Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810459M11Rik |
A |
C |
1: 85,973,893 (GRCm39) |
E70A |
possibly damaging |
Het |
Abcb5 |
C |
A |
12: 118,899,850 (GRCm39) |
Q272H |
probably damaging |
Het |
Acoxl |
T |
C |
2: 127,719,706 (GRCm39) |
Y156H |
probably damaging |
Het |
Alg9 |
T |
C |
9: 50,711,436 (GRCm39) |
F305L |
probably damaging |
Het |
Apobec4 |
T |
C |
1: 152,632,947 (GRCm39) |
V325A |
probably benign |
Het |
Aqp9 |
T |
G |
9: 71,069,651 (GRCm39) |
D46A |
probably benign |
Het |
Atp13a4 |
T |
A |
16: 29,288,130 (GRCm39) |
|
probably null |
Het |
BC051019 |
A |
G |
7: 109,315,466 (GRCm39) |
F263S |
probably damaging |
Het |
Bicc1 |
A |
T |
10: 70,776,828 (GRCm39) |
|
probably null |
Het |
Birc2 |
G |
A |
9: 7,861,028 (GRCm39) |
Q97* |
probably null |
Het |
Capn13 |
G |
T |
17: 73,633,362 (GRCm39) |
T533N |
probably benign |
Het |
Casp6 |
G |
A |
3: 129,699,559 (GRCm39) |
V13M |
probably benign |
Het |
Cdh10 |
A |
T |
15: 18,964,267 (GRCm39) |
E143V |
probably damaging |
Het |
Cobl |
T |
A |
11: 12,203,501 (GRCm39) |
Q1067L |
probably benign |
Het |
Cr2 |
A |
G |
1: 194,850,743 (GRCm39) |
V241A |
probably damaging |
Het |
Cyp2c23 |
C |
T |
19: 44,010,085 (GRCm39) |
V87M |
probably damaging |
Het |
Cyp2j9 |
G |
A |
4: 96,460,211 (GRCm39) |
Q431* |
probably null |
Het |
Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
Cyp4a12b |
A |
T |
4: 115,271,768 (GRCm39) |
M160L |
probably benign |
Het |
Ddhd2 |
T |
A |
8: 26,217,731 (GRCm39) |
K715N |
possibly damaging |
Het |
Ecscr |
T |
C |
18: 35,851,436 (GRCm39) |
Y32C |
probably damaging |
Het |
Ednra |
A |
T |
8: 78,446,934 (GRCm39) |
L48Q |
probably benign |
Het |
Eya4 |
C |
T |
10: 22,987,458 (GRCm39) |
|
probably null |
Het |
F13a1 |
C |
A |
13: 37,082,118 (GRCm39) |
V529L |
probably benign |
Het |
Fam151b |
A |
T |
13: 92,610,621 (GRCm39) |
I56K |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,903,504 (GRCm39) |
I2997T |
probably damaging |
Het |
Fgfr2 |
A |
T |
7: 129,765,763 (GRCm39) |
F817I |
probably damaging |
Het |
Fras1 |
G |
T |
5: 96,884,895 (GRCm39) |
C2591F |
probably damaging |
Het |
Fryl |
T |
C |
5: 73,215,134 (GRCm39) |
D2214G |
|
Het |
Galntl6 |
A |
T |
8: 58,290,410 (GRCm39) |
D394E |
probably damaging |
Het |
Ggcx |
C |
A |
6: 72,406,190 (GRCm39) |
N605K |
probably damaging |
Het |
Gja5 |
A |
G |
3: 96,958,801 (GRCm39) |
N286S |
|
Het |
Gm4553 |
A |
T |
7: 141,719,298 (GRCm39) |
C43* |
probably null |
Het |
Gpr158 |
T |
C |
2: 21,831,825 (GRCm39) |
V975A |
probably benign |
Het |
Greb1l |
T |
A |
18: 10,458,600 (GRCm39) |
D60E |
probably benign |
Het |
Hao2 |
A |
T |
3: 98,784,462 (GRCm39) |
L301H |
probably damaging |
Het |
Hic1 |
A |
G |
11: 75,060,131 (GRCm39) |
L72P |
possibly damaging |
Het |
Hs3st5 |
A |
C |
