Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
T |
C |
7: 45,772,364 (GRCm39) |
Y805C |
probably damaging |
Het |
Aoc1l3 |
T |
A |
6: 48,964,512 (GRCm39) |
D173E |
probably benign |
Het |
Cabp7 |
T |
A |
11: 4,688,886 (GRCm39) |
I195F |
probably damaging |
Het |
Camsap1 |
T |
C |
2: 25,835,201 (GRCm39) |
N317S |
probably damaging |
Het |
Ccdc127 |
T |
G |
13: 74,500,994 (GRCm39) |
L4V |
probably damaging |
Het |
Ccdc7a |
T |
C |
8: 129,774,100 (GRCm39) |
E145G |
probably damaging |
Het |
Cdh10 |
T |
A |
15: 19,013,287 (GRCm39) |
V629D |
probably damaging |
Het |
Cdh23 |
A |
C |
10: 60,214,530 (GRCm39) |
L1497R |
probably damaging |
Het |
Chsy3 |
A |
G |
18: 59,542,875 (GRCm39) |
K671R |
probably benign |
Het |
Clca4b |
T |
C |
3: 144,621,367 (GRCm39) |
Y569C |
probably damaging |
Het |
Cnga1 |
T |
C |
5: 72,786,696 (GRCm39) |
|
probably benign |
Het |
Cyp51 |
T |
A |
5: 4,150,188 (GRCm39) |
E178D |
probably damaging |
Het |
Defa30 |
T |
A |
8: 21,625,471 (GRCm39) |
N78K |
probably benign |
Het |
Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
Dnah14 |
G |
T |
1: 181,450,568 (GRCm39) |
C727F |
probably benign |
Het |
Egf |
A |
T |
3: 129,548,607 (GRCm39) |
W3R |
unknown |
Het |
Egfem1 |
G |
A |
3: 29,136,364 (GRCm39) |
|
probably null |
Het |
Epb41l1 |
G |
T |
2: 156,368,812 (GRCm39) |
V682L |
possibly damaging |
Het |
Etv1 |
A |
G |
12: 38,834,369 (GRCm39) |
|
probably null |
Het |
Faap100 |
A |
G |
11: 120,268,200 (GRCm39) |
F191S |
possibly damaging |
Het |
Fmo1 |
T |
A |
1: 162,667,263 (GRCm39) |
D184V |
possibly damaging |
Het |
Ghrl |
A |
G |
6: 113,696,344 (GRCm39) |
L16P |
probably damaging |
Het |
Gria4 |
T |
A |
9: 4,420,278 (GRCm39) |
L861F |
probably damaging |
Het |
Gsr |
T |
A |
8: 34,185,090 (GRCm39) |
M428K |
probably damaging |
Het |
Hspa5 |
C |
T |
2: 34,663,204 (GRCm39) |
P127L |
probably damaging |
Het |
Kbtbd12 |
A |
G |
6: 88,595,497 (GRCm39) |
M111T |
possibly damaging |
Het |
Krtap21-1 |
G |
T |
16: 89,200,623 (GRCm39) |
Y6* |
probably null |
Het |
Lin9 |
A |
G |
1: 180,494,935 (GRCm39) |
D219G |
probably damaging |
Het |
Lrrc38 |
A |
G |
4: 143,076,739 (GRCm39) |
M1V |
probably null |
Het |
Macc1 |
T |
G |
12: 119,410,773 (GRCm39) |
F514V |
probably benign |
Het |
Madcam1 |
C |
T |
10: 79,504,139 (GRCm39) |
R242C |
probably benign |
Het |
Mfhas1 |
T |
C |
8: 36,131,944 (GRCm39) |
S1037P |
probably benign |
Het |
Micall2 |
C |
T |
5: 139,694,699 (GRCm39) |
|
probably benign |
Het |
Mtr |
C |
A |
13: 12,205,095 (GRCm39) |
A1122S |
possibly damaging |
Het |
Muc6 |
T |
A |
7: 141,226,456 (GRCm39) |
|
probably benign |
Het |
Napsa |
T |
C |
7: 44,234,509 (GRCm39) |
V247A |
probably damaging |
Het |
Nr2c2 |
A |
G |
6: 92,135,338 (GRCm39) |
T309A |
probably damaging |
Het |
Or1e26 |
A |
T |
11: 73,480,558 (GRCm39) |
I2K |
probably benign |
Het |
Or1q1 |
T |
A |
2: 36,887,173 (GRCm39) |
V117E |
probably benign |
Het |
Or2n1b |
A |
T |
17: 38,459,691 (GRCm39) |
M71L |
probably benign |
Het |
Osgepl1 |
A |
T |
1: 53,360,710 (GRCm39) |
I384F |
possibly damaging |
Het |
Otud4 |
C |
T |
8: 80,377,671 (GRCm39) |
L111F |
possibly damaging |
Het |
Pds5b |
A |
G |
5: 150,673,385 (GRCm39) |
Y481C |
probably damaging |
Het |
Pdzrn4 |
T |
A |
15: 92,668,303 (GRCm39) |
Y818* |
probably null |
Het |
Pin1rt1 |
T |
C |
2: 104,544,767 (GRCm39) |
S122G |
probably benign |
Het |
Pkdcc |
A |
T |
17: 83,531,687 (GRCm39) |
Y487F |
probably damaging |
Het |
Plxna4 |
C |
T |
6: 32,493,440 (GRCm39) |
C392Y |
probably damaging |
Het |
Psd4 |
T |
G |
2: 24,284,985 (GRCm39) |
M283R |
probably benign |
Het |
Ralgds |
G |
T |
2: 28,430,741 (GRCm39) |
G68W |
probably damaging |
Het |
Rmdn2 |
T |
A |
17: 79,928,808 (GRCm39) |
I20N |
probably damaging |
Het |
Sestd1 |
A |
