Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
T |
A |
10: 14,302,521 (GRCm39) |
Y964F |
probably damaging |
Het |
Akap3 |
T |
A |
6: 126,842,521 (GRCm39) |
L380Q |
probably damaging |
Het |
Alpk1 |
A |
G |
3: 127,473,723 (GRCm39) |
I760T |
probably benign |
Het |
Aoc1l2 |
T |
A |
6: 48,910,412 (GRCm39) |
F701L |
probably damaging |
Het |
Arhgap20 |
G |
A |
9: 51,736,276 (GRCm39) |
|
probably benign |
Het |
Cacng3 |
T |
C |
7: 122,361,532 (GRCm39) |
F113S |
possibly damaging |
Het |
Ccdc158 |
G |
T |
5: 92,775,339 (GRCm39) |
N955K |
probably benign |
Het |
Ccdc63 |
T |
A |
5: 122,254,908 (GRCm39) |
M368L |
possibly damaging |
Het |
Cnot2 |
T |
C |
10: 116,363,851 (GRCm39) |
T18A |
probably damaging |
Het |
Ctnna2 |
A |
T |
6: 76,950,820 (GRCm39) |
D550E |
possibly damaging |
Het |
Dact2 |
A |
G |
17: 14,419,450 (GRCm39) |
S103P |
probably damaging |
Het |
Dek |
A |
G |
13: 47,255,077 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
CAGTTGCTTAAA |
CA |
11: 65,986,066 (GRCm39) |
|
probably null |
Het |
Dock4 |
A |
G |
12: 40,671,250 (GRCm39) |
Y23C |
probably damaging |
Het |
Edar |
T |
A |
10: 58,439,001 (GRCm39) |
S344C |
probably damaging |
Het |
Epg5 |
T |
C |
18: 78,073,270 (GRCm39) |
V2431A |
probably benign |
Het |
Evc2 |
C |
T |
5: 37,562,068 (GRCm39) |
|
probably benign |
Het |
Idh3b |
A |
T |
2: 130,125,948 (GRCm39) |
D41E |
probably benign |
Het |
Igkv8-24 |
A |
T |
6: 70,193,956 (GRCm39) |
V84D |
probably damaging |
Het |
Iqca1l |
A |
T |
5: 24,749,164 (GRCm39) |
L778Q |
probably benign |
Het |
Mgam |
T |
C |
6: 40,660,989 (GRCm39) |
I1118T |
probably benign |
Het |
Mtmr3 |
A |
G |
11: 4,432,925 (GRCm39) |
V1116A |
probably damaging |
Het |
Myoc |
A |
G |
1: 162,466,936 (GRCm39) |
Y35C |
probably damaging |
Het |
Ncr1 |
A |
T |
7: 4,347,573 (GRCm39) |
D246V |
probably benign |
Het |
Nphp3 |
A |
G |
9: 103,880,236 (GRCm39) |
E86G |
probably damaging |
Het |
Or2l13b |
A |
T |
16: 19,349,076 (GRCm39) |
V198E |
probably damaging |
Het |
Or52e5 |
A |
T |
7: 104,719,064 (GRCm39) |
Y130F |
probably benign |
Het |
Or8h7 |
A |
C |
2: 86,720,676 (GRCm39) |
V281G |
probably damaging |
Het |
Pbld1 |
A |
T |
10: 62,912,193 (GRCm39) |
I275L |
probably benign |
Het |
Pde12 |
A |
G |
14: 26,386,786 (GRCm39) |
V574A |
possibly damaging |
Het |
Pdxk |
G |
T |
10: 78,280,872 (GRCm39) |
D189E |
probably benign |
Het |
Pkhd1 |
C |
A |
1: 20,444,960 (GRCm39) |
E2276* |
probably null |
Het |
Ppp1r10 |
A |
G |
17: 36,237,739 (GRCm39) |
N237S |
possibly damaging |
Het |
Rheb |
T |
A |
5: 25,012,067 (GRCm39) |
Y131F |
probably benign |
Het |
Rpgrip1l |
T |
C |
8: 92,031,613 (GRCm39) |
D88G |
probably damaging |
Het |
Scgb2b33 |
T |
C |
7: 32,812,239 (GRCm39) |
|
noncoding transcript |
Het |
Snx9 |
C |
A |
17: 5,974,896 (GRCm39) |
N461K |
possibly damaging |
Het |
Tbc1d2b |
C |
A |
9: 90,091,777 (GRCm39) |
V842F |
probably damaging |
Het |
Tgfbi |
G |
A |
13: 56,784,418 (GRCm39) |
E615K |
possibly damaging |
Het |
Tmem51 |
A |
G |
4: 141,759,346 (GRCm39) |
M134T |
probably damaging |
Het |
Tox4 |
A |
