Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
T |
A |
7: 119,137,319 (GRCm39) |
C378* |
probably null |
Het |
Ago3 |
T |
C |
4: 126,311,045 (GRCm39) |
D56G |
possibly damaging |
Het |
Ahnak |
G |
T |
19: 8,986,492 (GRCm39) |
G2592V |
probably damaging |
Het |
Aldh6a1 |
C |
T |
12: 84,480,300 (GRCm39) |
G470D |
probably damaging |
Het |
Ankub1 |
T |
A |
3: 57,597,796 (GRCm39) |
N58I |
probably damaging |
Het |
Apol7b |
G |
T |
15: 77,309,728 (GRCm39) |
T23K |
probably benign |
Het |
Arap2 |
G |
A |
5: 62,763,474 (GRCm39) |
P1557S |
possibly damaging |
Het |
Arhgap24 |
T |
C |
5: 103,023,643 (GRCm39) |
Y136H |
probably damaging |
Het |
Atp1a1 |
A |
G |
3: 101,497,128 (GRCm39) |
F393L |
probably damaging |
Het |
Bcdin3d |
A |
T |
15: 99,368,873 (GRCm39) |
C109S |
probably damaging |
Het |
Catsperd |
A |
G |
17: 56,965,078 (GRCm39) |
K475R |
possibly damaging |
Het |
Cblb |
A |
G |
16: 52,024,843 (GRCm39) |
T913A |
probably benign |
Het |
Cbx6 |
A |
G |
15: 79,712,404 (GRCm39) |
L341P |
probably benign |
Het |
Cd177 |
T |
C |
7: 24,457,781 (GRCm39) |
Y159C |
probably damaging |
Het |
Cdh20 |
A |
G |
1: 110,027,844 (GRCm39) |
N530D |
probably damaging |
Het |
Cdk8 |
T |
C |
5: 146,235,682 (GRCm39) |
F270L |
probably damaging |
Het |
Ces2c |
A |
T |
8: 105,574,656 (GRCm39) |
T38S |
probably damaging |
Het |
Chst14 |
T |
C |
2: 118,758,202 (GRCm39) |
L357P |
probably damaging |
Het |
Clca3b |
T |
A |
3: 144,528,627 (GRCm39) |
|
probably benign |
Het |
Cluh |
A |
G |
11: 74,555,720 (GRCm39) |
S839G |
probably benign |
Het |
Cnga4 |
T |
A |
7: 105,056,947 (GRCm39) |
V350E |
probably damaging |
Het |
Creb1 |
G |
A |
1: 64,609,426 (GRCm39) |
G180R |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 48,320,907 (GRCm39) |
E301G |
probably benign |
Het |
Cyp4f18 |
A |
T |
8: 72,749,844 (GRCm39) |
D268E |
probably benign |
Het |
Dock5 |
A |
G |
14: 68,022,241 (GRCm39) |
|
probably benign |
Het |
Dpy19l4 |
T |
A |
4: 11,289,715 (GRCm39) |
H332L |
probably benign |
Het |
Dync2h1 |
T |
A |
9: 7,113,153 (GRCm39) |
H224L |
probably benign |
Het |
Dzip1l |
C |
A |
9: 99,545,134 (GRCm39) |
Q585K |
possibly damaging |
Het |
Erf |
C |
T |
7: 24,943,801 (GRCm39) |
G510D |
probably damaging |
Het |
Fanci |
T |
C |
7: 79,081,926 (GRCm39) |
L623P |
probably benign |
Het |
Fat1 |
T |
C |
8: 45,475,988 (GRCm39) |
V1655A |
probably damaging |
Het |
Fat4 |
T |
C |
3: 38,942,463 (GRCm39) |
V452A |
probably benign |
Het |
Gal3st4 |
C |
T |
5: 138,264,151 (GRCm39) |
G283S |
probably benign |
Het |
Gm5422 |
A |
G |
10: 31,126,318 (GRCm39) |
|
noncoding transcript |
Het |
Gnal |
C |
T |
18: 67,221,744 (GRCm39) |
T49I |
unknown |
Het |
Gng5 |
A |
G |
3: 146,209,103 (GRCm39) |
N57S |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,355,441 (GRCm39) |
I2231V |
probably damaging |
Het |
Hgfac |
G |
T |
5: 35,201,584 (GRCm39) |
G272W |
probably damaging |
Het |
Hmcn1 |
T |
A |
1: 150,618,092 (GRCm39) |
D1265V |
possibly damaging |
Het |
Ifi207 |
T |
A |
1: 173,563,878 (GRCm39) |
Q47L |
possibly damaging |
Het |
Klhl40 |
G |
A |
9: 121,607,133 (GRCm39) |
E98K |
probably damaging |
Het |
Lepr |
G |
T |
4: 101,630,207 (GRCm39) |
