Incidental Mutation 'R5119:Myh8'
ID |
392840 |
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 |
042707-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.825)
|
Stock # |
R5119 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
67167950-67199460 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 67189184 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 1120
(E1120G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000019625
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000019625]
|
AlphaFold |
P13542 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000019625
AA Change: E1120G
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000019625 Gene: ENSMUSG00000055775 AA Change: E1120G
Domain | Start | End | E-Value | Type |
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 |
noncoding transcript
Transcript: ENSMUST00000108686
|
Meta Mutation Damage Score |
0.2439 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.1%
|
Validation Efficiency |
100% (127/127) |
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: 120 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930470P17Rik |
C |
A |
2: 170,421,505 (GRCm39) |
G125V |
unknown |
Het |
Actr6 |
A |
T |
10: 89,561,717 (GRCm39) |
L143Q |
probably damaging |
Het |
Adamts18 |
A |
G |
8: 114,425,642 (GRCm39) |
Y1207H |
probably benign |
Het |
Adamts5 |
T |
A |
16: 85,696,466 (GRCm39) |
R230S |
probably benign |
Het |
Adat2 |
A |
T |
10: 13,432,650 (GRCm39) |
N51Y |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,567,546 (GRCm39) |
Y5209C |
possibly damaging |
Het |
Ahnak |
G |
T |
19: 8,991,008 (GRCm39) |
M4097I |
probably benign |
Het |
Akap13 |
A |
G |
7: 75,337,000 (GRCm39) |
T820A |
probably damaging |
Het |
Als2cl |
C |
T |
9: 110,719,887 (GRCm39) |
R492C |
probably damaging |
Het |
Aox3 |
G |
A |
1: 58,227,683 (GRCm39) |
|
probably null |
Het |
Arid4b |
G |
A |
13: 14,338,866 (GRCm39) |
V446M |
probably benign |
Het |
Armc2 |
A |
G |
10: 41,798,144 (GRCm39) |
L794P |
probably damaging |
Het |
Atp6v0a1 |
T |
A |
11: 100,911,341 (GRCm39) |
M80K |
probably benign |
Het |
Aup1 |
T |
C |
6: 83,032,115 (GRCm39) |
V94A |
probably damaging |
Het |
Bank1 |
A |
T |
3: 135,940,443 (GRCm39) |
I180K |
possibly damaging |
Het |
Becn1 |
A |
G |
11: 101,182,221 (GRCm39) |
L116P |
probably damaging |
Het |
Bsg |
A |
G |
10: 79,546,057 (GRCm39) |
|
probably benign |
Het |
Camk2a |
A |
T |
18: 61,076,208 (GRCm39) |
|
probably benign |
Het |
Ccdc180 |
A |
G |
4: 45,914,603 (GRCm39) |
E706G |
possibly damaging |
Het |
Cdk8 |
A |
T |
5: 146,220,437 (GRCm39) |
|
probably null |
Het |
Cpne4 |
A |
G |
9: 104,778,720 (GRCm39) |
|
probably null |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Cyp2c38 |
C |
A |
19: 39,449,065 (GRCm39) |
G96V |
probably damaging |
Het |
Dhx40 |
A |
G |
11: 86,667,462 (GRCm39) |
I261T |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,856,322 (GRCm39) |
F2038L |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,737,851 (GRCm39) |
D27E |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,545,711 (GRCm39) |
|
probably null |
Het |
Dst |
A |
T |
1: 34,235,050 (GRCm39) |
K3710* |
probably null |
Het |
Dtl |
G |
T |
1: 191,273,618 (GRCm39) |
A430D |
probably damaging |
Het |
Ece2 |
T |
C |
16: 20,437,381 (GRCm39) |
L241P |
probably damaging |
Het |
Ecel1 |
T |
A |
1: 87,078,861 (GRCm39) |
Y526F |
probably benign |
Het |
Enpp2 |
T |
A |
15: 54,733,701 (GRCm39) |
R420* |
probably null |
Het |
Epb41 |
A |
C |