G |
2: 77,022,910 (GRCm39) |
V486A |
probably benign |
Het |
Skic8 |
T |
A |
9: 54,626,539 (GRCm39) |
D275V |
probably damaging |
Het |
Spmap2 |
G |
T |
10: 79,422,796 (GRCm39) |
D35E |
probably benign |
Het |
Tango6 |
A |
G |
8: 107,533,748 (GRCm39) |
H958R |
possibly damaging |
Het |
Taok3 |
C |
T |
5: 117,411,771 (GRCm39) |
R857C |
probably damaging |
Het |
Tasor |
A |
T |
14: 27,194,392 (GRCm39) |
L1197F |
probably damaging |
Het |
Trio |
T |
C |
15: 27,832,137 (GRCm39) |
E1245G |
probably damaging |
Het |
Usp19 |
C |
T |
9: 108,374,334 (GRCm39) |
H763Y |
possibly damaging |
Het |
Vmn1r185 |
A |
G |
7: 26,310,651 (GRCm39) |
S285P |
probably damaging |
Het |
Vmn1r45 |
T |
G |
6: 89,910,538 (GRCm39) |
Y144S |
probably benign |
Het |
Vwa3b |
G |
A |
1: 37,212,959 (GRCm39) |
E152K |
probably benign |
Het |
Xrcc5 |
G |
A |
1: 72,433,875 (GRCm39) |
M731I |
probably benign |
Het |
Zfp619 |
G |
A |
7: 39,186,787 (GRCm39) |
S939N |
possibly damaging |
Het |
Zfp874a |
C |
A |
13: 67,590,418 (GRCm39) |
C422F |
probably damaging |
Het |
Zfp948 |
A |
G |
17: 21,808,719 (GRCm39) |
D637G |
possibly damaging |
Het |
|
Other mutations in Myh15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00943:Myh15
|
APN |
16 |
48,986,176 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01095:Myh15
|
APN |
16 |
48,952,378 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01343:Myh15
|
APN |
16 |
48,976,040 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01474:Myh15
|
APN |
16 |
48,952,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01572:Myh15
|
APN |
16 |
48,920,585 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01595:Myh15
|
APN |
16 |
48,993,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01632:Myh15
|
APN |
16 |
48,881,874 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01638:Myh15
|
APN |
16 |
48,889,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01667:Myh15
|
APN |
16 |
49,015,942 (GRCm39) |
missense |
probably benign |
0.20 |
IGL01715:Myh15
|
APN |
16 |
48,877,847 (GRCm39) |
unclassified |
probably benign |
|
IGL01833:Myh15
|
APN |
16 |
48,934,421 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02004:Myh15
|
APN |
16 |
48,930,892 (GRCm39) |
splice site |
probably benign |
|
IGL02033:Myh15
|
APN |
16 |
48,965,707 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02148:Myh15
|
APN |
16 |
48,936,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02225:Myh15
|
APN |
16 |
48,911,526 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02249:Myh15
|
APN |
16 |
48,930,847 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02505:Myh15
|
APN |
16 |
48,937,626 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02622:Myh15
|
APN |
16 |
48,997,317 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02814:Myh15
|
APN |
16 |
48,965,801 (GRCm39) |
splice site |
probably benign |
|
IGL02869:Myh15
|
APN |
16 |
48,965,767 (GRCm39) |
missense |
probably benign |
|
IGL02879:Myh15
|
APN |
16 |
48,993,422 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02881:Myh15
|
APN |
16 |
48,937,628 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03077:Myh15
|
APN |
16 |
48,916,901 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03354:Myh15
|
APN |
16 |
48,992,373 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03411:Myh15
|
APN |
16 |
48,980,330 (GRCm39) |
missense |
possibly damaging |
0.58 |
ANU74:Myh15
|
UTSW |
16 |
48,993,295 (GRCm39) |
missense |
possibly damaging |
0.58 |
P0027:Myh15
|
UTSW |
16 |
48,901,571 (GRCm39) |
missense |
possibly damaging |
0.77 |
PIT1430001:Myh15
|
UTSW |
16 |
49,017,254 (GRCm39) |
critical splice donor site |
probably null |
|
R0017:Myh15
|
UTSW |
16 |
48,983,423 (GRCm39) |
missense |
probably damaging |
