Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
A |
G |
16: 20,218,310 (GRCm39) |
I305T |
probably damaging |
Het |
Adamts18 |
G |
A |
8: 114,490,929 (GRCm39) |
Q513* |
probably null |
Het |
Adamts6 |
A |
G |
13: 104,450,842 (GRCm39) |
I342V |
possibly damaging |
Het |
Agtr1a |
A |
G |
13: 30,565,582 (GRCm39) |
T216A |
possibly damaging |
Het |
Coro1b |
A |
G |
19: 4,200,225 (GRCm39) |
|
probably benign |
Het |
Cyp4a10 |
G |
A |
4: 115,382,890 (GRCm39) |
|
probably null |
Het |
Cyp4x1 |
T |
A |
4: 114,965,982 (GRCm39) |
Q448L |
probably benign |
Het |
Ddx60 |
A |
T |
8: 62,430,916 (GRCm39) |
|
probably null |
Het |
Exoc1 |
C |
A |
5: 76,690,042 (GRCm39) |
A194D |
probably damaging |
Het |
Fastkd1 |
A |
C |
2: 69,537,703 (GRCm39) |
V293G |
probably damaging |
Het |
Gm5773 |
T |
C |
3: 93,681,264 (GRCm39) |
L312P |
probably damaging |
Het |
Hhla1 |
A |
G |
15: 65,802,078 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
A |
T |
2: 31,236,649 (GRCm39) |
E397D |
possibly damaging |
Het |
Lig1 |
C |
T |
7: 13,030,694 (GRCm39) |
R449C |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 36,164,018 (GRCm39) |
T1189A |
probably benign |
Het |
Muc4 |
G |
A |
16: 32,575,436 (GRCm39) |
M1397I |
probably benign |
Het |
Myh15 |
A |
G |
16: 48,980,330 (GRCm39) |
E1484G |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,182,890 (GRCm39) |
I1019V |
probably benign |
Het |
Nid1 |
T |
C |
13: 13,612,474 (GRCm39) |
L63P |
probably damaging |
Het |
Ogfod3 |
A |
T |
11: 121,068,630 (GRCm39) |
*316R |
probably null |
Het |
Or6z7 |
T |
C |
7: 6,483,435 (GRCm39) |
K240R |
probably benign |
Het |
Pdpk1 |
A |
T |
17: 24,320,618 (GRCm39) |
V193E |
probably damaging |
Het |
Phf3 |
G |
T |
1: 30,843,482 (GRCm39) |
P1826T |
probably damaging |
Het |
Pnliprp2 |
A |
G |
19: 58,748,847 (GRCm39) |
I51V |
probably benign |
Het |
Prpf4b |
C |
T |
13: 35,079,342 (GRCm39) |
L739F |
probably damaging |
Het |
Rcbtb1 |
T |
A |
14: 59,447,419 (GRCm39) |
M1K |
probably null |
Het |
Scgb2b7 |
A |
T |
7: 31,404,506 (GRCm39) |
C65S |
probably damaging |
Het |
Shpk |
A |
G |
11: 73,105,861 (GRCm39) |
T238A |
probably benign |
Het |
Tmem132d |
A |
T |
5: 128,061,347 (GRCm39) |
Y418* |
probably null |
Het |
Tpte |
T |
C |
8: 22,815,553 (GRCm39) |
V212A |
possibly damaging |
Het |
Trim55 |
A |
T |
3: 19,713,354 (GRCm39) |
Y135F |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,598,456 (GRCm39) |
A19486T |
probably damaging |
Het |
Vmn2r59 |
A |
T |
7: 41,708,340 (GRCm39) |
N22K |
probably benign |
Het |
Vmn2r63 |
T |
C |
7: 42,577,368 (GRCm39) |
D390G |
probably benign |
Het |
Vmn2r96 |
A |
G |
17: 18,806,634 (GRCm39) |
E527G |
possibly damaging |
Het |
Vps13d |
C |
T |
4: 144,875,894 (GRCm39) |
E1538K |
probably damaging |
Het |
Zfp64 |
T |
C |
2: 168,793,462 (GRCm39) |
|
probably null |
Het |
Zfp827 |
A |
G |
8: 79,803,116 (GRCm39) |
S563G |
probably 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 |
|
IGL03371:Rin2
|
APN |
2 |
145,727,846 (GRCm39) |
utr 3 prime |
probably benign |
|
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 |
|