Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553M12Rik |
T |
C |
4: 88,786,596 (GRCm39) |
I7M |
unknown |
Het |
Abca8a |
C |
T |
11: 109,921,705 (GRCm39) |
E1450K |
probably damaging |
Het |
B4galnt2 |
T |
C |
11: 95,756,985 (GRCm39) |
Y482C |
probably damaging |
Het |
Bud23 |
A |
G |
5: 135,092,775 (GRCm39) |
F9L |
probably damaging |
Het |
Cacna1s |
A |
T |
1: 136,039,816 (GRCm39) |
E1214V |
probably damaging |
Het |
Cdh20 |
T |
C |
1: 104,861,823 (GRCm39) |
M1T |
probably null |
Het |
Chkb |
T |
C |
15: 89,313,715 (GRCm39) |
E30G |
probably benign |
Het |
Crp |
A |
C |
1: 172,525,635 (GRCm39) |
|
probably benign |
Het |
Cyp11b1 |
T |
C |
15: 74,708,670 (GRCm39) |
R375G |
probably null |
Het |
Ddx11 |
C |
T |
17: 66,436,976 (GRCm39) |
S90L |
probably benign |
Het |
Flnc |
A |
C |
6: 29,459,429 (GRCm39) |
I2510L |
probably damaging |
Het |
Ftdc1 |
C |
A |
16: 58,436,075 (GRCm39) |
|
probably null |
Het |
Fyb1 |
T |
A |
15: 6,692,707 (GRCm39) |
|
probably benign |
Het |
Gbp3 |
C |
T |
3: 142,272,239 (GRCm39) |
P247L |
probably benign |
Het |
Ggn |
C |
T |
7: 28,871,981 (GRCm39) |
P454S |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,352,894 (GRCm39) |
S2127T |
probably benign |
Het |
Ipo11 |
A |
G |
13: 106,984,926 (GRCm39) |
|
probably benign |
Het |
Kcnh7 |
G |
A |
2: 62,546,582 (GRCm39) |
R1000W |
probably benign |
Het |
Kdm5b |
A |
T |
1: 134,516,511 (GRCm39) |
|
probably benign |
Het |
Klc3 |
C |
T |
7: 19,129,724 (GRCm39) |
|
probably null |
Het |
Lst1 |
A |
T |
17: 35,407,359 (GRCm39) |
M3K |
unknown |
Het |
Madd |
C |
T |
2: 90,982,878 (GRCm39) |
R1355Q |
probably damaging |
Het |
Map3k10 |
A |
G |
7: 27,356,159 (GRCm39) |
L920P |
probably damaging |
Het |
Mdga2 |
A |
G |
12: 66,702,109 (GRCm39) |
V423A |
probably damaging |
Het |
Mogat2 |
T |
C |
7: 98,869,112 (GRCm39) |
D302G |
possibly damaging |
Het |
Nkapl |
A |
C |
13: 21,652,593 (GRCm39) |
S7A |
unknown |
Het |
Npas2 |
A |
G |
1: 39,386,647 (GRCm39) |
S639G |
probably benign |
Het |
Nr1h5 |
T |
G |
3: 102,856,644 (GRCm39) |
H260P |
probably damaging |
Het |
Or2g25 |
T |
C |
17: 37,971,122 (GRCm39) |
Y34C |
probably damaging |
Het |
Or2t49 |
A |
T |
11: 58,392,464 (GRCm39) |
L306Q |
possibly damaging |
Het |
Or4c35 |
T |
C |
2: 89,808,787 (GRCm39) |
S222P |
probably damaging |
Het |
Or7a36 |
C |
T |
10: 78,820,023 (GRCm39) |
T133I |
possibly damaging |
Het |
Or8a1b |
T |
C |
9: 37,623,087 (GRCm39) |
M163V |
probably benign |
Het |
Pan2 |
T |
C |
10: 128,156,249 (GRCm39) |
L1142P |
probably damaging |
Het |
Pdik1l |
C |
T |
4: 134,014,474 (GRCm39) |
E11K |
possibly damaging |
Het |
Ppp1r15a |
A |
G |
7: 45,172,727 (GRCm39) |
V555A |
probably damaging |
Het |
Ppp6c |
G |
A |
2: 39,090,064 (GRCm39) |
Q81* |
probably null |
Het |
Ptprz1 |
A |
T |
6: 23,001,444 (GRCm39) |
Y1178F |
probably benign |
