Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat3 |
G |
C |
17: 13,147,405 (GRCm39) |
P204R |
probably damaging |
Het |
Aldh3b1 |
A |
G |
19: 3,968,803 (GRCm39) |
I250T |
possibly damaging |
Het |
Ankrd11 |
C |
T |
8: 123,622,718 (GRCm39) |
R378K |
probably damaging |
Het |
Arap1 |
G |
A |
7: 101,057,324 (GRCm39) |
R1355Q |
possibly damaging |
Het |
Arhgef19 |
T |
C |
4: 140,976,603 (GRCm39) |
V455A |
probably damaging |
Het |
BC051019 |
T |
C |
7: 109,315,286 (GRCm39) |
E323G |
probably damaging |
Het |
Bzw2 |
T |
C |
12: 36,184,943 (GRCm39) |
N2S |
possibly damaging |
Het |
Calm3 |
G |
C |
7: 16,651,398 (GRCm39) |
F66L |
probably damaging |
Het |
Carmil1 |
T |
A |
13: 24,338,704 (GRCm39) |
T191S |
probably benign |
Het |
Cemip2 |
T |
A |
19: 21,770,323 (GRCm39) |
S104T |
probably benign |
Het |
Cep170 |
A |
T |
1: 176,597,377 (GRCm39) |
C389S |
probably benign |
Het |
Clhc1 |
C |
T |
11: 29,510,533 (GRCm39) |
Q195* |
probably null |
Het |
Cttnbp2 |
A |
G |
6: 18,434,808 (GRCm39) |
L350P |
probably benign |
Het |
Cyp7a1 |
T |
C |
4: 6,271,238 (GRCm39) |
E306G |
possibly damaging |
Het |
Ddx25 |
T |
C |
9: 35,465,864 (GRCm39) |
N119S |
possibly damaging |
Het |
Ephx2 |
G |
T |
14: 66,322,441 (GRCm39) |
|
probably benign |
Het |
Ern2 |
C |
T |
7: 121,769,363 (GRCm39) |
A888T |
probably benign |
Het |
Fbln2 |
A |
T |
6: 91,246,072 (GRCm39) |
I973F |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,202,095 (GRCm39) |
I1259M |
probably damaging |
Het |
Glis1 |
A |
G |
4: 107,421,060 (GRCm39) |
H92R |
probably benign |
Het |
Gm13283 |
A |
C |
4: 88,679,516 (GRCm39) |
D169A |
probably benign |
Het |
Gpr61 |
A |
G |
3: 108,057,470 (GRCm39) |
L397P |
probably benign |
Het |
H4c11 |
T |
A |
13: 21,919,369 (GRCm39) |
I35N |
probably damaging |
Het |
Hip1 |
A |
T |
5: 135,460,297 (GRCm39) |
|
probably benign |
Het |
Hmgcs2 |
C |
T |
3: 98,203,557 (GRCm39) |
A222V |
probably damaging |
Het |
Ifna2 |
G |
A |
4: 88,601,712 (GRCm39) |
T102I |
probably benign |
Het |
Kat6b |
T |
C |
14: 21,674,995 (GRCm39) |
S387P |
probably damaging |
Het |
Ldlr |
G |
A |
9: 21,643,108 (GRCm39) |
V45M |
probably damaging |
Het |
Mc3r |
A |
T |
2: 172,091,515 (GRCm39) |
I246F |
possibly damaging |
Het |
Mug1 |
G |
C |
6: 121,861,296 (GRCm39) |
A1306P |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,368,020 (GRCm39) |
E260G |
probably benign |
Het |
Naa16 |
A |
G |
14: 79,582,395 (GRCm39) |
Y565H |
probably damaging |
Het |
Ndufaf7 |
A |
G |
17: 79,244,950 (GRCm39) |
Y23C |
possibly damaging |
Het |
Nop58 |
G |
A |
1: 59,731,549 (GRCm39) |
|
probably null |
Het |
Or6c33 |
A |
T |
10: 129,853,769 (GRCm39) |
T180S |
possibly damaging |
Het |
Or6c88 |
A |
T |
10: 129,406,550 (GRCm39) |
T9S |
probably benign |
Het |
Or7g19 |
T |
A |
9: 18,855,920 (GRCm39) |
|
probably benign |
Het |
Pcdh8 |
G |
A |
14: 80,006,971 (GRCm39) |
Q531* |
probably null |
Het |
Pik3c2g |
A |
G |
6: 139,821,093 (GRCm39) |
T297A |
probably benign |
Het |
Poc1b |
T |
C |
10: 99,028,861 (GRCm39) |
|
probably null |
Het |
Prb1c |
G |
A |
6: 132,338,897 (GRCm39) |
P107L |
|
Het |
Prokr2 |
A |
G |
2: 132,215,996 (GRCm39) |
V155A |
possibly damaging |
Het |
Rce1 |
C |
T |
19: 4,674,094 (GRCm39) |
|
probably benign |
Het |
Rnf148 |
A |
T |
6: 23,654,704 (GRCm39) |
N97K |
possibly damaging |
Het |
Setbp1 |
A |
G |
18: 78,899,723 (GRCm39) |
S1315P |
probably benign |
Het |
Sgcz |
A |
G |
8: 38,107,140 (GRCm39) |
V124A |
probably damaging |
Het |
Slc25a2 |
C |
A |
18: 37,771,089 (GRCm39) |
G147C |
probably damaging |
Het |
Slc28a2b |
C |
A |
2: 122,348,983 (GRCm39) |
P303Q |
|
Het |
Sod2 |
T |
C |
17: 13,227,193 (GRCm39) |
L49P |
probably damaging |
Het |
Tbc1d12 |
T |
C |
19: 38,854,098 (GRCm39) |
V260A |
probably benign |
Het |
Tcte2 |
C |
A |
17: 13,933,410 (GRCm39) |
|
probably benign |
Het |
Tenm3 |
T |
C |
8: 48,688,637 (GRCm39) |
T2317A |
probably damaging |
Het |
Tfcp2 |
T |
C |
15: 100,402,298 (GRCm39) |
I500V |
possibly damaging |
Het |
Trav14-3 |
C |
A |
