Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
A |
G |
17: 48,348,330 (GRCm39) |
S36P |
probably benign |
Het |
A530084C06Rik |
G |
T |
13: 31,742,978 (GRCm39) |
R92S |
unknown |
Het |
Ampd1 |
A |
G |
3: 103,003,028 (GRCm39) |
T582A |
probably benign |
Het |
Ank1 |
A |
C |
8: 23,555,011 (GRCm39) |
N57T |
probably damaging |
Het |
Atxn3 |
A |
G |
12: 101,914,261 (GRCm39) |
|
probably null |
Het |
Bace2 |
G |
A |
16: 97,200,882 (GRCm39) |
A117T |
probably benign |
Het |
Bcl2l15 |
A |
G |
3: 103,740,203 (GRCm39) |
N19S |
probably benign |
Het |
Bid |
C |
A |
6: 120,877,112 (GRCm39) |
|
probably null |
Het |
Cadps2 |
A |
T |
6: 23,626,607 (GRCm39) |
M227K |
probably benign |
Het |
Clip4 |
G |
A |
17: 72,135,697 (GRCm39) |
C483Y |
possibly damaging |
Het |
Dennd4a |
A |
G |
9: 64,780,326 (GRCm39) |
T621A |
probably damaging |
Het |
E2f3 |
G |
A |
13: 30,094,112 (GRCm39) |
S383L |
probably damaging |
Het |
F2r |
C |
T |
13: 95,754,858 (GRCm39) |
V9I |
probably benign |
Het |
Gm14226 |
T |
C |
2: 154,867,131 (GRCm39) |
S363P |
probably damaging |
Het |
Gstm5 |
T |
C |
3: 107,804,610 (GRCm39) |
Y65H |
probably damaging |
Het |
H2bc13 |
A |
G |
13: 21,900,040 (GRCm39) |
S92P |
probably benign |
Het |
Itgav |
G |
T |
2: 83,606,894 (GRCm39) |
G448* |
probably null |
Het |
Klrh1 |
T |
C |
6: 129,749,343 (GRCm39) |
H84R |
probably benign |
Het |
Lhx6 |
C |
T |
2: 35,993,357 (GRCm39) |
|
probably null |
Het |
Manba |
T |
A |
3: 135,276,007 (GRCm39) |
V816D |
probably benign |
Het |
Marchf10 |
G |
A |
11: 105,280,906 (GRCm39) |
P460S |
not run |
Het |
Mmp17 |
T |
A |
5: 129,673,653 (GRCm39) |
V244E |
probably damaging |
Het |
Mtrr |
C |
T |
13: 68,730,268 (GRCm39) |
|
probably benign |
Het |
Nup160 |
T |
C |
2: 90,515,402 (GRCm39) |
I170T |
probably damaging |
Het |
Or4c12b |
A |
G |
2: 89,647,363 (GRCm39) |
N225S |
probably benign |
Het |
Or4c12b |
A |
T |
2: 89,647,538 (GRCm39) |
L283F |
probably damaging |
Het |
Or51e1 |
T |
C |
7: 102,358,996 (GRCm39) |
S177P |
probably damaging |
Het |
Pappa |
G |
A |
4: 65,074,352 (GRCm39) |
S302N |
possibly damaging |
Het |
Plekhj1 |
G |
A |
10: 80,633,748 (GRCm39) |
A53V |
possibly damaging |
Het |
Pramel46 |
T |
A |
5: 95,418,171 (GRCm39) |
H275L |
possibly damaging |
Het |
Pramel48 |
C |
T |
5: 95,630,539 (GRCm39) |
R139C |
probably benign |
Het |
Prpf8 |
T |
C |
11: 75,399,200 (GRCm39) |
V2157A |
probably damaging |
Het |
Rps8 |
G |
A |
4: 117,011,104 (GRCm39) |
R200W |
probably damaging |
Het |
Sesn2 |
A |
G |
4: 132,227,154 (GRCm39) |
F93L |
probably damaging |
Het |
Skic3 |
C |
A |
13: 76,282,954 (GRCm39) |
L759M |
probably damaging |
Het |
Slf1 |
A |
G |
13: 77,197,311 (GRCm39) |
S768P |
probably benign |
Het |
Stat4 |
A |
G |
1: 52,137,622 (GRCm39) |
N471S |
probably damaging |
Het |
Trcg1 |
T |
C |
9: 57,155,621 (GRCm39) |
L758P |
probably benign |
Het |
Trim35 |
A |
G |
14: 66,540,696 (GRCm39) |
T183A |
probably benign |
Het |
Ttr |
C |
A |
18: 20,803,102 (GRCm39) |
Y89* |
probably null |
Het |
Zfp90 |
C |
A |
8: 107,151,323 (GRCm39) |
H345Q |
probably benign |
Het |
Zmym4 |
A |
G |
4: 126,757,961 (GRCm39) |
V1531A |
probably damaging |
Het |
|
Other mutations in H60c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01018:H60c
|
APN |
10 |
3,210,343 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01018:H60c
|
APN |
10 |
3,209,766 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02089:H60c
|
APN |
10 |
3,209,826 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03221:H60c
|
APN |
10 |
3,209,799 (GRCm39) |
nonsense |
probably null |
|
R0376:H60c
|
UTSW |
10 |
3,210,435 (GRCm39) |
splice site |
probably benign |
|
R1456:H60c
|
UTSW |
10 |
3,210,307 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1459:H60c
|
UTSW |
10 |
3,210,240 (GRCm39) |
missense |
probably benign |
0.27 |
R1737:H60c
|
UTSW |
10 |
3,209,914 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2041:H60c
|
UTSW |
10 |
3,209,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R3431:H60c
|
UTSW |
10 |
3,210,382 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4597:H60c
|
UTSW |
10 |
3,209,968 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5186:H60c
|
UTSW |
10 |
3,209,273 (GRCm39) |
splice site |
probably null |
|
R6658:H60c
|
UTSW |
10 |
3,210,270 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7516:H60c
|
UTSW |
10 |
3,209,746 (GRCm39) |
nonsense |
probably null |
|
R8067:H60c
|
UTSW |
10 |
3,209,338 (GRCm39) |
missense |
unknown |
|
R8192:H60c
|
UTSW |
10 |
3,209,781 (GRCm39) |
missense |
probably benign |
0.42 |
R8696:H60c
|
UTSW |
10 |
3,210,265 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8887:H60c
|
UTSW |
10 |
3,217,255 (GRCm39) |
missense |
probably benign |
0.34 |
|