric3 A G 7: 108,638,018 (GRCm39) V246A probably damaging Het
Robo3 A G 9: 37,340,900 (GRCm39) F124S probably damaging Het
Rpl27a C A 7: 109,118,837 (GRCm39) H17N probably benign Het
Rptn A G 3: 93,304,536 (GRCm39) D623G probably benign Het
Rtl1 G T 12: 109,556,713 (GRCm39) Q1709K probably benign Het
Sacs T A 14: 61,449,046 (GRCm39) D3697E probably damaging Het
Sec61b A G 4: 47,483,049 (GRCm39) Y93C probably damaging Het
Serpina3a A T 12: 104,084,886 (GRCm39) I94L probably benign Het
Skic2 C T 17: 35,063,758 (GRCm39) A562T probably benign Het
Skor2 C T 18: 76,946,376 (GRCm39) H33Y unknown Het
Slc12a3 G A 8: 95,082,983 (GRCm39) V874I probably benign Het
Slit1 T A 19: 41,591,861 (GRCm39) M1254L probably benign Het
Smg1 A G 7: 117,812,208 (GRCm39) S52P unknown Het
Sorl1 A G 9: 41,957,893 (GRCm39) Y584H probably damaging Het
Spata32 T A 11: 103,099,779 (GRCm39) Q242L possibly damaging Het
Sptbn4 T G 7: 27,117,504 (GRCm39) E415A probably damaging Het
St6galnac5 T C 3: 152,545,782 (GRCm39) R259G probably damaging Het
Stat3 T C 11: 100,784,614 (GRCm39) I589V probably benign Het
Tecta T A 9: 42,249,123 (GRCm39) K1913M probably damaging Het
Tek C A 4: 94,762,172 (GRCm39) N1103K probably damaging Het
Telo2 A G 17: 25,334,199 (GRCm39) I16T probably benign Het
Tmem207 G T 16: 26,335,499 (GRCm39) C79* probably null Het
Topaz1 C T 9: 122,579,219 (GRCm39) H710Y probably benign Het
Trim33 T A 3: 103,238,965 (GRCm39) S648T probably benign Het
Trpm6 A G 19: 18,851,240 (GRCm39) T1734A possibly damaging Het
Trpm8 A G 1: 88,254,158 (GRCm39) E127G possibly damaging Het
Ttc3 T A 16: 94,248,918 (GRCm39) C1139S probably benign Het
Ttn T C 2: 76,580,330 (GRCm39) E23521G probably damaging Het
Ush2a T C 1: 188,268,551 (GRCm39) I1669T possibly damaging Het
Vcpip1 C A 1: 9,817,456 (GRCm39) S309I possibly damaging Het
Vmn1r208 A G 13: 22,956,789 (GRCm39) V236A probably damaging Het
Vmn1r74 T C 7: 11,581,534 (GRCm39) F278S probably damaging Het
Vmn2r33 T C 7: 7,557,081 (GRCm39) S540G probably benign Het
Vmn2r52 T C 7: 9,905,182 (GRCm39) D219G probably benign Het
Wiz G T 17: 32,575,939 (GRCm39) D812E probably benign Het
Ylpm1 C T 12: 85,091,176 (GRCm39) P1787S probably benign Het
Zan T C 5: 137,404,688 (GRCm39) E3858G unknown Het
Zfp760 T G 17: 21,942,272 (GRCm39) H482Q possibly damaging Het
Zfp78 A G 7: 6,381,390 (GRCm39) T147A probably benign Het
Zfp808 T A 13: 62,320,661 (GRCm39) I630K possibly damaging Het
Zpld1 T A 16: 55,061,701 (GRCm39) R227* probably null Het
Other mutations in Myh8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00236:Myh8 APN 11 67,174,644 (GRCm39) missense probably damaging 0.97
IGL01020:Myh8 APN 11 67,174,229 (GRCm39) missense probably damaging 0.99
IGL01348:Myh8 APN 11 67,188,606 (GRCm39) missense probably damaging 1.00
IGL01382:Myh8 APN 11 67,192,799 (GRCm39) missense probably damaging 1.00
IGL01454:Myh8 APN 11 67,174,422 (GRCm39) missense probably damaging 1.00
IGL01457:Myh8 APN 11 67,183,505 (GRCm39) missense probably benign 0.00
IGL01472:Myh8 APN 11 67,179,205 (GRCm39) splice site probably benign
IGL01473:Myh8 APN 11 67,192,651 (GRCm39) critical splice donor site probably null
