Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110021N24Rik |
T |
C |
4: 108,637,744 (GRCm39) |
V37A |
unknown |
Het |
3425401B19Rik |
G |
A |
14: 32,382,614 (GRCm39) |
S1117L |
possibly damaging |
Het |
Abi3bp |
A |
G |
16: 56,456,590 (GRCm39) |
I1021V |
probably benign |
Het |
Agrn |
C |
A |
4: 156,253,264 (GRCm39) |
K1848N |
probably benign |
Het |
Anln |
A |
G |
9: 22,249,283 (GRCm39) |
V1005A |
probably benign |
Het |
Arb2a |
A |
G |
13: 78,311,725 (GRCm39) |
K356R |
possibly damaging |
Het |
Arid3b |
A |
G |
9: 57,741,327 (GRCm39) |
Y40H |
probably damaging |
Het |
Bco1 |
A |
C |
8: 117,859,917 (GRCm39) |
D540A |
probably benign |
Het |
Blnk |
A |
G |
19: 40,982,482 (GRCm39) |
I7T |
probably benign |
Het |
Brca2 |
T |
G |
5: 150,475,770 (GRCm39) |
D2493E |
probably benign |
Het |
Bsn |
T |
A |
9: 107,988,052 (GRCm39) |
M2567L |
unknown |
Het |
Cacna1e |
T |
A |
1: 154,355,064 (GRCm39) |
Y693F |
possibly damaging |
Het |
Catsperg1 |
G |
C |
7: 28,884,152 (GRCm39) |
T987R |
probably damaging |
Het |
Cpa4 |
G |
T |
6: 30,574,393 (GRCm39) |
D61Y |
possibly damaging |
Het |
Cpne1 |
A |
C |
2: 155,921,080 (GRCm39) |
V70G |
probably damaging |
Het |
Dnase1l3 |
A |
T |
14: 7,987,306 (GRCm38) |
N81K |
probably damaging |
Het |
Duxf3 |
GCCC |
GCC |
10: 58,066,944 (GRCm39) |
|
probably null |
Het |
Fbxo31 |
G |
A |
8: 122,281,136 (GRCm39) |
R337C |
probably damaging |
Het |
Fbxo34 |
C |
G |
14: 47,767,928 (GRCm39) |
H480Q |
probably benign |
Het |
Frmd4b |
T |
C |
6: 97,398,559 (GRCm39) |
E96G |
|
Het |
Gdpgp1 |
T |
A |
7: 79,888,216 (GRCm39) |
D82E |
probably benign |
Het |
Gjb3 |
GCCAGATGCGCCCA |
GCCAGATGCGCCCAGATGCGCCCA |
4: 127,220,458 (GRCm39) |
|
probably null |
Het |
Grpel1 |
A |
G |
5: 36,626,823 (GRCm39) |
N35S |
probably benign |
Het |
Il16 |
T |
C |
7: 83,301,559 (GRCm39) |
T886A |
probably benign |
Het |
Insig1 |
T |
A |
5: 28,278,570 (GRCm39) |
C128* |
probably null |
Het |
Kcnk10 |
T |
A |
12: 98,484,775 (GRCm39) |
E120D |
probably benign |
Het |
Kctd1 |
T |
C |
18: 15,195,369 (GRCm39) |
N418S |
possibly damaging |
Het |
Kifbp |
A |
G |
10: 62,395,037 (GRCm39) |
V535A |
probably damaging |
Het |
Klhl20 |
T |
A |
1: 160,933,055 (GRCm39) |
H251L |
probably damaging |
Het |
Ldlrad3 |
T |
C |
2: 101,888,326 (GRCm39) |
D127G |
probably damaging |
Het |
Lrp3 |
T |
C |
7: 34,903,182 (GRCm39) |
Y388C |
probably damaging |
Het |
Lrrc4 |
G |
A |
6: 28,830,206 (GRCm39) |
R47W |
possibly damaging |
Het |
Luzp1 |
A |
T |
4: 136,272,562 (GRCm39) |
D1022V |
probably damaging |
Het |
Mllt1 |
C |
A |
17: 57,212,737 (GRCm39) |
R132L |
probably damaging |
Het |
Ncoa1 |
G |
T |
12: 4,345,494 (GRCm39) |
H618N |
possibly damaging |
Het |
Nelfcd |
T |
C |
2: 174,265,861 (GRCm39) |
S318P |
probably damaging |
Het |
Ngly1 |
A |
C |
14: 16,280,721 (GRCm38) |
T301P |
probably damaging |
Het |
Npy5r |
G |
A |
8: 67,133,560 (GRCm39) |
T411I |
probably damaging |
Het |
Or55b10 |
T |
C |
7: 102,143,568 (GRCm39) |
E138G |
possibly damaging |
Het |
Or5d46 |
A |
G |
2: 88,170,248 (GRCm39) |
N113S |
probably benign |
Het |
Pcdha6 |
T |
A |
18: 37,101,593 (GRCm39) |
I262N |
probably damaging |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Pm20d1 |
C |
A |
1: 131,730,481 (GRCm39) |
A245D |
possibly damaging |
Het |
Rars1 |
T |
C |
11: 35,718,182 (GRCm39) |
|
probably benign |
Het |
Rbms2 |
T |
A |
10: 127,987,107 (GRCm39) |
I62F |
probably damaging |
Het |
Rev3l |
A |
T |
10: 39,700,809 (GRCm39) |
T1769S |
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,378,854 (GRCm39) |
Y1061H |
probably damaging |
Het |
Rgs3 |
A |
T |
4: 62,500,240 (GRCm39) |
