Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
G |
T |
6: 121,622,212 (GRCm39) |
V372F |
probably benign |
Het |
Adcy10 |
G |
A |
1: 165,347,464 (GRCm39) |
C393Y |
probably damaging |
Het |
Adgrg7 |
A |
C |
16: 56,550,669 (GRCm39) |
I681S |
possibly damaging |
Het |
Akap8l |
T |
C |
17: 32,540,485 (GRCm39) |
|
probably benign |
Het |
Akr1a1 |
A |
T |
4: 116,497,092 (GRCm39) |
V156E |
probably damaging |
Het |
Alk |
T |
G |
17: 72,202,734 (GRCm39) |
D1167A |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,620,453 (GRCm39) |
|
probably null |
Het |
Aspm |
T |
A |
1: 139,385,221 (GRCm39) |
N288K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,398,133 (GRCm39) |
|
probably null |
Het |
Asxl2 |
G |
A |
12: 3,524,618 (GRCm39) |
|
probably null |
Het |
Atp6v0a1 |
A |
G |
11: 100,946,413 (GRCm39) |
H802R |
probably damaging |
Het |
B4galnt1 |
A |
G |
10: 127,007,691 (GRCm39) |
T531A |
possibly damaging |
Het |
Cecr2 |
A |
G |
6: 120,733,530 (GRCm39) |
N506D |
possibly damaging |
Het |
Crebrf |
T |
C |
17: 26,978,839 (GRCm39) |
V509A |
probably damaging |
Het |
Cyp4f40 |
A |
T |
17: 32,894,590 (GRCm39) |
I413F |
probably null |
Het |
Defb12 |
C |
A |
8: 19,164,342 (GRCm39) |
|
probably null |
Het |
Dnah2 |
T |
C |
11: 69,312,674 (GRCm39) |
E4297G |
probably damaging |
Het |
Dpysl5 |
A |
T |
5: 30,948,857 (GRCm39) |
N371Y |
probably damaging |
Het |
Eef1d |
G |
T |
15: 75,775,038 (GRCm39) |
T207N |
probably benign |
Het |
Esrrb |
C |
T |
12: 86,565,783 (GRCm39) |
Q416* |
probably null |
Het |
Exd2 |
T |
C |
12: 80,536,222 (GRCm39) |
L284P |
probably damaging |
Het |
Fat3 |
T |
A |
9: 16,287,739 (GRCm39) |
I595F |
probably benign |
Het |
Gm9920 |
A |
G |
15: 54,972,371 (GRCm39) |
|
probably benign |
Het |
Hephl1 |
T |
C |
9: 14,981,084 (GRCm39) |
K783E |
probably damaging |
Het |
Irs2 |
A |
G |
8: 11,055,277 (GRCm39) |
S1052P |
probably benign |
Het |
Kctd18 |
T |
C |
1: 58,002,252 (GRCm39) |
I192V |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,586,803 (GRCm39) |
D722G |
probably damaging |
Het |
Lpin1 |
C |
T |
12: 16,613,656 (GRCm39) |
G504S |
probably damaging |
Het |
Lrit2 |
A |
C |
14: 36,791,140 (GRCm39) |
Q273P |
possibly damaging |
Het |
Mlkl |
T |
A |
8: 112,054,569 (GRCm39) |
E189D |
probably benign |
Het |
Mttp |
C |
T |
3: 137,810,790 (GRCm39) |
R608H |
probably benign |
Het |
Nav2 |
T |
C |
7: 49,238,908 (GRCm39) |
V2011A |
probably benign |
Het |
Nos2 |
A |
T |
11: 78,848,317 (GRCm39) |
I1075F |
probably benign |
Het |
Npat |
A |
G |
9: 53,461,336 (GRCm39) |
|
probably null |
Het |
Nucks1 |
T |
C |
1: 131,846,771 (GRCm39) |
F16L |
probably damaging |
Het |
Nus1 |
T |
C |
10: 52,305,309 (GRCm39) |
S150P |
possibly damaging |
Het |
Odad1 |
C |
T |
7: 45,591,506 (GRCm39) |
R257* |
probably null |
Het |
Oga |
A |
T |
19: 45,746,461 (GRCm39) |
Y779* |
probably null |
Het |
Or4c123 |
G |
T |
2: 89,127,506 (GRCm39) |
T36K |
probably damaging |
Het |
Or8b35 |
A |
T |
9: 37,903,908 (GRCm39) |
Y40F |
probably benign |
Het |
Pclo |
A |
G |
5: 14,731,367 (GRCm39) |
T3290A |
unknown |
Het |
Pign |
A |
T |
1: 105,585,537 (GRCm39) |
F4Y |
probably benign |
Het |
Rfx4 |
A |
G |
10: 84,696,406 (GRCm39) |
N233D |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,397,652 (GRCm39) |
M1325L |
possibly damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Scaf11 |
T |
A |
15: 96,315,001 (GRCm39) |
H1227L |
possibly damaging |
Het |
Sec31b |
G |
T |
19: 44,507,076 (GRCm39) |
P840T |
probably damaging |
Het |
Slc16a9 |
T |
A |