|
probably benign |
Het |
Lyst |
A |
G |
13: 13,812,600 (GRCm39) |
H1004R |
probably benign |
Het |
Mmp1b |
C |
A |
9: 7,387,013 (GRCm39) |
Q66H |
possibly damaging |
Het |
Mpo |
T |
C |
11: 87,694,330 (GRCm39) |
S107P |
probably benign |
Het |
Mroh9 |
T |
C |
1: 162,888,205 (GRCm39) |
H290R |
possibly damaging |
Het |
Myo7b |
A |
G |
18: 32,097,439 (GRCm39) |
|
probably null |
Het |
Myom1 |
T |
C |
17: 71,399,215 (GRCm39) |
|
probably benign |
Het |
Nalcn |
C |
T |
14: 123,834,026 (GRCm39) |
V50I |
possibly damaging |
Het |
Negr1 |
A |
G |
3: 156,866,385 (GRCm39) |
|
probably benign |
Het |
Nlrc5 |
T |
G |
8: 95,219,753 (GRCm39) |
|
probably benign |
Het |
Nyap2 |
G |
A |
1: 81,065,029 (GRCm39) |
D14N |
probably damaging |
Het |
Or10w1 |
T |
A |
19: 13,632,261 (GRCm39) |
I151N |
possibly damaging |
Het |
Or2h1 |
C |
A |
17: 37,404,203 (GRCm39) |
G188W |
probably damaging |
Het |
Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
Parp14 |
A |
T |
16: 35,661,779 (GRCm39) |
S1419T |
possibly damaging |
Het |
Piezo2 |
A |
G |
18: 63,160,615 (GRCm39) |
F2347S |
probably damaging |
Het |
Pigf |
A |
G |
17: 87,316,337 (GRCm39) |
V147A |
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,629,693 (GRCm39) |
M637K |
probably benign |
Het |
Plce1 |
T |
C |
19: 38,748,582 (GRCm39) |
I1771T |
probably benign |
Het |
Ppp6c |
A |
T |
2: 39,096,660 (GRCm39) |
|
probably benign |
Het |
Prag1 |
T |
C |
8: 36,570,854 (GRCm39) |
V479A |
possibly damaging |
Het |
Prss33 |
A |
T |
17: 24,054,079 (GRCm39) |
D42E |
probably benign |
Het |
Psmb10 |
A |
G |
8: 106,664,177 (GRCm39) |
V64A |
possibly damaging |
Het |
Psmd14 |
A |
G |
2: 61,630,407 (GRCm39) |
T306A |
probably benign |
Het |
Psmg1 |
C |
T |
16: 95,790,687 (GRCm39) |
|
probably benign |
Het |
Rc3h2 |
A |
T |
2: 37,266,671 (GRCm39) |
|
probably null |
Het |
Reln |
C |
T |
5: 22,125,494 (GRCm39) |
V2730I |
probably damaging |
Het |
Sec24a |
A |
T |
11: 51,634,622 (GRCm39) |
H101Q |
probably benign |
Het |
Selenoi |
A |
G |
5: 30,471,954 (GRCm39) |
N385S |
probably benign |
Het |
Slc24a4 |
T |
C |
12: 102,097,882 (GRCm39) |
|
probably null |
Het |
Slc4a10 |
G |
A |
2: 62,080,877 (GRCm39) |
S338N |
probably benign |
Het |
Slfn3 |
A |
T |
11: 83,103,986 (GRCm39) |
T286S |
probably damaging |
Het |
Snx29 |
A |
G |
16: 11,213,167 (GRCm39) |
D111G |
probably benign |
Het |
Sp8 |
T |
C |
12: 118,812,300 (GRCm39) |
S52P |
possibly damaging |
Het |
Srek1 |
G |
T |
13: 103,897,098 (GRCm39) |
T81K |
probably damaging |
Het |
Sry |
C |
G |
Y: 2,662,864 (GRCm39) |
Q265H |
unknown |
Het |
Taf3 |
A |
G |
2: 9,945,804 (GRCm39) |
V600A |
probably benign |
Het |
Tatdn2 |
C |
A |
6: 113,679,550 (GRCm39) |
D298E |
probably benign |
Het |
Tmem253 |
A |
T |
14: 52,254,663 (GRCm39) |
|
probably benign |
Het |
Tmem63a |
T |
A |
1: 180,785,614 (GRCm39) |
|
probably null |
Het |
Tmprss11b |
T |
C |
5: 86,809,499 (GRCm39) |
D331G |
probably damaging |
Het |
Tor1aip1 |
T |
A |
1: 155,883,420 (GRCm39) |
K143* |
probably null |
Het |
Trappc8 |
A |
T |
18: 20,977,245 (GRCm39) |
N841K |
possibly damaging |
Het |
Trio |
T |
C |
15: 27,855,049 (GRCm39) |
Q711R |
