Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700088E04Rik |
T |
A |
15: 79,019,842 (GRCm39) |
D158V |
probably benign |
Het |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Aadacl2fm1 |
T |
C |
3: 59,840,114 (GRCm39) |
I62T |
possibly damaging |
Het |
Acp5 |
G |
A |
9: 22,038,483 (GRCm39) |
Q273* |
probably null |
Het |
Apoa5 |
G |
C |
9: 46,181,944 (GRCm39) |
R340P |
probably damaging |
Het |
Atp2b1 |
T |
A |
10: 98,835,660 (GRCm39) |
N468K |
probably damaging |
Het |
Bltp3a |
A |
G |
17: 28,112,414 (GRCm39) |
D1201G |
probably damaging |
Het |
Bphl |
A |
T |
13: 34,234,312 (GRCm39) |
I143L |
probably benign |
Het |
Cd33 |
A |
T |
7: 43,182,150 (GRCm39) |
H98Q |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,917,286 (GRCm39) |
S229* |
probably null |
Het |
Cemip2 |
T |
A |
19: 21,779,249 (GRCm39) |
V353D |
probably damaging |
Het |
Cfap96 |
C |
T |
8: 46,409,458 (GRCm39) |
S287N |
probably damaging |
Het |
Colec10 |
A |
G |
15: 54,325,761 (GRCm39) |
D197G |
probably damaging |
Het |
Cpt1a |
T |
C |
19: 3,433,795 (GRCm39) |
M759T |
probably benign |
Het |
Ctc1 |
A |
G |
11: 68,913,593 (GRCm39) |
Y165C |
probably damaging |
Het |
Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
Dnah2 |
T |
C |
11: 69,345,208 (GRCm39) |
D2667G |
possibly damaging |
Het |
Dok1 |
T |
C |
6: 83,009,972 (GRCm39) |
K46E |
probably damaging |
Het |
Erv3 |
C |
A |
2: 131,697,975 (GRCm39) |
W128L |
possibly damaging |
Het |
Fam186a |
A |
G |
15: 99,844,766 (GRCm39) |
S493P |
unknown |
Het |
Fbn1 |
A |
T |
2: 125,160,984 (GRCm39) |
N2185K |
probably damaging |
Het |
Figla |
A |
C |
6: 85,997,689 (GRCm39) |
H139P |
probably benign |
Het |
Gemin4 |
A |
G |
11: 76,101,749 (GRCm39) |
L1004P |
probably damaging |
Het |
Gm11937 |
T |
C |
11: 99,500,646 (GRCm39) |
T124A |
unknown |
Het |
Gm17669 |
G |
T |
18: 67,695,682 (GRCm39) |
V76L |
probably benign |
Het |
H2ac21 |
A |
G |
3: 96,127,401 (GRCm39) |
E57G |
probably damaging |
Het |
Hcls1 |
A |
T |
16: 36,777,702 (GRCm39) |
M274L |
probably benign |
Het |
Il17rc |
T |
C |
6: 113,449,741 (GRCm39) |
S116P |
probably damaging |
Het |
Krt79 |
G |
A |
15: 101,840,288 (GRCm39) |
R303C |
probably damaging |
Het |
Lamb2 |
C |
T |
9: 108,358,006 (GRCm39) |
T149I |
probably damaging |
Het |
Lrrc41 |
T |
A |
4: 115,932,806 (GRCm39) |
|
probably null |
Het |
Mga |
C |
A |
2: 119,781,676 (GRCm39) |
T2234K |
possibly damaging |
Het |
Mix23 |
A |
G |
16: 35,892,491 (GRCm39) |
E12G |
probably benign |
Het |
Muc6 |
T |
A |
7: 141,237,398 (GRCm39) |
Q205L |
probably damaging |
Het |
Nlrp9b |
A |
T |
7: 19,760,462 (GRCm39) |
K624N |
possibly damaging |
Het |
Or1o4 |
G |
T |
17: 37,591,386 (GRCm39) |
|
probably benign |
Het |
Or4d2 |
C |
T |
11: 87,784,082 (GRCm39) |
V223M |
probably benign |
Het |
Or6e1 |
T |
C |
14: 54,520,137 (GRCm39) |
T72A |
probably damaging |
Het |
Otud4 |
T |
C |
8: 80,400,087 (GRCm39) |
S934P |
probably damaging |
Het |
Pcdha12 |
G |
T |
18: 37,155,526 (GRCm39) |
W748C |
probably damaging |
Het |
Pdc |
T |
C |
1: 150,208,919 (GRCm39) |
I134T |
probably damaging |
Het |
Peg10 |
T |
TCCC |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pkn1 |
C |
T |
8: 84,410,799 (GRCm39) |
R276Q |
possibly damaging |
Het |
Plin3 |
C |
A |
17: 56,587,824 (GRCm39) |
G297V |
probably benign |
Het |
Podn |
C |
T |
4: 107,876,106 (GRCm39) |
V517I |
probably benign |
Het |
Pomk |
T |
C |
8: 26,473,344 (GRCm39) |
D203G |
probably damaging |
Het |
Ppil4 |
A |
G |
10: 7,675,355 (GRCm39) |
