Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
G |
11: 109,846,002 (GRCm39) |
C811R |
possibly damaging |
Het |
Acvr1 |
G |
A |
2: 58,367,808 (GRCm39) |
Q118* |
probably null |
Het |
Als2 |
A |
G |
1: 59,250,296 (GRCm39) |
S483P |
probably damaging |
Het |
Ankrd40 |
T |
C |
11: 94,224,771 (GRCm39) |
V60A |
possibly damaging |
Het |
Armc2 |
C |
T |
10: 41,842,696 (GRCm39) |
|
probably null |
Het |
Atp12a |
A |
G |
14: 56,624,407 (GRCm39) |
R952G |
possibly damaging |
Het |
Atp13a2 |
T |
C |
4: 140,730,294 (GRCm39) |
I773T |
probably benign |
Het |
Atp6v1g1 |
A |
G |
4: 63,468,258 (GRCm39) |
Y87C |
probably benign |
Het |
Ccdc162 |
G |
T |
10: 41,531,095 (GRCm39) |
T537N |
possibly damaging |
Het |
Ccdc59 |
A |
T |
10: 105,677,388 (GRCm39) |
K9M |
possibly damaging |
Het |
Cd101 |
A |
T |
3: 100,911,164 (GRCm39) |
D831E |
probably benign |
Het |
Ch25h |
T |
A |
19: 34,452,210 (GRCm39) |
H106L |
probably benign |
Het |
Cimap1d |
G |
A |
10: 79,481,487 (GRCm39) |
T14I |
probably benign |
Het |
Csmd2 |
T |
C |
4: 128,451,511 (GRCm39) |
F113S |
unknown |
Het |
Cyp4a14 |
C |
A |
4: 115,344,498 (GRCm39) |
G456W |
probably damaging |
Het |
Cyp4a30b |
A |
G |
4: 115,315,559 (GRCm39) |
H260R |
possibly damaging |
Het |
Dennd2b |
A |
T |
7: 109,156,637 (GRCm39) |
Y38N |
probably benign |
Het |
Eif4enif1 |
C |
T |
11: 3,192,586 (GRCm39) |
P805S |
probably damaging |
Het |
Fan1 |
A |
G |
7: 64,012,938 (GRCm39) |
I668T |
probably benign |
Het |
Flnc |
A |
G |
6: 29,447,542 (GRCm39) |
D1115G |
probably damaging |
Het |
Ftdc1 |
A |
T |
16: 58,434,342 (GRCm39) |
I125K |
probably benign |
Het |
Gbp11 |
C |
T |
5: 105,478,866 (GRCm39) |
D191N |
probably benign |
Het |
Gm5519 |
A |
C |
19: 33,802,410 (GRCm39) |
D151A |
possibly damaging |
Het |
Grid2ip |
C |
A |
5: 143,343,684 (GRCm39) |
Q127K |
probably benign |
Het |
Hdhd2 |
T |
C |
18: 77,042,702 (GRCm39) |
F44L |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,614,467 (GRCm39) |
V1313D |
possibly damaging |
Het |
Kpna7 |
T |
C |
5: 144,930,745 (GRCm39) |
T367A |
probably benign |
Het |
Matr3 |
T |
A |
18: 35,705,349 (GRCm39) |
S91R |
probably benign |
Het |
Mdm1 |
A |
G |
10: 117,986,847 (GRCm39) |
T267A |
probably benign |
Het |
Mlxip |
A |
G |
5: 123,590,730 (GRCm39) |
M878V |
probably benign |
Het |
Mtor |
T |
A |
4: 148,624,487 (GRCm39) |
M2089K |
probably benign |
Het |
Myo9b |
G |
A |
8: 71,786,981 (GRCm39) |
R721Q |
probably benign |
Het |
Ndufs1 |
A |
G |
1: 63,203,882 (GRCm39) |
|
probably benign |
Het |
Nlrp4b |
C |
T |
7: 10,444,170 (GRCm39) |
Q40* |
probably null |
Het |
Nomo1 |
C |
A |
7: 45,696,361 (GRCm39) |
T293N |
probably damaging |
Het |
Notch1 |
A |
G |
2: 26,350,247 (GRCm39) |
C2298R |
possibly damaging |
Het |
Notum |
A |
G |
11: 120,551,022 (GRCm39) |
V48A |
probably benign |
Het |
Or10g1 |
T |
G |
14: 52,648,318 (GRCm39) |
T4P |
probably benign |
Het |
Or10z1 |
T |
C |
1: 174,078,092 (GRCm39) |
S134G |
probably benign |
Het |
Or6c211 |
A |
T |
10: 129,505,628 (GRCm39) |
C253* |
probably null |
Het |
Ostc |
T |
C |
3: 130,497,157 (GRCm39) |
N80S |
probably damaging |
Het |
Palmd |
T |
C |
3: 116,717,400 (GRCm39) |
R366G |
possibly damaging |
Het |
Parp1 |
A |
G |
1: 180,401,230 (GRCm39) |
D45G |
probably damaging |
Het |
Pcdhga9 |
T |
A |
18: 37,870,524 (GRCm39) |
Y118N |
possibly damaging |
Het |
Pes1 |
C |
A |
11: 3,926,834 (GRCm39) |
T372K |
probably benign |
Het |
Plcl1 |
A |
T |
1: 55,736,309 (GRCm39) |
D550V |
probably benign |
Het |
Plekhg5 |
T |
A |
4: 152,191,960 (GRCm39) |
C433S |
probably benign |
Het |
Plin2 |
A |
G |
4: 86,586,915 (GRCm39) |
M1T |
probably null |
Het |
Pms2 |
G |
A |
5: 143,848,732 (GRCm39) |
|
probably benign |
Het |
Ppp1r7 |
T |
A |
1: 93,285,585 (GRCm39) |
|
probably null |
Het |
Psmb8 |
T |
C |
17: 34,419,144 (GRCm39) |
I146T |
probably damaging |
Het |
Ptger4 |
T |
C |
15: 5,264,286 (GRCm39) |
R457G |
probably benign |
Het |
Pzp |
A |
T |
6: 128,462,519 (GRCm39) |
|
probably null |
Het |
Ralgds |
A |
G |
2: 28,438,781 (GRCm39) |
|
probably null |
