Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930011G23Rik |
A |
G |
5: 99,377,238 (GRCm39) |
V403A |
probably damaging |
Het |
Adpgk |
T |
C |
9: 59,221,088 (GRCm39) |
L298P |
probably damaging |
Het |
Akap6 |
A |
T |
12: 53,187,089 (GRCm39) |
D1501V |
probably damaging |
Het |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Ankhd1 |
T |
A |
18: 36,791,061 (GRCm39) |
Y2478* |
probably null |
Het |
Col6a3 |
A |
G |
1: 90,749,584 (GRCm39) |
Y417H |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 16,011,521 (GRCm39) |
F2511L |
probably damaging |
Het |
Dzip3 |
T |
C |
16: 48,762,446 (GRCm39) |
M602V |
possibly damaging |
Het |
Efna2 |
G |
A |
10: 80,024,346 (GRCm39) |
|
probably null |
Het |
Fzd8 |
T |
C |
18: 9,214,270 (GRCm39) |
S451P |
probably damaging |
Het |
Galntl6 |
A |
T |
8: 58,880,750 (GRCm39) |
D134E |
probably damaging |
Het |
Grid2 |
T |
C |
6: 64,040,888 (GRCm39) |
S277P |
probably damaging |
Het |
Lcn2 |
A |
G |
2: 32,277,716 (GRCm39) |
V91A |
possibly damaging |
Het |
Lrp1b |
G |
A |
2: 41,202,478 (GRCm39) |
|
probably benign |
Het |
Lrrc7 |
T |
A |
3: 157,866,696 (GRCm39) |
Y1015F |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,729,994 (GRCm39) |
C2779S |
possibly damaging |
Het |
Nlrp10 |
A |
T |
7: 108,524,118 (GRCm39) |
F454Y |
probably damaging |
Het |
Obox5 |
T |
A |
7: 15,492,684 (GRCm39) |
L213Q |
probably damaging |
Het |
Or1o2 |
T |
A |
17: 37,543,087 (GRCm39) |
Y58F |
probably damaging |
Het |
Piezo2 |
T |
C |
18: 63,248,043 (GRCm39) |
M486V |
probably benign |
Het |
Plcg1 |
A |
C |
2: 160,616,446 (GRCm39) |
|
probably null |
Het |
Polr1b |
G |
A |
2: 128,957,627 (GRCm39) |
V561I |
probably benign |
Het |
Polr3c |
A |
T |
3: 96,626,770 (GRCm39) |
|
probably benign |
Het |
Prkg1 |
T |
A |
19: 30,562,681 (GRCm39) |
K523* |
probably null |
Het |
Sema3b |
T |
A |
9: 107,476,995 (GRCm39) |
|
probably benign |
Het |
Sp9 |
A |
G |
2: 73,103,865 (GRCm39) |
T140A |
probably benign |
Het |
Zfp507 |
T |
C |
7: 35,493,631 (GRCm39) |
R471G |
probably damaging |
Het |
|
Other mutations in Prss3l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01094:Prss3l
|
APN |
6 |
41,420,357 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0379:Prss3l
|
UTSW |
6 |
41,422,190 (GRCm39) |
splice site |
probably benign |
|
R0387:Prss3l
|
UTSW |
6 |
41,420,303 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0452:Prss3l
|
UTSW |
6 |
41,422,271 (GRCm39) |
missense |
probably benign |
0.30 |
R0647:Prss3l
|
UTSW |
6 |
41,420,275 (GRCm39) |
missense |
probably benign |
|
R4622:Prss3l
|
UTSW |
6 |
41,422,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R4655:Prss3l
|
UTSW |
6 |
41,422,984 (GRCm39) |
missense |
probably benign |
|
R5340:Prss3l
|
UTSW |
6 |
41,422,307 (GRCm39) |
missense |
probably benign |
0.02 |
R6734:Prss3l
|
UTSW |
6 |
41,422,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R9026:Prss3l
|
UTSW |
6 |
41,422,990 (GRCm39) |
missense |
probably benign |
|
R9464:Prss3l
|
UTSW |
6 |
41,420,486 (GRCm39) |
missense |
probably benign |
0.05 |
|