IGL01613:Myh8 APN 11 67,192,536 (GRCm39) missense probably benign 0.11
IGL01763:Myh8 APN 11 67,177,245 (GRCm39) missense probably benign 0.01
IGL01828:Myh8 APN 11 67,194,652 (GRCm39) missense possibly damaging 0.82
IGL01862:Myh8 APN 11 67,180,520 (GRCm39) nonsense probably null
IGL01905:Myh8 APN 11 67,175,477 (GRCm39) missense possibly damaging 0.90
IGL02280:Myh8 APN 11 67,174,198 (GRCm39) unclassified probably benign
IGL02386:Myh8 APN 11 67,185,266 (GRCm39) missense probably damaging 0.99
IGL02449:Myh8 APN 11 67,185,440 (GRCm39) critical splice donor site probably null
IGL02500:Myh8 APN 11 67,196,536 (GRCm39) missense probably benign 0.00
IGL02745:Myh8 APN 11 67,188,327 (GRCm39) missense possibly damaging 0.88
IGL02799:Myh8 APN 11 67,192,418 (GRCm39) splice site probably benign
IGL03063:Myh8 APN 11 67,179,031 (GRCm39) missense probably benign 0.00
IGL03223:Myh8 APN 11 67,174,644 (GRCm39) missense probably damaging 0.97
IGL03336:Myh8 APN 11 67,175,528 (GRCm39) missense probably damaging 1.00
IGL03338:Myh8 APN 11 67,189,172 (GRCm39) missense probably damaging 1.00
IGL03351:Myh8 APN 11 67,194,739 (GRCm39) missense possibly damaging 0.94
IGL03392:Myh8 APN 11 67,185,244 (GRCm39) missense probably damaging 1.00
BB003:Myh8 UTSW 11 67,169,732 (GRCm39) missense possibly damaging 0.94
BB009:Myh8 UTSW 11 67,185,430 (GRCm39) missense probably benign 0.00
BB013:Myh8 UTSW 11 67,169,732 (GRCm39) missense possibly damaging 0.94
BB019:Myh8 UTSW 11 67,185,430 (GRCm39) missense probably benign 0.00
PIT4354001:Myh8 UTSW 11 67,180,456 (GRCm39) missense probably benign 0.01
R0012:Myh8 UTSW 11 67,190,847 (GRCm39) missense probably benign 0.02
R0016:Myh8 UTSW 11 67,189,351 (GRCm39) missense probably damaging 1.00
R0016:Myh8 UTSW 11 67,189,351 (GRCm39) missense probably damaging 1.00
R0115:Myh8 UTSW 11 67,197,090 (GRCm39) splice site probably benign
R0131:Myh8 UTSW 11 67,183,014 (GRCm39) missense probably damaging 0.96
R0131:Myh8 UTSW 11 67,183,014 (GRCm39) missense probably damaging 0.96
R0132:Myh8 UTSW 11 67,183,014 (GRCm39) missense probably damaging 0.96
R0238:Myh8 UTSW 11 67,192,518 (GRCm39) missense probably benign 0.00
R0238:Myh8 UTSW 11 67,192,518 (GRCm39) missense probably benign 0.00
R0239:Myh8 UTSW 11 67,192,518 (GRCm39) missense probably benign 0.00
R0239:Myh8 UTSW 11 67,192,518 (GRCm39) missense probably benign 0.00
R0393:Myh8 UTSW 11 67,196,843 (GRCm39) splice site probably benign
R0453:Myh8 UTSW 11 67,183,731 (GRCm39) missense probably benign 0.03
R0454:Myh8 UTSW 11 67,194,591 (GRCm39) nonsense probably null
R0466:Myh8 UTSW 11 67,189,405 (GRCm39) missense probably benign 0.01
R0487:Myh8 UTSW 11 67,192,837 (GRCm39) missense probably benign
R0511:Myh8 UTSW 11 67,175,333 (GRCm39) missense probably benign 0.01
R0557:Myh8 UTSW 11 67,192,624 (GRCm39) missense possibly damaging 0.88
R0589:Myh8 UTSW 11 67,189,453 (GRCm39) missense probably benign 0.00
R0658:Myh8 UTSW 11 67,175,358 (GRCm39) critical splice donor site probably null
R0782:Myh8 UTSW 11 67,180,580 (GRCm39) missense probably benign 0.16
R0829:Myh8 UTSW 11 67,174,326 (GRCm39) unclassified probably benign