10: 36,709,370 (GRCm39) |
N302H |
probably benign |
Het |
Htr1d |
A |
G |
4: 136,169,663 (GRCm39) |
|
probably benign |
Het |
Inka1 |
A |
G |
9: 107,861,938 (GRCm39) |
V128A |
probably benign |
Het |
Kdm7a |
T |
C |
6: 39,128,253 (GRCm39) |
D526G |
probably damaging |
Het |
Kif5a |
T |
C |
10: 127,079,353 (GRCm39) |
S282G |
probably damaging |
Het |
Klhdc7b |
T |
C |
15: 89,272,463 (GRCm39) |
V457A |
possibly damaging |
Het |
Lcorl |
A |
G |
5: 45,891,339 (GRCm39) |
V421A |
probably benign |
Het |
Ltc4s |
A |
G |
11: 50,127,386 (GRCm39) |
S150P |
unknown |
Het |
Mdfic |
C |
T |
6: 15,720,852 (GRCm39) |
R18W |
unknown |
Het |
Mdfic |
T |
G |
6: 15,770,508 (GRCm39) |
D171E |
probably benign |
Het |
Meis2 |
T |
C |
2: 115,694,724 (GRCm39) |
D473G |
possibly damaging |
Het |
Mettl17 |
A |
T |
14: 52,129,029 (GRCm39) |
Q433L |
unknown |
Het |
Mettl25 |
T |
C |
10: 105,677,090 (GRCm39) |
R31G |
probably damaging |
Het |
Mroh2b |
T |
A |
15: 4,950,845 (GRCm39) |
I581N |
probably damaging |
Het |
Myh7 |
A |
T |
14: 55,217,841 (GRCm39) |
N1091K |
probably benign |
Het |
Mysm1 |
T |
C |
4: 94,848,635 (GRCm39) |
D466G |
probably benign |
Het |
Ncoa6 |
T |
C |
2: 155,248,238 (GRCm39) |
T1689A |
probably damaging |
Het |
Ndfip2 |
A |
G |
14: 105,542,245 (GRCm39) |
T332A |
probably benign |
Het |
Nfkbil1 |
G |
A |
17: 35,439,605 (GRCm39) |
P303S |
probably damaging |
Het |
Nfx1 |
T |
G |
4: 40,994,104 (GRCm39) |
N604K |
probably benign |
Het |
Npb |
T |
C |
11: 120,499,473 (GRCm39) |
F47L |
probably benign |
Het |
Nt5el |
G |
T |
13: 105,236,987 (GRCm39) |
L79F |
probably damaging |
Het |
Obsl1 |
C |
T |
1: 75,467,484 (GRCm39) |
C1430Y |
probably damaging |
Het |
Or10al5 |
T |
A |
17: 38,062,942 (GRCm39) |
Y66N |
probably damaging |
Het |
Or10b1 |
A |
G |
10: 78,355,738 (GRCm39) |
I99V |
probably benign |
Het |
Or10g6 |
A |
T |
9: 39,934,616 (GRCm39) |
H309L |
probably benign |
Het |
Or4d5 |
G |
A |
9: 40,011,935 (GRCm39) |
P284S |
probably damaging |
Het |
Or4n4b |
C |
T |
14: 50,536,362 (GRCm39) |
V135I |
probably benign |
Het |
Or6c202 |
C |
A |
10: 128,996,464 (GRCm39) |
V130L |
probably benign |
Het |
Or6f1 |
G |
A |
7: 85,970,989 (GRCm39) |
T57M |
probably damaging |
Het |
Pdcd6 |
A |
T |
13: 74,453,695 (GRCm39) |
F148I |
probably damaging |
Het |
Pih1d1 |
A |
T |
7: 44,803,789 (GRCm39) |
Q16L |
unknown |
Het |
Ppp1r10 |
T |
C |
17: 36,235,786 (GRCm39) |
S123P |
probably damaging |
Het |
Ppp1r13b |
A |
T |
12: 111,807,446 (GRCm39) |
M305K |
probably benign |
Het |
Prg2 |
A |
G |
2: 84,811,685 (GRCm39) |
K2E |
possibly damaging |
Het |
Prkd1 |
A |
T |
12: 50,438,107 (GRCm39) |
|
probably null |
Het |
Rfx7 |
T |
A |
9: 72,526,423 (GRCm39) |
H1204Q |
probably benign |
Het |
Serpina3k |
A |
C |
12: 104,309,430 (GRCm39) |
Q291H |
probably benign |
