Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
A |
T |
1: 11,950,964 (GRCm38) |
D383V |
probably damaging |
Het |
Abca4 |
A |
T |
3: 122,054,232 (GRCm38) |
L67F |
probably damaging |
Het |
Abcc9 |
C |
A |
6: 142,656,676 (GRCm38) |
|
probably null |
Het |
Atp2a3 |
T |
C |
11: 72,972,882 (GRCm38) |
V175A |
probably damaging |
Het |
B3galt4 |
T |
A |
17: 33,950,757 (GRCm38) |
D169V |
probably damaging |
Het |
Bsn |
C |
T |
9: 108,113,009 (GRCm38) |
R1848Q |
possibly damaging |
Het |
Camkk2 |
T |
C |
5: 122,734,244 (GRCm38) |
E90G |
probably damaging |
Het |
Cdon |
T |
A |
9: 35,454,420 (GRCm38) |
I155N |
probably damaging |
Het |
Cep70 |
A |
G |
9: 99,296,405 (GRCm38) |
N519D |
probably damaging |
Het |
Clgn |
T |
C |
8: 83,425,614 (GRCm38) |
S582P |
probably damaging |
Het |
Cnga3 |
T |
C |
1: 37,260,925 (GRCm38) |
F280S |
probably damaging |
Het |
Dennd4c |
C |
T |
4: 86,811,453 (GRCm38) |
T764M |
probably benign |
Het |
Dis3 |
A |
T |
14: 99,099,664 (GRCm38) |
S4T |
probably damaging |
Het |
Dlgap1 |
T |
C |
17: 70,766,091 (GRCm38) |
|
probably null |
Het |
Dnah17 |
C |
T |
11: 118,036,446 (GRCm38) |
V3839I |
possibly damaging |
Het |
Dnajc1 |
A |
G |
2: 18,284,739 (GRCm38) |
Y286H |
probably benign |
Het |
Dynap |
T |
A |
18: 70,241,002 (GRCm38) |
D151V |
unknown |
Het |
Ednrb |
A |
G |
14: 103,821,714 (GRCm38) |
F292S |
probably damaging |
Het |
Eef1a1 |
A |
G |
9: 78,479,036 (GRCm38) |
S396P |
probably damaging |
Het |
Fancg |
A |
G |
4: 43,006,582 (GRCm38) |
F324S |
probably benign |
Het |
Fbxw11 |
T |
A |
11: 32,711,790 (GRCm38) |
S56T |
probably benign |
Het |
Gm13178 |
T |
A |
4: 144,703,636 (GRCm38) |
D261V |
probably damaging |
Het |
Gm14409 |
T |
C |
2: 177,265,256 (GRCm38) |
T150A |
possibly damaging |
Het |
Gm17535 |
G |
C |
9: 3,035,758 (GRCm38) |
V209L |
probably benign |
Homo |
Gm20767 |
G |
A |
13: 120,154,913 (GRCm38) |
S96N |
possibly damaging |
Het |
Gm5592 |
C |
T |
7: 41,219,105 (GRCm38) |
|
probably benign |
Het |
Gm7030 |
A |
G |
17: 36,111,287 (GRCm38) |
|
probably benign |
Het |
Gpr137 |
C |
T |
19: 6,942,005 (GRCm38) |
W51* |
probably null |
Het |
Hbb-bs |
T |
C |
7: 103,826,672 (GRCm38) |
Y146C |
probably damaging |
Het |
Herc1 |
G |
T |
9: 66,462,878 (GRCm38) |
C2982F |
probably damaging |
Het |
Hnrnpa3 |
T |
A |
2: 75,665,056 (GRCm38) |
N309K |
unknown |
Het |
Hydin |
A |
T |
8: 110,452,060 (GRCm38) |
I1096F |
possibly damaging |
Het |
Klf12 |
A |
G |
14: 100,022,894 (GRCm38) |
V133A |
probably benign |
Het |
Lats2 |
A |
T |
14: 57,694,418 (GRCm38) |
Y848N |
probably damaging |
Het |
Loxl3 |
A |
G |
6: 83,049,289 (GRCm38) |
T453A |
possibly damaging |
Het |
Ltn1 |
T |
G |
16: 87,415,681 (GRCm38) |
H664P |
probably benign |
Het |
Lypd6 |
C |
T |
2: 50,173,601 (GRCm38) |
T40I |
probably benign |
Het |
Nbeal1 |
A |
T |
1: 60,272,221 (GRCm38) |
T1817S |
probably benign |
Het |
Nub1 |
A |
C |
5: 24,702,441 (GRCm38) |
Y350S |
possibly damaging |
Het |
Pbp2 |
A |
G |
