Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp13a5 |
C |
T |
16: 29,133,422 (GRCm39) |
V410M |
probably benign |
Het |
Cdkn2aip |
G |
T |
8: 48,166,653 (GRCm39) |
D51E |
probably benign |
Het |
Chd6 |
A |
G |
2: 160,802,282 (GRCm39) |
V2184A |
probably benign |
Het |
Clcn1 |
C |
T |
6: 42,288,153 (GRCm39) |
T797I |
probably benign |
Het |
Cntnap4 |
A |
G |
8: 113,500,208 (GRCm39) |
D500G |
probably benign |
Het |
Cog5 |
A |
T |
12: 31,944,037 (GRCm39) |
I641F |
possibly damaging |
Het |
Cr2 |
A |
T |
1: 194,852,067 (GRCm39) |
V94E |
probably damaging |
Het |
Creg2 |
T |
G |
1: 39,689,915 (GRCm39) |
D65A |
probably damaging |
Het |
Dennd4a |
A |
G |
9: 64,795,808 (GRCm39) |
R711G |
possibly damaging |
Het |
Efr3b |
A |
G |
12: 4,034,648 (GRCm39) |
V58A |
probably damaging |
Het |
Fbxo3 |
A |
G |
2: 103,880,639 (GRCm39) |
T250A |
probably damaging |
Het |
Fzr1 |
T |
C |
10: 81,205,018 (GRCm39) |
T300A |
probably benign |
Het |
Gabrg1 |
A |
T |
5: 70,935,474 (GRCm39) |
Y227N |
possibly damaging |
Het |
Gins3 |
A |
G |
8: 96,369,903 (GRCm39) |
I197V |
probably benign |
Het |
Gm17079 |
T |
C |
14: 51,930,420 (GRCm39) |
T142A |
possibly damaging |
Het |
Gna15 |
T |
C |
10: 81,338,879 (GRCm39) |
Y320C |
probably damaging |
Het |
H2-T5 |
C |
A |
17: 36,479,001 (GRCm39) |
D83Y |
probably damaging |
Het |
Hibch |
G |
A |
1: 52,959,539 (GRCm39) |
|
probably benign |
Het |
Kif5b |
G |
A |
18: 6,222,767 (GRCm39) |
R355W |
probably damaging |
Het |
Klf1 |
T |
C |
8: 85,629,561 (GRCm39) |
S129P |
probably benign |
Het |
Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
Nat8f5 |
A |
G |
6: 85,794,640 (GRCm39) |
S107P |
probably damaging |
Het |
Or2t49 |
A |
G |
11: 58,392,581 (GRCm39) |
L267P |
possibly damaging |
Het |
Or8g24 |
T |
A |
9: 38,989,258 (GRCm39) |
Q261L |
probably damaging |
Het |
Or8g24 |
C |
A |
9: 38,989,257 (GRCm39) |
Q261H |
probably benign |
Het |
Pcdhb18 |
G |
A |
18: 37,622,674 (GRCm39) |
M1I |
probably null |
Het |
Plcb3 |
A |
G |
19: 6,932,420 (GRCm39) |
F1080L |
probably benign |
Het |
Polr2g |
T |
C |
19: 8,775,669 (GRCm39) |
H14R |
probably damaging |
Het |
Rp1l1 |
A |
G |
14: 64,266,889 (GRCm39) |
D825G |
probably benign |
Het |
Scn3a |
G |
A |
2: 65,367,016 (GRCm39) |
A2V |
probably damaging |
Het |
Slc25a54 |
T |
C |
3: 108,993,046 (GRCm39) |
|
probably benign |
Het |
Smad9 |
C |
A |
3: 54,696,636 (GRCm39) |
Q234K |
probably benign |
Het |
Tie1 |
T |
C |
4: 118,330,025 (GRCm39) |
Y1066C |
probably damaging |
Het |
Traf1 |
T |
C |
2: 34,838,484 (GRCm39) |
E118G |
probably benign |
Het |
Ttc21b |
T |
C |
2: 66,068,192 (GRCm39) |
D278G |
possibly damaging |
Het |
Uaca |
C |
A |
9: 60,761,600 (GRCm39) |
T204K |
probably damaging |
Het |
Utrn |
A |
T |
10: 12,401,096 (GRCm39) |
Y154N |
probably benign |
Het |
Virma |
A |
G |
4: 11,518,984 (GRCm39) |
T694A |
probably benign |
Het |
Vmn2r50 |
T |
C |
7: 9,779,929 (GRCm39) |
D500G |
probably damaging |
Het |
Vmn2r59 |
T |
A |
7: 41,693,253 (GRCm39) |
H449L |
probably benign |
Het |
|
Other mutations in Cldn23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01667:Cldn23
|
APN |
8 |
36,293,074 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01767:Cldn23
|
APN |
8 |
36,292,816 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02078:Cldn23
|
APN |
8 |
36,293,359 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1610:Cldn23
|
UTSW |
8 |
36,293,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Cldn23
|
UTSW |
8 |
36,293,140 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1915:Cldn23
|
UTSW |
8 |
36,293,099 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2121:Cldn23
|
UTSW |
8 |
36,293,389 (GRCm39) |
missense |
probably benign |
|
R4342:Cldn23
|
UTSW |
8 |
36,292,652 (GRCm39) |
missense |
probably benign |
0.00 |
R5167:Cldn23
|
UTSW |
8 |
36,293,474 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5207:Cldn23
|
UTSW |
8 |
36,293,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R6102:Cldn23
|
UTSW |
8 |
36,292,705 (GRCm39) |
missense |
probably benign |
0.00 |
R7106:Cldn23
|
UTSW |
8 |
36,293,069 (GRCm39) |
missense |
probably benign |
|
R7363:Cldn23
|
UTSW |
8 |
36,292,659 (GRCm39) |
critical splice donor site |
probably null |
|
R7721:Cldn23
|
UTSW |
8 |
36,293,417 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8119:Cldn23
|
UTSW |
8 |
36,293,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R9011:Cldn23
|
UTSW |
8 |
36,292,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R9504:Cldn23
|
UTSW |
8 |
36,293,470 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cldn23
|
UTSW |
8 |
36,293,431 (GRCm39) |
missense |
probably damaging |
0.99 |
|