Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,188,908 (GRCm39) |
F850L |
probably benign |
Het |
Adam1a |
A |
T |
5: 121,657,411 (GRCm39) |
D627E |
probably damaging |
Het |
Add2 |
C |
A |
6: 86,081,459 (GRCm39) |
|
probably benign |
Het |
Anpep |
T |
C |
7: 79,491,785 (GRCm39) |
N72S |
probably benign |
Het |
Aqp6 |
A |
G |
15: 99,501,655 (GRCm39) |
T238A |
possibly damaging |
Het |
Arhgef38 |
G |
T |
3: 132,912,706 (GRCm39) |
T111K |
|
Het |
Atg10 |
A |
G |
13: 91,189,032 (GRCm39) |
Y93H |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Cald1 |
A |
G |
6: 34,732,682 (GRCm39) |
N286S |
unknown |
Het |
Caps2 |
A |
T |
10: 112,031,829 (GRCm39) |
I322F |
possibly damaging |
Het |
Cbx3 |
T |
A |
6: 51,455,533 (GRCm39) |
S95T |
probably benign |
Het |
Ccdc24 |
T |
C |
4: 117,727,102 (GRCm39) |
T83A |
unknown |
Het |
Cntn1 |
T |
C |
15: 92,140,864 (GRCm39) |
Y197H |
probably damaging |
Het |
Cpd |
A |
G |
11: 76,675,275 (GRCm39) |
I1282T |
possibly damaging |
Het |
Crat |
A |
T |
2: 30,295,052 (GRCm39) |
S454R |
probably damaging |
Het |
D2hgdh |
G |
A |
1: 93,754,338 (GRCm39) |
V126I |
probably benign |
Het |
Dcst1 |
A |
G |
3: 89,271,558 (GRCm39) |
V75A |
probably benign |
Het |
Dnm1l |
T |
C |
16: 16,176,668 (GRCm39) |
D21G |
probably benign |
Het |
Evc2 |
A |
G |
5: 37,504,823 (GRCm39) |
N74D |
probably benign |
Het |
Gm19965 |
A |
T |
1: 116,748,942 (GRCm39) |
M208L |
|
Het |
Gprc6a |
T |
G |
10: 51,497,182 (GRCm39) |
T454P |
possibly damaging |
Het |
Gprin1 |
C |
T |
13: 54,886,778 (GRCm39) |
V499M |
probably benign |
Het |
Gtf3c5 |
A |
G |
2: 28,463,577 (GRCm39) |
Y194H |
probably damaging |
Het |
Hcn4 |
T |
C |
9: 58,767,880 (GRCm39) |
V1147A |
possibly damaging |
Het |
Ighv1-82 |
A |
C |
12: 115,916,342 (GRCm39) |
V56G |
probably damaging |
Het |
Ins2 |
T |
C |
7: 142,232,505 (GRCm39) |
D93G |
possibly damaging |
Het |
Itgb8 |
A |
G |
12: 119,130,535 (GRCm39) |
S658P |
probably benign |
Het |
Kcnmb1 |
T |
C |
11: 33,920,263 (GRCm39) |
F159L |
probably benign |
Het |
Klf1 |
C |
T |
8: 85,629,954 (GRCm39) |
L260F |
probably benign |
Het |
Larp4 |
T |
A |
15: 99,888,205 (GRCm39) |
S140T |
possibly damaging |
Het |
Maneal |
C |
A |
4: 124,755,542 (GRCm39) |
R140L |
probably benign |
Het |
Mfsd11 |
T |
A |
11: 116,750,323 (GRCm39) |
V114D |
|
Het |
Muc4 |
A |
G |
16: 32,752,617 (GRCm38) |
T832A |
probably benign |
Het |
Myh11 |
T |
G |
16: 14,050,439 (GRCm39) |
I509L |
|
Het |
Myh7b |
A |
G |
2: 155,474,439 (GRCm39) |
E1718G |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,807,871 (GRCm39) |
|
probably benign |
Het |
Notch1 |
A |
T |
2: 26,367,939 (GRCm39) |
L656Q |
probably benign |
Het |
Nova1 |
A |
G |
12: 46,746,813 (GRCm39) |
I488T |
probably damaging |
Het |
Or51r1 |
A |
T |
7: 102,228,500 (GRCm39) |
E266V |
probably damaging |
Het |
Or5b113 |
A |
T |
19: 13,342,222 (GRCm39) |
T77S |
possibly damaging |
Het |
Or5b21 |
A |
G |
19: 12,839,976 (GRCm39) |
Y279C |
probably damaging |
Het |
Or5d18 |
A |
G |
2: 87,864,697 (GRCm39) |
V262A |
probably damaging |
Het |
Or6c35 |
A |
G |
10: 129,169,623 (GRCm39) |
N291S |
probably damaging |