6: 135,309,876 (GRCm38) |
Y158H |
possibly damaging |
Het |
Ptpru |
C |
T |
4: 131,788,377 (GRCm38) |
E827K |
possibly damaging |
Het |
Rap1a |
A |
G |
3: 105,745,936 (GRCm38) |
Y32H |
probably damaging |
Het |
Raph1 |
T |
C |
1: 60,488,673 (GRCm38) |
N1143S |
possibly damaging |
Het |
Rbl1 |
T |
C |
2: 157,161,433 (GRCm38) |
T859A |
probably benign |
Het |
Rom1 |
A |
G |
19: 8,928,824 (GRCm38) |
L117P |
probably damaging |
Het |
Senp6 |
T |
C |
9: 80,118,644 (GRCm38) |
|
probably benign |
Het |
Sirpb1c |
T |
C |
3: 15,832,076 (GRCm38) |
M379V |
probably benign |
Het |
Slc6a4 |
C |
T |
11: 77,019,236 (GRCm38) |
T439M |
probably damaging |
Het |
Srsf12 |
G |
T |
4: 33,230,929 (GRCm38) |
R141L |
probably damaging |
Het |
Stk10 |
C |
T |
11: 32,596,748 (GRCm38) |
P335L |
probably benign |
Het |
Tecpr1 |
A |
T |
5: 144,206,546 (GRCm38) |
N670K |
probably benign |
Het |
Tgds |
T |
C |
14: 118,132,707 (GRCm38) |
E8G |
probably benign |
Het |
Tmem129 |
A |
G |
5: 33,657,716 (GRCm38) |
S38P |
probably damaging |
Het |
Trappc9 |
T |
C |
15: 72,685,339 (GRCm38) |
E812G |
probably damaging |
Het |
Wapl |
A |
G |
14: 34,692,320 (GRCm38) |
T380A |
probably damaging |
Het |
Xylt1 |
A |
T |
7: 117,656,691 (GRCm38) |
T829S |
probably benign |
Het |
Zc3h6 |
C |
T |
2: 129,015,559 (GRCm38) |
P666L |
possibly damaging |
Het |
Zfp703 |
C |
T |
8: 26,979,205 (GRCm38) |
P299L |
probably damaging |
Het |
|
Other mutations in Trmt10b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01064:Trmt10b
|
APN |
4 |
45,314,347 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL01743:Trmt10b
|
APN |
4 |
45,305,879 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02012:Trmt10b
|
APN |
4 |
45,315,045 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02174:Trmt10b
|
APN |
4 |
45,308,508 (GRCm38) |
missense |
possibly damaging |
0.88 |
R0454:Trmt10b
|
UTSW |
4 |
45,304,286 (GRCm38) |
missense |
probably damaging |
1.00 |
R0506:Trmt10b
|
UTSW |
4 |
45,304,306 (GRCm38) |
missense |
probably damaging |
0.98 |
R1757:Trmt10b
|
UTSW |
4 |
45,307,946 (GRCm38) |
missense |
probably damaging |
1.00 |
R1962:Trmt10b
|
UTSW |
4 |
45,314,378 (GRCm38) |
nonsense |
probably null |
|
R2944:Trmt10b
|
UTSW |
4 |
45,300,445 (GRCm38) |
start codon destroyed |
probably null |
0.99 |
R4781:Trmt10b
|
UTSW |
4 |
45,305,817 (GRCm38) |
missense |
probably damaging |
0.98 |
R6400:Trmt10b
|
UTSW |
4 |
45,308,562 (GRCm38) |
missense |
probably damaging |
1.00 |
R6460:Trmt10b
|
UTSW |
4 |
45,314,322 (GRCm38) |
missense |
possibly damaging |
0.81 |
R7165:Trmt10b
|
UTSW |
4 |
45,308,549 (GRCm38) |
missense |
probably damaging |
1.00 |
R7182:Trmt10b
|
UTSW |
4 |
45,308,520 (GRCm38) |
missense |
probably benign |
0.36 |
R8399:Trmt10b
|
UTSW |
4 |
45,305,870 (GRCm38) |
missense |
possibly damaging |
0.70 |
R8805:Trmt10b
|
UTSW |
4 |
45,301,281 (GRCm38) |
missense |
probably benign |
0.31 |
R9778:Trmt10b
|
UTSW |
4 |
45,314,374 (GRCm38) |
missense |
probably damaging |
1.00 |
|