Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019A02Rik |
T |
C |
1: 53,216,972 (GRCm39) |
H81R |
probably benign |
Het |
Alg10b |
A |
T |
15: 90,112,532 (GRCm39) |
K459* |
probably null |
Het |
C8g |
A |
T |
2: 25,388,824 (GRCm39) |
*203K |
probably null |
Het |
Cacna1b |
T |
C |
2: 24,652,821 (GRCm39) |
E80G |
probably damaging |
Het |
Cdh12 |
T |
A |
15: 21,583,826 (GRCm39) |
N555K |
probably benign |
Het |
Cenpf |
T |
A |
1: 189,387,273 (GRCm39) |
N1669I |
probably damaging |
Het |
Cpsf1 |
A |
G |
15: 76,480,203 (GRCm39) |
|
probably null |
Het |
Ear1 |
A |
G |
14: 44,056,575 (GRCm39) |
S98P |
probably benign |
Het |
Elfn2 |
A |
T |
15: 78,557,670 (GRCm39) |
D292E |
possibly damaging |
Het |
Fbxw24 |
T |
C |
9: 109,430,316 (GRCm39) |
S443G |
probably damaging |
Het |
Fnip2 |
T |
C |
3: 79,388,583 (GRCm39) |
E716G |
possibly damaging |
Het |
Gabra1 |
G |
T |
11: 42,024,345 (GRCm39) |
N443K |
probably damaging |
Het |
Grik5 |
A |
T |
7: 24,714,894 (GRCm39) |
V700E |
probably damaging |
Het |
Ifi27l2a |
T |
A |
12: 103,405,772 (GRCm39) |
N162K |
probably damaging |
Het |
Myom2 |
A |
T |
8: 15,115,731 (GRCm39) |
T49S |
probably benign |
Het |
Obsl1 |
T |
C |
1: 75,463,443 (GRCm39) |
M1750V |
probably benign |
Het |
Or10g9b |
A |
T |
9: 39,917,802 (GRCm39) |
W148R |
probably benign |
Het |
Or2l13b |
A |
T |
16: 19,349,667 (GRCm39) |
M1K |
probably null |
Het |
Or2y1 |
A |
T |
11: 49,385,873 (GRCm39) |
H171L |
probably benign |
Het |
Ppp2r5e |
A |
G |
12: 75,511,667 (GRCm39) |
V352A |
probably damaging |
Het |
Prkca |
T |
A |
11: 108,231,489 (GRCm39) |
Q63L |
probably benign |
Het |
Scgb2b7 |
A |
T |
7: 31,404,506 (GRCm39) |
C65S |
probably damaging |
Het |
Slfn14 |
T |
C |
11: 83,167,139 (GRCm39) |
K792R |
probably benign |
Het |
Slfn3 |
C |
T |
11: 83,104,257 (GRCm39) |
T376M |
probably damaging |
Het |
Snx19 |
A |
T |
9: 30,351,430 (GRCm39) |
I135F |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,805,165 (GRCm39) |
V271E |
probably benign |
Het |
Urb2 |
T |
C |
8: 124,756,588 (GRCm39) |
V765A |
possibly damaging |
Het |
Vmn2r61 |
A |
G |
7: 41,909,679 (GRCm39) |
H68R |
probably benign |
Het |
Vps8 |
T |
C |
16: 21,267,148 (GRCm39) |
I177T |
possibly damaging |
Het |
Zfp810 |
A |
C |
9: 22,190,441 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Trpv1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Trpv1
|
APN |
11 |
73,151,188 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01348:Trpv1
|
APN |
11 |
73,129,078 (GRCm39) |
splice site |
probably null |
|
IGL01568:Trpv1
|
APN |
11 |
73,129,269 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01638:Trpv1
|
APN |
11 |
73,144,155 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02092:Trpv1
|
APN |
11 |
73,136,905 (GRCm39) |
splice site |
probably benign |
|
IGL02167:Trpv1
|
APN |
11 |
73,145,623 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02649:Trpv1
|
APN |
11 |
73,141,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03396:Trpv1
|
APN |
11 |
73,143,882 (GRCm39) |
missense |
probably benign |
0.01 |
R0112:Trpv1
|
UTSW |
11 |
73,144,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Trpv1
|
UTSW |
11 |
73,143,834 (GRCm39) |
splice site |
probably benign |
|
R0482:Trpv1
|
UTSW |
11 |
73,130,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Trpv1
|
UTSW |
11 |
73,151,268 (GRCm39) |
missense |
probably benign |
|
R1401:Trpv1
|
UTSW |
11 |
73,130,952 (GRCm39) |
splice site |
probably null |
|
R2032:Trpv1
|
UTSW |
11 |
73,129,211 (GRCm39) |
missense |
probably benign |
|
R2199:Trpv1
|
UTSW |
11 |
73,131,077 (GRCm39) |
missense |
probably damaging |
0.96 |
R2263:Trpv1
|
UTSW |
11 |
73,132,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R2939:Trpv1
|
UTSW |
11 |
73,145,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R2940:Trpv1
|
UTSW |
11 |
73,145,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R3743:Trpv1
|
UTSW |
11 |
73,145,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R3805:Trpv1
|
UTSW |
11 |
73,143,879 (GRCm39) |
missense |
probably damaging |
0.99 |
R4073:Trpv1
|
UTSW |
11 |
73,141,606 (GRCm39) |
missense |
probably damaging |
0.96 |
R4294:Trpv1
|
UTSW |
11 |
