Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bcor |
A |
G |
X: 11,905,498 (GRCm39) |
S1556P |
possibly damaging |
Het |
Brd10 |
A |
G |
19: 29,694,259 (GRCm39) |
S1745P |
possibly damaging |
Het |
Ccdc6 |
T |
A |
10: 70,004,978 (GRCm39) |
I241N |
probably benign |
Het |
Cd81 |
T |
C |
7: 142,619,986 (GRCm39) |
I48T |
probably damaging |
Het |
Cfap52 |
A |
G |
11: 67,837,118 (GRCm39) |
|
probably null |
Het |
Cfap54 |
T |
C |
10: 92,897,347 (GRCm39) |
M264V |
probably damaging |
Het |
Cmya5 |
G |
A |
13: 93,221,043 (GRCm39) |
|
probably benign |
Het |
Csn2 |
A |
G |
5: 87,843,941 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
G |
A |
7: 55,548,101 (GRCm39) |
R567Q |
probably damaging |
Het |
Ehbp1 |
A |
G |
11: 22,235,486 (GRCm39) |
|
probably null |
Het |
Ermp1 |
G |
A |
19: 29,623,359 (GRCm39) |
|
probably benign |
Het |
Erv3 |
C |
T |
2: 131,697,934 (GRCm39) |
V142I |
possibly damaging |
Het |
Fzd2 |
A |
G |
11: 102,495,730 (GRCm39) |
N58S |
probably damaging |
Het |
Gcm2 |
G |
A |
13: 41,259,269 (GRCm39) |
R67C |
probably damaging |
Het |
Gm17019 |
A |
G |
5: 15,080,266 (GRCm39) |
I182T |
possibly damaging |
Het |
Gpr45 |
T |
C |
1: 43,072,478 (GRCm39) |
*374Q |
probably null |
Het |
Haus8 |
T |
C |
8: 71,708,202 (GRCm39) |
N165S |
probably damaging |
Het |
Hoxd4 |
T |
A |
2: 74,558,750 (GRCm39) |
L191Q |
probably damaging |
Het |
I830077J02Rik |
A |
G |
3: 105,834,565 (GRCm39) |
|
probably benign |
Het |
Lpl |
T |
C |
8: 69,333,424 (GRCm39) |
L7P |
possibly damaging |
Het |
Lrp1b |
T |
A |
2: 41,158,382 (GRCm39) |
K1612* |
probably null |
Het |
Nbea |
A |
G |
3: 55,875,577 (GRCm39) |
S1698P |
probably damaging |
Het |
Or10p22 |
A |
T |
10: 128,826,570 (GRCm39) |
Q263L |
probably benign |
Het |
Or4c112 |
C |
T |
2: 88,854,015 (GRCm39) |
V111M |
probably benign |
Het |
Or52e7 |
C |
A |
7: 104,684,597 (GRCm39) |
T64N |
probably benign |
Het |
Or5p51 |
G |
A |
7: 107,444,385 (GRCm39) |
T185I |
probably benign |
Het |
Otog |
A |
T |
7: 45,945,417 (GRCm39) |
K40* |
probably null |
Het |
Rgma |
C |
A |
7: 73,067,181 (GRCm39) |
H145Q |
probably damaging |
Het |
Rpgrip1l |
A |
T |
8: 91,977,776 (GRCm39) |
|
probably null |
Het |
Ssxb2 |
T |
A |
X: 8,324,743 (GRCm39) |
|
probably benign |
Het |
Tmem175 |
C |
T |
5: 108,790,002 (GRCm39) |
T118I |
probably damaging |
Het |
Wdhd1 |
A |
G |
14: 47,498,808 (GRCm39) |
V542A |
probably benign |
Het |
Zfp977 |
G |
A |
7: 42,230,136 (GRCm39) |
P130S |
probably damaging |
Het |
|
Other mutations in Myh14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01139:Myh14
|
APN |
7 |
44,255,716 (GRCm39) |
unclassified |
probably benign |
|
IGL01431:Myh14
|
APN |
7 |
44,263,782 (GRCm39) |
missense |
probably null |
0.00 |
IGL01722:Myh14
|
APN |
7 |
44,292,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01806:Myh14
|
APN |
7 |
44,307,363 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02260:Myh14
|
APN |
7 |
44,260,995 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02590:Myh14
|
APN |
7 |
44,273,503 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02696:Myh14
|
APN |
7 |
44,314,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02705:Myh14
|
APN |
7 |
44,257,960 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03193:Myh14
|
APN |
7 |
44,279,369 (GRCm39) |