10: 70,118,958 (GRCm39) |
L426I |
probably damaging |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Slc34a1 |
T |
C |
13: 23,996,575 (GRCm39) |
S27P |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,299 (GRCm39) |
S310P |
possibly damaging |
Het |
Tmem245 |
G |
A |
4: 56,947,084 (GRCm39) |
R110C |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,735,152 (GRCm39) |
Y953C |
probably damaging |
Het |
Trpm7 |
C |
A |
2: 126,684,775 (GRCm39) |
|
probably null |
Het |
Ush2a |
G |
A |
1: 188,644,320 (GRCm39) |
V4561I |
probably benign |
Het |
Vmn1r192 |
C |
T |
13: 22,371,801 (GRCm39) |
V140I |
probably benign |
Het |
Vmn2r66 |
A |
T |
7: 84,656,026 (GRCm39) |
I330N |
probably damaging |
Het |
Vmn2r99 |
T |
C |
17: 19,599,531 (GRCm39) |
V405A |
probably damaging |
Het |
Wdhd1 |
A |
C |
14: 47,509,678 (GRCm39) |
V172G |
probably benign |
Het |
Zfhx3 |
C |
T |
8: 109,677,817 (GRCm39) |
R2956C |
possibly damaging |
Het |
Zfp446 |
T |
C |
7: 12,716,178 (GRCm39) |
L283P |
possibly damaging |
Het |
Zfp82 |
T |
C |
7: 29,756,591 (GRCm39) |
K164E |
probably damaging |
Het |
|
Other mutations in Lepr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Lepr
|
APN |
4 |
101,672,232 (GRCm39) |
missense |
probably benign |
|
IGL01111:Lepr
|
APN |
4 |
101,671,852 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01324:Lepr
|
APN |
4 |
101,625,265 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01372:Lepr
|
APN |
4 |
101,592,774 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01626:Lepr
|
APN |
4 |
101,590,731 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01733:Lepr
|
APN |
4 |
101,622,279 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01815:Lepr
|
APN |
4 |
101,671,987 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01899:Lepr
|
APN |
4 |
101,637,184 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02138:Lepr
|
APN |
4 |
101,625,264 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02161:Lepr
|
APN |
4 |
101,602,875 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02653:Lepr
|
APN |
4 |
101,622,141 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02735:Lepr
|
APN |
4 |
101,639,835 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03035:Lepr
|
APN |
4 |
101,622,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03083:Lepr
|
APN |
4 |
101,671,876 (GRCm39) |
nonsense |
probably null |
|
IGL03160:Lepr
|
APN |
4 |
101,622,103 (GRCm39) |
missense |
probably damaging |
1.00 |
aufsetzigen
|
UTSW |
4 |
101,609,372 (GRCm39) |
missense |
probably damaging |
1.00 |
beastly
|
UTSW |
4 |
101,671,788 (GRCm39) |
missense |
probably benign |
|
business_class
|
UTSW |
4 |
101,622,069 (GRCm39) |
missense |
probably damaging |
1.00 |
cherub
|
UTSW |
4 |
101,625,259 (GRCm39) |
missense |
probably benign |
0.25 |
clodhopper
|
UTSW |
4 |
101,622,487 (GRCm39) |
splice site |
probably null |
|
donner
|
UTSW |
4 |
101,672,398 (GRCm39) |
missense |
probably damaging |
1.00 |
fluffy
|
UTSW |
4 |
101,649,220 (GRCm39) |
missense |
probably damaging |
1.00 |
giant
|
UTSW |
4 |
101,622,349 (GRCm39) |
critical splice donor site |
probably null |
|
gordo
|
UTSW |
4 |
101,622,502 (GRCm39) |
missense |
probably damaging |
0.97 |
Immunoglutton
|
UTSW |
4 |
101,622,498 (GRCm39) |
splice site |
probably benign |
|
Jumbo_shrimp
|
UTSW |
4 |
101,622,151 (GRCm39) |
nonsense |
probably null |
|
lowleaning
|
UTSW |
4 |
101,671,588 (GRCm39) |
splice site |
probably null |
|
odd
|
UTSW |
4 |
101,585,271 (GRCm39) |
splice site |
probably benign |
|
paleo
|
UTSW |