Het |
Or6d13 |
A |
T |
6: 116,517,990 (GRCm39) |
N192I |
possibly damaging |
Het |
Pax6 |
C |
T |
2: 105,523,097 (GRCm39) |
S325L |
probably benign |
Het |
Phldb1 |
T |
C |
9: 44,619,740 (GRCm39) |
D142G |
probably null |
Het |
Phldb3 |
T |
G |
7: 24,324,048 (GRCm39) |
|
probably benign |
Het |
Pikfyve |
G |
T |
1: 65,235,898 (GRCm39) |
R190L |
probably damaging |
Het |
Plagl2 |
A |
T |
2: 153,074,540 (GRCm39) |
H120Q |
probably damaging |
Het |
Pou2f1 |
A |
T |
1: 165,703,640 (GRCm39) |
|
probably benign |
Het |
Pramel58 |
A |
G |
5: 94,831,836 (GRCm39) |
Y281C |
possibly damaging |
Het |
Prpf6 |
A |
G |
2: 181,250,001 (GRCm39) |
R54G |
possibly damaging |
Het |
Prss33 |
T |
C |
17: 24,052,966 (GRCm39) |
E236G |
probably benign |
Het |
Ptpru |
T |
C |
4: 131,522,278 (GRCm39) |
Y709C |
probably benign |
Het |
Rcc1l |
A |
G |
5: 134,197,057 (GRCm39) |
V212A |
probably benign |
Het |
Rtl1 |
G |
A |
12: 109,560,007 (GRCm39) |
L611F |
|
Het |
Scp2 |
A |
G |
4: 107,931,603 (GRCm39) |
I344T |
possibly damaging |
Het |
Serpinb2 |
A |
T |
1: 107,449,890 (GRCm39) |
D101V |
possibly damaging |
Het |
Slc13a1 |
T |
C |
6: 24,097,662 (GRCm39) |
T422A |
probably damaging |
Het |
Slc38a10 |
G |
T |
11: 120,007,762 (GRCm39) |
T406K |
probably benign |
Het |
Smad4 |
T |
C |
18: 73,782,806 (GRCm39) |
E376G |
probably damaging |
Het |
Smarcb1 |
T |
C |
10: 75,750,916 (GRCm39) |
E115G |
probably benign |
Het |
Spata31h1 |
A |
T |
10: 82,120,928 (GRCm39) |
H4027Q |
probably damaging |
Het |
Taf5 |
G |
A |
19: 47,063,370 (GRCm39) |
V307I |
probably damaging |
Het |
Tnc |
T |
C |
4: 63,938,686 (GRCm39) |
N51S |
possibly damaging |
Het |
Trp53inp2 |
G |
T |
2: 155,228,558 (GRCm39) |
R171L |
possibly damaging |
Het |
Ttc13 |
A |
T |
8: 125,402,021 (GRCm39) |
D579E |
probably benign |
Het |
Ttn |
A |
T |
2: 76,775,896 (GRCm39) |
N1761K |
unknown |
Het |
Ttpa |
C |
T |
4: 20,008,401 (GRCm39) |
|
probably benign |
Het |
Ugt3a1 |
G |
A |
15: 9,362,051 (GRCm39) |
V276I |
probably benign |
Het |
Usp4 |
T |
A |
9: 108,244,011 (GRCm39) |
H296Q |
probably benign |
Het |
Vmn1r119 |
T |
A |
7: 20,745,593 (GRCm39) |
H263L |
possibly damaging |
Het |
Vmn2r81 |
A |
G |
10: 79,103,905 (GRCm39) |
D176G |
|
Het |
Wdr1 |
A |
T |
5: 38,687,468 (GRCm39) |
|
probably benign |
Het |
Zfp488 |
T |
G |
14: 33,692,695 (GRCm39) |
Q156P |
possibly damaging |
Het |
|
Other mutations in Myh13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00497:Myh13
|
APN |
11 |
67,233,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00808:Myh13
|
APN |
11 |
67,225,830 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00822:Myh13
|
APN |
11 |
67,252,154 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00823:Myh13
|
APN |
11 |
67,246,773 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00945:Myh13
|
APN |
11 |
67,238,832 (GRCm39) |
missense |
probably null |
1.00 |
IGL01414:Myh13
|
APN |
11 |
67,233,298 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01482:Myh13
|
APN |
11 |
67,242,894 (GRCm39) |
missense |
probably benign |
|
IGL01523:Myh13
|
APN |
11 |