missense |
possibly damaging |
0.91 |
PIT4581001:Myh14
|
UTSW |
7 |
44,262,906 (GRCm39) |
missense |
probably benign |
0.04 |
R0067:Myh14
|
UTSW |
7 |
44,272,551 (GRCm39) |
missense |
probably benign |
0.05 |
R0083:Myh14
|
UTSW |
7 |
44,283,943 (GRCm39) |
missense |
probably damaging |
0.98 |
R0108:Myh14
|
UTSW |
7 |
44,283,943 (GRCm39) |
missense |
probably damaging |
0.98 |
R0152:Myh14
|
UTSW |
7 |
44,272,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Myh14
|
UTSW |
7 |
44,310,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Myh14
|
UTSW |
7 |
44,263,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R0699:Myh14
|
UTSW |
7 |
44,274,395 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0763:Myh14
|
UTSW |
7 |
44,314,791 (GRCm39) |
missense |
probably damaging |
0.98 |
R1079:Myh14
|
UTSW |
7 |
44,279,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R1388:Myh14
|
UTSW |
7 |
44,314,546 (GRCm39) |
missense |
probably damaging |
0.98 |
R1432:Myh14
|
UTSW |
7 |
44,265,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R1568:Myh14
|
UTSW |
7 |
44,261,122 (GRCm39) |
nonsense |
probably null |
|
R1579:Myh14
|
UTSW |
7 |
44,305,118 (GRCm39) |
splice site |
probably null |
|
R1598:Myh14
|
UTSW |
7 |
44,287,818 (GRCm39) |
missense |
probably damaging |
0.96 |
R1848:Myh14
|
UTSW |
7 |
44,281,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R1869:Myh14
|
UTSW |
7 |
44,261,067 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1917:Myh14
|
UTSW |
7 |
44,307,349 (GRCm39) |
missense |
probably benign |
|
R1933:Myh14
|
UTSW |
7 |
44,264,772 (GRCm39) |
missense |
probably benign |
0.09 |
R1984:Myh14
|
UTSW |
7 |
44,288,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R2154:Myh14
|
UTSW |
7 |
44,301,853 (GRCm39) |
critical splice donor site |
probably null |
|
R2190:Myh14
|
UTSW |
7 |
44,310,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R2217:Myh14
|
UTSW |
7 |
44,283,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Myh14
|
UTSW |
7 |
44,314,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R2918:Myh14
|
UTSW |
7 |
44,265,687 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4091:Myh14
|
UTSW |
7 |
44,282,415 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4110:Myh14
|
UTSW |
7 |
44,277,974 (GRCm39) |
missense |
probably benign |
0.00 |
R4199:Myh14
|
UTSW |
7 |
44,264,927 (GRCm39) |
nonsense |
probably null |
|
R4507:Myh14
|
UTSW |
7 |
44,279,415 (GRCm39) |
missense |
probably benign |
0.00 |
R4539:Myh14
|
UTSW |
7 |
44,276,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4550:Myh14
|
UTSW |
7 |
44,283,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Myh14
|
UTSW |
7 |
44,273,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R4768:Myh14
|
UTSW |
7 |
44,263,099 (GRCm39) |
missense |
probably benign |
0.19 |
R4832:Myh14
|
UTSW |
7 |
44,274,566 (GRCm39) |
missense |
probably benign |
0.31 |
R4853:Myh14
|
UTSW |
7 |
44,257,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Myh14
|
UTSW |
7 |
44,310,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Myh14
|
UTSW |
7 |
44,284,926 (GRCm39) |
missense |
probably benign |
0.00 |
R5070:Myh14
|
UTSW |
7 |
44,265,672 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5166:Myh14
|
UTSW |
7 |
44,278,279 (GRCm39) |
missense |
probably damaging |
