Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg2 |
C |
T |
X: 159,275,704 (GRCm39) |
T931I |
probably damaging |
Het |
Atp5mc3 |
A |
G |
2: 73,741,293 (GRCm39) |
|
probably benign |
Het |
Btd |
T |
A |
14: 31,389,733 (GRCm39) |
F485I |
probably benign |
Het |
Camk2d |
A |
G |
3: 126,591,934 (GRCm39) |
|
probably benign |
Het |
Cd300lg |
A |
T |
11: 101,945,047 (GRCm39) |
|
probably benign |
Het |
Col9a1 |
A |
G |
1: 24,263,726 (GRCm39) |
|
probably null |
Het |
Cybb |
T |
A |
X: 9,312,983 (GRCm39) |
N367I |
possibly damaging |
Het |
Dcaf17 |
T |
C |
2: 70,920,149 (GRCm39) |
V479A |
probably benign |
Het |
Dscaml1 |
G |
T |
9: 45,660,930 (GRCm39) |
|
probably null |
Het |
Espl1 |
T |
C |
15: 102,231,373 (GRCm39) |
F51S |
probably damaging |
Het |
Gsdmc3 |
T |
A |
15: 63,733,306 (GRCm39) |
D258V |
probably benign |
Het |
Gvin-ps3 |
A |
T |
7: 105,682,021 (GRCm39) |
N411K |
unknown |
Het |
Ifngr1 |
C |
T |
10: 19,473,161 (GRCm39) |
|
probably benign |
Het |
Kcnip1 |
A |
T |
11: 33,583,202 (GRCm39) |
D194E |
probably damaging |
Het |
Lrrtm1 |
C |
T |
6: 77,221,436 (GRCm39) |
R298C |
probably damaging |
Het |
Mmp16 |
A |
G |
4: 18,112,066 (GRCm39) |
K481E |
possibly damaging |
Het |
Myh1 |
A |
T |
11: 67,111,486 (GRCm39) |
M1642L |
probably benign |
Het |
Nol9 |
G |
T |
4: 152,131,066 (GRCm39) |
C363F |
probably damaging |
Het |
Nsd1 |
T |
C |
13: 55,393,430 (GRCm39) |
S344P |
probably damaging |
Het |
Or52e5 |
A |
T |
7: 104,718,808 (GRCm39) |
I45F |
probably benign |
Het |
Phf20 |
G |
A |
2: 156,145,104 (GRCm39) |
|
probably null |
Het |
Ppp3cc |
G |
T |
14: 70,455,701 (GRCm39) |
H467Q |
probably damaging |
Het |
Rab28 |
A |
G |
5: 41,793,237 (GRCm39) |
M136T |
probably benign |
Het |
Rag1 |
A |
G |
2: 101,472,346 (GRCm39) |
I932T |
probably damaging |
Het |
Sez6 |
T |
C |
11: 77,868,115 (GRCm39) |
|
probably benign |
Het |
Slc49a3 |
A |
G |
5: 108,592,458 (GRCm39) |
|
probably benign |
Het |
Sorcs1 |
T |
C |
19: 50,216,639 (GRCm39) |
T647A |
probably damaging |
Het |
Sspo |
T |
A |
6: 48,469,822 (GRCm39) |
C4507S |
probably damaging |
Het |
Traf3ip3 |
T |
C |
1: 192,866,772 (GRCm39) |
|
probably null |
Het |
Vmn2r121 |
T |
A |
X: 123,042,504 (GRCm39) |
I218F |
probably damaging |
Het |
Vmn2r61 |
A |
G |
7: 41,909,550 (GRCm39) |
Y25C |
probably damaging |
Het |
|
Other mutations in Map3k4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Map3k4
|
APN |
17 |
12,451,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01124:Map3k4
|
APN |
17 |
12,474,087 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01585:Map3k4
|
APN |
17 |
12,467,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02194:Map3k4
|
APN |
17 |
12,482,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02194:Map3k4
|
APN |
17 |
12,467,882 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02292:Map3k4
|
APN |
17 |
12,454,045 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02326:Map3k4
|
APN |
17 |
12,467,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02388:Map3k4
|
APN |
17 |
12,490,497 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02621:Map3k4
|
APN |
17 |
12,482,900 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02668:Map3k4
|
APN |
17 |
12,454,840 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02850:Map3k4
|
APN |
17 |
12,490,801 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Map3k4
|
APN |
17 |
12,491,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03148:Map3k4
|
APN |
17 |
12,457,045 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03238:Map3k4
|
APN |
17 |
12,490,045 (GRCm39) |
missense |
probably benign |
0.10 |
ANU74:Map3k4
|
UTSW |
17 |
12,451,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Map3k4
|
UTSW |
17 |
12,457,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Map3k4
|
UTSW |
17 |
12,457,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:Map3k4
|
UTSW |
17 |
12,466,950 (GRCm39) |
missense |
probably damaging |
0.99 |
R0183:Map3k4
|
UTSW |
17 |
12,454,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Map3k4
|
UTSW |
17 |
12,489,902 (GRCm39) |
frame shift |
probably null |
|
R0355:Map3k4
|
UTSW |
17 |
12,473,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R0367:Map3k4
|
UTSW |
17 |
12,476,928 (GRCm39) |
splice site |
probably benign |
|
R1103:Map3k4
|
UTSW |
17 |
12,455,950 (GRCm39) |
splice site |
probably null |
|
R1446:Map3k4
|
UTSW |
17 |
12,475,681 (GRCm39) |
nonsense |
probably null |
|
R1542:Map3k4
|
UTSW |
17 |
12,454,793 (GRCm39) |
missense |
probably damaging |
0.97 |
R1713:Map3k4
|
UTSW |
17 |
12,468,458 (GRCm39) |
missense |
probably benign |
0.39 |
R1777:Map3k4
|
UTSW |
17 |
12,490,617 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1797:Map3k4
|
UTSW |
17 |
12,482,906 (GRCm39) |
missense |
probably benign |
0.30 |
R1997:Map3k4
|
UTSW |
17 |
12,473,882 (GRCm39) |
critical splice donor site |
probably null |
|
R2042:Map3k4
|
UTSW |
17 |
12,496,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R2878:Map3k4
|
UTSW |
17 |
