Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700024B05Rik |
T |
A |
14: 41,818,174 (GRCm39) |
H23Q |
possibly damaging |
Het |
Abca14 |
T |
C |
7: 119,877,691 (GRCm39) |
S1069P |
probably benign |
Het |
Abo |
A |
G |
2: 26,733,720 (GRCm39) |
W160R |
probably damaging |
Het |
Adgrb1 |
A |
T |
15: 74,435,807 (GRCm39) |
|
probably benign |
Het |
Ahnak2 |
T |
C |
12: 112,745,978 (GRCm39) |
Q1624R |
|
Het |
Amy2a1 |
T |
A |
3: 113,325,324 (GRCm39) |
N90I |
possibly damaging |
Het |
Bod1l |
C |
T |
5: 41,974,619 (GRCm39) |
V2232I |
probably benign |
Het |
Brsk2 |
T |
A |
7: 141,538,149 (GRCm39) |
H98Q |
probably damaging |
Het |
Caskin2 |
C |
T |
11: 115,694,576 (GRCm39) |
V342I |
probably damaging |
Het |
Ccdc13 |
T |
C |
9: 121,627,156 (GRCm39) |
N707S |
probably benign |
Het |
Cdv3 |
T |
C |
9: 103,241,240 (GRCm39) |
E109G |
probably damaging |
Het |
Coro2a |
C |
T |
4: 46,540,558 (GRCm39) |
E454K |
probably benign |
Het |
Cpq |
A |
T |
15: 33,213,391 (GRCm39) |
I137F |
possibly damaging |
Het |
Ctsj |
G |
A |
13: 61,151,838 (GRCm39) |
T73I |
possibly damaging |
Het |
Dchs2 |
A |
G |
3: 83,146,284 (GRCm39) |
D710G |
probably damaging |
Het |
Drd4 |
T |
C |
7: 140,872,162 (GRCm39) |
V71A |
probably damaging |
Het |
Eef2k |
T |
C |
7: 120,457,694 (GRCm39) |
C18R |
probably benign |
Het |
F2rl2 |
A |
C |
13: 95,837,622 (GRCm39) |
L222F |
probably benign |
Het |
Fkbp4 |
T |
C |
6: 128,413,580 (GRCm39) |
D68G |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,806,132 (GRCm39) |
D817V |
probably damaging |
Het |
Gm19410 |
G |
A |
8: 36,239,652 (GRCm39) |
R116H |
possibly damaging |
Het |
Gm9376 |
A |
T |
14: 118,504,502 (GRCm39) |
|
probably benign |
Het |
Golim4 |
A |
T |
3: 75,813,775 (GRCm39) |
F150I |
probably damaging |
Het |
Gtpbp2 |
G |
A |
17: 46,478,757 (GRCm39) |
V525M |
probably damaging |
Het |
Hook1 |
A |
G |
4: 95,901,499 (GRCm39) |
N486D |
probably benign |
Het |
Hook1 |
A |
G |
4: 95,903,049 (GRCm39) |
S513G |
probably benign |
Het |
Hoxd9 |
A |
T |
2: 74,528,415 (GRCm39) |
T6S |
probably damaging |
Het |
Hsd3b2 |
A |
T |
3: 98,619,051 (GRCm39) |
L298Q |
possibly damaging |
Het |
Idh3b |
A |
C |
2: 130,123,572 (GRCm39) |
S172A |
probably benign |
Het |
Ifnar1 |
C |
T |
16: 91,292,367 (GRCm39) |
P207L |
probably benign |
Het |
Ighv5-17 |
T |
A |
12: 113,822,858 (GRCm39) |
T88S |
possibly damaging |
Het |
Il16 |
T |
A |
7: 83,337,380 (GRCm39) |
K112* |
probably null |
Het |
Irag1 |
A |
T |
7: 110,545,161 (GRCm39) |
I45N |
possibly damaging |
Het |
Kalrn |
T |
A |
16: 33,805,600 (GRCm39) |
I2646F |
probably benign |
Het |
Kcnt1 |
G |
T |
2: 25,767,959 (GRCm39) |
G23C |
probably damaging |
Het |
Kirrel2 |
T |
A |
7: 30,150,260 (GRCm39) |
I523F |
probably damaging |
Het |
Lrrc3b |
A |
T |
14: 15,358,552 (GRCm38) |
L18H |
probably damaging |
Het |
Med13l |
T |
A |
5: 118,862,214 (GRCm39) |
S386T |
probably benign |
Het |
Mettl6 |
C |
T |
14: 31,209,527 (GRCm39) |
|
probably null |
Het |
Mocs2 |
C |
T |
13: 114,961,879 (GRCm39) |
A120V |
possibly damaging |
Het |
Mrpl39 |
T |
C |
16: 84,531,346 (GRCm39) |
T74A |
probably benign |
Het |
Myh2 |
T |
C |
11: 67,069,754 (GRCm39) |
F367L |
probably damaging |
Het |
N4bp1 |
G |
A |
8: 87,587,238 (GRCm39) |
