Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930009A15Rik |
A |
T |
10: 115,415,717 (GRCm39) |
|
probably benign |
Het |
Acaa2 |
T |
C |
18: 74,937,223 (GRCm39) |
L369S |
probably damaging |
Het |
Akna |
A |
G |
4: 63,313,140 (GRCm39) |
S328P |
probably damaging |
Het |
Albfm1 |
A |
G |
5: 90,719,546 (GRCm39) |
Y214C |
probably damaging |
Het |
Apc |
A |
G |
18: 34,354,140 (GRCm39) |
|
probably benign |
Het |
Brca2 |
C |
T |
5: 150,466,716 (GRCm39) |
T2160I |
probably damaging |
Het |
Camsap2 |
A |
G |
1: 136,204,330 (GRCm39) |
S1251P |
probably damaging |
Het |
Ccdc110 |
A |
G |
8: 46,395,573 (GRCm39) |
E488G |
probably damaging |
Het |
Ccdc158 |
T |
A |
5: 92,797,908 (GRCm39) |
I411F |
probably damaging |
Het |
Cd163 |
C |
T |
6: 124,297,595 (GRCm39) |
Q914* |
probably null |
Het |
Cd22 |
T |
C |
7: 30,566,083 (GRCm39) |
D827G |
probably damaging |
Het |
Ces1e |
A |
G |
8: 93,946,001 (GRCm39) |
|
probably null |
Het |
Col14a1 |
T |
C |
15: 55,315,779 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
A |
15: 47,713,135 (GRCm39) |
D1509V |
probably damaging |
Het |
Ddx51 |
A |
G |
5: 110,804,717 (GRCm39) |
D543G |
probably damaging |
Het |
Diaph3 |
T |
A |
14: 87,222,261 (GRCm39) |
I408F |
probably damaging |
Het |
Dld |
G |
A |
12: 31,390,325 (GRCm39) |
P213L |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,037,262 (GRCm39) |
T3327A |
probably benign |
Het |
Dnttip2 |
T |
A |
3: 122,078,817 (GRCm39) |
|
probably benign |
Het |
Dock10 |
T |
C |
1: 80,546,225 (GRCm39) |
E791G |
possibly damaging |
Het |
Ehd3 |
G |
T |
17: 74,134,356 (GRCm39) |
W238C |
probably damaging |
Het |
Ehd3 |
T |
G |
17: 74,134,361 (GRCm39) |
L240R |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,824,766 (GRCm39) |
V2357A |
unknown |
Het |
Fam20c |
T |
C |
5: 138,741,932 (GRCm39) |
V181A |
probably damaging |
Het |
Gm4781 |
T |
C |
10: 100,232,814 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch8 |
A |
T |
11: 102,371,058 (GRCm39) |
S827T |
unknown |
Het |
Grm3 |
A |
T |
5: 9,561,930 (GRCm39) |
I640N |
probably damaging |
Het |
Gstm7 |
A |
G |
3: 107,838,747 (GRCm39) |
|
probably benign |
Het |
Hdac7 |
G |
T |
15: 97,700,372 (GRCm39) |
H572Q |
probably damaging |
Het |
Ift140 |
C |
T |
17: 25,313,735 (GRCm39) |
Q1389* |
probably null |
Het |
Igfn1 |
A |
G |
1: 135,893,152 (GRCm39) |
V2099A |
probably damaging |
Het |
Ik |
A |
G |
18: 36,888,531 (GRCm39) |
N443S |
possibly damaging |
Het |
Impact |
A |
G |
18: 13,123,601 (GRCm39) |
K315E |
probably benign |
Het |
Insr |
C |
A |
8: 3,308,697 (GRCm39) |
R113L |
probably benign |
Het |
Jak2 |
T |
A |
19: 29,260,954 (GRCm39) |
Y317N |
possibly damaging |
Het |
Kif18a |
T |
A |
2: 109,122,411 (GRCm39) |