4 |
101,602,842 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0140_Lepr_245
|
UTSW |
4 |
101,625,264 (GRCm39) |
missense |
probably damaging |
1.00 |
well-upholstered
|
UTSW |
4 |
101,630,155 (GRCm39) |
synonymous |
probably benign |
|
worldly
|
UTSW |
4 |
101,625,425 (GRCm39) |
missense |
possibly damaging |
0.96 |
PIT4651001:Lepr
|
UTSW |
4 |
101,649,194 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4696001:Lepr
|
UTSW |
4 |
101,637,180 (GRCm39) |
missense |
probably benign |
0.10 |
R0140:Lepr
|
UTSW |
4 |
101,625,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:Lepr
|
UTSW |
4 |
101,609,349 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0279:Lepr
|
UTSW |
4 |
101,607,541 (GRCm39) |
missense |
probably benign |
0.05 |
R0487:Lepr
|
UTSW |
4 |
101,625,290 (GRCm39) |
nonsense |
probably null |
|
R0498:Lepr
|
UTSW |
4 |
101,602,889 (GRCm39) |
missense |
probably benign |
0.01 |
R0506:Lepr
|
UTSW |
4 |
101,630,207 (GRCm39) |
splice site |
probably benign |
|
R0512:Lepr
|
UTSW |
4 |
101,671,901 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0512:Lepr
|
UTSW |
4 |
101,649,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R0726:Lepr
|
UTSW |
4 |
101,622,131 (GRCm39) |
missense |
probably benign |
0.01 |
R1054:Lepr
|
UTSW |
4 |
101,639,793 (GRCm39) |
missense |
probably damaging |
0.97 |
R1109:Lepr
|
UTSW |
4 |
101,628,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R1398:Lepr
|
UTSW |
4 |
101,649,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Lepr
|
UTSW |
4 |
101,592,878 (GRCm39) |
missense |
probably benign |
0.08 |
R1464:Lepr
|
UTSW |
4 |
101,592,878 (GRCm39) |
missense |
probably benign |
0.08 |
R1519:Lepr
|
UTSW |
4 |
101,646,541 (GRCm39) |
missense |
probably damaging |
0.97 |
R1602:Lepr
|
UTSW |
4 |
101,602,842 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1830:Lepr
|
UTSW |
4 |
101,592,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R1850:Lepr
|
UTSW |
4 |
101,590,620 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1918:Lepr
|
UTSW |
4 |
101,630,033 (GRCm39) |
missense |
probably benign |
0.08 |
R1928:Lepr
|
UTSW |
4 |
101,639,927 (GRCm39) |
splice site |
probably benign |
|
R2099:Lepr
|
UTSW |
4 |
101,630,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Lepr
|
UTSW |
4 |
101,630,178 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2175:Lepr
|
UTSW |
4 |
101,622,576 (GRCm39) |
missense |
probably benign |
0.01 |
R2254:Lepr
|
UTSW |
4 |
101,672,309 (GRCm39) |
missense |
probably benign |
0.26 |
R2396:Lepr
|
UTSW |
4 |
101,590,725 (GRCm39) |
missense |
probably benign |
0.19 |
R2508:Lepr
|
UTSW |
4 |
101,648,093 (GRCm39) |
missense |
probably damaging |
0.98 |
R2571:Lepr
|
UTSW |
4 |
101,625,369 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3790:Lepr
|
UTSW |
4 |
101,648,111 (GRCm39) |
splice site |
probably benign |
|
R3882:Lepr
|
UTSW |
4 |
101,672,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R3933:Lepr
|
UTSW |
4 |
101,622,498 (GRCm39) |
splice site |
probably benign |
|
R4211:Lepr
|
UTSW |
4 |
101,590,611 (GRCm39) |
missense |
probably benign |
0.19 |
R4343:Lepr
|
UTSW |
4 |
101,622,349 (GRCm39) |
critical splice donor site |
probably null |
|
R4345:Lepr
|
UTSW |
4 |
101,622,349 (GRCm39) |
critical splice donor site |
probably null |
|
R4544:Lepr
|
UTSW |
4 |
101,625,425 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4546:Lepr
|
UTSW |
4 |
101,671,838 (GRCm39) |
missense |
probably benign |
0.35 |
R4724:Lepr
|
UTSW |
4 |
101,622,562 (GRCm39) |
nonsense |
