Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4732465J04Rik |
T |
C |
10: 95,629,659 (GRCm39) |
I29T |
probably damaging |
Het |
Agps |
G |
A |
2: 75,740,045 (GRCm39) |
|
probably null |
Het |
Agxt2 |
A |
G |
15: 10,393,794 (GRCm39) |
|
probably null |
Het |
Ahnak |
T |
C |
19: 8,992,273 (GRCm39) |
V4519A |
possibly damaging |
Het |
Aktip |
T |
C |
8: 91,852,853 (GRCm39) |
D159G |
probably damaging |
Het |
Ankrd44 |
T |
C |
1: 54,806,125 (GRCm39) |
I94V |
probably damaging |
Het |
Asph |
T |
C |
4: 9,474,904 (GRCm39) |
E674G |
possibly damaging |
Het |
Atat1 |
T |
A |
17: 36,219,735 (GRCm39) |
|
probably benign |
Het |
Ccar1 |
G |
A |
10: 62,626,714 (GRCm39) |
A20V |
possibly damaging |
Het |
Cdc26 |
T |
C |
4: 62,321,001 (GRCm39) |
D14G |
probably damaging |
Het |
Cdh15 |
T |
C |
8: 123,586,089 (GRCm39) |
F156S |
probably damaging |
Het |
Dctn1 |
A |
G |
6: 83,168,326 (GRCm39) |
T525A |
possibly damaging |
Het |
Dnah8 |
T |
G |
17: 31,074,869 (GRCm39) |
|
probably benign |
Het |
Dnajc10 |
T |
A |
2: 80,151,648 (GRCm39) |
|
probably benign |
Het |
Dtl |
C |
A |
1: 191,300,489 (GRCm39) |
W125L |
probably damaging |
Het |
Fam3c |
G |
A |
6: 22,318,954 (GRCm39) |
T149I |
probably damaging |
Het |
Fgd6 |
A |
G |
10: 93,974,170 (GRCm39) |
T1304A |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm6578 |
A |
G |
6: 12,099,766 (GRCm39) |
|
noncoding transcript |
Het |
Gnai1 |
A |
G |
5: 18,478,568 (GRCm39) |
F199S |
probably damaging |
Het |
Grb7 |
T |
A |
11: 98,345,480 (GRCm39) |
V480D |
probably damaging |
Het |
Hdc |
A |
G |
2: 126,436,452 (GRCm39) |
L473P |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,479,622 (GRCm39) |
N4614S |
probably benign |
Het |
Il20ra |
A |
G |
10: 19,634,791 (GRCm39) |
D344G |
probably benign |
Het |
Ints1 |
C |
T |
5: 139,745,843 (GRCm39) |
R1342Q |
possibly damaging |
Het |
Itga9 |
T |
A |
9: 118,465,562 (GRCm39) |
|
probably benign |
Het |
Kat14 |
T |
C |
2: 144,236,285 (GRCm39) |
L339P |
probably damaging |
Het |
Klhl22 |
A |
G |
16: 17,594,326 (GRCm39) |
I152V |
probably benign |
Het |
Krtap5-2 |
C |
A |
7: 141,729,459 (GRCm39) |
G74* |
probably null |
Het |
Lrrc59 |
C |
A |
11: 94,529,354 (GRCm39) |
|
probably null |
Het |
Map3k13 |
A |
G |
16: 21,710,873 (GRCm39) |
Q52R |
probably benign |
Het |
Mb21d2 |
A |
G |
16: 28,646,495 (GRCm39) |
|
probably benign |
Het |
Mphosph9 |
A |
T |
5: 124,463,053 (GRCm39) |
|
probably benign |
Het |
Myrf |
A |
G |
19: 10,187,742 (GRCm39) |
|
probably benign |
Het |
Nek11 |
T |
C |
9: 105,177,502 (GRCm39) |
T250A |
probably benign |
Het |
Nek5 |
A |
T |
8: 22,586,842 (GRCm39) |
V323E |
probably benign |
Het |
Nfasc |
A |
T |
1: 132,536,176 (GRCm39) |
C586* |
probably null |
Het |
Nup210l |
T |
A |
3: 90,111,231 (GRCm39) |
L1711Q |
possibly damaging |
Het |
Parp8 |
T |
G |
13: 117,013,108 (GRCm39) |
K644Q |
probably benign |
Het |
Pcnt |
G |
T |
10: 76,269,513 (GRCm39) |
Q252K |
probably damaging |
Het |
Pianp |
A |
G |
6: 124,977,646 (GRCm39) |
T181A |
possibly damaging |
Het |
Pkd1 |
T |
C |
17: 24,799,298 (GRCm39) |
V2839A |
probably damaging |
Het |
Poli |
C |
T |
18: 70,659,657 (GRCm39) |
R58H |
possibly damaging |
Het |
Ptk7 |
T |
C |
17: 46,890,353 (GRCm39) |
