Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg1 |
T |
C |
8: 95,739,559 (GRCm39) |
S670P |
probably damaging |
Het |
Ap5m1 |
T |
A |
14: 49,317,797 (GRCm39) |
F351L |
probably damaging |
Het |
Cacnb2 |
A |
G |
2: 14,619,079 (GRCm39) |
Y38C |
probably damaging |
Het |
Ccdc28a |
C |
T |
10: 18,095,262 (GRCm39) |
A151T |
possibly damaging |
Het |
Cgnl1 |
T |
C |
9: 71,557,604 (GRCm39) |
E976G |
probably damaging |
Het |
Cyp2c39 |
A |
G |
19: 39,525,264 (GRCm39) |
Y189C |
probably damaging |
Het |
Dbt |
T |
C |
3: 116,326,954 (GRCm39) |
V101A |
probably damaging |
Het |
Evc |
A |
G |
5: 37,477,578 (GRCm39) |
|
probably null |
Het |
Fastkd5 |
A |
G |
2: 130,457,532 (GRCm39) |
Y353H |
probably benign |
Het |
Gm6408 |
G |
A |
5: 146,418,892 (GRCm39) |
R30H |
probably damaging |
Het |
Lhx8 |
A |
G |
3: 154,027,992 (GRCm39) |
S156P |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,300,686 (GRCm39) |
I1449M |
probably damaging |
Het |
Mtrr |
A |
T |
13: 68,728,719 (GRCm39) |
V27E |
possibly damaging |
Het |
Nek1 |
T |
C |
8: 61,577,246 (GRCm39) |
S1076P |
possibly damaging |
Het |
Or52z14 |
C |
T |
7: 103,253,548 (GRCm39) |
A229V |
probably benign |
Het |
Or6ae1 |
G |
T |
7: 139,742,841 (GRCm39) |
N7K |
probably benign |
Het |
Pcdhb7 |
A |
G |
18: 37,475,548 (GRCm39) |
D228G |
possibly damaging |
Het |
Pias3 |
T |
C |
3: 96,611,073 (GRCm39) |
S414P |
probably benign |
Het |
Plcd4 |
G |
A |
1: 74,591,192 (GRCm39) |
V196I |
probably benign |
Het |
Proca1 |
A |
G |
11: 78,095,737 (GRCm39) |
D123G |
probably damaging |
Het |
Ptpn3 |
A |
G |
4: 57,254,915 (GRCm39) |
|
probably null |
Het |
Ptprq |
C |
A |
10: 107,535,469 (GRCm39) |
R432L |
probably damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,838,475 (GRCm39) |
K108E |
possibly damaging |
Het |
Siglecg |
A |
G |
7: 43,060,888 (GRCm39) |
|
probably null |
Het |
Srpra |
A |
G |
9: 35,126,201 (GRCm39) |
T465A |
possibly damaging |
Het |
Tmpo |
G |
A |
10: 90,999,104 (GRCm39) |
R228C |
probably benign |
Het |
Zeb1 |
G |
A |
18: 5,767,867 (GRCm39) |
V793M |
possibly 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 |
IGL02034:Myh14
|
APN |
7 |
44,265,717 (GRCm39) |
missense |
possibly damaging |
0.58 |
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 |
|