probably benign |
Het |
Trmt10b |
C |
A |
4: 45,304,306 (GRCm39) |
T114N |
probably damaging |
Het |
Trpv2 |
C |
A |
11: 62,473,732 (GRCm39) |
A129D |
probably benign |
Het |
Ttll4 |
T |
G |
1: 74,727,777 (GRCm39) |
D846E |
probably benign |
Het |
Ugt2a3 |
A |
G |
5: 87,484,508 (GRCm39) |
L172P |
possibly damaging |
Het |
Usp19 |
T |
A |
9: 108,371,686 (GRCm39) |
F355Y |
probably damaging |
Het |
Vmn1r209 |
C |
T |
13: 22,990,114 (GRCm39) |
G192D |
probably damaging |
Het |
Vmn2r107 |
T |
G |
17: 20,578,021 (GRCm39) |
D443E |
probably benign |
Het |
Wee2 |
A |
T |
6: 40,440,187 (GRCm39) |
E445V |
probably benign |
Het |
Zer1 |
A |
T |
2: 29,991,819 (GRCm39) |
I680N |
probably damaging |
Het |
Zfhx4 |
T |
C |
3: 5,467,795 (GRCm39) |
L2651P |
probably damaging |
Het |
Zfp692 |
C |
T |
11: 58,199,881 (GRCm39) |
Q157* |
probably null |
Het |
Zfp964 |
T |
A |
8: 70,116,587 (GRCm39) |
C396S |
unknown |
Het |
|
Other mutations in Map3k1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01594:Map3k1
|
APN |
13 |
111,894,723 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01686:Map3k1
|
APN |
13 |
111,891,196 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02104:Map3k1
|
APN |
13 |
111,892,777 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03071:Map3k1
|
APN |
13 |
111,892,059 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03087:Map3k1
|
APN |
13 |
111,885,559 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03213:Map3k1
|
APN |
13 |
111,885,426 (GRCm39) |
utr 3 prime |
probably benign |
|
Nepal
|
UTSW |
13 |
111,888,983 (GRCm39) |
missense |
probably benign |
0.07 |
Snow_leopard
|
UTSW |
13 |
111,892,298 (GRCm39) |
nonsense |
probably null |
|
R0005:Map3k1
|
UTSW |
13 |
111,892,238 (GRCm39) |
missense |
probably benign |
0.00 |
R0025:Map3k1
|
UTSW |
13 |
111,892,663 (GRCm39) |
missense |
probably benign |
|
R0540:Map3k1
|
UTSW |
13 |
111,900,044 (GRCm39) |
missense |
probably benign |
0.05 |
R0607:Map3k1
|
UTSW |
13 |
111,900,044 (GRCm39) |
missense |
probably benign |
0.05 |
R0898:Map3k1
|
UTSW |
13 |
111,904,490 (GRCm39) |
unclassified |
probably benign |
|
R1171:Map3k1
|
UTSW |
13 |
111,892,177 (GRCm39) |
missense |
probably benign |
0.29 |
R1464:Map3k1
|
UTSW |
13 |
111,892,405 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1464:Map3k1
|
UTSW |
13 |
111,892,405 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1682:Map3k1
|
UTSW |
13 |
111,893,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R1718:Map3k1
|
UTSW |
13 |
111,891,953 (GRCm39) |
missense |
probably benign |
0.23 |
R1893:Map3k1
|
UTSW |
13 |
111,904,567 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2174:Map3k1
|
UTSW |
13 |
111,889,016 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2215:Map3k1
|
UTSW |
13 |
111,892,322 (GRCm39) |
missense |
probably benign |
0.00 |
R2239:Map3k1
|
UTSW |
13 |
111,885,478 (GRCm39) |
missense |
probably benign |
0.00 |
R3686:Map3k1
|
UTSW |
13 |
111,890,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R3783:Map3k1
|
UTSW |
13 |
111,892,754 (GRCm39) |
missense |
probably benign |
0.00 |
R4094:Map3k1
|
UTSW |
13 |
111,892,696 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4231:Map3k1