Het |
Relch |
G |
A |
1: 105,646,581 (GRCm39) |
V660M |
probably damaging |
Het |
Rictor |
G |
A |
15: 6,823,487 (GRCm39) |
E1555K |
probably benign |
Het |
Rims2 |
T |
A |
15: 39,339,886 (GRCm39) |
L860Q |
probably damaging |
Het |
Sdr39u1 |
A |
G |
14: 56,135,196 (GRCm39) |
V249A |
probably benign |
Het |
Serhl |
T |
C |
15: 83,000,528 (GRCm39) |
V305A |
probably benign |
Het |
Slc5a11 |
T |
C |
7: 122,851,654 (GRCm39) |
I201T |
probably damaging |
Het |
Stk32a |
A |
T |
18: 43,446,552 (GRCm39) |
E334V |
probably benign |
Het |
Tmem217 |
A |
G |
17: 29,745,529 (GRCm39) |
L67P |
probably damaging |
Het |
Tnnt1 |
A |
T |
7: 4,519,345 (GRCm39) |
L12* |
probably null |
Het |
Trim80 |
C |
T |
11: 115,338,747 (GRCm39) |
R526C |
probably damaging |
Het |
Unc5b |
A |
T |
10: 60,608,306 (GRCm39) |
F635I |
possibly damaging |
Het |
Utp20 |
T |
G |
10: 88,653,147 (GRCm39) |
N311T |
probably benign |
Het |
Zfp276 |
A |
G |
8: 123,982,457 (GRCm39) |
T74A |
probably benign |
Het |
|
Other mutations in Pramel18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02430:Pramel18
|
APN |
4 |
101,767,477 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02683:Pramel18
|
APN |
4 |
101,767,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03403:Pramel18
|
APN |
4 |
101,767,125 (GRCm39) |
missense |
probably benign |
0.40 |
R0833:Pramel18
|
UTSW |
4 |
101,767,294 (GRCm39) |
missense |
probably damaging |
0.97 |
R1054:Pramel18
|
UTSW |
4 |
101,766,361 (GRCm39) |
missense |
probably benign |
0.00 |
R1953:Pramel18
|
UTSW |
4 |
101,767,312 (GRCm39) |
missense |
probably benign |
|
R2216:Pramel18
|
UTSW |
4 |
101,767,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R3746:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3747:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3750:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4931:Pramel18
|
UTSW |
4 |
101,766,367 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5102:Pramel18
|
UTSW |
4 |
101,766,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Pramel18
|
UTSW |
4 |
101,767,317 (GRCm39) |
missense |
probably benign |
0.00 |
R6395:Pramel18
|
UTSW |
4 |
101,767,189 (GRCm39) |
missense |
probably benign |
|
R6904:Pramel18
|
UTSW |
4 |
101,767,291 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7544:Pramel18
|
UTSW |
4 |
101,768,599 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7768:Pramel18
|
UTSW |
4 |
101,769,010 (GRCm39) |
missense |
probably benign |
|
R8342:Pramel18
|
UTSW |
4 |
101,767,581 (GRCm39) |
missense |
probably benign |
0.01 |
R8917:Pramel18
|
UTSW |
4 |
101,768,935 (GRCm39) |
missense |
probably benign |
0.09 |
Z1088:Pramel18
|
UTSW |
4 |
101,766,315 (GRCm39) |
splice site |
probably null |
|
Z1088:Pramel18
|
UTSW |
4 |
101,767,383 (GRCm39) |
missense |
probably benign |
0.00 |
|