Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd13 |
T |
A |
8: 10,037,600 (GRCm39) |
Y66N |
probably damaging |
Het |
Apol6 |
C |
T |
15: 76,935,147 (GRCm39) |
Q139* |
probably null |
Het |
Armh1 |
C |
A |
4: 117,072,753 (GRCm39) |
E244* |
probably null |
Het |
Cd1d1 |
A |
T |
3: 86,904,880 (GRCm39) |
H219Q |
probably benign |
Het |
Cdca2 |
A |
G |
14: 67,950,568 (GRCm39) |
L121P |
probably benign |
Het |
Cdin1 |
T |
C |
2: 115,607,411 (GRCm39) |
Y255H |
possibly damaging |
Het |
Cog4 |
T |
A |
8: 111,580,328 (GRCm39) |
L133I |
possibly damaging |
Het |
Csf1 |
T |
C |
3: 107,655,922 (GRCm39) |
M370V |
probably benign |
Het |
Ddi2 |
G |
A |
4: 141,412,834 (GRCm39) |
T26M |
probably benign |
Het |
Dhcr7 |
A |
G |
7: 143,391,507 (GRCm39) |
D32G |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,581,706 (GRCm39) |
V16A |
probably benign |
Het |
Exd1 |
T |
C |
2: 119,354,047 (GRCm39) |
N337S |
possibly damaging |
Het |
Flii |
T |
C |
11: 60,612,683 (GRCm39) |
D227G |
probably damaging |
Het |
Hsf1 |
A |
G |
15: 76,384,679 (GRCm39) |
T485A |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,884,505 (GRCm39) |
R2614* |
probably null |
Het |
Iqch |
T |
C |
9: 63,408,158 (GRCm39) |
T630A |
probably benign |
Het |
Itgal |
T |
A |
7: 126,921,253 (GRCm39) |
D770E |
probably damaging |
Het |
Mroh1 |
T |
A |
15: 76,316,449 (GRCm39) |
V759E |
probably damaging |
Het |
Mrps17 |
A |
G |
5: 129,795,209 (GRCm39) |
|
probably benign |
Het |
Mtpap |
A |
G |
18: 4,396,195 (GRCm39) |
S496G |
possibly damaging |
Het |
Nkd1 |
T |
A |
8: 89,311,844 (GRCm39) |
Y39* |
probably null |
Het |
Nmd3 |
A |
G |
3: 69,650,907 (GRCm39) |
Y359C |
probably damaging |
Het |
Nr1h3 |
G |
A |
2: 91,022,170 (GRCm39) |
L153F |
possibly damaging |
Het |
Nuf2 |
T |
A |
1: 169,341,112 (GRCm39) |
|
probably null |
Het |
Or4b1b |
T |
C |
2: 90,112,926 (GRCm39) |
|
probably null |
Het |
Or4c113 |
T |
A |
2: 88,885,700 (GRCm39) |
K23N |
probably benign |
Het |
Or8b12i |
A |
T |
9: 20,082,032 (GRCm39) |
Y278* |
probably null |
Het |
Pnn |
T |
C |
12: 59,113,903 (GRCm39) |
|
probably null |
Het |
Ppm1j |
A |
G |
3: 104,690,687 (GRCm39) |
D230G |
probably benign |
Het |
Ppp1r15a |
A |
T |
7: 45,172,442 (GRCm39) |
L650Q |
probably damaging |
Het |
Rbm19 |
T |
C |
5: 120,266,372 (GRCm39) |
V465A |
possibly damaging |
Het |
Rubcnl |
G |
T |
14: 75,278,331 (GRCm39) |
V372F |
probably damaging |
Het |
Sema6a |
G |
T |
18: 47,403,785 (GRCm39) |
D595E |
probably benign |
Het |
Slc35c1 |
A |
G |
2: 92,289,377 (GRCm39) |
F43S |
probably damaging |
Het |
Slc39a5 |
C |
T |
10: 128,232,619 (GRCm39) |
|
probably null |
Het |
Slco4c1 |
A |
G |
1: 96,756,574 (GRCm39) |
F583L |
probably benign |
Het |
Sox9 |
A |
G |
11: 112,675,702 (GRCm39) |
Y297C |
probably damaging |
Het |
Taf1b |
A |
G |
12: 24,564,884 (GRCm39) |
D167G |
possibly damaging |
Het |
Trpm6 |
T |
C |
19: 18,861,321 (GRCm39) |
|
probably null |
Het |
Uba6 |
A |
C |
5: 86,292,237 (GRCm39) |
V402G |
possibly damaging |
Het |
Usp43 |
T |
C |
11: 67,767,324 (GRCm39) |
Y682C |
probably damaging |
Het |
Vmn1r195 |
A |
G |
13: 22,463,403 (GRCm39) |
D291G |
probably damaging |
Het |
Xpr1 |
A |
T |
1: 155,206,214 (GRCm39) |
F156Y |
probably damaging |
Het |
Yju2b |
C |
T |
8: 84,987,277 (GRCm39) |
E99K |
probably damaging |
Het |
Zfp318 |
T |
A |
17: 46,724,124 (GRCm39) |
H2042Q |
probably benign |
Het |
Zfp937 |
T |
A |
2: 150,081,222 (GRCm39) |
D417E |
possibly damaging |
Het |
|
Other mutations in Prss37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02282:Prss37
|
APN |
6 |
40,492,317 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03110:Prss37
|
APN |
6 |
40,495,984 (GRCm39) |
missense |
probably benign |
0.00 |
R0201:Prss37
|
UTSW |
6 |
40,493,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Prss37
|
UTSW |
6 |
40,492,294 (GRCm39) |
nonsense |
probably null |
|
R2120:Prss37
|
UTSW |
6 |
40,492,294 (GRCm39) |
nonsense |
probably null |
|
R2124:Prss37
|
UTSW |
6 |
40,492,294 (GRCm39) |
nonsense |
probably null |
|
R2504:Prss37
|
UTSW |
6 |
40,494,760 (GRCm39) |
splice site |
probably null |
|
R4711:Prss37
|
UTSW |
6 |
40,492,381 (GRCm39) |
missense |
probably benign |
0.21 |
R4938:Prss37
|
UTSW |
6 |
40,491,917 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4983:Prss37
|
UTSW |
6 |
40,493,070 (GRCm39) |
missense |
probably benign |
0.01 |
R6652:Prss37
|
UTSW |
6 |
40,496,090 (GRCm39) |
start gained |
probably benign |
|
R8111:Prss37
|
UTSW |
6 |
40,494,747 (GRCm39) |
missense |
probably benign |
0.00 |
R8425:Prss37
|
UTSW |
6 |
40,493,052 (GRCm39) |
nonsense |
probably null |
|
R8859:Prss37
|
UTSW |
6 |
40,491,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R9297:Prss37
|
UTSW |
6 |
40,491,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Prss37
|
UTSW |
6 |
40,491,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R9778:Prss37
|
UTSW |
6 |
40,494,713 (GRCm39) |
missense |
probably damaging |
0.99 |
X0063:Prss37
|
UTSW |
6 |
40,493,149 (GRCm39) |
missense |
possibly damaging |
0.65 |
|