Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
T |
A |
4: 144,504,594 (GRCm39) |
T186S |
probably benign |
Het |
AI467606 |
C |
T |
7: 126,691,998 (GRCm39) |
P191L |
probably benign |
Het |
Aoc1l1 |
C |
A |
6: 48,952,728 (GRCm39) |
Q218K |
possibly damaging |
Het |
Arl9 |
T |
C |
5: 77,154,440 (GRCm39) |
V56A |
probably damaging |
Het |
Cacng5 |
T |
C |
11: 107,768,248 (GRCm39) |
Q253R |
probably benign |
Het |
Cc2d1b |
T |
C |
4: 108,483,556 (GRCm39) |
M331T |
possibly damaging |
Het |
Cep97 |
A |
G |
16: 55,735,659 (GRCm39) |
S380P |
probably benign |
Het |
Clpx |
A |
T |
9: 65,224,730 (GRCm39) |
K153* |
probably null |
Het |
Dclk2 |
A |
G |
3: 86,827,147 (GRCm39) |
S111P |
probably damaging |
Het |
E2f7 |
A |
G |
10: 110,595,806 (GRCm39) |
E167G |
probably damaging |
Het |
Edn1 |
T |
C |
13: 42,455,436 (GRCm39) |
|
probably null |
Het |
Farp1 |
C |
T |
14: 121,472,489 (GRCm39) |
P208L |
probably damaging |
Het |
Fbxw18 |
G |
T |
9: 109,520,589 (GRCm39) |
H257N |
probably benign |
Het |
Ftsj3 |
T |
C |
11: 106,146,414 (GRCm39) |
T22A |
probably benign |
Het |
Gm17019 |
A |
T |
5: 15,082,819 (GRCm39) |
M45K |
possibly damaging |
Het |
Gpr162 |
T |
C |
6: 124,837,876 (GRCm39) |
D258G |
probably damaging |
Het |
Grk1 |
T |
A |
8: 13,459,305 (GRCm39) |
D285E |
probably benign |
Het |
Herc6 |
A |
T |
6: 57,624,105 (GRCm39) |
D625V |
possibly damaging |
Het |
Igkv1-135 |
C |
T |
6: 67,587,324 (GRCm39) |
P65L |
possibly damaging |
Het |
Nphp3 |
A |
G |
9: 103,901,872 (GRCm39) |
S689G |
probably benign |
Het |
Or14c44 |
T |
A |
7: 86,062,064 (GRCm39) |
S165T |
probably benign |
Het |
Or5w20 |
T |
C |
2: 87,726,753 (GRCm39) |
|
probably benign |
Het |
Phf8-ps |
A |
G |
17: 33,284,367 (GRCm39) |
Y812H |
probably benign |
Het |
Plxnb2 |
T |
G |
15: 89,051,746 (GRCm39) |
T158P |
possibly damaging |
Het |
Pramel32 |
A |
C |
4: 88,548,277 (GRCm39) |
S43A |
probably damaging |
Het |
R3hcc1 |
T |
A |
14: 69,936,057 (GRCm39) |
K437* |
probably null |
Het |
Rnf213 |
C |
A |
11: 119,324,325 (GRCm39) |
H1428Q |
probably damaging |
Het |
Ro60 |
A |
T |
1: 143,646,509 (GRCm39) |
S79T |
probably benign |
Het |
Spata31e2 |
A |
T |
1: 26,724,900 (GRCm39) |
N93K |
probably benign |
Het |
Ssx2ip |
G |
A |
3: 146,143,066 (GRCm39) |
R548H |
probably benign |
Het |
Trim23 |
C |
T |
13: 104,324,035 (GRCm39) |
R165C |
probably damaging |
Het |
Ulk2 |
T |
G |
11: 61,698,970 (GRCm39) |
T405P |
probably damaging |
Het |
Unkl |
G |
A |
17: 25,424,584 (GRCm39) |
V204I |
probably damaging |
Het |
Vmn1r43 |
T |
C |
6: 89,846,728 (GRCm39) |
T253A |
probably damaging |
Het |
Zfp534 |
T |
C |
4: 147,759,887 (GRCm39) |
I261V |
possibly 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 |
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 |
|