G |
14: 52,524,241 (GRCm39) |
D125G |
probably damaging |
Het |
Trappc3 |
A |
T |
4: 126,167,771 (GRCm39) |
N110I |
probably damaging |
Het |
Trim11 |
T |
A |
11: 58,881,419 (GRCm39) |
D437E |
probably damaging |
Het |
Ttc23l |
T |
C |
15: 10,537,682 (GRCm39) |
N196S |
probably benign |
Het |
Wnk1 |
C |
A |
6: 119,969,369 (GRCm39) |
G362V |
probably damaging |
Het |
Wwc1 |
A |
G |
11: 35,758,153 (GRCm39) |
F731S |
probably damaging |
Het |
Wwp1 |
A |
T |
4: 19,662,174 (GRCm39) |
D140E |
possibly damaging |
Het |
Zfp24 |
G |
A |
18: 24,151,095 (GRCm39) |
P17L |
possibly damaging |
Het |
Zfp354b |
T |
C |
11: 50,814,043 (GRCm39) |
E294G |
probably damaging |
Het |
Zfp853 |
C |
T |
5: 143,274,424 (GRCm39) |
V399M |
unknown |
Het |
Zfp868 |
T |
C |
8: 70,064,303 (GRCm39) |
H344R |
probably damaging |
Het |
|
Other mutations in Cyp2c37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Cyp2c37
|
APN |
19 |
39,990,441 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01307:Cyp2c37
|
APN |
19 |
39,981,023 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01959:Cyp2c37
|
APN |
19 |
39,984,277 (GRCm39) |
nonsense |
probably null |
|
IGL02580:Cyp2c37
|
APN |
19 |
39,982,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02611:Cyp2c37
|
APN |
19 |
39,982,309 (GRCm39) |
missense |
probably benign |
0.00 |
R0124:Cyp2c37
|
UTSW |
19 |
39,982,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R0391:Cyp2c37
|
UTSW |
19 |
39,982,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R0420:Cyp2c37
|
UTSW |
19 |
39,984,238 (GRCm39) |
missense |
probably benign |
0.00 |
R0782:Cyp2c37
|
UTSW |
19 |
39,982,269 (GRCm39) |
missense |
probably benign |
0.00 |
R1413:Cyp2c37
|
UTSW |
19 |
39,982,542 (GRCm39) |
missense |
probably benign |
0.21 |
R1637:Cyp2c37
|
UTSW |
19 |
39,990,426 (GRCm39) |
nonsense |
probably null |
|
R1688:Cyp2c37
|
UTSW |
19 |
39,982,887 (GRCm39) |
splice site |
probably null |
|
R2258:Cyp2c37
|
UTSW |
19 |
39,984,303 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4353:Cyp2c37
|
UTSW |
19 |
39,988,989 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4640:Cyp2c37
|
UTSW |
19 |
40,000,276 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4965:Cyp2c37
|
UTSW |
19 |
40,000,206 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5053:Cyp2c37
|
UTSW |
19 |
39,990,331 (GRCm39) |
missense |
probably benign |
0.00 |
R5645:Cyp2c37
|
UTSW |
19 |
39,982,596 (GRCm39) |
missense |
probably benign |
0.04 |
R6487:Cyp2c37
|
UTSW |
19 |
39,983,025 (GRCm39) |
missense |
probably benign |
|
R6631:Cyp2c37
|
UTSW |
19 |
39,998,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R7062:Cyp2c37
|
UTSW |
19 |
39,983,990 (GRCm39) |
splice site |
probably null |
|
R7937:Cyp2c37
|
UTSW |
19 |
39,982,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R9640:Cyp2c37
|
UTSW |
19 |
40,000,180 (GRCm39) |
missense |
probably benign |
0.01 |
R9779:Cyp2c37
|
UTSW |
19 |
39,998,323 (GRCm39) |
missense |
probably benign |
0.09 |
R9784:Cyp2c37
|
UTSW |
19 |
39,988,943 (GRCm39) |
missense |
possibly damaging |
0.85 |
|