0.97 |
R0038:Myh15
|
UTSW |
16 |
48,891,504 (GRCm39) |
splice site |
probably benign |
|
R0149:Myh15
|
UTSW |
16 |
48,934,368 (GRCm39) |
missense |
probably benign |
0.01 |
R0361:Myh15
|
UTSW |
16 |
48,934,368 (GRCm39) |
missense |
probably benign |
0.01 |
R0373:Myh15
|
UTSW |
16 |
49,003,322 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0433:Myh15
|
UTSW |
16 |
48,965,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R0525:Myh15
|
UTSW |
16 |
48,952,414 (GRCm39) |
missense |
probably benign |
0.03 |
R0586:Myh15
|
UTSW |
16 |
48,992,250 (GRCm39) |
splice site |
probably benign |
|
R0601:Myh15
|
UTSW |
16 |
48,881,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R0717:Myh15
|
UTSW |
16 |
48,963,356 (GRCm39) |
missense |
probably benign |
0.03 |
R0963:Myh15
|
UTSW |
16 |
48,952,512 (GRCm39) |
missense |
probably damaging |
0.97 |
R1075:Myh15
|
UTSW |
16 |
48,940,417 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1143:Myh15
|
UTSW |
16 |
48,885,449 (GRCm39) |
missense |
probably benign |
0.02 |
R1200:Myh15
|
UTSW |
16 |
48,916,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R1644:Myh15
|
UTSW |
16 |
48,952,566 (GRCm39) |
missense |
probably benign |
0.12 |
R1646:Myh15
|
UTSW |
16 |
49,015,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R1720:Myh15
|
UTSW |
16 |
48,913,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Myh15
|
UTSW |
16 |
48,983,498 (GRCm39) |
missense |
probably benign |
0.27 |
R1881:Myh15
|
UTSW |
16 |
48,891,446 (GRCm39) |
missense |
probably damaging |
0.98 |
R2048:Myh15
|
UTSW |
16 |
48,975,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R2064:Myh15
|
UTSW |
16 |
48,975,984 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2184:Myh15
|
UTSW |
16 |
48,957,874 (GRCm39) |
missense |
probably damaging |
0.99 |
R2212:Myh15
|
UTSW |
16 |
48,959,095 (GRCm39) |
missense |
probably benign |
0.02 |
R2216:Myh15
|
UTSW |
16 |
48,986,201 (GRCm39) |
nonsense |
probably null |
|
R2321:Myh15
|
UTSW |
16 |
48,933,436 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2327:Myh15
|
UTSW |
16 |
48,963,313 (GRCm39) |
missense |
probably benign |
0.01 |
R2395:Myh15
|
UTSW |
16 |
48,889,877 (GRCm39) |
missense |
probably benign |
0.04 |
R2399:Myh15
|
UTSW |
16 |
48,957,952 (GRCm39) |
missense |
probably damaging |
0.97 |
R3413:Myh15
|
UTSW |
16 |
48,959,095 (GRCm39) |
missense |
probably benign |
0.02 |
R4234:Myh15
|
UTSW |
16 |
48,983,405 (GRCm39) |
missense |
probably benign |
0.04 |
R4382:Myh15
|
UTSW |
16 |
48,963,306 (GRCm39) |
missense |
probably benign |
0.03 |
R4421:Myh15
|
UTSW |
16 |
48,929,707 (GRCm39) |
missense |
probably damaging |
0.99 |
R4580:Myh15
|
UTSW |
16 |
48,885,388 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4657:Myh15
|
UTSW |
16 |
48,992,421 (GRCm39) |
nonsense |
probably null |
|
R4780:Myh15
|
UTSW |
16 |
48,940,420 (GRCm39) |
missense |
probably benign |
0.13 |
R5004:Myh15
|
UTSW |
16 |
48,952,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R5175:Myh15
|
UTSW |
16 |
48,889,789 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5189:Myh15
|
UTSW |
16 |
48,921,870 (GRCm39) |
missense |
probably benign |
0.20 |
R5311:Myh15
|
UTSW |
16 |
48,986,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5318:Myh15
|
UTSW |
16 |
48,930,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R5404:Myh15
|
UTSW |
16 |
48,980,341 (GRCm39) |
missense |
probably benign |
0.15 |
R5415:Myh15
|
UTSW |
16 |
48,937,658 (GRCm39) |
missense |
probably null |
1.00 |
R5558:Myh15
|
UTSW |
16 |
48,889,900 (GRCm39) |
missense |
probably benign |
0.32 |
R5977:Myh15
|
UTSW |
16 |
48,973,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R6004:Myh15
|
UTSW |
16 |
48,980,062 (GRCm39) |
missense |
probably benign |
0.00 |