Q567* |
probably null |
Het |
Naf1 |
A |
G |
8: 67,336,097 (GRCm39) |
I341M |
probably damaging |
Het |
Ncoa6 |
A |
T |
2: 155,250,063 (GRCm39) |
N1080K |
probably benign |
Het |
Nell1 |
C |
A |
7: 49,632,474 (GRCm39) |
L36I |
possibly damaging |
Het |
Nrxn2 |
A |
G |
19: 6,522,448 (GRCm39) |
D446G |
probably damaging |
Het |
Nrxn3 |
T |
A |
12: 89,499,737 (GRCm39) |
C709* |
probably null |
Het |
Or13p4 |
T |
G |
4: 118,547,416 (GRCm39) |
T78P |
probably damaging |
Het |
Or2ag17 |
A |
G |
7: 106,389,464 (GRCm39) |
V248A |
probably damaging |
Het |
Or2n1 |
A |
C |
17: 38,486,694 (GRCm39) |
T240P |
probably damaging |
Het |
Or2t26 |
C |
G |
11: 49,039,879 (GRCm39) |
A265G |
probably benign |
Het |
Or8g19 |
T |
A |
9: 39,055,766 (GRCm39) |
Y123* |
probably null |
Het |
Ovgp1 |
T |
C |
3: 105,893,883 (GRCm39) |
|
probably benign |
Het |
Pbx3 |
A |
G |
2: 34,114,555 (GRCm39) |
|
probably benign |
Het |
Pcnx1 |
T |
C |
12: 81,964,981 (GRCm39) |
S383P |
probably damaging |
Het |
Pde6h |
T |
G |
6: 136,936,359 (GRCm39) |
F34C |
probably damaging |
Het |
Pnliprp1 |
A |
G |
19: 58,720,628 (GRCm39) |
|
probably benign |
Het |
Pramel21 |
T |
C |
4: 143,343,795 (GRCm39) |
L365P |
probably damaging |
Het |
Prl8a9 |
C |
T |
13: 27,748,498 (GRCm39) |
|
probably null |
Het |
Qdpr |
T |
C |
5: 45,596,669 (GRCm39) |
N165S |
probably benign |
Het |
Rabl2 |
A |
G |
15: 89,468,148 (GRCm39) |
F158L |
probably damaging |
Het |
Rrp7a |
G |
T |
15: 83,004,084 (GRCm39) |
C117* |
probably null |
Het |
Ryr2 |
T |
C |
13: 11,787,463 (GRCm39) |
Y970C |
probably damaging |
Het |
Sf3b3 |
T |
C |
8: 111,552,774 (GRCm39) |
T503A |
possibly damaging |
Het |
Sipa1 |
T |
C |
19: 5,704,198 (GRCm39) |
E708G |
probably damaging |
Het |
Skor2 |
T |
A |
18: 76,948,811 (GRCm39) |
S844R |
possibly damaging |
Het |
Slc6a7 |
C |
T |
18: 61,138,815 (GRCm39) |
C231Y |
probably damaging |
Het |
Smgc |
A |
T |
15: 91,729,665 (GRCm39) |
E206D |
probably benign |
Het |
Tanc2 |
T |
C |
11: 105,758,290 (GRCm39) |
S684P |
possibly damaging |
Het |
Tep1 |
T |
C |
14: 51,082,967 (GRCm39) |
T1014A |
possibly damaging |
Het |
Tex19.1 |
A |
G |
11: 121,038,283 (GRCm39) |
S214G |
probably benign |
Het |
Trmt6 |
G |
A |
2: 132,650,774 (GRCm39) |
S278L |
probably benign |
Het |
Use1 |
T |
C |
8: 71,821,200 (GRCm39) |
S156P |
probably benign |
Het |
Znrf1 |
G |
A |
8: 112,335,954 (GRCm39) |
V152M |
probably damaging |
Het |
|
Other mutations in Ercc4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00781:Ercc4
|
APN |
16 |
12,943,233 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00805:Ercc4
|
APN |
16 |
12,939,868 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01348:Ercc4
|
APN |
16 |
12,950,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02406:Ercc4
|
APN |
16 |
12,941,400 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03248:Ercc4
|
APN |
16 |
12,945,457 (GRCm39) |
missense |
probably damaging |
1.00 |
Rapscallion
|
UTSW |
16 |
12,944,331 (GRCm39) |
missense |
probably benign |
|
Rascal
|
UTSW |
16 |
12,950,811 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4812001:Ercc4
|
UTSW |
16 |
12,962,311 (GRCm39) |
missense |
probably benign |
0.29 |
R0212:Ercc4
|
UTSW |
16 |
