Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
A2ml1 |
A |
T |
6: 128,529,271 (GRCm39) |
M957K |
probably benign |
Het |
Adam7 |
C |
A |
14: 68,742,610 (GRCm39) |
V668F |
probably benign |
Het |
Adcy7 |
T |
G |
8: 89,038,902 (GRCm39) |
L306R |
probably damaging |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Alox12e |
G |
A |
11: 70,206,828 (GRCm39) |
R620W |
probably damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Ano7 |
T |
C |
1: 93,318,035 (GRCm39) |
V249A |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,098,351 (GRCm39) |
|
probably null |
Het |
Asah2 |
A |
T |
19: 32,002,274 (GRCm39) |
V290E |
probably damaging |
Het |
Ascc2 |
A |
T |
11: 4,631,496 (GRCm39) |
M646L |
probably benign |
Het |
Atxn2l |
T |
A |
7: 126,095,038 (GRCm39) |
K421N |
probably damaging |
Het |
Cars2 |
T |
C |
8: 11,597,747 (GRCm39) |
I110V |
probably damaging |
Het |
Ccdc74a |
A |
G |
16: 17,467,890 (GRCm39) |
N249S |
probably benign |
Het |
Cenpe |
T |
C |
3: 134,928,082 (GRCm39) |
|
probably benign |
Het |
Clptm1l |
C |
T |
13: 73,755,842 (GRCm39) |
Q153* |
probably null |
Het |
Cnep1r1 |
G |
T |
8: 88,845,445 (GRCm39) |
|
probably benign |
Het |
Cyp2d37-ps |
C |
T |
15: 82,574,289 (GRCm39) |
|
noncoding transcript |
Het |
Cyp3a25 |
A |
G |
5: 145,923,779 (GRCm39) |
|
probably benign |
Het |
Dis3l |
G |
T |
9: 64,246,855 (GRCm39) |
Q67K |
probably benign |
Het |
Dnah1 |
A |
G |
14: 30,993,086 (GRCm39) |
V2936A |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,366,416 (GRCm39) |
R2710C |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Dvl3 |
G |
A |
16: 20,345,101 (GRCm39) |
S361N |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,881,181 (GRCm39) |
V1085A |
probably benign |
Het |
Eif3b |
T |
C |
5: 140,412,208 (GRCm39) |
Y226H |
probably damaging |
Het |
Endov |
T |
C |
11: 119,390,408 (GRCm39) |
F12S |
probably damaging |
Het |
Ercc1 |
A |
G |
7: 19,088,295 (GRCm39) |
*37W |
probably null |
Het |
Evi2a |
G |
A |
11: 79,418,593 (GRCm39) |
Q6* |
probably null |
Het |
Faah |
C |
T |
4: 115,855,770 (GRCm39) |
V552M |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,477,369 (GRCm39) |
N2138K |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,479,741 (GRCm39) |
V2929E |
probably damaging |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm6327 |
A |
T |
16: 12,578,979 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Gtf2f2 |
A |
G |
14: 76,155,136 (GRCm39) |
S142P |
possibly damaging |
Het |
Hspg2 |
A |
T |
4: 137,286,678 (GRCm39) |
T3666S |
possibly damaging |
Het |
Htt |
C |
T |
5: 34,983,326 (GRCm39) |
T975I |
probably benign |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Iqgap1 |
G |
A |
7: 80,373,727 (GRCm39) |
Q1421* |
probably null |
Het |
Itga3 |
T |
A |
11: 94,944,902 (GRCm39) |
Q802L |
possibly damaging |
Het |
Lonp2 |
A |
G |
8: 87,392,403 (GRCm39) |
T490A |
probably damaging |
Het |
Lztr1 |
T |
C |
16: 17,327,534 (GRCm39) |
V79A |
probably damaging |
Het |
Mast4 |
C |
T |
13: 102,895,601 (GRCm39) |
E736K |
probably benign |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Myof |
A |
G |
19: 37,904,194 (GRCm39) |
V2A |
possibly damaging |
Het |
Naf1 |
A |
G |
8: 67,340,432 (GRCm39) |
D414G |
probably damaging |
Het |
Nav3 |
G |
A |
10: 109,555,882 (GRCm39) |
T1683M |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,993,578 (GRCm39) |
