Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503B20Rik |
A |
C |
3: 146,356,613 (GRCm39) |
D98E |
probably benign |
Het |
Ackr3 |
T |
C |
1: 90,141,790 (GRCm39) |
I83T |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,994,411 (GRCm39) |
M5232L |
probably benign |
Het |
Ano1 |
A |
C |
7: 144,161,653 (GRCm39) |
|
probably null |
Het |
Arap1 |
T |
A |
7: 101,053,208 (GRCm39) |
I532N |
probably damaging |
Het |
Bsn |
A |
G |
9: 107,991,153 (GRCm39) |
V1533A |
possibly damaging |
Het |
Ccdc83 |
T |
C |
7: 89,875,885 (GRCm39) |
S329G |
possibly damaging |
Het |
Ccno |
T |
A |
13: 113,124,719 (GRCm39) |
D96E |
probably benign |
Het |
Cpsf1 |
CCCCTGCATGAGGCAGGTCCC |
CCCC |
15: 76,481,655 (GRCm39) |
|
probably null |
Het |
Degs1 |
T |
C |
1: 182,106,638 (GRCm39) |
Y207C |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,495,693 (GRCm39) |
|
probably null |
Het |
Dnah9 |
C |
T |
11: 66,059,107 (GRCm39) |
A63T |
probably benign |
Het |
Eif4e1b |
T |
C |
13: 54,932,711 (GRCm39) |
F100S |
probably damaging |
Het |
Eps8 |
A |
T |
6: 137,460,596 (GRCm39) |
Y722* |
probably null |
Het |
Etfa |
A |
T |
9: 55,402,910 (GRCm39) |
I96N |
probably damaging |
Het |
Flt4 |
A |
G |
11: 49,516,199 (GRCm39) |
T101A |
probably benign |
Het |
Gabra4 |
A |
G |
5: 71,781,268 (GRCm39) |
I381T |
probably benign |
Het |
Gria2 |
A |
G |
3: 80,596,603 (GRCm39) |
V821A |
probably damaging |
Het |
Gss |
G |
T |
2: 155,423,931 (GRCm39) |
T51K |
probably damaging |
Het |
Igkv13-84 |
C |
A |
6: 68,916,977 (GRCm39) |
Y91* |
probably null |
Het |
Iqcb1 |
A |
T |
16: 36,691,863 (GRCm39) |
Q487H |
probably damaging |
Het |
Itga8 |
G |
A |
2: 12,234,972 (GRCm39) |
H429Y |
probably benign |
Het |
Myo1c |
T |
G |
11: 75,547,124 (GRCm39) |
|
probably benign |
Het |
Odad2 |
C |
A |
18: 7,129,394 (GRCm39) |
|
probably null |
Het |
Pcdhga5 |
T |
C |
18: 37,828,434 (GRCm39) |
L294P |
probably damaging |
Het |
Pkd2l2 |
T |
C |
18: 34,558,134 (GRCm39) |
L271P |
probably damaging |
Het |
Plcb2 |
T |
C |
2: 118,549,654 (GRCm39) |
D290G |
probably damaging |
Het |
Pmp22 |
C |
T |
11: 63,049,099 (GRCm39) |
A114V |
probably damaging |
Het |
Ppp1r15a |
T |
C |
7: 45,173,533 (GRCm39) |
D425G |
probably benign |
Het |
Ppp2r3d |
G |
A |
9: 101,071,584 (GRCm39) |
P678L |
probably benign |
Het |
Ptbp2 |
T |
G |
3: 119,541,596 (GRCm39) |
Q147P |
probably damaging |
Het |
Sez6l |
A |
G |
5: 112,724,692 (GRCm39) |
S15P |
possibly damaging |
Het |
Slc25a10 |
T |
C |
11: 120,387,903 (GRCm39) |
F199L |
probably benign |
Het |
Slc4a8 |
A |
G |
15: 100,705,197 (GRCm39) |
N801S |
probably damaging |
Het |
Sucnr1 |
T |
C |
3: 59,994,020 (GRCm39) |
Y183H |
probably damaging |
Het |
Tmem67 |
T |
C |
4: 12,063,086 (GRCm39) |
D520G |
possibly damaging |
Het |
Trrap |
G |
T |
5: 144,752,360 (GRCm39) |
|
probably null |
Het |
Tubgcp5 |
C |
T |
7: 55,473,331 (GRCm39) |
P803L |
probably benign |
Het |
Ubash3a |
A |
T |
17: 31,451,370 (GRCm39) |
Q423L |
probably damaging |
Het |
Ucp1 |
G |
A |
8: 84,020,718 (GRCm39) |
|
probably null |
Het |
Vmn2r94 |
G |
T |
17: 18,476,421 (GRCm39) |
N425K |
probably damaging |
Het |
Vps52 |
A |
G |
17: 34,181,452 (GRCm39) |
M418V |
probably null |
Het |
|
Other mutations in Trgc3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4449001:Trgc3
|
UTSW |
13 |
19,447,532 (GRCm39) |
nonsense |
probably null |
|
R0498:Trgc3
|
UTSW |
13 |
19,445,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R1322:Trgc3
|
UTSW |
13 |
19,445,364 (GRCm39) |
missense |
probably benign |
0.26 |
R1834:Trgc3
|
UTSW |
13 |
19,447,535 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1852:Trgc3
|
UTSW |
13 |
19,445,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Trgc3
|
UTSW |
13 |
19,445,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Trgc3
|
UTSW |
13 |
19,445,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R6086:Trgc3
|
UTSW |
13 |
19,447,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R7209:Trgc3
|
UTSW |
13 |
19,445,334 (GRCm39) |
missense |
probably benign |
0.34 |
R9366:Trgc3
|
UTSW |
13 |
19,446,825 (GRCm39) |
missense |
probably benign |
0.05 |
|