R0845:Myh8 UTSW 11 67,177,090 (GRCm39) missense probably damaging 1.00
R0930:Myh8 UTSW 11 67,196,824 (GRCm39) missense possibly damaging 0.93
R0972:Myh8 UTSW 11 67,188,585 (GRCm39) missense probably damaging 1.00
R1132:Myh8 UTSW 11 67,187,957 (GRCm39) nonsense probably null
R1417:Myh8 UTSW 11 67,197,011 (GRCm39) missense probably damaging 1.00
R1478:Myh8 UTSW 11 67,183,551 (GRCm39) missense probably benign 0.23
R1497:Myh8 UTSW 11 67,180,638 (GRCm39) missense probably benign 0.00
R1605:Myh8 UTSW 11 67,192,497 (GRCm39) missense probably damaging 0.99
R1701:Myh8 UTSW 11 67,170,964 (GRCm39) missense probably damaging 1.00
R1950:Myh8 UTSW 11 67,169,830 (GRCm39) missense possibly damaging 0.75
R1989:Myh8 UTSW 11 67,183,550 (GRCm39) missense probably benign 0.00
R2010:Myh8 UTSW 11 67,187,990 (GRCm39) nonsense probably null
R2095:Myh8 UTSW 11 67,177,050 (GRCm39) missense probably benign 0.00
R2132:Myh8 UTSW 11 67,183,702 (GRCm39) missense probably damaging 1.00
R2152:Myh8 UTSW 11 67,185,295 (GRCm39) missense probably damaging 0.97
R2229:Myh8 UTSW 11 67,199,174 (GRCm39) missense probably damaging 0.98
R2302:Myh8 UTSW 11 67,177,065 (GRCm39) missense probably damaging 1.00
R2364:Myh8 UTSW 11 67,185,344 (GRCm39) missense probably benign 0.03
R2429:Myh8 UTSW 11 67,194,723 (GRCm39) missense probably benign 0.21
R2880:Myh8 UTSW 11 67,188,090 (GRCm39) missense probably damaging 0.97
R3692:Myh8 UTSW 11 67,192,744 (GRCm39) missense probably damaging 0.98
R3756:Myh8 UTSW 11 67,175,443 (GRCm39) unclassified probably benign
R3924:Myh8 UTSW 11 67,187,963 (GRCm39) missense probably damaging 0.99
R4172:Myh8 UTSW 11 67,183,247 (GRCm39) missense probably damaging 1.00
R4255:Myh8 UTSW 11 67,190,560 (GRCm39) missense probably benign
R4621:Myh8 UTSW 11 67,177,084 (GRCm39) missense probably damaging 1.00
R4623:Myh8 UTSW 11 67,177,084 (GRCm39) missense probably damaging 1.00
R4790:Myh8 UTSW 11 67,170,789 (GRCm39) missense probably damaging 0.99
R4914:Myh8 UTSW 11 67,183,510 (GRCm39) missense probably damaging 1.00
R5074:Myh8 UTSW 11 67,196,742 (GRCm39) missense possibly damaging 0.79
R5119:Myh8 UTSW 11 67,189,184 (GRCm39) missense probably damaging 1.00
R5159:Myh8 UTSW 11 67,179,179 (GRCm39) missense probably damaging 0.99
R5229:Myh8 UTSW 11 67,175,310 (GRCm39) missense probably damaging 0.96
R5320:Myh8 UTSW 11 67,177,089 (GRCm39) missense probably damaging 1.00
R5455:Myh8 UTSW 11 67,192,244 (GRCm39) missense possibly damaging 0.59
R5523:Myh8 UTSW 11 67,196,788 (GRCm39) missense possibly damaging 0.95
R5540:Myh8 UTSW 11 67,177,266 (GRCm39) missense probably benign 0.00
R5726:Myh8 UTSW 11 67,185,392 (GRCm39) missense possibly damaging 0.79
R5770:Myh8 UTSW 11 67,188,026 (GRCm39) missense probably damaging 1.00
R6135:Myh8 UTSW 11 67,188,326 (GRCm39) missense possibly damaging 0.51
R6253:Myh8 UTSW 11 67,192,793 (GRCm39) missense probably benign 0.06
R6318:Myh8 UTSW 11 67,190,167 (GRCm39) missense probably benign 0.00
R6432:Myh8 UTSW 11 67,189,405 (GRCm39) missense probably benign 0.01
R6452:Myh8 UTSW 11 67,196,565 (GRCm39) missense possibly damaging 0.88
R6452:Myh8 UTSW 11 67,183,275 (GRCm39) missense probably benign 0.27