|
probably benign |
Het |
Nebl |
A |
T |
2: 17,401,932 (GRCm39) |
M427K |
probably benign |
Het |
Ngdn |
T |
C |
14: 55,259,564 (GRCm39) |
V205A |
possibly damaging |
Het |
Nup133 |
C |
A |
8: 124,641,314 (GRCm39) |
D869Y |
probably damaging |
Het |
Oas1g |
T |
C |
5: 121,023,946 (GRCm39) |
E121G |
probably damaging |
Het |
Or10j3b |
T |
C |
1: 173,043,277 (GRCm39) |
F20L |
probably benign |
Het |
Or2ab1 |
A |
G |
11: 58,488,396 (GRCm39) |
N58S |
probably damaging |
Het |
Or2w3 |
G |
T |
11: 58,556,808 (GRCm39) |
C141F |
probably damaging |
Het |
Or5m9 |
A |
G |
2: 85,877,299 (GRCm39) |
T158A |
probably damaging |
Het |
Or6c205 |
T |
A |
10: 129,087,001 (GRCm39) |
Y199* |
probably null |
Het |
Park7 |
T |
C |
4: 150,989,732 (GRCm39) |
N76S |
probably benign |
Het |
Pcdh8 |
A |
T |
14: 80,005,651 (GRCm39) |
S912R |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,271,559 (GRCm39) |
I2998T |
probably damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Ppard |
A |
G |
17: 28,518,663 (GRCm39) |
H388R |
probably damaging |
Het |
Psma1 |
A |
G |
7: 113,869,001 (GRCm39) |
S142P |
possibly damaging |
Het |
Pth2r |
T |
C |
1: 65,382,721 (GRCm39) |
I158T |
probably damaging |
Het |
Rbl2 |
C |
A |
8: 91,833,367 (GRCm39) |
P714Q |
probably damaging |
Het |
Rexo2 |
A |
T |
9: 48,385,813 (GRCm39) |
S104T |
possibly damaging |
Het |
Sema5a |
T |
C |
15: 32,609,363 (GRCm39) |
|
probably benign |
Het |
Spmip10 |
C |
T |
18: 56,721,535 (GRCm39) |
Q25* |
probably null |
Het |
Sun2 |
A |
G |
15: 79,622,852 (GRCm39) |
L109P |
probably damaging |
Het |
Tdg |
A |
G |
10: 82,477,368 (GRCm39) |
T116A |
probably benign |
Het |
Tmcc1 |
C |
T |
6: 116,020,019 (GRCm39) |
V118M |
probably benign |
Het |
Tnfsf11 |
T |
A |
14: 78,516,362 (GRCm39) |
N202I |
probably damaging |
Het |
Togaram2 |
T |
C |
17: 72,023,360 (GRCm39) |
S759P |
probably benign |
Het |
Ttc7b |
G |
A |
12: 100,291,948 (GRCm39) |
A208V |
probably damaging |
Het |
Tti2 |
T |
C |
8: 31,644,338 (GRCm39) |
|
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,905,118 (GRCm39) |
|
probably null |
Het |
Zfyve26 |
T |
C |
12: 79,330,806 (GRCm39) |
|
probably null |
Het |
Zfyve28 |
T |
C |
5: 34,391,681 (GRCm39) |
M157V |
probably null |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
probably damaging |
Het |
|
Other mutations in Terb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00787:Terb1
|
APN |
8 |
105,178,439 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01468:Terb1
|
APN |
8 |
105,208,799 (GRCm39) |
intron |
probably benign |
|
IGL01619:Terb1
|
APN |
8 |
105,199,646 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01631:Terb1
|
APN |
8 |
105,199,496 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02041:Terb1
|
APN |
8 |
105,221,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02413:Terb1
|
APN |
8 |
105,221,500 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02974:Terb1
|
APN |
8 |
105,221,600 (GRCm39) |
nonsense |
probably null |
|
IGL03091:Terb1
|
APN |
8 |
105,195,786 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03410:Terb1
|
APN |
8 |
105,199,674 (GRCm39) |
splice site |
probably benign |
|
R0825:Terb1
|
UTSW |
8 |
105,195,380 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0906:Terb1
|
UTSW |
8 |
105,179,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R1175:Terb1