I26F |
probably damaging |
Het |
Rsf1 |
G |
GACGGCGGCC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Rtkn |
A |
T |
6: 83,128,018 (GRCm39) |
N406Y |
possibly damaging |
Het |
Rtn4r |
A |
T |
16: 17,969,708 (GRCm39) |
I379F |
possibly damaging |
Het |
Sez6 |
G |
A |
11: 77,865,121 (GRCm39) |
E623K |
possibly damaging |
Het |
Slmap |
T |
C |
14: 26,137,355 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
A |
T |
9: 41,975,050 (GRCm39) |
N519K |
possibly damaging |
Het |
Srebf2 |
A |
T |
15: 82,056,975 (GRCm39) |
I237F |
possibly damaging |
Het |
Szt2 |
T |
C |
4: 118,242,651 (GRCm39) |
S1479G |
possibly damaging |
Het |
Tbc1d24 |
C |
A |
17: 24,400,274 (GRCm39) |
E537* |
probably null |
Het |
Ttf1 |
T |
A |
2: 28,957,080 (GRCm39) |
I450K |
probably benign |
Het |
Ube2e2 |
A |
G |
14: 18,893,288 (GRCm38) |
S2P |
unknown |
Het |
Utp20 |
T |
C |
10: 88,611,180 (GRCm39) |
N1379S |
probably damaging |
Het |
Vmn2r25 |
C |
T |
6: 123,805,391 (GRCm39) |
V489I |
probably benign |
Het |
Wfdc8 |
C |
T |
2: 164,439,245 (GRCm39) |
R379H |
unknown |
Het |
Zeb2 |
C |
T |
2: 45,003,136 (GRCm39) |
|
probably benign |
Het |
Zfp3 |
C |
T |
11: 70,663,241 (GRCm39) |
T400I |
probably benign |
Het |
Zfp760 |
T |
C |
17: 21,941,932 (GRCm39) |
I369T |
possibly damaging |
Het |
|
Other mutations in Il12rb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02056:Il12rb1
|
APN |
8 |
71,263,831 (GRCm39) |
nonsense |
probably null |
|
IGL03065:Il12rb1
|
APN |
8 |
71,273,202 (GRCm39) |
missense |
possibly damaging |
0.51 |
P0026:Il12rb1
|
UTSW |
8 |
71,265,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R0140:Il12rb1
|
UTSW |
8 |
71,272,415 (GRCm39) |
splice site |
probably benign |
|
R0763:Il12rb1
|
UTSW |
8 |
71,265,934 (GRCm39) |
splice site |
probably benign |
|
R1554:Il12rb1
|
UTSW |
8 |
71,266,016 (GRCm39) |
critical splice donor site |
probably null |
|
R1577:Il12rb1
|
UTSW |
8 |
71,263,250 (GRCm39) |
missense |
probably damaging |
0.99 |
R1688:Il12rb1
|
UTSW |
8 |
71,272,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R1918:Il12rb1
|
UTSW |
8 |
71,266,324 (GRCm39) |
missense |
probably benign |
0.04 |
R2848:Il12rb1
|
UTSW |
8 |
71,268,446 (GRCm39) |
nonsense |
probably null |
|
R3735:Il12rb1
|
UTSW |
8 |
71,269,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R4791:Il12rb1
|
UTSW |
8 |
71,266,012 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4857:Il12rb1
|
UTSW |
8 |
71,263,232 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5189:Il12rb1
|
UTSW |
8 |
71,263,702 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5493:Il12rb1
|
UTSW |
8 |
71,262,483 (GRCm39) |
missense |
probably benign |
0.00 |
R5590:Il12rb1
|
UTSW |
8 |
71,266,411 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6484:Il12rb1
|
UTSW |
8 |
71,262,348 (GRCm39) |
splice site |
probably null |
|
R7213:Il12rb1
|
UTSW |
8 |
71,269,097 (GRCm39) |
missense |
probably benign |
0.00 |
R7301:Il12rb1
|
UTSW |
8 |
71,266,343 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7388:Il12rb1
|
UTSW |
8 |
71,263,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7992:Il12rb1
|
UTSW |
8 |
71,265,233 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8409:Il12rb1
|
UTSW |
8 |
71,269,187 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9697:Il12rb1
|
UTSW |
8 |
71,263,874 (GRCm39) |
nonsense |
probably null |
|
R9698:Il12rb1
|
UTSW |
8 |
71,263,848 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9774:Il12rb1
|
UTSW |
8 |
71,272,040 (GRCm39) |
missense |
possibly damaging |
0.85 |
X0061:Il12rb1
|
UTSW |
8 |
71,267,279 (GRCm39) |
missense |
probably benign |
|
|