Het |
Tafa4 |
T |
A |
6: 96,820,831 (GRCm39) |
I93F |
possibly damaging |
Het |
Tas2r107 |
G |
T |
6: 131,636,549 (GRCm39) |
Q167K |
probably benign |
Het |
Tle1 |
A |
C |
4: 72,071,135 (GRCm39) |
|
probably benign |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Trpa1 |
C |
T |
1: 14,989,026 (GRCm39) |
E12K |
probably benign |
Het |
Vmn2r7 |
T |
C |
3: 64,614,474 (GRCm39) |
T447A |
probably benign |
Het |
Wdr86 |
T |
C |
5: 24,920,538 (GRCm39) |
Y283C |
probably benign |
Het |
Zfp329 |
A |
T |
7: 12,544,215 (GRCm39) |
Y436* |
probably null |
Het |
|
Other mutations in Nr2c2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00596:Nr2c2
|
APN |
6 |
92,126,700 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01129:Nr2c2
|
APN |
6 |
92,135,397 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01578:Nr2c2
|
APN |
6 |
92,139,019 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02281:Nr2c2
|
APN |
6 |
92,131,495 (GRCm39) |
missense |
probably benign |
0.20 |
R1385:Nr2c2
|
UTSW |
6 |
92,131,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1397:Nr2c2
|
UTSW |
6 |
92,126,745 (GRCm39) |
missense |
probably benign |
0.34 |
R1503:Nr2c2
|
UTSW |
6 |
92,082,312 (GRCm39) |
missense |
probably benign |
|
R1691:Nr2c2
|
UTSW |
6 |
92,133,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R1779:Nr2c2
|
UTSW |
6 |
92,136,224 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2655:Nr2c2
|
UTSW |
6 |
92,140,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R3840:Nr2c2
|
UTSW |
6 |
92,140,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R3841:Nr2c2
|
UTSW |
6 |
92,140,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R3923:Nr2c2
|
UTSW |
6 |
92,137,382 (GRCm39) |
missense |
probably damaging |
0.98 |
R3926:Nr2c2
|
UTSW |
6 |
92,137,382 (GRCm39) |
missense |
probably damaging |
0.98 |
R3945:Nr2c2
|
UTSW |
6 |
92,140,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R3946:Nr2c2
|
UTSW |
6 |
92,140,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R4721:Nr2c2
|
UTSW |
6 |
92,116,828 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5038:Nr2c2
|
UTSW |
6 |
92,116,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R5101:Nr2c2
|
UTSW |
6 |
92,131,497 (GRCm39) |
critical splice donor site |
probably null |
|
R5524:Nr2c2
|
UTSW |
6 |
92,116,746 (GRCm39) |
splice site |
probably null |
|
R6884:Nr2c2
|
UTSW |
6 |
92,135,374 (GRCm39) |
missense |
probably benign |
0.05 |
R7046:Nr2c2
|
UTSW |
6 |
92,135,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Nr2c2
|
UTSW |
6 |
92,136,359 (GRCm39) |
missense |
probably damaging |
0.96 |
R7316:Nr2c2
|
UTSW |
6 |
92,131,444 (GRCm39) |
missense |
probably damaging |
0.99 |
R9238:Nr2c2
|
UTSW |
6 |
92,144,530 (GRCm39) |
missense |
probably damaging |
1.00 |
|