|
UTSW |
8 |
105,210,938 (GRCm39) |
missense |
probably benign |
0.07 |
R1494:Terb1
|
UTSW |
8 |
105,225,122 (GRCm39) |
splice site |
probably benign |
|
R1657:Terb1
|
UTSW |
8 |
105,215,123 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2018:Terb1
|
UTSW |
8 |
105,179,331 (GRCm39) |
missense |
probably benign |
0.00 |
R2029:Terb1
|
UTSW |
8 |
105,224,732 (GRCm39) |
splice site |
probably benign |
|
R2047:Terb1
|
UTSW |
8 |
105,212,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R2179:Terb1
|
UTSW |
8 |
105,199,369 (GRCm39) |
missense |
probably benign |
0.08 |
R2179:Terb1
|
UTSW |
8 |
105,179,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R2187:Terb1
|
UTSW |
8 |
105,199,516 (GRCm39) |
missense |
probably benign |
|
R2420:Terb1
|
UTSW |
8 |
105,225,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2867:Terb1
|
UTSW |
8 |
105,174,485 (GRCm39) |
unclassified |
probably benign |
|
R3749:Terb1
|
UTSW |
8 |
105,223,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Terb1
|
UTSW |
8 |
105,212,057 (GRCm39) |
missense |
probably benign |
0.02 |
R4930:Terb1
|
UTSW |
8 |
105,174,580 (GRCm39) |
missense |
probably benign |
0.00 |
R4963:Terb1
|
UTSW |
8 |
105,208,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4969:Terb1
|
UTSW |
8 |
105,221,795 (GRCm39) |
missense |
probably benign |
0.00 |
R5100:Terb1
|
UTSW |
8 |
105,221,805 (GRCm39) |
nonsense |
probably null |
|
R5440:Terb1
|
UTSW |
8 |
105,215,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R5824:Terb1
|
UTSW |
8 |
105,212,079 (GRCm39) |
missense |
probably benign |
0.08 |
R5950:Terb1
|
UTSW |
8 |
105,215,117 (GRCm39) |
critical splice donor site |
probably null |
|
R5985:Terb1
|
UTSW |
8 |
105,208,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R5985:Terb1
|
UTSW |
8 |
105,178,439 (GRCm39) |
missense |
probably benign |
0.09 |
R6320:Terb1
|
UTSW |
8 |
105,173,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6432:Terb1
|
UTSW |
8 |
105,212,078 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6473:Terb1
|
UTSW |
8 |
105,199,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Terb1
|
UTSW |
8 |
105,199,388 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7013:Terb1
|
UTSW |
8 |
105,215,222 (GRCm39) |
nonsense |
probably null |
|
R7064:Terb1
|
UTSW |
8 |
105,215,186 (GRCm39) |
missense |
probably benign |
0.00 |
R7237:Terb1
|
UTSW |
8 |
105,221,959 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7361:Terb1
|
UTSW |
8 |
105,195,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Terb1
|
UTSW |
8 |
105,224,716 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7915:Terb1
|
UTSW |
8 |
105,173,848 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8112:Terb1
|
UTSW |
8 |
105,195,399 (GRCm39) |
missense |
probably benign |
0.32 |
R8256:Terb1
|
UTSW |
8 |
105,199,579 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8329:Terb1
|
UTSW |
8 |
105,211,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R8807:Terb1
|
UTSW |
8 |
105,195,741 (GRCm39) |
critical splice donor site |
probably null |
|
R8953:Terb1
|
UTSW |
8 |
105,195,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8984:Terb1
|
UTSW |
8 |
105,212,036 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9614:Terb1
|
UTSW |
8 |
105,223,476 (GRCm39) |
missense |
probably benign |
0.13 |
|