Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
T |
9: 57,161,292 (GRCm39) |
S152T |
probably benign |
Het |
Aass |
A |
G |
6: 23,093,901 (GRCm39) |
V140A |
probably damaging |
Het |
Add1 |
A |
G |
5: 34,776,740 (GRCm39) |
N32S |
probably null |
Het |
Agap2 |
T |
C |
10: 126,918,865 (GRCm39) |
S414P |
unknown |
Het |
Arhgef38 |
A |
G |
3: 132,846,638 (GRCm39) |
F376L |
probably benign |
Het |
Cd22 |
A |
T |
7: 30,577,127 (GRCm39) |
I60N |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,274,626 (GRCm39) |
D488V |
probably damaging |
Het |
Cfap251 |
G |
A |
5: 123,392,729 (GRCm39) |
|
probably benign |
Het |
Cox16 |
T |
G |
12: 81,519,115 (GRCm39) |
D148A |
probably damaging |
Het |
Dclre1b |
G |
A |
3: 103,715,471 (GRCm39) |
T9I |
probably damaging |
Het |
Dennd4c |
T |
C |
4: 86,743,686 (GRCm39) |
V1176A |
probably benign |
Het |
Echdc1 |
A |
C |
10: 29,220,522 (GRCm39) |
|
probably null |
Het |
Efcab3 |
A |
G |
11: 104,784,533 (GRCm39) |
K2772E |
probably benign |
Het |
Efnb3 |
G |
A |
11: 69,446,966 (GRCm39) |
A248V |
probably benign |
Het |
Glud1 |
A |
G |
14: 34,033,173 (GRCm39) |
R107G |
probably benign |
Het |
Gtf2h4 |
A |
G |
17: 35,980,647 (GRCm39) |
S279P |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,791,402 (GRCm39) |
C2579R |
probably damaging |
Het |
Igkv15-103 |
A |
G |
6: 68,414,441 (GRCm39) |
|
probably benign |
Het |
Ivl |
CCTGCTGCTGCTGCT |
CCTGCTGCTGCT |
3: 92,479,217 (GRCm39) |
|
probably benign |
Het |
Krtap5-2 |
T |
C |
7: 141,729,119 (GRCm39) |
|
probably benign |
Het |
Lrrtm3 |
G |
A |
10: 63,765,943 (GRCm39) |
T548M |
probably benign |
Het |
Map3k2 |
A |
T |
18: 32,345,023 (GRCm39) |
T283S |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,872,493 (GRCm39) |
K2292E |
possibly damaging |
Het |
Med23 |
G |
T |
10: 24,764,311 (GRCm39) |
C98F |
probably damaging |
Het |
Morc1 |
T |
A |
16: 48,257,652 (GRCm39) |
F26Y |
probably damaging |
Het |
Muc5ac |
T |
A |
7: 141,366,416 (GRCm39) |
M2160K |
probably benign |
Het |
Myocd |
T |
C |
11: 65,109,396 (GRCm39) |
|
probably null |
Het |
Nup160 |
T |
A |
2: 90,542,279 (GRCm39) |
|
probably null |
Het |
Obi1 |
A |
G |
14: 104,716,313 (GRCm39) |
S687P |
probably damaging |
Het |
Olr1 |
A |
T |
6: 129,470,522 (GRCm39) |
L215Q |
probably benign |
Het |
Or5ak23 |
T |
A |
2: 85,245,031 (GRCm39) |
Q64L |
probably damaging |
Het |
Or6c216 |
T |
A |
10: 129,678,477 (GRCm39) |
S145C |
probably benign |
Het |
Pik3c2a |
T |
C |
7: 115,947,440 (GRCm39) |
K1414R |
possibly damaging |
Het |
Ppfibp2 |
T |
C |
7: 107,280,976 (GRCm39) |
V96A |
probably benign |
Het |
Prim1 |
T |
A |
10: 127,859,704 (GRCm39) |
Y299N |
probably damaging |
Het |
Rsf1 |
T |
C |
7: 97,311,141 (GRCm39) |
S624P |
probably benign |
Het |
Samd4b |
A |
T |
7: 28,101,018 (GRCm39) |
I687N |
probably damaging |
Het |
Sbf2 |
A |
T |
7: 109,971,830 (GRCm39) |
F801L |
probably damaging |
Het |
St6gal2 |
T |
C |
17: 55,789,014 (GRCm39) |
I16T |
probably damaging |
Het |
Tiam2 |
CGGG |
CGGGG |
17: 3,464,897 (GRCm39) |
|
probably null |
Het |
Trim8 |
T |
G |
19: 46,503,797 (GRCm39) |
S450A |
probably benign |
Het |
Trp53bp2 |
A |
G |
1: 182,276,562 (GRCm39) |
T848A |
probably benign |
Het |
Vmn2r24 |
A |
G |
6: 123,783,368 (GRCm39) |
S523G |
possibly damaging |
Het |
Vmn2r52 |
T |
A |
7: 9,902,926 (GRCm39) |
M501L |
probably benign |
Het |
Vmn2r68 |
C |
T |
7: 84,883,048 (GRCm39) |
V235M |
possibly damaging |
Het |
Zfhx3 |
G |
A |
8: 109,673,251 (GRCm39) |
V1434M |
probably damaging |
Het |
Zmym5 |
A |
T |
14: 57,031,622 (GRCm39) |
N495K |
possibly damaging |
Het |
|
Other mutations in Lcn11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02904:Lcn11
|
APN |
2 |
25,669,278 (GRCm39) |
missense |
probably null |
0.00 |
R0220:Lcn11
|
UTSW |
2 |
25,667,843 (GRCm39) |
missense |
probably benign |
0.02 |
R0607:Lcn11
|
UTSW |
2 |
25,669,305 (GRCm39) |
missense |
probably benign |
0.00 |
R1104:Lcn11
|
UTSW |
2 |
25,669,115 (GRCm39) |
unclassified |
probably benign |
|
R2021:Lcn11
|
UTSW |
2 |
25,668,097 (GRCm39) |
missense |
probably benign |
0.34 |
R2331:Lcn11
|
UTSW |
2 |
25,670,188 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4295:Lcn11
|
UTSW |
2 |
25,668,111 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6109:Lcn11
|
UTSW |
2 |
25,669,308 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6502:Lcn11
|
UTSW |
2 |
25,669,103 (GRCm39) |
missense |
probably benign |
0.08 |
R7754:Lcn11
|
UTSW |
2 |
25,667,830 (GRCm39) |
missense |
probably benign |
0.06 |
R7920:Lcn11
|
UTSW |
2 |
25,669,343 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8389:Lcn11
|
UTSW |
2 |
25,669,043 (GRCm39) |
missense |
probably damaging |
0.97 |
R8752:Lcn11
|
UTSW |
2 |
25,668,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R8765:Lcn11
|
UTSW |
2 |
25,668,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Lcn11
|
UTSW |
2 |
25,669,296 (GRCm39) |
missense |
probably benign |
0.33 |
R8954:Lcn11
|
UTSW |
2 |
25,669,265 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Lcn11
|
UTSW |
2 |
25,667,736 (GRCm39) |
missense |
probably benign |
0.00 |
|