73,131,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R4650:Trpv1
|
UTSW |
11 |
73,129,089 (GRCm39) |
missense |
probably benign |
0.04 |
R4700:Trpv1
|
UTSW |
11 |
73,142,110 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5114:Trpv1
|
UTSW |
11 |
73,132,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Trpv1
|
UTSW |
11 |
73,129,342 (GRCm39) |
missense |
probably benign |
0.32 |
R5319:Trpv1
|
UTSW |
11 |
73,130,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R5516:Trpv1
|
UTSW |
11 |
73,136,809 (GRCm39) |
missense |
probably benign |
0.44 |
R5845:Trpv1
|
UTSW |
11 |
73,131,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R6134:Trpv1
|
UTSW |
11 |
73,135,143 (GRCm39) |
missense |
probably benign |
0.01 |
R6232:Trpv1
|
UTSW |
11 |
73,141,636 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6383:Trpv1
|
UTSW |
11 |
73,136,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R7200:Trpv1
|
UTSW |
11 |
73,130,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7319:Trpv1
|
UTSW |
11 |
73,141,620 (GRCm39) |
missense |
probably benign |
0.01 |
R7323:Trpv1
|
UTSW |
11 |
73,151,163 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7361:Trpv1
|
UTSW |
11 |
73,151,203 (GRCm39) |
missense |
probably damaging |
0.99 |
R7373:Trpv1
|
UTSW |
11 |
73,131,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R7444:Trpv1
|
UTSW |
11 |
73,135,030 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7488:Trpv1
|
UTSW |
11 |
73,129,355 (GRCm39) |
missense |
probably benign |
0.00 |
R7513:Trpv1
|
UTSW |
11 |
73,131,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Trpv1
|
UTSW |
11 |
73,145,048 (GRCm39) |
missense |
probably benign |
0.01 |
R7991:Trpv1
|
UTSW |
11 |
73,132,583 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8213:Trpv1
|
UTSW |
11 |
73,145,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Trpv1
|
UTSW |
11 |
73,145,593 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8753:Trpv1
|
UTSW |
11 |
73,135,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R9176:Trpv1
|
UTSW |
11 |
73,130,481 (GRCm39) |
missense |
probably benign |
0.37 |
R9183:Trpv1
|
UTSW |
11 |
73,135,039 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9190:Trpv1
|
UTSW |
11 |
73,145,148 (GRCm39) |
critical splice donor site |
probably null |
|
R9222:Trpv1
|
UTSW |
11 |
73,141,681 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9241:Trpv1
|
UTSW |
11 |
73,151,182 (GRCm39) |
missense |
probably benign |
0.01 |
R9508:Trpv1
|
UTSW |
11 |
73,145,090 (GRCm39) |
missense |
|
|
R9727:Trpv1
|
UTSW |
11 |
73,130,347 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Trpv1
|
UTSW |
11 |
73,135,027 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Trpv1
|
UTSW |
11 |
73,131,333 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Trpv1
|
UTSW |
11 |
73,131,014 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Trpv1
|
UTSW |
11 |
73,145,599 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Trpv1
|
UTSW |
11 |
73,145,117 (GRCm39) |
missense |
probably benign |
0.12 |
Z1186:Trpv1
|
UTSW |
11 |
73,131,427 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1187:Trpv1
|
UTSW |
11 |
73,145,117 (GRCm39) |
missense |
probably benign |
0.12 |
Z1187:Trpv1
|
UTSW |
11 |
73,131,427 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1188:Trpv1
|
UTSW |
11 |
73,145,117 (GRCm39) |
missense |
probably benign |
0.12 |
Z1188:Trpv1
|
UTSW |
11 |
73,131,427 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1189:Trpv1
|
UTSW |
11 |
73,145,117 (GRCm39) |
missense |
probably benign |
0.12 |
Z1189:Trpv1
|
UTSW |
11 |
73,131,427 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1190:Trpv1
|
UTSW |
11 |
73,145,117 (GRCm39) |
missense |
probably benign |
0.12 |
Z1190:Trpv1
|
UTSW |
11 |
73,131,427 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1191:Trpv1
|
UTSW |
11 |
73,145,117 (GRCm39) |
missense |
probably benign |
0.12 |
Z1191:Trpv1
|
UTSW |
11 |
73,131,427 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1192:Trpv1
|
UTSW |
11 |
73,145,117 (GRCm39) |
missense |
probably benign |
0.12 |
Z1192:Trpv1
|
UTSW |
11 |
73,131,427 (GRCm39) |
missense |
possibly damaging |
0.90 |
|