Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd3 |
T |
C |
1: 180,560,748 (GRCm39) |
F99L |
possibly damaging |
Het |
Arg1 |
T |
C |
10: 24,796,702 (GRCm39) |
|
probably null |
Het |
Bsnd |
C |
T |
4: 106,343,809 (GRCm39) |
E166K |
probably benign |
Het |
Cxcl9 |
A |
G |
5: 92,474,709 (GRCm39) |
C30R |
probably damaging |
Het |
Ect2l |
C |
T |
10: 18,041,290 (GRCm39) |
R296H |
probably benign |
Het |
Epha5 |
C |
A |
5: 84,254,644 (GRCm39) |
D632Y |
probably damaging |
Het |
Fbxw11 |
T |
C |
11: 32,661,859 (GRCm39) |
Y79H |
probably benign |
Het |
Fh1 |
A |
G |
1: 175,437,310 (GRCm39) |
M263T |
probably benign |
Het |
Mrgprb1 |
A |
T |
7: 48,097,177 (GRCm39) |
I245N |
possibly damaging |
Het |
Ms4a13 |
A |
T |
19: 11,161,251 (GRCm39) |
I96N |
probably damaging |
Het |
Nipa2 |
G |
A |
7: 55,594,256 (GRCm39) |
L38F |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,269,840 (GRCm39) |
|
probably benign |
Het |
Rnf111 |
A |
T |
9: 70,361,098 (GRCm39) |
D454E |
possibly damaging |
Het |
Rp1 |
C |
T |
1: 4,418,193 (GRCm39) |
G973D |
probably benign |
Het |
Rtn3 |
A |
G |
19: 7,408,376 (GRCm39) |
V922A |
possibly damaging |
Het |
Setbp1 |
T |
C |
18: 78,826,573 (GRCm39) |
M1347V |
probably benign |
Het |
Slc6a6 |
A |
G |
6: 91,703,016 (GRCm39) |
I130V |
probably benign |
Het |
Smad7 |
T |
C |
18: 75,509,016 (GRCm39) |
S48P |
probably benign |
Het |
Star |
A |
G |
8: 26,299,865 (GRCm39) |
D69G |
probably benign |
Het |
Syne1 |
C |
A |
10: 4,998,925 (GRCm39) |
|
probably benign |
Het |
Synj1 |
A |
T |
16: 90,743,743 (GRCm39) |
N1212K |
probably benign |
Het |
Tep1 |
T |
C |
14: 51,090,556 (GRCm39) |
M721V |
probably benign |
Het |
Txndc11 |
T |
C |
16: 10,934,678 (GRCm39) |
D223G |
possibly damaging |
Het |
Vit |
G |
A |
17: 78,932,629 (GRCm39) |
D579N |
probably damaging |
Het |
Zan |
T |
C |
5: 137,464,173 (GRCm39) |
|
probably benign |
Het |
Zfp1005 |
A |
T |
2: 150,108,070 (GRCm39) |
H10L |
possibly damaging |
Het |
Zfp318 |
A |
G |
17: 46,724,189 (GRCm39) |
E2064G |
probably damaging |
Het |
Zftraf1 |
T |
A |
15: 76,533,376 (GRCm39) |
T121S |
probably damaging |
Het |
Zic5 |
T |
G |
14: 122,697,191 (GRCm39) |
|
probably benign |
Het |
Zzef1 |
T |
C |
11: 72,784,240 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rin2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02928:Rin2
|
APN |
2 |
145,701,926 (GRCm39) |
splice site |
probably benign |
|
IGL03222:Rin2
|
APN |
2 |
145,702,115 (GRCm39) |
nonsense |
probably null |
|
IGL03371:Rin2
|
APN |
2 |
145,727,846 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL03411:Rin2
|
APN |
2 |
145,702,864 (GRCm39) |
missense |
probably damaging |
0.99 |
D4043:Rin2
|
UTSW |
2 |
145,664,283 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0025:Rin2
|
UTSW |
2 |
145,720,752 (GRCm39) |
splice site |
probably benign |
|
R0110:Rin2
|
UTSW |
2 |
145,702,953 (GRCm39) |
missense |
probably benign |
|
R0144:Rin2
|
UTSW |
2 |
145,718,559 (GRCm39) |
missense |
probably damaging |
0.96 |
R0510:Rin2
|
UTSW |
2 |
145,702,953 (GRCm39) |
missense |
probably benign |
|
R1326:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R1328:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R1329:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R1330:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R1544:Rin2
|
UTSW |
2 |
145,700,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R1658:Rin2
|
UTSW |
2 |
145,718,376 (GRCm39) |
missense |
probably benign |
0.04 |
R1832:Rin2
|
UTSW |
2 |
145,703,091 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1986:Rin2
|
UTSW |
2 |
145,720,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R2167:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R2170:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R2260:Rin2
