Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
G |
A |
10: 79,841,615 (GRCm39) |
|
probably null |
Het |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Dsg3 |
T |
A |
18: 20,653,615 (GRCm39) |
F54I |
probably benign |
Het |
Ehbp1 |
G |
A |
11: 22,045,892 (GRCm39) |
S619L |
probably benign |
Het |
Eif1ad3 |
A |
G |
12: 87,843,446 (GRCm39) |
Y31C |
probably damaging |
Het |
Eif1ad5 |
A |
G |
12: 87,946,852 (GRCm39) |
D98G |
probably benign |
Het |
Erlec1 |
G |
A |
11: 30,898,442 (GRCm39) |
Q10* |
probably null |
Het |
Fbxw14 |
A |
G |
9: 109,107,750 (GRCm39) |
|
probably null |
Het |
Fhod1 |
C |
T |
8: 106,056,224 (GRCm39) |
R1163H |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gm4846 |
G |
A |
1: 166,311,462 (GRCm39) |
P466S |
probably damaging |
Het |
Ift122 |
A |
T |
6: 115,865,726 (GRCm39) |
K339* |
probably null |
Het |
Il6st |
T |
C |
13: 112,625,064 (GRCm39) |
S227P |
probably damaging |
Het |
Letmd1 |
A |
G |
15: 100,375,708 (GRCm39) |
Y198C |
probably damaging |
Het |
Mdc1 |
C |
G |
17: 36,168,361 (GRCm39) |
R1656G |
probably benign |
Het |
Megf11 |
C |
T |
9: 64,597,407 (GRCm39) |
S662L |
possibly damaging |
Het |
Mrps25 |
T |
C |
6: 92,160,881 (GRCm39) |
E25G |
probably benign |
Het |
Myh2 |
G |
T |
11: 67,085,520 (GRCm39) |
G1815C |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,393,867 (GRCm39) |
D2353G |
probably damaging |
Het |
Naip5 |
T |
A |
13: 100,356,338 (GRCm39) |
E1092D |
probably benign |
Het |
P2rx5 |
A |
T |
11: 73,058,390 (GRCm39) |
H275L |
possibly damaging |
Het |
Pyroxd1 |
C |
G |
6: 142,300,467 (GRCm39) |
S199* |
probably null |
Het |
Rnf123 |
T |
C |
9: 107,935,786 (GRCm39) |
D920G |
probably damaging |
Het |
Slc44a2 |
A |
G |
9: 21,258,178 (GRCm39) |
Y474C |
probably damaging |
Het |
Slc9a4 |
T |
A |
1: 40,646,285 (GRCm39) |
F439I |
probably damaging |
Het |
Snap91 |
A |
G |
9: 86,761,528 (GRCm39) |
V26A |
probably damaging |
Het |
Spata31d1c |
C |
A |
13: 65,182,862 (GRCm39) |
Q135K |
probably benign |
Het |
Stard8 |
AGAGGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGAGGA |
X: 98,110,114 (GRCm39) |
|
probably benign |
Het |
Tlk2 |
T |
C |
11: 105,166,809 (GRCm39) |
I669T |
probably benign |
Het |
Tmem273 |
A |
G |
14: 32,528,839 (GRCm39) |
D68G |
probably damaging |
Het |
Ttc38 |
T |
C |
15: 85,728,659 (GRCm39) |
S204P |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,617,155 (GRCm39) |
Y16403F |
probably damaging |
Het |
Ttyh2 |
G |
T |
11: 114,592,609 (GRCm39) |
W213L |
probably damaging |
Het |
Ugt2a2 |
A |
T |
5: 87,610,755 (GRCm39) |
D360E |
probably damaging |
Het |
Vwa5b2 |
A |
T |
16: 20,423,393 (GRCm39) |
H1102L |
probably damaging |
Het |
Zbtb41 |
A |
T |
1: 139,370,557 (GRCm39) |
T665S |
probably damaging |
Het |
Zfp292 |
T |
C |
4: 34,807,828 (GRCm39) |
I1739V |
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 |
IGL01125:Map3k4
|
APN |
17 |
12,490,849 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
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 |
|