Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
A |
G |
13: 81,620,597 (GRCm39) |
V3950A |
probably damaging |
Het |
App |
A |
G |
16: 84,917,455 (GRCm39) |
I63T |
probably damaging |
Het |
Bpifb4 |
A |
T |
2: 153,803,467 (GRCm39) |
K381N |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,603,607 (GRCm39) |
A529T |
probably damaging |
Het |
Cdh18 |
T |
A |
15: 23,446,159 (GRCm39) |
N536K |
probably damaging |
Het |
Dpy19l1 |
C |
A |
9: 24,414,158 (GRCm39) |
R90L |
possibly damaging |
Het |
E2f3 |
A |
G |
13: 30,102,568 (GRCm39) |
V231A |
possibly damaging |
Het |
F930015N05Rik |
A |
T |
11: 64,326,229 (GRCm39) |
|
probably benign |
Het |
Fcer2a |
T |
C |
8: 3,739,830 (GRCm39) |
H47R |
possibly damaging |
Het |
Hcar2 |
A |
G |
5: 124,003,330 (GRCm39) |
S58P |
probably benign |
Het |
Hivep3 |
A |
G |
4: 119,953,558 (GRCm39) |
T625A |
possibly damaging |
Het |
Insrr |
C |
T |
3: 87,720,873 (GRCm39) |
R1044C |
probably damaging |
Het |
Itgax |
C |
T |
7: 127,734,236 (GRCm39) |
A336V |
probably damaging |
Het |
Lin37 |
A |
T |
7: 30,256,341 (GRCm39) |
V140E |
probably damaging |
Het |
Malrd1 |
T |
A |
2: 15,874,595 (GRCm39) |
I1341K |
unknown |
Het |
Map4k5 |
T |
C |
12: 69,864,799 (GRCm39) |
I561V |
probably benign |
Het |
Mcc |
A |
G |
18: 44,857,627 (GRCm39) |
S163P |
probably benign |
Het |
Nlrp12 |
T |
C |
7: 3,290,039 (GRCm39) |
T158A |
probably damaging |
Het |
Or5an6 |
A |
T |
19: 12,372,292 (GRCm39) |
I222F |
probably damaging |
Het |
Or5b119 |
A |
G |
19: 13,457,278 (GRCm39) |
C95R |
probably damaging |
Het |
Paqr5 |
C |
T |
9: 61,871,065 (GRCm39) |
R171Q |
probably damaging |
Het |
Pax8 |
A |
T |
2: 24,331,098 (GRCm39) |
M200K |
probably benign |
Het |
Plcd4 |
T |
C |
1: 74,601,229 (GRCm39) |
S498P |
probably benign |
Het |
Poglut1 |
T |
C |
16: 38,349,972 (GRCm39) |
Y267C |
probably damaging |
Het |
Pom121l2 |
T |
C |
13: 22,167,694 (GRCm39) |
I655T |
probably benign |
Het |
Proca1 |
G |
T |
11: 78,085,754 (GRCm39) |
R19L |
probably benign |
Het |
Ranbp17 |
T |
C |
11: 33,167,398 (GRCm39) |
S1022G |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rpgrip1 |
A |
G |
14: 52,387,469 (GRCm39) |
H1037R |
probably damaging |
Het |
Rpl34 |
G |
T |
3: 130,522,926 (GRCm39) |
T6K |
probably damaging |
Het |
Scaper |
T |
C |
9: 55,771,711 (GRCm39) |
T402A |
probably benign |
Het |
Selenow |
A |
T |
7: 15,653,996 (GRCm39) |
V52E |
probably damaging |
Het |
Septin14 |
T |
A |
5: 129,774,822 (GRCm39) |
I118L |
probably benign |
Het |
Sis |
A |
T |
3: 72,872,951 (GRCm39) |
N62K |
probably benign |
Het |
Sit1 |
A |
T |
4: 43,482,761 (GRCm39) |
C133S |
probably benign |
Het |
Susd3 |
ACC |
AC |
13: 49,391,041 (GRCm39) |
|
probably null |
Het |
Svep1 |
A |
G |
4: 58,064,275 (GRCm39) |
V3236A |
probably benign |
Het |
Taf12 |
G |
A |
4: 132,016,725 (GRCm39) |
V168I |
possibly damaging |
Het |
Tas2r139 |
A |
T |
6: 42,118,526 (GRCm39) |
R219S |
probably damaging |
Het |
Tmc1 |
A |
T |
19: 20,776,400 (GRCm39) |
V653D |
probably damaging |
Het |
Utp23 |
T |
A |
15: 51,741,007 (GRCm39) |
L30Q |
probably damaging |
Het |
|
Other mutations in Prr30 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02434:Prr30
|
APN |
14 |
101,435,804 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02504:Prr30
|
APN |
14 |
101,436,056 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02824:Prr30
|
APN |
14 |
101,435,954 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02898:Prr30
|
APN |
14 |
101,435,917 (GRCm39) |
missense |
probably benign |
|
IGL03333:Prr30
|
APN |
14 |
101,435,827 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4453001:Prr30
|
UTSW |
14 |
101,436,371 (GRCm39) |
missense |
probably benign |
0.23 |
R1004:Prr30
|
UTSW |
14 |
101,436,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R1950:Prr30
|
UTSW |
14 |
101,435,377 (GRCm39) |
missense |
probably benign |
0.00 |
R2290:Prr30
|
UTSW |
14 |
101,436,211 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3123:Prr30
|
UTSW |
14 |
101,436,425 (GRCm39) |
missense |
probably benign |
|
R4854:Prr30
|
UTSW |
14 |
101,435,879 (GRCm39) |
missense |
probably benign |
|
R7919:Prr30
|
UTSW |
14 |
101,436,547 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8270:Prr30
|
UTSW |
14 |
101,435,822 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8749:Prr30
|
UTSW |
14 |
101,436,365 (GRCm39) |
missense |
probably benign |
0.12 |
R9140:Prr30
|
UTSW |
14 |
101,436,430 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Prr30
|
UTSW |
14 |
101,435,576 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Prr30
|
UTSW |
14 |
101,436,068 (GRCm39) |
missense |
probably damaging |
0.97 |
|