|
UTSW |
2 |
145,720,824 (GRCm39) |
missense |
probably damaging |
0.97 |
R2312:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R2884:Rin2
|
UTSW |
2 |
145,702,911 (GRCm39) |
missense |
probably benign |
0.07 |
R3155:Rin2
|
UTSW |
2 |
145,702,771 (GRCm39) |
missense |
probably benign |
0.17 |
R3771:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3772:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3773:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3822:Rin2
|
UTSW |
2 |
145,664,550 (GRCm39) |
missense |
probably benign |
0.02 |
R3824:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3825:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3885:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3893:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3939:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3940:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4012:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4058:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4214:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4231:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4232:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4236:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4372:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4410:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4415:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4471:Rin2
|
UTSW |
2 |
145,702,366 (GRCm39) |
missense |
probably benign |
0.00 |
R4490:Rin2
|
UTSW |
2 |
145,664,194 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4597:Rin2
|
UTSW |
2 |
145,702,825 (GRCm39) |
missense |
probably benign |
0.01 |
R5099:Rin2
|
UTSW |
2 |
145,720,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Rin2
|
UTSW |
2 |
145,686,680 (GRCm39) |
missense |
probably benign |
|
R5493:Rin2
|
UTSW |
2 |
145,702,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5622:Rin2
|
UTSW |
2 |
145,702,299 (GRCm39) |
missense |
probably benign |
0.07 |
R5947:Rin2
|
UTSW |
2 |
145,686,863 (GRCm39) |
intron |
probably benign |
|
R6280:Rin2
|
UTSW |
2 |
145,702,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Rin2
|
UTSW |
2 |
145,725,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7531:Rin2
|
UTSW |
2 |
145,700,419 (GRCm39) |
missense |
probably benign |
|
R7824:Rin2
|
UTSW |
2 |
145,703,037 (GRCm39) |
missense |
probably benign |
0.00 |
R8065:Rin2
|
UTSW |
2 |
145,702,977 (GRCm39) |
missense |
probably damaging |
0.99 |
R8067:Rin2
|
UTSW |
2 |
145,702,977 (GRCm39) |
missense |
probably damaging |
0.99 |
R8144:Rin2
|
UTSW |
2 |
145,664,225 (GRCm39) |
missense |
probably benign |
|
R8510:Rin2
|
UTSW |
2 |
145,727,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R8853:Rin2
|
UTSW |
2 |
145,718,475 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8880:Rin2
|
UTSW |
2 |
145,690,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Rin2
|
UTSW |
2 |
145,720,822 (GRCm39) |
nonsense |
probably null |
|
R9325:Rin2
|
UTSW |
2 |
145,727,819 (GRCm39) |
missense |
probably benign |
0.15 |
R9417:Rin2
|
UTSW |
2 |
145,686,713 (GRCm39) |
missense |
probably benign |
0.02 |
R9555:Rin2
|
UTSW |
2 |
145,718,415 (GRCm39) |
nonsense |
probably null |
|
R9631:Rin2
|
UTSW |
2 |
145,718,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R9667:Rin2
|
UTSW |
2 |
145,702,202 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9691:Rin2
|
UTSW |
2 |
145,690,764 (GRCm39) |
missense |
probably damaging |
0.97 |
R9727:Rin2
|
UTSW |
2 |
145,702,506 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9780:Rin2
|
UTSW |
2 |
145,718,551 (GRCm39) |
missense |
probably damaging |
1.00 |
|