14: 54,001,112 (GRCm39) |
Q108K |
probably damaging |
Het |
Trbv14 |
T |
C |
6: 41,112,364 (GRCm39) |
Y54H |
probably damaging |
Het |
Trpm3 |
T |
A |
19: 22,744,034 (GRCm39) |
V337E |
probably damaging |
Het |
Uox |
A |
T |
3: 146,318,047 (GRCm39) |
I14F |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,065,421 (GRCm39) |
V1249A |
probably benign |
Het |
Zfp511 |
T |
C |
7: 139,617,194 (GRCm39) |
Y97H |
probably damaging |
Het |
Zfp536 |
G |
T |
7: 37,268,721 (GRCm39) |
Q232K |
probably benign |
Het |
Zng1 |
T |
G |
19: 24,932,780 (GRCm39) |
K84N |
probably damaging |
Het |
|
Other mutations in Tsbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00668:Tsbp1
|
APN |
17 |
34,639,394 (GRCm39) |
unclassified |
probably benign |
|
IGL01516:Tsbp1
|
APN |
17 |
34,668,234 (GRCm39) |
missense |
possibly damaging |
0.90 |
FR4304:Tsbp1
|
UTSW |
17 |
34,679,051 (GRCm39) |
unclassified |
probably benign |
|
FR4304:Tsbp1
|
UTSW |
17 |
34,679,029 (GRCm39) |
unclassified |
probably benign |
|
FR4340:Tsbp1
|
UTSW |
17 |
34,679,051 (GRCm39) |
unclassified |
probably benign |
|
FR4340:Tsbp1
|
UTSW |
17 |
34,679,042 (GRCm39) |
unclassified |
probably benign |
|
FR4340:Tsbp1
|
UTSW |
17 |
34,679,034 (GRCm39) |
nonsense |
probably null |
|
FR4548:Tsbp1
|
UTSW |
17 |
34,679,039 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Tsbp1
|
UTSW |
17 |
34,679,047 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Tsbp1
|
UTSW |
17 |
34,679,027 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Tsbp1
|
UTSW |
17 |
34,679,042 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Tsbp1
|
UTSW |
17 |
34,679,025 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Tsbp1
|
UTSW |
17 |
34,679,035 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Tsbp1
|
UTSW |
17 |
34,679,032 (GRCm39) |
unclassified |
probably benign |
|
R0046:Tsbp1
|
UTSW |
17 |
34,679,095 (GRCm39) |
critical splice donor site |
probably null |
|
R0046:Tsbp1
|
UTSW |
17 |
34,679,095 (GRCm39) |
critical splice donor site |
probably null |
|
R0523:Tsbp1
|
UTSW |
17 |
34,664,473 (GRCm39) |
critical splice donor site |
probably null |
|
R0661:Tsbp1
|
UTSW |
17 |
34,678,887 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2224:Tsbp1
|
UTSW |
17 |
34,667,737 (GRCm39) |
splice site |
probably null |
|
R2937:Tsbp1
|
UTSW |
17 |
34,640,836 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3932:Tsbp1
|
UTSW |
17 |
34,662,417 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4210:Tsbp1
|
UTSW |
17 |
34,679,257 (GRCm39) |
unclassified |
probably benign |
|
R4924:Tsbp1
|
UTSW |
17 |
34,678,951 (GRCm39) |
missense |
probably damaging |
0.96 |
R5055:Tsbp1
|
UTSW |
17 |
34,667,770 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5446:Tsbp1
|
UTSW |
17 |
34,659,867 (GRCm39) |
splice site |
probably null |
|
R6147:Tsbp1
|
UTSW |
17 |
34,637,897 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6851:Tsbp1
|
UTSW |
17 |
34,679,146 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6866:Tsbp1
|
UTSW |
17 |
34,678,935 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7035:Tsbp1
|
UTSW |
17 |
34,679,305 (GRCm39) |
unclassified |
probably benign |
|
R7077:Tsbp1
|
UTSW |
17 |
34,659,856 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7468:Tsbp1
|
UTSW |
17 |
34,636,539 (GRCm39) |
splice site |
probably null |
|
R7556:Tsbp1
|
UTSW |
17 |
34,656,691 (GRCm39) |
missense |
unknown |
|
R7843:Tsbp1
|
UTSW |
17 |
34,668,798 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8503:Tsbp1
|
UTSW |
17 |
34,667,100 (GRCm39) |
splice site |
probably benign |
|
R8529:Tsbp1
|
UTSW |
17 |
34,679,143 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8683:Tsbp1
|
UTSW |
17 |
34,667,782 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8941:Tsbp1
|
UTSW |
17 |
34,678,973 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9222:Tsbp1
|
UTSW |
17 |
34,648,922 (GRCm39) |
missense |
|
|
R9560:Tsbp1
|
UTSW |
17 |
34,663,016 (GRCm39) |
missense |
probably damaging |
0.97 |
|