Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn2 |
T |
C |
13: 12,293,853 (GRCm39) |
T62A |
probably benign |
Het |
Adam33 |
G |
A |
2: 130,897,530 (GRCm39) |
T265I |
probably damaging |
Het |
Afap1l2 |
T |
C |
19: 56,904,560 (GRCm39) |
T654A |
probably benign |
Het |
Agrn |
A |
G |
4: 156,258,066 (GRCm39) |
S992P |
probably damaging |
Het |
Anapc1 |
A |
G |
2: 128,492,292 (GRCm39) |
F939L |
probably damaging |
Het |
Anks1 |
G |
A |
17: 28,276,304 (GRCm39) |
V1016I |
probably benign |
Het |
Ankzf1 |
A |
G |
1: 75,173,238 (GRCm39) |
T401A |
probably benign |
Het |
Atad1 |
G |
T |
19: 32,678,987 (GRCm39) |
D105E |
probably benign |
Het |
Carmil2 |
A |
G |
8: 106,415,664 (GRCm39) |
T313A |
possibly damaging |
Het |
Cdk15 |
T |
C |
1: 59,304,792 (GRCm39) |
V131A |
probably damaging |
Het |
Cldnd1 |
A |
T |
16: 58,551,663 (GRCm39) |
|
probably null |
Het |
Col16a1 |
A |
T |
4: 129,948,882 (GRCm39) |
|
probably benign |
Het |
Dnah7b |
A |
C |
1: 46,165,828 (GRCm39) |
K498Q |
probably benign |
Het |
Dnase2b |
A |
G |
3: 146,290,318 (GRCm39) |
Y218H |
probably benign |
Het |
Dsg2 |
T |
A |
18: 20,712,506 (GRCm39) |
V170D |
probably damaging |
Het |
Dst |
T |
C |
1: 34,309,955 (GRCm39) |
V1543A |
probably damaging |
Het |
Ell3 |
A |
T |
2: 121,272,258 (GRCm39) |
I72K |
probably damaging |
Het |
Fank1 |
A |
G |
7: 133,463,927 (GRCm39) |
Y41C |
probably benign |
Het |
Foxd3 |
T |
C |
4: 99,545,261 (GRCm39) |
Y134H |
probably damaging |
Het |
Frmd6 |
A |
G |
12: 70,910,685 (GRCm39) |
|
probably benign |
Het |
Gale |
A |
G |
4: 135,692,916 (GRCm39) |
E53G |
possibly damaging |
Het |
Glis3 |
A |
G |
19: 28,294,702 (GRCm39) |
S699P |
probably damaging |
Het |
Gm12830 |
T |
A |
4: 114,702,246 (GRCm39) |
M136K |
unknown |
Het |
Grik3 |
T |
C |
4: 125,553,582 (GRCm39) |
V438A |
probably benign |
Het |
Gsap |
A |
G |
5: 21,422,429 (GRCm39) |
N133D |
probably damaging |
Het |
Gsg1 |
T |
A |
6: 135,217,110 (GRCm39) |
D239V |
probably damaging |
Het |
H2-T10 |
A |
T |
17: 36,431,975 (GRCm39) |
W23R |
probably damaging |
Het |
Itgae |
A |
G |
11: 73,031,583 (GRCm39) |
T1100A |
probably benign |
Het |
Kcnh7 |
A |
T |
2: 62,607,903 (GRCm39) |
F559L |
probably damaging |
Het |
Kdm5b |
G |
T |
1: 134,536,616 (GRCm39) |
R612L |
probably damaging |
Het |
Lrrc74a |
T |
A |
12: 86,795,231 (GRCm39) |
N253K |
possibly damaging |
Het |
Mcm3ap |
A |
G |
10: 76,351,540 (GRCm39) |
H1961R |
possibly damaging |
Het |
Ncam1 |
C |
T |
9: 49,476,304 (GRCm39) |
E262K |
probably benign |
Het |
Nckap1 |
A |
G |
2: 80,339,125 (GRCm39) |
S968P |
possibly damaging |
Het |
Nkapd1 |
T |
C |
9: 50,519,070 (GRCm39) |
T181A |
possibly damaging |
Het |
Nr2f2 |
T |
G |
7: 70,009,744 (GRCm39) |
S112R |
probably benign |
Het |
Nup93 |
T |
C |
8: 95,013,165 (GRCm39) |
W137R |
probably damaging |
Het |
Or10ag53 |
A |
G |
2: 87,082,736 (GRCm39) |
S152G |
probably benign |
Het |
Or2t26 |
A |
G |
11: 49,039,660 (GRCm39) |
D192G |
possibly damaging |
Het |
Or4a78 |
A |
T |
2: 89,497,333 (GRCm39) |
L299H |
probably damaging |
Het |
Or52n1 |
A |
T |
7: 104,383,243 (GRCm39) |
F109L |
probably damaging |
Het |
Or8b12 |
T |
A |
9: 37,657,433 (GRCm39) |
M1K |
probably null |
Het |
Or8b55 |
T |
C |
9: 38,727,666 (GRCm39) |
I289T |
probably damaging |
Het |
Otogl |
A |
T |
10: 107,607,067 (GRCm39) |
Y2105* |
probably null |
Het |
Pibf1 |
A |
G |
14: 99,338,555 (GRCm39) |
S24G |
probably damaging |
Het |
Pitx2 |
C |
T |
3: 129,009,491 (GRCm39) |
R130W |
probably damaging |
Het |
Pkd1l1 |
T |
C |
11: 8,851,287 (GRCm39) |
N715S |
probably benign |
Het |
Pou6f2 |
A |
T |
13: 18,303,739 (GRCm39) |
I123N |
possibly damaging |
Het |
Prss29 |
T |
A |
17: 25,539,513 (GRCm39) |
H35Q |
possibly damaging |
Het |
Ptpn21 |
A |
G |
12: 98,646,375 (GRCm39) |
F1028L |
probably benign |
Het |