R6275:Myh15
|
UTSW |
16 |
48,965,610 (GRCm39) |
missense |
probably benign |
0.00 |
R6381:Myh15
|
UTSW |
16 |
48,921,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R6448:Myh15
|
UTSW |
16 |
48,992,295 (GRCm39) |
missense |
probably damaging |
0.99 |
R6516:Myh15
|
UTSW |
16 |
48,957,996 (GRCm39) |
missense |
probably benign |
0.19 |
R6752:Myh15
|
UTSW |
16 |
49,003,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R6847:Myh15
|
UTSW |
16 |
48,965,451 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6868:Myh15
|
UTSW |
16 |
48,889,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R6889:Myh15
|
UTSW |
16 |
48,973,474 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6896:Myh15
|
UTSW |
16 |
48,933,434 (GRCm39) |
missense |
probably benign |
0.44 |
R6955:Myh15
|
UTSW |
16 |
48,901,598 (GRCm39) |
critical splice donor site |
probably null |
|
R6984:Myh15
|
UTSW |
16 |
48,930,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7095:Myh15
|
UTSW |
16 |
48,992,272 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7098:Myh15
|
UTSW |
16 |
48,997,420 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7134:Myh15
|
UTSW |
16 |
48,901,705 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7159:Myh15
|
UTSW |
16 |
48,881,937 (GRCm39) |
missense |
probably damaging |
0.97 |
R7244:Myh15
|
UTSW |
16 |
49,017,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Myh15
|
UTSW |
16 |
48,911,468 (GRCm39) |
missense |
probably damaging |
0.98 |
R7309:Myh15
|
UTSW |
16 |
48,916,828 (GRCm39) |
missense |
probably benign |
0.34 |
R7327:Myh15
|
UTSW |
16 |
48,993,369 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7418:Myh15
|
UTSW |
16 |
48,975,900 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7937:Myh15
|
UTSW |
16 |
48,976,009 (GRCm39) |
missense |
probably benign |
0.00 |
R8053:Myh15
|
UTSW |
16 |
48,963,302 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8313:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8315:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8316:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8317:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8342:Myh15
|
UTSW |
16 |
48,913,120 (GRCm39) |
missense |
probably benign |
|
R8379:Myh15
|
UTSW |
16 |
48,901,551 (GRCm39) |
missense |
probably benign |
|
R8445:Myh15
|
UTSW |
16 |
48,940,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R8707:Myh15
|
UTSW |
16 |
48,973,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R8729:Myh15
|
UTSW |
16 |
48,881,851 (GRCm39) |
missense |
probably damaging |
0.97 |
R8773:Myh15
|
UTSW |
16 |
49,015,900 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8869:Myh15
|
UTSW |
16 |
48,997,366 (GRCm39) |
missense |
probably benign |
|
R8890:Myh15
|
UTSW |
16 |
48,959,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9026:Myh15
|
UTSW |
16 |
49,007,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9063:Myh15
|
UTSW |
16 |
48,913,118 (GRCm39) |
missense |
probably benign |
0.00 |
R9290:Myh15
|
UTSW |
16 |
48,997,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R9630:Myh15
|
UTSW |
16 |
48,980,341 (GRCm39) |
missense |
probably benign |
0.15 |
R9710:Myh15
|
UTSW |
16 |
48,959,044 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Myh15
|
UTSW |
16 |
48,963,341 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Myh15
|
UTSW |
16 |
48,986,237 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myh15
|
UTSW |
16 |
48,916,894 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Myh15
|
UTSW |
16 |
48,980,189 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:Myh15
|
UTSW |
16 |
48,975,981 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Myh15
|
UTSW |
16 |
48,901,591 (GRCm39) |
missense |
probably benign |
0.02 |
|