V162E |
probably damaging |
Het |
L3mbtl3 |
A |
G |
10: 26,207,762 (GRCm39) |
V319A |
unknown |
Het |
Lmo7 |
C |
T |
14: 102,137,938 (GRCm39) |
T647I |
possibly damaging |
Het |
Mindy3 |
C |
T |
2: 12,405,854 (GRCm39) |
R147Q |
probably benign |
Het |
Mtr |
T |
C |
13: 12,230,453 (GRCm39) |
|
probably null |
Het |
Muc4 |
A |
T |
16: 32,576,652 (GRCm39) |
|
probably benign |
Het |
Nrip1 |
G |
A |
16: 76,090,471 (GRCm39) |
T362M |
possibly damaging |
Het |
Or1j17 |
G |
T |
2: 36,578,074 (GRCm39) |
R20L |
probably null |
Het |
Or1q1 |
T |
C |
2: 36,886,957 (GRCm39) |
I45T |
possibly damaging |
Het |
Or5d45 |
A |
G |
2: 88,153,222 (GRCm39) |
S276P |
probably benign |
Het |
Ovol1 |
G |
A |
19: 5,601,630 (GRCm39) |
R131C |
probably damaging |
Het |
Pcca |
T |
C |
14: 122,905,998 (GRCm39) |
V323A |
probably damaging |
Het |
Pcdhb14 |
A |
T |
18: 37,581,295 (GRCm39) |
M134L |
probably benign |
Het |
Pecam1 |
G |
A |
11: 106,581,887 (GRCm39) |
T252M |
probably benign |
Het |
Rnd3 |
T |
A |
2: 51,022,536 (GRCm39) |
I169F |
probably damaging |
Het |
Rnmt |
T |
A |
18: 68,444,689 (GRCm39) |
D219E |
probably benign |
Het |
Rufy1 |
A |
T |
11: 50,292,315 (GRCm39) |
F491L |
probably benign |
Het |
Ryr2 |
G |
T |
13: 11,677,124 (GRCm39) |
C3242* |
probably null |
Het |
Smurf2 |
G |
T |
11: 106,766,727 (GRCm39) |
R31S |
possibly damaging |
Het |
Sptbn1 |
A |
G |
11: 30,074,873 (GRCm39) |
I1333T |
probably damaging |
Het |
Stard9 |
G |
A |
2: 120,527,580 (GRCm39) |
C1279Y |
probably damaging |
Het |
Sugp2 |
T |
C |
8: 70,704,753 (GRCm39) |
|
probably null |
Het |
Sulf1 |
A |
T |
1: 12,929,636 (GRCm39) |
D301V |
probably benign |
Het |
Tbcd |
G |
T |
11: 121,492,737 (GRCm39) |
|
probably benign |
Het |
Tlr11 |
T |
C |
14: 50,599,712 (GRCm39) |
I566T |
probably benign |
Het |
Tm9sf2 |
T |
A |
14: 122,374,921 (GRCm39) |
|
probably benign |
Het |
Tnfaip8l1 |
T |
C |
17: 56,478,799 (GRCm39) |
F30L |
probably benign |
Het |
Trav15-2-dv6-2 |
T |
A |
14: 53,887,433 (GRCm39) |
C118S |
probably damaging |
Het |
Ttc13 |
A |
G |
8: 125,408,959 (GRCm39) |
|
probably benign |
Het |
Ubqln3 |
A |
T |
7: 103,790,906 (GRCm39) |
S395T |
probably benign |
Het |
Urb2 |
A |
G |
8: 124,754,827 (GRCm39) |
D178G |
probably benign |
Het |
Usf3 |
A |
G |
16: 44,041,222 (GRCm39) |
I1901V |
probably benign |
Het |
Vmn1r173 |
A |
T |
7: 23,402,112 (GRCm39) |
I116F |
probably benign |
Het |
Vmn1r69 |
T |
A |
7: 10,314,717 (GRCm39) |
T5S |
probably benign |
Het |
Wbp1l |
C |
T |
19: 46,642,619 (GRCm39) |
R191* |
probably null |
Het |
Wfikkn2 |
C |
T |
11: 94,129,688 (GRCm39) |
R151H |
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 |
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 |
|