67,238,769 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01723:Myh13
|
APN |
11 |
67,260,045 (GRCm39) |
unclassified |
probably benign |
|
IGL01997:Myh13
|
APN |
11 |
67,257,992 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02369:Myh13
|
APN |
11 |
67,251,100 (GRCm39) |
unclassified |
probably benign |
|
IGL02478:Myh13
|
APN |
11 |
67,260,204 (GRCm39) |
missense |
probably benign |
|
IGL02663:Myh13
|
APN |
11 |
67,245,753 (GRCm39) |
nonsense |
probably null |
|
IGL02851:Myh13
|
APN |
11 |
67,239,742 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02863:Myh13
|
APN |
11 |
67,223,367 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02929:Myh13
|
APN |
11 |
67,257,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02979:Myh13
|
APN |
11 |
67,225,788 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03065:Myh13
|
APN |
11 |
67,235,679 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03214:Myh13
|
APN |
11 |
67,244,411 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03223:Myh13
|
APN |
11 |
67,241,068 (GRCm39) |
missense |
probably benign |
0.39 |
IGL03231:Myh13
|
APN |
11 |
67,242,817 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03407:Myh13
|
APN |
11 |
67,242,978 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Myh13
|
UTSW |
11 |
67,242,777 (GRCm39) |
splice site |
probably benign |
|
P0042:Myh13
|
UTSW |
11 |
67,225,817 (GRCm39) |
missense |
probably benign |
0.00 |
R0047:Myh13
|
UTSW |
11 |
67,258,063 (GRCm39) |
missense |
probably benign |
0.00 |
R0047:Myh13
|
UTSW |
11 |
67,258,063 (GRCm39) |
missense |
probably benign |
0.00 |
R0379:Myh13
|
UTSW |
11 |
67,260,121 (GRCm39) |
unclassified |
probably benign |
|
R0496:Myh13
|
UTSW |
11 |
67,239,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R0584:Myh13
|
UTSW |
11 |
67,251,200 (GRCm39) |
nonsense |
probably null |
|
R0595:Myh13
|
UTSW |
11 |
67,235,672 (GRCm39) |
missense |
probably benign |
0.03 |
R0621:Myh13
|
UTSW |
11 |
67,232,058 (GRCm39) |
missense |
probably damaging |
0.98 |
R0834:Myh13
|
UTSW |
11 |
67,240,436 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0893:Myh13
|
UTSW |
11 |
67,225,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964:Myh13
|
UTSW |
11 |
67,235,828 (GRCm39) |
missense |
probably benign |
0.02 |
R0973:Myh13
|
UTSW |
11 |
67,223,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Myh13
|
UTSW |
11 |
67,223,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Myh13
|
UTSW |
11 |
67,223,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R1028:Myh13
|
UTSW |
11 |
67,247,007 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1112:Myh13
|
UTSW |
11 |
67,245,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R1283:Myh13
|
UTSW |
11 |
67,261,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1288:Myh13
|
UTSW |
11 |
67,244,544 (GRCm39) |
missense |
probably benign |
0.00 |
R1386:Myh13
|
UTSW |
11 |
67,261,776 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1457:Myh13
|
UTSW |
11 |
67,221,872 (GRCm39) |
missense |
probably damaging |
0.97 |
R1503:Myh13
|
UTSW |
11 |
67,244,500 (GRCm39) |
missense |
probably benign |
0.43 |