0.99 |
R5726:Myh14
|
UTSW |
7 |
44,292,886 (GRCm39) |
critical splice donor site |
probably null |
|
R5786:Myh14
|
UTSW |
7 |
44,262,887 (GRCm39) |
missense |
probably benign |
0.23 |
R5895:Myh14
|
UTSW |
7 |
44,256,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R5961:Myh14
|
UTSW |
7 |
44,272,518 (GRCm39) |
missense |
probably damaging |
0.96 |
R6014:Myh14
|
UTSW |
7 |
44,274,502 (GRCm39) |
missense |
probably null |
|
R6080:Myh14
|
UTSW |
7 |
44,305,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R6187:Myh14
|
UTSW |
7 |
44,276,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Myh14
|
UTSW |
7 |
44,287,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R6833:Myh14
|
UTSW |
7 |
44,273,803 (GRCm39) |
nonsense |
probably null |
|
R6894:Myh14
|
UTSW |
7 |
44,282,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R6916:Myh14
|
UTSW |
7 |
44,278,737 (GRCm39) |
missense |
probably damaging |
0.96 |
R6962:Myh14
|
UTSW |
7 |
44,307,363 (GRCm39) |
missense |
probably benign |
0.36 |
R7066:Myh14
|
UTSW |
7 |
44,280,179 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7261:Myh14
|
UTSW |
7 |
44,273,761 (GRCm39) |
nonsense |
probably null |
|
R7303:Myh14
|
UTSW |
7 |
44,261,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R7304:Myh14
|
UTSW |
7 |
44,279,415 (GRCm39) |
missense |
probably benign |
0.00 |
R7327:Myh14
|
UTSW |
7 |
44,260,977 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7380:Myh14
|
UTSW |
7 |
44,310,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Myh14
|
UTSW |
7 |
44,281,850 (GRCm39) |
missense |
probably benign |
0.37 |
R7622:Myh14
|
UTSW |
7 |
44,281,846 (GRCm39) |
missense |
probably benign |
0.25 |
R7681:Myh14
|
UTSW |
7 |
44,273,572 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7718:Myh14
|
UTSW |
7 |
44,310,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R7910:Myh14
|
UTSW |
7 |
44,281,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Myh14
|
UTSW |
7 |
44,274,551 (GRCm39) |
missense |
probably damaging |
0.97 |
R8088:Myh14
|
UTSW |
7 |
44,314,920 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R8164:Myh14
|
UTSW |
7 |
44,274,457 (GRCm39) |
missense |
probably benign |
0.01 |
R8260:Myh14
|
UTSW |
7 |
44,264,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R8299:Myh14
|
UTSW |
7 |
44,276,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R8410:Myh14
|
UTSW |
7 |
44,282,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R8723:Myh14
|
UTSW |
7 |
44,272,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R8853:Myh14
|
UTSW |
7 |
44,265,678 (GRCm39) |
missense |
probably benign |
0.08 |
R8934:Myh14
|
UTSW |
7 |
44,306,852 (GRCm39) |
missense |
probably benign |
|
R9169:Myh14
|
UTSW |
7 |
44,271,281 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9395:Myh14
|
UTSW |
7 |
44,274,584 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9451:Myh14
|
UTSW |
7 |
44,273,743 (GRCm39) |
critical splice donor site |
probably null |
|
X0026:Myh14
|
UTSW |
7 |
44,263,818 (GRCm39) |
missense |
probably benign |
0.00 |
X0063:Myh14
|
UTSW |
7 |
44,273,557 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myh14
|
UTSW |
7 |
44,287,733 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Myh14
|
UTSW |
7 |
44,257,939 (GRCm39) |
missense |
probably damaging |
1.00 |
|