D168G |
probably damaging |
Het |
Ptgr2 |
T |
C |
12: 84,354,647 (GRCm39) |
I276T |
probably benign |
Het |
Ptk7 |
T |
A |
17: 46,887,744 (GRCm39) |
I563F |
possibly damaging |
Het |
Rbm12 |
G |
T |
2: 155,939,738 (GRCm39) |
T178K |
unknown |
Het |
Sctr |
T |
C |
1: 119,959,403 (GRCm39) |
|
probably null |
Het |
Sh2b1 |
GGGACC |
GGGACCGGCTCAGCCACGTGGACC |
7: 126,066,744 (GRCm39) |
|
probably benign |
Het |
Spata31e4 |
T |
A |
13: 50,855,465 (GRCm39) |
S368T |
possibly damaging |
Het |
Steap1 |
A |
T |
5: 5,786,458 (GRCm39) |
D326E |
probably damaging |
Het |
Stra6 |
G |
A |
9: 58,059,175 (GRCm39) |
V513I |
probably benign |
Het |
Tbx19 |
A |
G |
1: 164,966,546 (GRCm39) |
S443P |
unknown |
Het |
Tfr2 |
G |
A |
5: 137,572,701 (GRCm39) |
V171I |
probably benign |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmem129 |
A |
G |
5: 33,815,122 (GRCm39) |
V17A |
probably benign |
Het |
Tmem87b |
T |
C |
2: 128,660,353 (GRCm39) |
L32P |
probably damaging |
Het |
Tor1aip1 |
T |
A |
1: 155,906,177 (GRCm39) |
D205V |
probably damaging |
Het |
Trim33 |
T |
C |
3: 103,239,074 (GRCm39) |
V684A |
probably benign |
Het |
Triobp |
C |
T |
15: 78,877,378 (GRCm39) |
R1637C |
probably damaging |
Het |
Ulbp1 |
C |
A |
10: 7,406,371 (GRCm39) |
M196I |
probably benign |
Het |
Vash1 |
G |
A |
12: 86,738,663 (GRCm39) |
G370E |
probably damaging |
Het |
Vmn2r23 |
A |
G |
6: 123,689,672 (GRCm39) |
T183A |
probably benign |
Het |
Vta1 |
A |
G |
10: 14,531,583 (GRCm39) |
I264T |
probably benign |
Het |
Zcchc8 |
A |
T |
5: 123,838,633 (GRCm39) |
M635K |
probably benign |
Het |
|
Other mutations in Tcea3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00588:Tcea3
|
APN |
4 |
136,001,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01647:Tcea3
|
APN |
4 |
136,002,087 (GRCm39) |
splice site |
probably benign |
|
IGL02153:Tcea3
|
APN |
4 |
136,000,945 (GRCm39) |
splice site |
probably benign |
|
IGL02832:Tcea3
|
APN |
4 |
135,995,424 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Tcea3
|
APN |
4 |
135,985,299 (GRCm39) |
critical splice donor site |
probably null |
|
R0281:Tcea3
|
UTSW |
4 |
135,998,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Tcea3
|
UTSW |
4 |
135,975,382 (GRCm39) |
nonsense |
probably null |
|
R3937:Tcea3
|
UTSW |
4 |
135,982,454 (GRCm39) |
splice site |
probably benign |
|
R4944:Tcea3
|
UTSW |
4 |
135,995,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R5028:Tcea3
|
UTSW |
4 |
135,985,246 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5169:Tcea3
|
UTSW |
4 |
135,992,181 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5245:Tcea3
|
UTSW |
4 |
135,991,813 (GRCm39) |
missense |
probably benign |
0.01 |
R5511:Tcea3
|
UTSW |
4 |
135,998,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R5730:Tcea3
|
UTSW |
4 |
135,992,204 (GRCm39) |
missense |
probably benign |
0.00 |
R6208:Tcea3
|
UTSW |
4 |
135,975,360 (GRCm39) |
start codon destroyed |
probably damaging |
0.96 |
R7106:Tcea3
|
UTSW |
4 |
135,998,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R8018:Tcea3
|
UTSW |
4 |
135,985,229 (GRCm39) |
splice site |
probably benign |
|
R8076:Tcea3
|
UTSW |
4 |
135,995,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R8078:Tcea3
|
UTSW |
4 |
135,981,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R8158:Tcea3
|
UTSW |
4 |
136,001,027 (GRCm39) |
critical splice donor site |
probably null |
|
R8861:Tcea3
|
UTSW |
4 |
135,981,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|