R1574:Myh13
|
UTSW |
11 |
67,253,407 (GRCm39) |
unclassified |
probably benign |
|
R1673:Myh13
|
UTSW |
11 |
67,242,945 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1693:Myh13
|
UTSW |
11 |
67,232,310 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1763:Myh13
|
UTSW |
11 |
67,225,402 (GRCm39) |
missense |
probably benign |
|
R2029:Myh13
|
UTSW |
11 |
67,252,115 (GRCm39) |
missense |
probably benign |
0.03 |
R2030:Myh13
|
UTSW |
11 |
67,241,064 (GRCm39) |
missense |
probably benign |
|
R2247:Myh13
|
UTSW |
11 |
67,225,384 (GRCm39) |
missense |
probably damaging |
0.96 |
R2393:Myh13
|
UTSW |
11 |
67,231,184 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2395:Myh13
|
UTSW |
11 |
67,255,748 (GRCm39) |
missense |
probably benign |
0.12 |
R2884:Myh13
|
UTSW |
11 |
67,228,469 (GRCm39) |
missense |
probably benign |
0.27 |
R3696:Myh13
|
UTSW |
11 |
67,235,870 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3786:Myh13
|
UTSW |
11 |
67,218,014 (GRCm39) |
missense |
probably benign |
0.01 |
R3875:Myh13
|
UTSW |
11 |
67,249,020 (GRCm39) |
missense |
probably benign |
0.26 |
R3918:Myh13
|
UTSW |
11 |
67,220,064 (GRCm39) |
missense |
probably benign |
0.00 |
R4061:Myh13
|
UTSW |
11 |
67,221,715 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4160:Myh13
|
UTSW |
11 |
67,255,636 (GRCm39) |
intron |
probably benign |
|
R4183:Myh13
|
UTSW |
11 |
67,240,436 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4392:Myh13
|
UTSW |
11 |
67,235,707 (GRCm39) |
splice site |
probably null |
|
R4639:Myh13
|
UTSW |
11 |
67,232,377 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4670:Myh13
|
UTSW |
11 |
67,255,564 (GRCm39) |
nonsense |
probably null |
|
R4783:Myh13
|
UTSW |
11 |
67,232,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R4877:Myh13
|
UTSW |
11 |
67,228,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R5250:Myh13
|
UTSW |
11 |
67,218,085 (GRCm39) |
nonsense |
probably null |
|
R5278:Myh13
|
UTSW |
11 |
67,225,390 (GRCm39) |
missense |
probably benign |
0.00 |
R5371:Myh13
|
UTSW |
11 |
67,235,616 (GRCm39) |
splice site |
probably null |
|
R5479:Myh13
|
UTSW |
11 |
67,239,648 (GRCm39) |
missense |
probably damaging |
0.97 |
R5510:Myh13
|
UTSW |
11 |
67,228,549 (GRCm39) |
missense |
probably benign |
0.05 |
R5690:Myh13
|
UTSW |
11 |
67,220,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Myh13
|
UTSW |
11 |
67,225,828 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5823:Myh13
|
UTSW |
11 |
67,251,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Myh13
|
UTSW |
11 |
67,244,484 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6041:Myh13
|
UTSW |
11 |
67,255,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Myh13
|
UTSW |
11 |
67,245,588 (GRCm39) |
missense |
probably benign |
0.00 |
R6244:Myh13
|
UTSW |
11 |
67,253,327 (GRCm39) |
missense |
probably benign |
0.00 |
R6454:Myh13
|
UTSW |
11 |
67,241,191 (GRCm39) |
missense |
probably benign |
0.03 |
R6617:Myh13
|
UTSW |
11 |
67,252,226 (GRCm39) |
missense |
probably benign |
0.00 |
R6707:Myh13
|
UTSW |
11 |
67,241,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Myh13
