Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agk |
C |
T |
6: 40,371,576 (GRCm39) |
R358C |
probably benign |
Het |
Ahnak |
G |
T |
19: 8,981,592 (GRCm39) |
V959F |
possibly damaging |
Het |
Aoc1 |
C |
T |
6: 48,883,380 (GRCm39) |
R419C |
probably benign |
Het |
Brf2 |
T |
C |
8: 27,615,872 (GRCm39) |
D171G |
probably benign |
Het |
Cnot1 |
T |
C |
8: 96,501,344 (GRCm39) |
I75V |
possibly damaging |
Het |
D430041D05Rik |
A |
G |
2: 104,078,719 (GRCm39) |
V1199A |
probably damaging |
Het |
Dpp9 |
G |
A |
17: 56,494,377 (GRCm39) |
H861Y |
probably benign |
Het |
Eddm3b |
G |
A |
14: 51,354,422 (GRCm39) |
D137N |
probably damaging |
Het |
Erich3 |
A |
T |
3: 154,433,114 (GRCm39) |
I363F |
probably damaging |
Het |
F13b |
T |
A |
1: 139,434,674 (GRCm39) |
C147S |
probably damaging |
Het |
Fam186b |
T |
C |
15: 99,178,258 (GRCm39) |
E356G |
probably benign |
Het |
Fat2 |
T |
A |
11: 55,201,990 (GRCm39) |
R361S |
probably benign |
Het |
Fat4 |
A |
T |
3: 39,037,336 (GRCm39) |
I3663F |
possibly damaging |
Het |
Haus3 |
C |
A |
5: 34,323,687 (GRCm39) |
E308* |
probably null |
Het |
Ifna11 |
A |
G |
4: 88,738,412 (GRCm39) |
K73E |
probably benign |
Het |
Itga10 |
A |
G |
3: 96,562,104 (GRCm39) |
K664E |
possibly damaging |
Het |
L3mbtl4 |
G |
A |
17: 68,768,563 (GRCm39) |
V224M |
probably damaging |
Het |
Mcf2l |
C |
A |
8: 13,051,298 (GRCm39) |
A378D |
probably damaging |
Het |
Mixl1 |
T |
C |
1: 180,522,191 (GRCm39) |
N230S |
probably benign |
Het |
Ncbp1 |
T |
A |
4: 46,171,991 (GRCm39) |
C786* |
probably null |
Het |
Nup153 |
C |
T |
13: 46,836,628 (GRCm39) |
S1327N |
probably benign |
Het |
Or4c12b |
A |
T |
2: 89,647,509 (GRCm39) |
T280S |
possibly damaging |
Het |
Or8k18 |
A |
T |
2: 86,085,935 (GRCm39) |
I34N |
possibly damaging |
Het |
Osr2 |
C |
A |
15: 35,301,000 (GRCm39) |
Y185* |
probably null |
Het |
Ppp1r3b |
T |
C |
8: 35,851,403 (GRCm39) |
F81L |
possibly damaging |
Het |
Ppp3r2 |
T |
A |
4: 49,681,630 (GRCm39) |
I107F |
probably damaging |
Het |
Rpap1 |
A |
T |
2: 119,605,538 (GRCm39) |
|
probably benign |
Het |
Slc12a4 |
A |
G |
8: 106,677,137 (GRCm39) |
Y466H |
probably null |
Het |
Slc25a40 |
C |
T |
5: 8,477,442 (GRCm39) |
P9L |
probably benign |
Het |
Slc27a1 |
T |
C |
8: 72,038,052 (GRCm39) |
S567P |
probably benign |
Het |
Sox8 |
G |
A |
17: 25,786,414 (GRCm39) |
R430C |
probably damaging |
Het |
Tacc2 |
T |
C |
7: 130,227,791 (GRCm39) |
V1492A |
possibly damaging |
Het |
Taf5l |
A |
G |
8: 124,724,725 (GRCm39) |
S365P |
possibly damaging |
Het |
Tet2 |
T |
A |
3: 133,173,312 (GRCm39) |
H1650L |
possibly damaging |
Het |
Tmem117 |
G |
A |
15: 94,909,274 (GRCm39) |
R229H |
probably damaging |
Het |
Ttc17 |
A |
G |
2: 94,216,450 (GRCm39) |
L79P |
probably damaging |
Het |
Usp54 |
A |
T |
14: 20,639,436 (GRCm39) |
|
probably benign |
Het |
Zfp455 |
T |
A |
13: 67,355,066 (GRCm39) |
C111* |
probably null |
Het |
Zmym4 |
A |
C |
4: 126,808,881 (GRCm39) |
C389G |
possibly damaging |
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 |
|
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 |
R1327: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 |
|