D447G |
probably benign |
Het |
Rapgef5 |
A |
G |
12: 117,694,386 (GRCm39) |
I637V |
probably benign |
Het |
Relt |
A |
G |
7: 100,500,350 (GRCm39) |
V113A |
probably benign |
Het |
Rnf215 |
G |
T |
11: 4,090,317 (GRCm39) |
C345F |
probably damaging |
Het |
Scart2 |
T |
C |
7: 139,854,040 (GRCm39) |
C348R |
probably damaging |
Het |
Scn2a |
A |
G |
2: 65,532,173 (GRCm39) |
D595G |
probably damaging |
Het |
Serpina3k |
G |
A |
12: 104,307,316 (GRCm39) |
V183M |
probably damaging |
Het |
Snapc4 |
T |
C |
2: 26,256,452 (GRCm39) |
|
probably benign |
Het |
Sparcl1 |
A |
T |
5: 104,240,406 (GRCm39) |
D339E |
probably benign |
Het |
Tg |
T |
C |
15: 66,631,335 (GRCm39) |
F535L |
probably benign |
Het |
Zbtb45 |
C |
A |
7: 12,740,203 (GRCm39) |
A471S |
probably benign |
Het |
Zfp106 |
T |
A |
2: 120,365,288 (GRCm39) |
K373M |
probably benign |
Het |
|
Other mutations in Rasip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01995:Rasip1
|
APN |
7 |
45,286,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R0208:Rasip1
|
UTSW |
7 |
45,281,999 (GRCm39) |
missense |
probably damaging |
0.97 |
R0373:Rasip1
|
UTSW |
7 |
45,284,668 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0869:Rasip1
|
UTSW |
7 |
45,284,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R0870:Rasip1
|
UTSW |
7 |
45,284,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R0871:Rasip1
|
UTSW |
7 |
45,284,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R0872:Rasip1
|
UTSW |
7 |
45,284,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R1388:Rasip1
|
UTSW |
7 |
45,279,656 (GRCm39) |
missense |
probably damaging |
0.98 |
R1780:Rasip1
|
UTSW |
7 |
45,284,742 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2348:Rasip1
|
UTSW |
7 |
45,278,507 (GRCm39) |
critical splice donor site |
probably null |
|
R2517:Rasip1
|
UTSW |
7 |
45,284,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R4587:Rasip1
|
UTSW |
7 |
45,282,159 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4678:Rasip1
|
UTSW |
7 |
45,277,247 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4679:Rasip1
|
UTSW |
7 |
45,277,247 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4714:Rasip1
|
UTSW |
7 |
45,281,820 (GRCm39) |
frame shift |
probably null |
|
R5572:Rasip1
|
UTSW |
7 |
45,286,153 (GRCm39) |
missense |
probably benign |
0.00 |
R6182:Rasip1
|
UTSW |
7 |
45,277,879 (GRCm39) |
small deletion |
probably benign |
|
R7443:Rasip1
|
UTSW |
7 |
45,288,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R7769:Rasip1
|
UTSW |
7 |
45,278,239 (GRCm39) |
missense |
probably damaging |
0.98 |
R8146:Rasip1
|
UTSW |
7 |
45,279,704 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8158:Rasip1
|
UTSW |
7 |
45,281,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R8493:Rasip1
|
UTSW |
7 |
45,284,467 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9047:Rasip1
|
UTSW |
7 |
45,282,066 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9352:Rasip1
|
UTSW |
7 |
45,278,280 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9679:Rasip1
|
UTSW |
7 |
45,277,327 (GRCm39) |
missense |
possibly damaging |
0.85 |
X0018:Rasip1
|
UTSW |
7 |
45,288,292 (GRCm39) |
missense |
probably damaging |
0.98 |
|