Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
C |
5: 8,957,278 (GRCm39) |
T136P |
probably damaging |
Het |
Abcc3 |
A |
T |
11: 94,254,886 (GRCm39) |
L639Q |
possibly damaging |
Het |
Adam10 |
T |
A |
9: 70,655,400 (GRCm39) |
N289K |
probably damaging |
Het |
Akap12 |
A |
G |
10: 4,306,289 (GRCm39) |
E1138G |
probably benign |
Het |
Akr1e1 |
C |
A |
13: 4,648,793 (GRCm39) |
L167F |
probably damaging |
Het |
Cars1 |
T |
C |
7: 143,123,766 (GRCm39) |
K506E |
possibly damaging |
Het |
Castor1 |
T |
C |
11: 4,170,165 (GRCm39) |
V81A |
probably damaging |
Het |
Cfap46 |
C |
A |
7: 139,260,902 (GRCm39) |
R65S |
possibly damaging |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Clec16a |
C |
A |
16: 10,559,487 (GRCm39) |
T920K |
probably benign |
Het |
Coro2b |
C |
T |
9: 62,333,842 (GRCm39) |
E351K |
probably damaging |
Het |
Diablo |
T |
C |
5: 123,655,829 (GRCm39) |
E163G |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,115,757 (GRCm39) |
L1547P |
probably damaging |
Het |
Dynll2 |
G |
T |
11: 87,874,719 (GRCm39) |
D37E |
probably benign |
Het |
Eml4 |
A |
T |
17: 83,755,656 (GRCm39) |
Q408L |
probably damaging |
Het |
F2rl3 |
T |
C |
8: 73,489,963 (GRCm39) |
*397R |
probably null |
Het |
Fance |
T |
A |
17: 28,545,155 (GRCm39) |
L127Q |
unknown |
Het |
Fat4 |
T |
C |
3: 39,033,824 (GRCm39) |
V2492A |
possibly damaging |
Het |
Ggta1 |
C |
T |
2: 35,292,573 (GRCm39) |
D245N |
probably damaging |
Het |
Gli1 |
T |
C |
10: 127,166,106 (GRCm39) |
N1049S |
probably benign |
Het |
Grin2c |
A |
G |
11: 115,148,215 (GRCm39) |
V354A |
probably benign |
Het |
Kank4 |
T |
A |
4: 98,666,729 (GRCm39) |
I573F |
probably damaging |
Het |
Kdm3a |
A |
G |
6: 71,588,881 (GRCm39) |
V376A |
probably benign |
Het |
Kndc1 |
T |
C |
7: 139,481,121 (GRCm39) |
V69A |
probably damaging |
Het |
Lcmt1 |
T |
A |
7: 123,020,825 (GRCm39) |
L250Q |
probably damaging |
Het |
Ldhb |
A |
T |
6: 142,444,356 (GRCm39) |
V99D |
probably damaging |
Het |
Lipe |
G |
T |
7: 25,080,017 (GRCm39) |
N710K |
probably damaging |
Het |
Med1 |
C |
A |
11: 98,060,240 (GRCm39) |
D230Y |
probably damaging |
Het |
Mpv17l |
T |
A |
16: 13,758,864 (GRCm39) |
I96K |
probably benign |
Het |
Obox1 |
A |
T |
7: 15,289,541 (GRCm39) |
Q110L |
probably damaging |
Het |
Or11h6 |
T |
C |
14: 50,880,008 (GRCm39) |
V84A |
probably benign |
Het |
Or4f4b |
T |
A |
2: 111,314,101 (GRCm39) |
Y137N |
probably damaging |
Het |
Or4k37 |
T |
A |
2: 111,159,307 (GRCm39) |
I181N |
possibly damaging |
Het |
Or5t16 |
T |
A |
2: 86,818,885 (GRCm39) |
I212F |
probably benign |
Het |
Or6c76 |
T |
G |
10: 129,612,371 (GRCm39) |
M211R |
possibly damaging |
Het |
Or9s14 |
C |
A |
1: 92,535,494 (GRCm39) |
|
probably benign |
Het |
Pah |
T |
C |
10: 87,417,827 (GRCm39) |
|
probably null |
Het |
Pate1 |
A |
T |
9: 35,597,631 (GRCm39) |
N40K |
probably benign |
Het |
Pclo |
C |
A |
5: 14,731,423 (GRCm39) |
D182E |
|
Het |
Prl7a2 |
A |
T |
13: 27,849,941 (GRCm39) |
S44T |
possibly damaging |
Het |
Pwp2 |
T |
A |
10: 78,007,873 (GRCm39) |
D894V |
probably benign |
Het |
Ripor2 |
T |
A |
13: 24,907,771 (GRCm39) |
L1014Q |
probably damaging |
Het |
Rpe |
G |
A |
1: 66,740,188 (GRCm39) |
|
probably null |
Het |
Sh2d3c |
A |
G |
2: 32,642,671 (GRCm39) |
T706A |
probably damaging |
Het |
Slc34a1 |
T |
C |
13: 24,006,309 (GRCm39) |
F445S |
possibly damaging |
Het |
Spata20 |
C |
A |
11: 94,373,080 (GRCm39) |
L515F |
probably damaging |
Het |
Tcf20 |
G |
A |
15: 82,737,437 (GRCm39) |
S1338F |
possibly damaging |
Het |
Tm9sf2 |
C |
A |
14: 122,377,180 (GRCm39) |
P236Q |
probably damaging |
Het |
Tmem135 |
T |
C |
7: 88,803,240 (GRCm39) |
Y311C |
probably damaging |
Het |
Tmem245 |
T |
C |
4: 56,906,261 (GRCm39) |
Q548R |
probably benign |
Het |
Tmem94 |
G |
T |
11: 115,688,023 (GRCm39) |
C1190F |
possibly damaging |
Het |
Tmem94 |
G |
A |
11: 115,688,696 (GRCm39) |
R1301H |
probably benign |
Het |
Zp3 |
G |
A |
5: 136,013,244 (GRCm39) |
G192E |
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 |
R5377:Lepr
|
UTSW |
4 |
101,672,216 (GRCm39) |
missense |
possibly damaging |
0.71 |
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 |
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 |
|