12,482,954 (GRCm39) |
missense |
probably benign |
0.00 |
R2939:Map3k4
|
UTSW |
17 |
12,480,157 (GRCm39) |
missense |
probably damaging |
0.98 |
R2940:Map3k4
|
UTSW |
17 |
12,480,157 (GRCm39) |
missense |
probably damaging |
0.98 |
R3405:Map3k4
|
UTSW |
17 |
12,475,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R3930:Map3k4
|
UTSW |
17 |
12,454,880 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4291:Map3k4
|
UTSW |
17 |
12,474,147 (GRCm39) |
missense |
probably benign |
0.08 |
R4410:Map3k4
|
UTSW |
17 |
12,467,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R4632:Map3k4
|
UTSW |
17 |
12,451,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R4641:Map3k4
|
UTSW |
17 |
12,482,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Map3k4
|
UTSW |
17 |
12,451,851 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4730:Map3k4
|
UTSW |
17 |
12,467,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R4832:Map3k4
|
UTSW |
17 |
12,490,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R4896:Map3k4
|
UTSW |
17 |
12,490,906 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4934:Map3k4
|
UTSW |
17 |
12,490,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Map3k4
|
UTSW |
17 |
12,468,382 (GRCm39) |
critical splice donor site |
probably null |
|
R4980:Map3k4
|
UTSW |
17 |
12,490,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R5211:Map3k4
|
UTSW |
17 |
12,451,321 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5337:Map3k4
|
UTSW |
17 |
12,490,497 (GRCm39) |
missense |
probably damaging |
0.99 |
R5356:Map3k4
|
UTSW |
17 |
12,466,195 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5550:Map3k4
|
UTSW |
17 |
12,462,445 (GRCm39) |
nonsense |
probably null |
|
R5824:Map3k4
|
UTSW |
17 |
12,448,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Map3k4
|
UTSW |
17 |
12,490,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R6285:Map3k4
|
UTSW |
17 |
12,482,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6380:Map3k4
|
UTSW |
17 |
12,490,954 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6383:Map3k4
|
UTSW |
17 |
12,468,470 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6571:Map3k4
|
UTSW |
17 |
12,461,579 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6584:Map3k4
|
UTSW |
17 |
12,479,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R6616:Map3k4
|
UTSW |
17 |
12,490,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R6644:Map3k4
|
UTSW |
17 |
12,451,297 (GRCm39) |
critical splice donor site |
probably null |
|
R6909:Map3k4
|
UTSW |
17 |
12,489,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Map3k4
|
UTSW |
17 |
12,479,456 (GRCm39) |
nonsense |
probably null |
|
R6970:Map3k4
|
UTSW |
17 |
12,467,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7120:Map3k4
|
UTSW |
17 |
12,490,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7253:Map3k4
|
UTSW |
17 |
12,490,955 (GRCm39) |
missense |
probably benign |
0.00 |
R7267:Map3k4
|
UTSW |
17 |
12,490,536 (GRCm39) |
nonsense |
probably null |
|
R7322:Map3k4
|
UTSW |
17 |
12,489,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R7522:Map3k4
|
UTSW |
17 |
12,480,219 (GRCm39) |
missense |
probably benign |
0.39 |
R7554:Map3k4
|
UTSW |
17 |
12,451,301 (GRCm39) |
nonsense |
probably null |
|
R7554:Map3k4
|
UTSW |
17 |
12,451,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R7681:Map3k4
|
UTSW |
17 |
12,537,430 (GRCm39) |
missense |
unknown |
|
R7734:Map3k4
|
UTSW |
17 |
12,482,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Map3k4
|
UTSW |
17 |
12,490,030 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8013:Map3k4
|
UTSW |
17 |
12,489,918 (GRCm39) |
nonsense |
probably null |
|
R8014:Map3k4
|
UTSW |
17 |
12,489,918 (GRCm39) |
nonsense |
probably null |
|
R8235:Map3k4
|
UTSW |
17 |
12,458,968 (GRCm39) |
splice site |
probably null |
|
R8294:Map3k4
|
UTSW |
17 |
12,537,500 (GRCm39) |
missense |
unknown |
|
R8528:Map3k4
|
UTSW |
17 |
12,451,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R8858:Map3k4
|
UTSW |
17 |
12,490,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Map3k4
|
UTSW |
17 |
12,490,433 (GRCm39) |
missense |
probably benign |
0.00 |
R9063:Map3k4
|
UTSW |
17 |
12,482,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Map3k4
|
UTSW |
17 |
12,456,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R9446:Map3k4
|
UTSW |
17 |
12,451,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R9486:Map3k4
|
UTSW |
17 |
12,489,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9488:Map3k4
|
UTSW |
17 |
12,489,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9591:Map3k4
|
UTSW |
17 |
12,454,795 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9617:Map3k4
|
UTSW |
17 |
12,476,871 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9722:Map3k4
|
UTSW |
17 |
12,490,523 (GRCm39) |
missense |
probably benign |
0.01 |
X0067:Map3k4
|
UTSW |
17 |
12,482,981 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Map3k4
|
UTSW |
17 |
12,490,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|