4: 131,664,747 (GRCm39) |
|
probably benign |
Het |
Eppin |
T |
C |
2: 164,431,371 (GRCm39) |
Y85C |
probably damaging |
Het |
Fam171a2 |
G |
A |
11: 102,329,559 (GRCm39) |
A400V |
probably damaging |
Het |
Fem1c |
A |
C |
18: 46,639,436 (GRCm39) |
C189G |
probably damaging |
Het |
Frmd4b |
A |
G |
6: 97,277,275 (GRCm39) |
V560A |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,818,535 (GRCm39) |
D4756V |
probably damaging |
Het |
Gabbr1 |
T |
C |
17: 37,359,330 (GRCm39) |
S102P |
probably damaging |
Het |
Garin3 |
G |
A |
11: 46,297,863 (GRCm39) |
G389D |
probably damaging |
Het |
Gm28042 |
G |
A |
2: 119,865,124 (GRCm39) |
A250T |
probably damaging |
Het |
Gm30275 |
T |
C |
14: 54,312,978 (GRCm39) |
|
probably benign |
Het |
Gm9762 |
A |
T |
3: 78,873,707 (GRCm39) |
|
noncoding transcript |
Het |
Gpr183 |
G |
T |
14: 122,192,275 (GRCm39) |
T82N |
possibly damaging |
Het |
Gps2 |
A |
G |
11: 69,805,617 (GRCm39) |
K45R |
probably benign |
Het |
Gramd2a |
A |
G |
9: 59,621,603 (GRCm39) |
|
probably benign |
Het |
Grap2 |
G |
A |
15: 80,530,345 (GRCm39) |
R155Q |
possibly damaging |
Het |
Hsdl1 |
T |
A |
8: 120,292,606 (GRCm39) |
Y203F |
possibly damaging |
Het |
Ifi204 |
A |
T |
1: 173,583,234 (GRCm39) |
I328N |
probably damaging |
Het |
Igsf3 |
T |
A |
3: 101,346,677 (GRCm39) |
|
probably null |
Het |
Il1rap |
T |
C |
16: 26,442,949 (GRCm39) |
I15T |
probably benign |
Het |
Il23r |
A |
T |
6: 67,443,300 (GRCm39) |
C268S |
probably damaging |
Het |
Irx4 |
A |
G |
13: 73,417,040 (GRCm39) |
T479A |
probably benign |
Het |
Kcnk7 |
G |
A |
19: 5,756,352 (GRCm39) |
V193I |
probably benign |
Het |
Kcnt1 |
G |
T |
2: 25,799,334 (GRCm39) |
|
probably benign |
Het |
Kif13b |
T |
G |
14: 64,994,902 (GRCm39) |
C885G |
probably benign |
Het |
Kif21b |
C |
A |
1: 136,090,838 (GRCm39) |
D1215E |
probably benign |
Het |
Klhdc2 |
A |
G |
12: 69,343,736 (GRCm39) |
|
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,745,075 (GRCm39) |
|
probably benign |
Het |
Lama4 |
A |
G |
10: 38,924,050 (GRCm39) |
N486S |
probably benign |
Het |
Ldah |
G |
A |
12: 8,277,237 (GRCm39) |
A58T |
probably benign |
Het |
Lrrc24 |
T |
C |
15: 76,600,200 (GRCm39) |
Q313R |
probably benign |
Het |
Luzp1 |
A |
G |
4: 136,270,708 (GRCm39) |
D977G |
possibly damaging |
Het |
Meak7 |
A |
C |
8: 120,494,882 (GRCm39) |
L292R |
probably damaging |
Het |
Mrgpra4 |
A |
G |
7: 47,631,466 (GRCm39) |
L45P |
probably damaging |
Het |
Mrps28 |
C |
T |
3: 8,988,756 (GRCm39) |
G34D |
possibly damaging |
Het |
Myt1l |
A |
G |
12: 29,882,302 (GRCm39) |
E499G |
unknown |
Het |
Ncan |
C |
T |
8: 70,567,675 (GRCm39) |
E146K |
probably damaging |
Het |
Nlgn1 |
A |
T |
3: 25,487,958 (GRCm39) |
D763E |
probably damaging |
Het |
Or11g26 |
T |
C |
14: 50,752,966 (GRCm39) |
F102L |
probably benign |
Het |
Or13c7c |
G |
T |
4: 43,836,433 (GRCm39) |
A19D |
probably benign |
Het |
Or1e17 |
A |
T |
11: 73,831,378 (GRCm39) |
Y102F |
possibly damaging |
Het |
Or4c12 |
A |
T |
2: 89,774,147 (GRCm39) |
I104N |
possibly damaging |
Het |
Or5b118 |
C |
T |
19: 13,448,910 (GRCm39) |
T192I |
probably benign |
Het |
Or6c8b |
T |
A |
10: 128,882,711 (GRCm39) |
I74F |
possibly damaging |
Het |
Pak6 |
A |
T |
2: 118,525,029 (GRCm39) |
I552F |
probably damaging |
Het |
Pcbp1 |
G |
A |
6: 86,501,897 (GRCm39) |
A334V |
probably damaging |
Het |
Pclaf |
T |
C |
9: 65,798,062 (GRCm39) |
V32A |
probably benign |
Het |
Pga5 |
T |
A |
19: 10,654,053 (GRCm39) |
H50L |
probably benign |
Het |
Phyhipl |
A |
T |