|
UTSW |
13 |
111,905,028 (GRCm39) |
missense |
probably benign |
0.01 |
R4902:Map3k1
|
UTSW |
13 |
111,909,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R4967:Map3k1
|
UTSW |
13 |
111,909,272 (GRCm39) |
missense |
probably damaging |
0.96 |
R5465:Map3k1
|
UTSW |
13 |
111,892,654 (GRCm39) |
missense |
probably benign |
0.20 |
R5855:Map3k1
|
UTSW |
13 |
111,892,513 (GRCm39) |
missense |
probably benign |
0.37 |
R6384:Map3k1
|
UTSW |
13 |
111,887,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R6389:Map3k1
|
UTSW |
13 |
111,905,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R6400:Map3k1
|
UTSW |
13 |
111,892,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R6509:Map3k1
|
UTSW |
13 |
111,890,363 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6644:Map3k1
|
UTSW |
13 |
111,888,983 (GRCm39) |
missense |
probably benign |
0.07 |
R6900:Map3k1
|
UTSW |
13 |
111,890,350 (GRCm39) |
missense |
probably benign |
0.01 |
R6943:Map3k1
|
UTSW |
13 |
111,909,246 (GRCm39) |
missense |
probably benign |
0.30 |
R6946:Map3k1
|
UTSW |
13 |
111,905,035 (GRCm39) |
nonsense |
probably null |
|
R7059:Map3k1
|
UTSW |
13 |
111,909,312 (GRCm39) |
missense |
probably benign |
|
R7271:Map3k1
|
UTSW |
13 |
111,893,231 (GRCm39) |
missense |
probably benign |
0.32 |
R7290:Map3k1
|
UTSW |
13 |
111,904,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R7397:Map3k1
|
UTSW |
13 |
111,891,742 (GRCm39) |
missense |
probably damaging |
0.98 |
R7457:Map3k1
|
UTSW |
13 |
111,892,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R7827:Map3k1
|
UTSW |
13 |
111,892,663 (GRCm39) |
missense |
probably benign |
|
R7990:Map3k1
|
UTSW |
13 |
111,892,696 (GRCm39) |
missense |
probably benign |
0.28 |
R8110:Map3k1
|
UTSW |
13 |
111,891,847 (GRCm39) |
missense |
probably damaging |
0.98 |
R8119:Map3k1
|
UTSW |
13 |
111,909,156 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8179:Map3k1
|
UTSW |
13 |
111,885,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R8317:Map3k1
|
UTSW |
13 |
111,894,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8397:Map3k1
|
UTSW |
13 |
111,892,138 (GRCm39) |
missense |
probably damaging |
0.99 |
R8745:Map3k1
|
UTSW |
13 |
111,893,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R8829:Map3k1
|
UTSW |
13 |
111,889,015 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8832:Map3k1
|
UTSW |
13 |
111,889,015 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8939:Map3k1
|
UTSW |
13 |
111,892,837 (GRCm39) |
nonsense |
probably null |
|
R9640:Map3k1
|
UTSW |
13 |
111,900,699 (GRCm39) |
nonsense |
probably null |
|
R9649:Map3k1
|
UTSW |
13 |
111,885,478 (GRCm39) |
missense |
probably damaging |
0.97 |
R9653:Map3k1
|
UTSW |
13 |
111,890,296 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9763:Map3k1
|
UTSW |
13 |
111,912,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R9768:Map3k1
|
UTSW |
13 |
111,904,630 (GRCm39) |
missense |
probably benign |
0.04 |
X0065:Map3k1
|
UTSW |
13 |
111,893,639 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Map3k1
|
UTSW |
13 |
111,892,480 (GRCm39) |
missense |
probably benign |
0.00 |
|