probably null |
|
R4797:Lepr
|
UTSW |
4 |
101,637,244 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4860:Lepr
|
UTSW |
4 |
101,646,534 (GRCm39) |
missense |
probably benign |
0.14 |
R4860:Lepr
|
UTSW |
4 |
101,646,534 (GRCm39) |
missense |
probably benign |
0.14 |
R4929:Lepr
|
UTSW |
4 |
101,672,314 (GRCm39) |
missense |
probably benign |
0.00 |
R4939:Lepr
|
UTSW |
4 |
101,590,635 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5520:Lepr
|
UTSW |
4 |
101,602,734 (GRCm39) |
missense |
probably benign |
0.00 |
R5966:Lepr
|
UTSW |
4 |
101,649,324 (GRCm39) |
intron |
probably benign |
|
R6092:Lepr
|
UTSW |
4 |
101,649,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R6130:Lepr
|
UTSW |
4 |
101,622,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R6168:Lepr
|
UTSW |
4 |
101,592,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R6232:Lepr
|
UTSW |
4 |
101,671,588 (GRCm39) |
splice site |
probably null |
|
R6380:Lepr
|
UTSW |
4 |
101,622,151 (GRCm39) |
nonsense |
probably null |
|
R6427:Lepr
|
UTSW |
4 |
101,631,454 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6428:Lepr
|
UTSW |
4 |
101,637,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R6641:Lepr
|
UTSW |
4 |
101,622,502 (GRCm39) |
missense |
probably damaging |
0.97 |
R6650:Lepr
|
UTSW |
4 |
101,672,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6859:Lepr
|
UTSW |
4 |
101,622,487 (GRCm39) |
splice site |
probably null |
|
R7023:Lepr
|
UTSW |
4 |
101,646,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R7145:Lepr
|
UTSW |
4 |
101,609,394 (GRCm39) |
missense |
probably benign |
0.00 |
R7174:Lepr
|
UTSW |
4 |
101,607,535 (GRCm39) |
missense |
probably benign |
0.01 |
R7179:Lepr
|
UTSW |
4 |
101,602,856 (GRCm39) |
missense |
probably benign |
0.06 |
R7189:Lepr
|
UTSW |
4 |
101,671,961 (GRCm39) |
missense |
probably benign |
0.00 |
R7426:Lepr
|
UTSW |
4 |
101,602,853 (GRCm39) |
missense |
probably benign |
0.03 |
R7531:Lepr
|
UTSW |
4 |
101,609,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R7620:Lepr
|
UTSW |
4 |
101,609,270 (GRCm39) |
missense |
probably benign |
0.41 |
R7804:Lepr
|
UTSW |
4 |
101,639,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Lepr
|
UTSW |
4 |
101,639,754 (GRCm39) |
missense |
probably benign |
0.32 |
R8142:Lepr
|
UTSW |
4 |
101,622,616 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8227:Lepr
|
UTSW |
4 |
101,628,559 (GRCm39) |
missense |
probably damaging |
0.99 |
R8426:Lepr
|
UTSW |
4 |
101,671,841 (GRCm39) |
missense |
probably benign |
0.12 |
R8447:Lepr
|
UTSW |
4 |
101,671,688 (GRCm39) |
missense |
probably benign |
0.08 |
R8531:Lepr
|
UTSW |
4 |
101,622,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R8682:Lepr
|
UTSW |
4 |
101,649,269 (GRCm39) |
missense |
probably benign |
0.00 |
R8897:Lepr
|
UTSW |
4 |
101,649,233 (GRCm39) |
missense |
probably damaging |
0.98 |
R9096:Lepr
|
UTSW |
4 |
101,631,418 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9177:Lepr
|
UTSW |
4 |
101,602,798 (GRCm39) |
nonsense |
probably null |
|
R9241:Lepr
|
UTSW |
4 |
101,671,788 (GRCm39) |
missense |
probably benign |
|
R9604:Lepr
|
UTSW |
4 |
101,590,473 (GRCm39) |
missense |
probably benign |
0.01 |
R9711:Lepr
|
UTSW |
4 |
101,592,851 (GRCm39) |
nonsense |
probably null |
|
X0026:Lepr
|
UTSW |
4 |
101,590,524 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1176:Lepr
|
UTSW |
4 |
101,602,811 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Lepr
|
UTSW |
4 |
101,592,792 (GRCm39) |
missense |
probably damaging |
1.00 |
|