10: 70,404,904 (GRCm39) |
D56E |
probably damaging |
Het |
Pik3ap1 |
C |
T |
19: 41,270,415 (GRCm39) |
R758H |
probably benign |
Het |
Plekha1 |
A |
G |
7: 130,507,094 (GRCm39) |
|
probably benign |
Het |
Plekhm1 |
A |
T |
11: 103,278,141 (GRCm39) |
N318K |
possibly damaging |
Het |
Ppargc1b |
G |
A |
18: 61,440,725 (GRCm39) |
A731V |
probably benign |
Het |
Pptc7 |
T |
C |
5: 122,451,844 (GRCm39) |
V100A |
possibly damaging |
Het |
Prl7a1 |
A |
T |
13: 27,817,564 (GRCm39) |
H233Q |
possibly damaging |
Het |
Prpf40a |
A |
G |
2: 53,034,861 (GRCm39) |
F776L |
probably damaging |
Het |
Prrc2c |
T |
C |
1: 162,533,009 (GRCm39) |
|
probably benign |
Het |
Psmb1 |
T |
C |
17: 15,718,524 (GRCm39) |
M1V |
probably null |
Het |
Ptpn3 |
A |
G |
4: 57,218,513 (GRCm39) |
F650S |
possibly damaging |
Het |
Ranbp17 |
A |
T |
11: 33,354,181 (GRCm39) |
*577R |
probably null |
Het |
Reln |
T |
A |
5: 22,176,868 (GRCm39) |
N1933Y |
probably benign |
Het |
Rgl2 |
T |
A |
17: 34,156,094 (GRCm39) |
H727Q |
probably benign |
Het |
Rhpn2 |
A |
G |
7: 35,070,549 (GRCm39) |
T160A |
probably damaging |
Het |
Rlf |
G |
A |
4: 121,004,652 (GRCm39) |
H1443Y |
probably damaging |
Het |
Rpgrip1l |
T |
C |
8: 92,007,444 (GRCm39) |
E382G |
probably damaging |
Het |
Rxrb |
T |
C |
17: 34,252,562 (GRCm39) |
S50P |
probably benign |
Het |
Scn4b |
A |
T |
9: 45,059,056 (GRCm39) |
E109V |
probably damaging |
Het |
Scrib |
C |
T |
15: 75,923,602 (GRCm39) |
|
probably null |
Het |
Slc22a29 |
A |
T |
19: 8,195,194 (GRCm39) |
V147D |
probably damaging |
Het |
Slc4a4 |
A |
T |
5: 89,102,721 (GRCm39) |
E53V |
probably null |
Het |
Slx4 |
A |
G |
16: 3,819,063 (GRCm39) |
S37P |
possibly damaging |
Het |
Spag9 |
G |
A |
11: 94,013,548 (GRCm39) |
G1127D |
probably damaging |
Het |
Srek1 |
T |
A |
13: 103,889,064 (GRCm39) |
|
probably benign |
Het |
Supt5 |
G |
T |
7: 28,015,795 (GRCm39) |
P849Q |
probably damaging |
Het |
Tex14 |
T |
C |
11: 87,324,639 (GRCm39) |
S2P |
probably damaging |
Het |
Them7 |
A |
G |
2: 105,209,153 (GRCm39) |
T158A |
probably benign |
Het |
Tll2 |
A |
G |
19: 41,118,948 (GRCm39) |
V260A |
possibly damaging |
Het |
Tlr6 |
A |
G |
5: 65,111,644 (GRCm39) |
V421A |
probably benign |
Het |
Tmc3 |
T |
G |
7: 83,264,218 (GRCm39) |
C649G |
probably damaging |
Het |
Tnn |
A |
G |
1: 159,948,122 (GRCm39) |
W864R |
probably damaging |
Het |
Tsc2 |
A |
C |
17: 24,822,254 (GRCm39) |
V1095G |
probably benign |
Het |
Vmn1r124 |
C |
T |
7: 20,994,172 (GRCm39) |
G124D |
probably damaging |
Het |
Vmn2r116 |
T |
C |
17: 23,606,138 (GRCm39) |
V350A |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,832,468 (GRCm39) |
S2813P |
possibly damaging |
Het |
Wrap53 |
T |
A |
11: 69,454,758 (GRCm39) |
M204L |
possibly damaging |
Het |
Zfp277 |
A |
G |
12: 40,378,687 (GRCm39) |
V390A |
possibly damaging |
Het |
Zfp687 |
A |
T |
3: 94,918,987 (GRCm39) |
S262T |
probably benign |
Het |
Zfp831 |
T |
A |
2: 174,547,103 (GRCm39) |
S1429T |
probably benign |
Het |
Znfx1 |
G |
A |
2: 166,907,307 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Myh8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |
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 |
R9564:Myh8
|
UTSW |
11 |
67,177,215 (GRCm39) |
missense |
probably benign |
0.40 |
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'- AGTTGCAGGTGACTCTTCTCTC -3'
(R):5'- CCCGGCGAAGTTTCTGAAAC -3'
Sequencing Primer
(F):5'- GCTAAACTATGTAACCCAGGTTGAC -3'
(R):5'- GAAACTCAGTTTCCCGCTTC -3'
|
Posted On |
2016-06-15 |