Ptpn21 |
A |
T |
12: 98,681,431 (GRCm39) |
Y68N |
probably damaging |
Het |
Ptprk |
A |
G |
10: 28,440,099 (GRCm39) |
T856A |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rpl22l1 |
A |
G |
3: 28,860,676 (GRCm39) |
T13A |
possibly damaging |
Het |
Rptn |
C |
G |
3: 93,305,437 (GRCm39) |
H923Q |
possibly damaging |
Het |
Sec14l5 |
G |
A |
16: 4,994,429 (GRCm39) |
V408I |
probably damaging |
Het |
Serpina5 |
T |
C |
12: 104,068,037 (GRCm39) |
S33P |
possibly damaging |
Het |
Sgip1 |
A |
G |
4: 102,823,392 (GRCm39) |
N524S |
probably damaging |
Het |
Shkbp1 |
C |
A |
7: 27,051,405 (GRCm39) |
R218M |
probably null |
Het |
Sorcs1 |
T |
A |
19: 50,169,852 (GRCm39) |
I970F |
probably damaging |
Het |
Spg11 |
A |
G |
2: 121,918,743 (GRCm39) |
V962A |
possibly damaging |
Het |
Sptbn1 |
A |
G |
11: 30,086,054 (GRCm39) |
M1205T |
probably damaging |
Het |
Sufu |
G |
A |
19: 46,462,093 (GRCm39) |
V369M |
probably damaging |
Het |
Tmem98 |
T |
C |
11: 80,712,220 (GRCm39) |
F219S |
probably benign |
Het |
Trim27 |
T |
C |
13: 21,365,086 (GRCm39) |
|
probably benign |
Het |
Trim43b |
T |
C |
9: 88,973,328 (GRCm39) |
E135G |
possibly damaging |
Het |
Ube2m |
A |
G |
7: 12,769,815 (GRCm39) |
V110A |
probably damaging |
Het |
Ugt2b36 |
A |
G |
5: 87,239,989 (GRCm39) |
V132A |
probably damaging |
Het |
Usp36 |
A |
T |
11: 118,168,100 (GRCm39) |
S86T |
probably damaging |
Het |
Zfp941 |
A |
T |
7: 140,392,398 (GRCm39) |
D320E |
probably benign |
Het |
|
Other mutations in Cts3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Cts3
|
APN |
13 |
61,715,988 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02662:Cts3
|
APN |
13 |
61,715,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R0455:Cts3
|
UTSW |
13 |
61,716,024 (GRCm39) |
unclassified |
probably benign |
|
R1673:Cts3
|
UTSW |
13 |
61,715,368 (GRCm39) |
nonsense |
probably null |
|
R1793:Cts3
|
UTSW |
13 |
61,715,967 (GRCm39) |
missense |
probably benign |
0.00 |
R2403:Cts3
|
UTSW |
13 |
61,712,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R3897:Cts3
|
UTSW |
13 |
61,712,800 (GRCm39) |
missense |
probably benign |
0.04 |
R4012:Cts3
|
UTSW |
13 |
61,715,868 (GRCm39) |
critical splice donor site |
probably null |
|
R4052:Cts3
|
UTSW |
13 |
61,716,535 (GRCm39) |
missense |
probably benign |
0.27 |
R4669:Cts3
|
UTSW |
13 |
61,714,637 (GRCm39) |
missense |
probably benign |
0.01 |
R4907:Cts3
|
UTSW |
13 |
61,714,634 (GRCm39) |
missense |
probably benign |
0.01 |
R5121:Cts3
|
UTSW |
13 |
61,715,409 (GRCm39) |
missense |
probably benign |
0.09 |
R5572:Cts3
|
UTSW |
13 |
61,712,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R5774:Cts3
|
UTSW |
13 |
61,716,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R5796:Cts3
|
UTSW |
13 |
61,716,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Cts3
|
UTSW |
13 |
61,716,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R6159:Cts3
|
UTSW |
13 |
61,714,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7346:Cts3
|
UTSW |
13 |
61,715,434 (GRCm39) |
missense |
probably benign |
0.00 |
R7642:Cts3
|
UTSW |
13 |
61,716,589 (GRCm39) |
missense |
probably benign |
0.02 |
R7948:Cts3
|
UTSW |
13 |
61,713,863 (GRCm39) |
missense |
probably benign |
0.04 |
R8060:Cts3
|
UTSW |
13 |
61,714,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Cts3
|
UTSW |
13 |
61,715,235 (GRCm39) |
nonsense |
probably null |
|
R9145:Cts3
|
UTSW |
13 |
61,712,800 (GRCm39) |
missense |
probably benign |
0.04 |
R9218:Cts3
|
UTSW |
13 |
61,716,583 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9707:Cts3
|
UTSW |
13 |
61,714,649 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9717:Cts3
|
UTSW |
13 |
61,712,799 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Cts3
|
UTSW |
13 |
61,716,561 (GRCm39) |
nonsense |
probably null |
|
|