|
UTSW |
11 |
67,241,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R6823:Myh13
|
UTSW |
11 |
67,246,984 (GRCm39) |
missense |
probably benign |
|
R6911:Myh13
|
UTSW |
11 |
67,245,753 (GRCm39) |
nonsense |
probably null |
|
R6997:Myh13
|
UTSW |
11 |
67,217,980 (GRCm39) |
nonsense |
probably null |
|
R7033:Myh13
|
UTSW |
11 |
67,260,142 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7145:Myh13
|
UTSW |
11 |
67,245,566 (GRCm39) |
missense |
probably benign |
0.08 |
R7232:Myh13
|
UTSW |
11 |
67,239,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7428:Myh13
|
UTSW |
11 |
67,223,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Myh13
|
UTSW |
11 |
67,255,286 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7474:Myh13
|
UTSW |
11 |
67,258,537 (GRCm39) |
missense |
|
|
R7474:Myh13
|
UTSW |
11 |
67,217,990 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7766:Myh13
|
UTSW |
11 |
67,249,155 (GRCm39) |
missense |
probably benign |
0.37 |
R7809:Myh13
|
UTSW |
11 |
67,241,167 (GRCm39) |
missense |
probably benign |
0.14 |
R7813:Myh13
|
UTSW |
11 |
67,218,056 (GRCm39) |
missense |
probably benign |
0.27 |
R7953:Myh13
|
UTSW |
11 |
67,231,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Myh13
|
UTSW |
11 |
67,225,613 (GRCm39) |
missense |
probably benign |
0.00 |
R8397:Myh13
|
UTSW |
11 |
67,241,113 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8434:Myh13
|
UTSW |
11 |
67,254,011 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8490:Myh13
|
UTSW |
11 |
67,255,351 (GRCm39) |
missense |
probably damaging |
0.98 |
R8676:Myh13
|
UTSW |
11 |
67,233,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R8681:Myh13
|
UTSW |
11 |
67,242,960 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8777:Myh13
|
UTSW |
11 |
67,252,161 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8777-TAIL:Myh13
|
UTSW |
11 |
67,252,161 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8965:Myh13
|
UTSW |
11 |
67,255,432 (GRCm39) |
missense |
probably benign |
0.00 |
R9088:Myh13
|
UTSW |
11 |
67,242,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R9154:Myh13
|
UTSW |
11 |
67,253,318 (GRCm39) |
missense |
probably benign |
|
R9182:Myh13
|
UTSW |
11 |
67,228,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R9332:Myh13
|
UTSW |
11 |
67,254,109 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9393:Myh13
|
UTSW |
11 |
67,242,894 (GRCm39) |
missense |
probably benign |
|
R9446:Myh13
|
UTSW |
11 |
67,255,325 (GRCm39) |
missense |
probably benign |
0.01 |
R9474:Myh13
|
UTSW |
11 |
67,255,712 (GRCm39) |
missense |
|
|
R9690:Myh13
|
UTSW |
11 |
67,249,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Myh13
|
UTSW |
11 |
67,251,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R9778:Myh13
|
UTSW |
11 |
67,249,016 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Myh13
|
UTSW |
11 |
67,220,121 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Myh13
|
UTSW |
11 |
67,255,417 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Myh13
|
UTSW |
11 |
67,241,278 (GRCm39) |
missense |
possibly damaging |
0.55 |
|