12,941,196 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0505:Ercc4
|
UTSW |
16 |
12,944,331 (GRCm39) |
missense |
probably benign |
|
R0962:Ercc4
|
UTSW |
16 |
12,948,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R1078:Ercc4
|
UTSW |
16 |
12,948,061 (GRCm39) |
missense |
probably benign |
0.00 |
R1356:Ercc4
|
UTSW |
16 |
12,943,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R1420:Ercc4
|
UTSW |
16 |
12,948,073 (GRCm39) |
missense |
probably benign |
0.01 |
R1554:Ercc4
|
UTSW |
16 |
12,965,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Ercc4
|
UTSW |
16 |
12,965,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Ercc4
|
UTSW |
16 |
12,965,798 (GRCm39) |
missense |
probably damaging |
0.99 |
R2214:Ercc4
|
UTSW |
16 |
12,927,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R3757:Ercc4
|
UTSW |
16 |
12,962,360 (GRCm39) |
missense |
probably benign |
0.28 |
R4072:Ercc4
|
UTSW |
16 |
12,948,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R4073:Ercc4
|
UTSW |
16 |
12,948,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R4075:Ercc4
|
UTSW |
16 |
12,948,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R4076:Ercc4
|
UTSW |
16 |
12,948,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:Ercc4
|
UTSW |
16 |
12,965,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Ercc4
|
UTSW |
16 |
12,965,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R4756:Ercc4
|
UTSW |
16 |
12,941,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4767:Ercc4
|
UTSW |
16 |
12,939,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Ercc4
|
UTSW |
16 |
12,941,445 (GRCm39) |
intron |
probably benign |
|
R5013:Ercc4
|
UTSW |
16 |
12,941,445 (GRCm39) |
intron |
probably benign |
|
R5301:Ercc4
|
UTSW |
16 |
12,948,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R5308:Ercc4
|
UTSW |
16 |
12,948,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R5684:Ercc4
|
UTSW |
16 |
12,948,465 (GRCm39) |
missense |
probably benign |
0.35 |
R6083:Ercc4
|
UTSW |
16 |
12,927,903 (GRCm39) |
nonsense |
probably null |
|
R6092:Ercc4
|
UTSW |
16 |
12,943,125 (GRCm39) |
missense |
probably benign |
0.04 |
R6815:Ercc4
|
UTSW |
16 |
12,941,299 (GRCm39) |
missense |
probably damaging |
0.99 |
R6953:Ercc4
|
UTSW |
16 |
12,948,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R7062:Ercc4
|
UTSW |
16 |
12,950,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Ercc4
|
UTSW |
16 |
12,965,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R7317:Ercc4
|
UTSW |
16 |
12,939,977 (GRCm39) |
missense |
probably benign |
0.12 |
R7858:Ercc4
|
UTSW |
16 |
12,943,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R7948:Ercc4
|
UTSW |
16 |
12,948,049 (GRCm39) |
missense |
probably benign |
0.00 |
R8245:Ercc4
|
UTSW |
16 |
12,948,001 (GRCm39) |
missense |
probably benign |
0.00 |
R8408:Ercc4
|
UTSW |
16 |
12,948,001 (GRCm39) |
missense |
probably benign |
0.00 |
R8409:Ercc4
|
UTSW |
16 |
12,948,001 (GRCm39) |
missense |
probably benign |
0.00 |
R9173:Ercc4
|
UTSW |
16 |
12,939,973 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9696:Ercc4
|
UTSW |
16 |
12,950,810 (GRCm39) |
missense |
probably damaging |
1.00 |
RF007:Ercc4
|
UTSW |
16 |
12,941,371 (GRCm39) |
missense |
possibly damaging |
0.67 |
|