Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adora2a |
A |
T |
10: 75,169,049 (GRCm39) |
Y171F |
probably damaging |
Het |
Agpat4 |
C |
T |
17: 12,429,203 (GRCm39) |
R152W |
probably damaging |
Het |
Aldh1a2 |
A |
G |
9: 71,188,964 (GRCm39) |
N293D |
possibly damaging |
Het |
Ash2l |
T |
C |
8: 26,312,913 (GRCm39) |
N441S |
probably damaging |
Het |
Asrgl1 |
A |
T |
19: 9,093,864 (GRCm39) |
|
probably null |
Het |
Capn3 |
C |
A |
2: 120,316,902 (GRCm39) |
S277* |
probably null |
Het |
Ccdc168 |
A |
T |
1: 44,096,339 (GRCm39) |
S1586R |
possibly damaging |
Het |
Ccp110 |
T |
C |
7: 118,329,167 (GRCm39) |
|
probably benign |
Het |
Cdh17 |
T |
C |
4: 11,799,676 (GRCm39) |
V491A |
probably benign |
Het |
Cep170b |
T |
C |
12: 112,707,339 (GRCm39) |
S362P |
probably damaging |
Het |
Cfap57 |
A |
G |
4: 118,463,849 (GRCm39) |
S335P |
possibly damaging |
Het |
Cmklr1 |
A |
T |
5: 113,752,107 (GRCm39) |
L298Q |
probably damaging |
Het |
Col4a4 |
A |
T |
1: 82,466,730 (GRCm39) |
|
probably null |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
Cyp2d26 |
A |
G |
15: 82,677,068 (GRCm39) |
|
probably benign |
Het |
Cyth3 |
T |
C |
5: 143,688,575 (GRCm39) |
Y240H |
probably damaging |
Het |
Dhx9 |
G |
A |
1: 153,334,109 (GRCm39) |
T1017I |
probably damaging |
Het |
Edar |
T |
C |
10: 58,464,453 (GRCm39) |
Y62C |
probably damaging |
Het |
Esyt3 |
C |
T |
9: 99,200,097 (GRCm39) |
G699D |
possibly damaging |
Het |
Fgb |
T |
C |
3: 82,950,564 (GRCm39) |
T397A |
probably damaging |
Het |
Foxc1 |
C |
A |
13: 31,992,668 (GRCm39) |
A493E |
unknown |
Het |
Grid1 |
T |
C |
14: 34,542,186 (GRCm39) |
M1T |
probably null |
Het |
Ipo4 |
T |
C |
14: 55,871,816 (GRCm39) |
K113R |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,080,114 (GRCm39) |
E550G |
probably damaging |
Het |
Krt1 |
T |
C |
15: 101,757,416 (GRCm39) |
K265E |
possibly damaging |
Het |
Lmx1a |
G |
A |
1: 167,618,968 (GRCm39) |
R109H |
probably damaging |
Het |
Mcm5 |
A |
G |
8: 75,852,919 (GRCm39) |
K677R |
probably benign |
Het |
Metap1 |
A |
T |
3: 138,180,791 (GRCm39) |
L130* |
probably null |
Het |
Mylip |
G |
A |
13: 45,560,178 (GRCm39) |
E205K |
probably damaging |
Het |
Myo3b |
A |
C |
2: 70,161,224 (GRCm39) |
E1128A |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Nlrp4d |
T |
C |
7: 10,098,194 (GRCm39) |
I823V |
probably benign |
Het |
Odad1 |
C |
T |
7: 45,592,182 (GRCm39) |
|
probably benign |
Het |
Rec114 |
A |
T |
9: 58,573,103 (GRCm39) |
|
probably benign |
Het |
Rimbp2 |
C |
T |
5: 128,865,351 (GRCm39) |
A666T |
probably benign |
Het |
Siva1 |
C |
T |
12: 112,613,355 (GRCm39) |
Q68* |
probably null |
Het |
Slc22a27 |
T |
A |
19: 7,904,033 (GRCm39) |
I35F |
probably benign |
Het |
Slco1a5 |
T |
A |
6: 142,200,100 (GRCm39) |
N228I |
probably damaging |
Het |
St8sia4 |
G |
A |
1: 95,581,464 (GRCm39) |
R93C |
probably damaging |
Het |
Tprg1 |
T |
C |
16: 25,231,593 (GRCm39) |
S190P |
probably damaging |
Het |
Trpc6 |
A |
G |
9: 8,658,287 (GRCm39) |
|
