Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700064H15Rik |
T |
C |
3: 19,682,685 (GRCm39) |
T30A |
unknown |
Het |
Abca12 |
A |
G |
1: 71,342,649 (GRCm39) |
Y944H |
possibly damaging |
Het |
Adgrv1 |
T |
C |
13: 81,656,887 (GRCm39) |
N2869S |
probably benign |
Het |
Ank1 |
C |
A |
8: 23,574,825 (GRCm39) |
Q140K |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,384,923 (GRCm39) |
M189K |
probably benign |
Het |
Atp2b1 |
G |
T |
10: 98,837,178 (GRCm39) |
R539L |
possibly damaging |
Het |
Camsap1 |
A |
G |
2: 25,845,304 (GRCm39) |
S152P |
|
Het |
Catsperd |
A |
T |
17: 56,958,821 (GRCm39) |
I276L |
probably benign |
Het |
Cbarp |
A |
G |
10: 79,967,861 (GRCm39) |
V460A |
probably damaging |
Het |
Ccdc168 |
T |
C |
1: 44,096,935 (GRCm39) |
I1388V |
probably benign |
Het |
Cd40 |
A |
T |
2: 164,904,162 (GRCm39) |
|
probably benign |
Het |
Cdk11b |
A |
T |
4: 155,724,302 (GRCm39) |
T307S |
unknown |
Het |
Chfr |
C |
T |
5: 110,317,056 (GRCm39) |
T643I |
probably damaging |
Het |
Cnbd1 |
T |
C |
4: 19,098,156 (GRCm39) |
Q88R |
probably benign |
Het |
Col15a1 |
G |
C |
4: 47,288,200 (GRCm39) |
|
probably benign |
Het |
Ghdc |
G |
T |
11: 100,661,081 (GRCm39) |
A28D |
probably damaging |
Het |
Gm5114 |
T |
C |
7: 39,057,540 (GRCm39) |
H693R |
possibly damaging |
Het |
H2-M1 |
G |
T |
17: 36,981,231 (GRCm39) |
A268E |
probably damaging |
Het |
Hsf5 |
A |
G |
11: 87,528,935 (GRCm39) |
N557D |
probably benign |
Het |
Ighg2c |
A |
G |
12: 113,251,015 (GRCm39) |
|
probably benign |
Het |
Il17ra |
C |
A |
6: 120,458,255 (GRCm39) |
Q469K |
possibly damaging |
Het |
Ipo8 |
T |
A |
6: 148,686,064 (GRCm39) |
N809Y |
probably benign |
Het |
Klra10 |
T |
A |
6: 130,256,435 (GRCm39) |
Q73L |
probably damaging |
Het |
Lamb2 |
T |
C |
9: 108,356,959 (GRCm39) |
V3A |
unknown |
Het |
Map3k9 |
T |
C |
12: 81,827,341 (GRCm39) |
Y103C |
probably damaging |
Het |
Map4 |
T |
C |
9: 109,882,029 (GRCm39) |
S298P |
possibly damaging |
Het |
Mtus2 |
T |
A |
5: 148,243,451 (GRCm39) |
N1254K |
probably damaging |
Het |
Nap1l5 |
T |
A |
6: 58,883,952 (GRCm39) |
M1L |
probably benign |
Het |
Nfxl1 |
G |
A |
5: 72,716,641 (GRCm39) |
|
probably benign |
Het |
Nmd3 |
T |
C |
3: 69,643,349 (GRCm39) |
I227T |
probably benign |
Het |
Or8c10 |
T |
G |
9: 38,279,162 (GRCm39) |
C97G |
probably damaging |
Het |
Ptchd3 |
G |
A |
11: 121,732,356 (GRCm39) |
M415I |
possibly damaging |
Het |
Rab28 |
A |
T |
5: 41,793,182 (GRCm39) |
S154R |
possibly damaging |
Het |
Rin1 |
A |
G |
19: 5,103,735 (GRCm39) |
E567G |
probably damaging |
Het |
Rrbp1 |
A |
C |
2: 143,811,436 (GRCm39) |
V806G |
probably benign |
Het |
Sec63 |
T |
A |
10: 42,679,901 (GRCm39) |
L326Q |
probably damaging |
Het |
Serinc2 |
T |
C |
4: 130,149,315 (GRCm39) |
T296A |
probably damaging |
Het |
Skint10 |
G |
A |
4: 112,572,981 (GRCm39) |
L272F |
probably damaging |
Het |
Slc4a11 |
C |
T |
2: 130,533,664 (GRCm39) |
A100T |
probably damaging |
Het |
Stag1 |
A |
G |
9: 100,811,967 (GRCm39) |
Q815R |
probably benign |
Het |
Stat3 |
A |
G |
11: 100,780,357 (GRCm39) |
M735T |
possibly damaging |
Het |
Stat3 |
A |
G |
11: 100,784,738 (GRCm39) |
I576T |
probably benign |
Het |
Styxl2 |
T |
C |
1: 165,927,755 (GRCm39) |
Q619R |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,155,071 (GRCm39) |
K5623E |
probably benign |
Het |
Tas1r2 |
T |
C |
4: 139,387,036 (GRCm39) |
V165A |
possibly damaging |
Het |
Tcaf3 |
A |
T |
6: 42,573,716 (GRCm39) |
D165E |
probably benign |
Het |
Tex2 |
G |
A |
11: 106,457,835 (GRCm39) |
Q532* |
probably null |
Het |
Utrn |
T |
C |
10: 12,564,125 (GRCm39) |
E1245G |
probably damaging |
Het |
|
Other mutations in Pramel39-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R2366:Pramel39-ps
|
UTSW |
5 |
94,450,972 (GRCm39) |
missense |
probably benign |
0.00 |
R7218:Pramel39-ps
|
UTSW |
5 |
94,451,113 (GRCm39) |
missense |
probably benign |
|
R7651:Pramel39-ps
|
UTSW |
5 |
94,451,236 (GRCm39) |
missense |
probably benign |
0.13 |
R9141:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9216:Pramel39-ps
|
UTSW |
5 |
94,450,952 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9237:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9238:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9242:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9360:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9361:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9362:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9363:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9391:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9418:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9420:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9421:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R9426:Pramel39-ps
|
UTSW |
5 |
94,451,001 (GRCm39) |
missense |
probably damaging |
1.00 |
|