Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abitram |
T |
C |
4: 56,806,131 (GRCm39) |
V181A |
possibly damaging |
Het |
Aff4 |
T |
C |
11: 53,300,198 (GRCm39) |
|
probably benign |
Het |
Ap1g2 |
T |
C |
14: 55,338,104 (GRCm39) |
|
probably null |
Het |
Aspn |
A |
T |
13: 49,705,363 (GRCm39) |
Y75F |
possibly damaging |
Het |
Atm |
G |
A |
9: 53,359,453 (GRCm39) |
T2783I |
probably damaging |
Het |
Cacnb1 |
A |
T |
11: 97,913,199 (GRCm39) |
I18N |
probably damaging |
Het |
Casr |
T |
C |
16: 36,336,017 (GRCm39) |
I97M |
probably damaging |
Het |
Cnga2 |
T |
A |
X: 71,048,655 (GRCm39) |
|
probably benign |
Het |
Coasy |
T |
A |
11: 100,976,147 (GRCm39) |
L425Q |
probably damaging |
Het |
Cps1 |
A |
G |
1: 67,162,396 (GRCm39) |
T25A |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,006,772 (GRCm39) |
Y2181C |
probably benign |
Het |
Efna3 |
A |
C |
3: 89,222,749 (GRCm39) |
S230A |
probably damaging |
Het |
Eng |
A |
G |
2: 32,563,286 (GRCm39) |
I281V |
probably damaging |
Het |
Erlec1 |
T |
A |
11: 30,898,430 (GRCm39) |
R14* |
probably null |
Het |
Gbp9 |
C |
T |
5: 105,231,431 (GRCm39) |
|
probably benign |
Het |
Gzmg |
T |
C |
14: 56,394,160 (GRCm39) |
M245V |
probably damaging |
Het |
Kdm5a |
A |
G |
6: 120,341,680 (GRCm39) |
I36V |
probably damaging |
Het |
Krt87 |
A |
G |
15: 101,389,095 (GRCm39) |
V79A |
probably damaging |
Het |
Lmo4 |
T |
C |
3: 143,899,683 (GRCm39) |
S155G |
probably benign |
Het |
Mrpl44 |
G |
A |
1: 79,753,862 (GRCm39) |
V5I |
probably benign |
Het |
Mrpl49 |
T |
C |
19: 6,104,931 (GRCm39) |
T146A |
possibly damaging |
Het |
Mrpl58 |
T |
C |
11: 115,301,457 (GRCm39) |
|
probably benign |
Het |
Nab1 |
C |
T |
1: 52,529,292 (GRCm39) |
V202M |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,527,997 (GRCm39) |
M2229L |
probably benign |
Het |
Notch2 |
C |
T |
3: 98,024,013 (GRCm39) |
|
probably benign |
Het |
Nub1 |
A |
G |
5: 24,897,931 (GRCm39) |
I106V |
probably benign |
Het |
Prom1 |
A |
T |
5: 44,172,117 (GRCm39) |
S595T |
probably benign |
Het |
Rbfox1 |
T |
A |
16: 7,110,078 (GRCm39) |
S165R |
probably damaging |
Het |
Sipa1l2 |
G |
A |
8: 126,174,507 (GRCm39) |
T1257I |
probably damaging |
Het |
Smarcc2 |
T |
C |
10: 128,305,556 (GRCm39) |
S327P |
probably damaging |
Het |
Tdpoz1 |
T |
C |
3: 93,578,056 (GRCm39) |
M243V |
probably benign |
Het |
Ttn |
G |
T |
2: 76,549,289 (GRCm39) |
T23469K |
probably damaging |
Het |
Ube2u |
T |
C |
4: 100,339,971 (GRCm39) |
|
probably benign |
Het |
Umodl1 |
T |
C |
17: 31,208,462 (GRCm39) |
Y836H |
probably damaging |
Het |
Vmn2r45 |
A |
G |
7: 8,488,728 (GRCm39) |
Y101H |
probably benign |
Het |
Vps13a |
T |
A |
19: 16,697,772 (GRCm39) |
Q781L |
possibly damaging |
Het |
Vwce |
G |
A |
19: 10,625,858 (GRCm39) |
V457M |
probably damaging |
Het |
|
Other mutations in Limd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00953:Limd1
|
APN |
9 |
123,308,948 (GRCm39) |
missense |
probably benign |
0.31 |
IGL00972:Limd1
|
APN |
9 |
123,309,141 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01815:Limd1
|
APN |
9 |
123,308,801 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02598:Limd1
|
APN |
9 |
123,309,236 (GRCm39) |
missense |
probably benign |
|
IGL02598:Limd1
|
APN |
9 |
123,345,933 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02999:Limd1
|
APN |
9 |
123,345,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0314:Limd1
|
UTSW |
9 |
123,345,892 (GRCm39) |
missense |
probably benign |
0.04 |
R1612:Limd1
|
UTSW |
9 |
123,347,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R2009:Limd1
|
UTSW |
9 |
123,308,564 (GRCm39) |
missense |
probably benign |
|
R2299:Limd1
|
UTSW |
9 |
123,345,942 (GRCm39) |
nonsense |
probably null |
|
R3791:Limd1
|
UTSW |
9 |
123,309,439 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4453:Limd1
|
UTSW |
9 |
123,309,359 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5979:Limd1
|
UTSW |
9 |
123,308,479 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7493:Limd1
|
UTSW |
9 |
123,308,748 (GRCm39) |
missense |
probably benign |
0.00 |
R8101:Limd1
|
UTSW |
9 |
123,329,216 (GRCm39) |
nonsense |
probably null |
|
R8332:Limd1
|
UTSW |
9 |
123,308,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R9060:Limd1
|
UTSW |
9 |
123,309,514 (GRCm39) |
missense |
probably benign |
0.08 |
R9679:Limd1
|
UTSW |
9 |
123,308,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R9681:Limd1
|
UTSW |
9 |
123,345,903 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9726:Limd1
|
UTSW |
9 |
123,308,984 (GRCm39) |
missense |
probably benign |
0.00 |
X0028:Limd1
|
UTSW |
9 |
123,345,927 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Limd1
|
UTSW |
9 |
123,309,086 (GRCm39) |
missense |
probably damaging |
0.99 |
|