Het |
Rnf6 |
T |
C |
5: 146,147,215 (GRCm39) |
Y601C |
probably benign |
Het |
Sgk2 |
A |
G |
2: 162,836,449 (GRCm39) |
|
probably benign |
Het |
Shoc1 |
A |
C |
4: 59,093,850 (GRCm39) |
L226R |
probably damaging |
Het |
Slc39a8 |
T |
A |
3: 135,592,554 (GRCm39) |
|
probably null |
Het |
Slc4a4 |
G |
T |
5: 89,283,623 (GRCm39) |
V481L |
probably damaging |
Het |
Slc5a8 |
A |
G |
10: 88,740,825 (GRCm39) |
I247V |
probably benign |
Het |
Slit3 |
G |
T |
11: 35,435,620 (GRCm39) |
E184* |
probably null |
Het |
Sppl2c |
C |
T |
11: 104,078,141 (GRCm39) |
P314S |
probably benign |
Het |
St7 |
C |
T |
6: 17,819,276 (GRCm39) |
P60L |
probably damaging |
Het |
Tafa2 |
A |
T |
10: 123,540,270 (GRCm39) |
H42L |
possibly damaging |
Het |
Tbc1d8 |
A |
G |
1: 39,444,398 (GRCm39) |
F187S |
probably damaging |
Het |
Tet2 |
C |
T |
3: 133,192,715 (GRCm39) |
G573E |
probably damaging |
Het |
Tnni3k |
C |
T |
3: 154,644,387 (GRCm39) |
|
probably null |
Het |
Trpa1 |
A |
G |
1: 14,957,844 (GRCm39) |
C705R |
probably damaging |
Het |
Usp9y |
T |
A |
Y: 1,310,502 (GRCm39) |
|
probably benign |
Het |
Vmn2r68 |
A |
C |
7: 84,882,834 (GRCm39) |
M306R |
probably benign |
Het |
Vwa7 |
G |
A |
17: 35,240,218 (GRCm39) |
M395I |
probably damaging |
Het |
Ybx3 |
G |
A |
6: 131,347,376 (GRCm39) |
A253V |
probably damaging |
Het |
Zfp53 |
A |
T |
17: 21,728,340 (GRCm39) |
E124D |
probably benign |
Het |
|
Other mutations in Chek2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01025:Chek2
|
APN |
5 |
110,996,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01830:Chek2
|
APN |
5 |
111,021,374 (GRCm39) |
missense |
probably benign |
|
IGL01943:Chek2
|
APN |
5 |
110,989,093 (GRCm39) |
unclassified |
probably benign |
|
IGL02319:Chek2
|
APN |
5 |
111,014,877 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03147:Chek2
|
UTSW |
5 |
110,996,536 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Chek2
|
UTSW |
5 |
111,011,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Chek2
|
UTSW |
5 |
110,996,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R1486:Chek2
|
UTSW |
5 |
110,989,093 (GRCm39) |
unclassified |
probably benign |
|
R1732:Chek2
|
UTSW |
5 |
111,019,968 (GRCm39) |
missense |
probably benign |
0.26 |
R2041:Chek2
|
UTSW |
5 |
110,996,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R2071:Chek2
|
UTSW |
5 |
110,989,112 (GRCm39) |
unclassified |
probably benign |
|
R2935:Chek2
|
UTSW |
5 |
111,015,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R3899:Chek2
|
UTSW |
5 |
111,013,479 (GRCm39) |
splice site |
probably benign |
|
R4662:Chek2
|
UTSW |
5 |
111,014,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:Chek2
|
UTSW |
5 |
111,003,705 (GRCm39) |
splice site |
probably null |
|
R5358:Chek2
|
UTSW |
5 |
110,989,148 (GRCm39) |
unclassified |
probably benign |
|
R5582:Chek2
|
UTSW |
5 |
111,015,901 (GRCm39) |
missense |
probably damaging |
0.96 |
R5594:Chek2
|
UTSW |
5 |
111,003,700 (GRCm39) |
critical splice donor site |
probably null |
|
R6526:Chek2
|
UTSW |
5 |
110,996,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R6972:Chek2
|
UTSW |
5 |
111,003,705 (GRCm39) |
splice site |
probably null |
|
R7232:Chek2
|
UTSW |
5 |
111,008,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7338:Chek2
|
UTSW |
5 |
111,021,380 (GRCm39) |
missense |
probably benign |
|
R7395:Chek2
|
UTSW |
5 |
111,019,974 (GRCm39) |
critical splice donor site |
probably null |
|
R7714:Chek2
|
UTSW |
5 |
110,989,319 (GRCm39) |
missense |
probably benign |
0.10 |
R7743:Chek2
|
UTSW |
5 |
110,987,916 (GRCm39) |
critical splice donor site |
probably null |
|
R8290:Chek2
|
UTSW |
5 |
111,008,766 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8297:Chek2
|
UTSW |
5 |
110,996,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R8719:Chek2
|
UTSW |
5 |
111,014,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R8898:Chek2
|
UTSW |
5 |
111,011,175 (GRCm39) |
missense |
probably benign |
0.00 |
R8906:Chek2
|
UTSW |
5 |
111,013,458 (GRCm39) |
utr 3 prime |
probably benign |
|
|