R6512:Myh8 UTSW 11 67,180,488 (GRCm39) nonsense probably null
R6714:Myh8 UTSW 11 67,197,775 (GRCm39) missense probably damaging 1.00
R6842:Myh8 UTSW 11 67,175,481 (GRCm39) missense probably damaging 1.00
R7007:Myh8 UTSW 11 67,179,142 (GRCm39) missense probably benign 0.03
R7025:Myh8 UTSW 11 67,188,365 (GRCm39) missense probably benign 0.02
R7086:Myh8 UTSW 11 67,183,453 (GRCm39) splice site probably null
R7098:Myh8 UTSW 11 67,169,879 (GRCm39) missense probably benign 0.03
R7498:Myh8 UTSW 11 67,174,263 (GRCm39) missense possibly damaging 0.80
R7716:Myh8 UTSW 11 67,189,478 (GRCm39) missense possibly damaging 0.51
R7765:Myh8 UTSW 11 67,194,481 (GRCm39) missense probably benign 0.44
R7825:Myh8 UTSW 11 67,194,538 (GRCm39) missense possibly damaging 0.94
R7921:Myh8 UTSW 11 67,174,644 (GRCm39) missense probably damaging 0.97
R7926:Myh8 UTSW 11 67,169,732 (GRCm39) missense possibly damaging 0.94
R7932:Myh8 UTSW 11 67,185,430 (GRCm39) missense probably benign 0.00
R8003:Myh8 UTSW 11 67,190,586 (GRCm39) missense probably damaging 1.00
R8028:Myh8 UTSW 11 67,194,502 (GRCm39) missense possibly damaging 0.65
R8121:Myh8 UTSW 11 67,180,647 (GRCm39) missense probably benign 0.00
R8125:Myh8 UTSW 11 67,190,598 (GRCm39) missense possibly damaging 0.94
R8170:Myh8 UTSW 11 67,179,092 (GRCm39) missense probably benign 0.30
R8277:Myh8 UTSW 11 67,183,735 (GRCm39) missense probably benign 0.10
R8304:Myh8 UTSW 11 67,195,162 (GRCm39) missense possibly damaging 0.72
R8431:Myh8 UTSW 11 67,174,440 (GRCm39) missense possibly damaging 0.94
R8535:Myh8 UTSW 11 67,169,741 (GRCm39) missense probably damaging 1.00
R8795:Myh8 UTSW 11 67,174,203 (GRCm39) critical splice acceptor site probably benign
R8858:Myh8 UTSW 11 67,192,820 (GRCm39) missense possibly damaging 0.67
R8927:Myh8 UTSW 11 67,174,081 (GRCm39) missense probably benign 0.10
R8928:Myh8 UTSW 11 67,174,081 (GRCm39) missense probably benign 0.10
R9031:Myh8 UTSW 11 67,190,141 (GRCm39) missense possibly damaging 0.49
R9172:Myh8 UTSW 11 67,183,260 (GRCm39) missense possibly damaging 0.82
R9252:Myh8 UTSW 11 67,177,302 (GRCm39) missense probably damaging 1.00
R9365:Myh8 UTSW 11 67,174,632 (GRCm39) missense probably benign 0.42
R9468:Myh8 UTSW 11 67,197,730 (GRCm39) missense probably damaging 1.00
R9565:Myh8 UTSW 11 67,177,215 (GRCm39) missense probably benign 0.40
T0722:Myh8 UTSW 11 67,195,262 (GRCm39) missense probably benign 0.41
Z1088:Myh8 UTSW 11 67,189,418 (GRCm39) missense probably damaging 1.00
Z1176:Myh8 UTSW 11 67,194,500 (GRCm39) missense probably damaging 1.00
Z1177:Myh8 UTSW 11 67,199,181 (GRCm39) missense possibly damaging 0.64
Z1177:Myh8 UTSW 11 67,192,250 (GRCm39) missense probably damaging 0.99
Z1187:Myh8 UTSW 11 67,188,312 (GRCm39) missense probably benign
Z1188:Myh8 UTSW 11 67,188,312 (GRCm39) missense probably benign
Z1190:Myh8 UTSW 11 67,188,312 (GRCm39) missense probably benign
Z1191:Myh8 UTSW 11 67,188,312 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- TCACCACAGTGGCTGACAAG -3'
(R):5'- GTTCAAAATTGTGTCCCTCACTTCG -3'

Sequencing Primer
(F):5'- GAACTCTGCTGATCTGCTCAAAG -3'
(R):5'- GTGTCCCTCACTTCGTATTATTATG -3'
Posted On 2022-08-09