probably null |
Het |
Vmn2r70 |
C |
T |
7: 85,208,269 (GRCm39) |
C736Y |
probably damaging |
Het |
Zfp629 |
C |
T |
7: 127,211,916 (GRCm39) |
|
probably benign |
Het |
Zswim4 |
A |
G |
8: 84,946,601 (GRCm39) |
V685A |
possibly damaging |
Het |
|
Other mutations in Mrgpra4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00790:Mrgpra4
|
APN |
7 |
47,631,052 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02083:Mrgpra4
|
APN |
7 |
47,630,808 (GRCm39) |
nonsense |
probably null |
|
IGL02155:Mrgpra4
|
APN |
7 |
47,631,292 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02577:Mrgpra4
|
APN |
7 |
47,630,981 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02674:Mrgpra4
|
APN |
7 |
47,630,690 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02696:Mrgpra4
|
APN |
7 |
47,631,251 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0357:Mrgpra4
|
UTSW |
7 |
47,631,574 (GRCm39) |
missense |
probably benign |
|
R0543:Mrgpra4
|
UTSW |
7 |
47,631,058 (GRCm39) |
missense |
probably benign |
0.00 |
R0677:Mrgpra4
|
UTSW |
7 |
47,630,728 (GRCm39) |
missense |
probably benign |
0.00 |
R1163:Mrgpra4
|
UTSW |
7 |
47,631,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R2255:Mrgpra4
|
UTSW |
7 |
47,631,523 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4191:Mrgpra4
|
UTSW |
7 |
47,630,867 (GRCm39) |
missense |
probably benign |
0.00 |
R4303:Mrgpra4
|
UTSW |
7 |
47,630,684 (GRCm39) |
missense |
probably benign |
0.02 |
R4472:Mrgpra4
|
UTSW |
7 |
47,631,539 (GRCm39) |
missense |
probably benign |
0.05 |
R4757:Mrgpra4
|
UTSW |
7 |
47,630,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Mrgpra4
|
UTSW |
7 |
47,631,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Mrgpra4
|
UTSW |
7 |
47,631,535 (GRCm39) |
missense |
probably benign |
0.26 |
R5034:Mrgpra4
|
UTSW |
7 |
47,631,317 (GRCm39) |
missense |
probably benign |
0.00 |
R5119:Mrgpra4
|
UTSW |
7 |
47,631,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R5722:Mrgpra4
|
UTSW |
7 |
47,630,755 (GRCm39) |
missense |
probably benign |
|
R6800:Mrgpra4
|
UTSW |
7 |
47,631,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R7163:Mrgpra4
|
UTSW |
7 |
47,631,238 (GRCm39) |
missense |
probably benign |
0.42 |
R7585:Mrgpra4
|
UTSW |
7 |
47,631,377 (GRCm39) |
missense |
probably benign |
0.24 |
R7636:Mrgpra4
|
UTSW |
7 |
47,630,721 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8162:Mrgpra4
|
UTSW |
7 |
47,631,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8352:Mrgpra4
|
UTSW |
7 |
47,631,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R8452:Mrgpra4
|
UTSW |
7 |
47,631,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R8812:Mrgpra4
|
UTSW |
7 |
47,631,481 (GRCm39) |
missense |
probably benign |
|
R8996:Mrgpra4
|
UTSW |
7 |
47,630,945 (GRCm39) |
missense |
probably benign |
0.28 |
R9026:Mrgpra4
|
UTSW |
7 |
47,631,208 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0028:Mrgpra4
|
UTSW |
7 |
47,631,168 (GRCm39) |
nonsense |
probably null |
|
|