Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
A |
13: 81,707,648 (GRCm39) |
V1253F |
probably damaging |
Het |
Apbb2 |
A |
G |
5: 66,557,574 (GRCm39) |
W296R |
probably damaging |
Het |
Armh3 |
G |
A |
19: 45,808,792 (GRCm39) |
T633I |
probably damaging |
Het |
Btbd3 |
T |
C |
2: 138,126,043 (GRCm39) |
V409A |
possibly damaging |
Het |
C130050O18Rik |
A |
T |
5: 139,400,820 (GRCm39) |
D291V |
probably damaging |
Het |
Catsper3 |
A |
G |
13: 55,955,848 (GRCm39) |
N318D |
probably benign |
Het |
Chd1 |
T |
A |
17: 15,945,543 (GRCm39) |
D22E |
possibly damaging |
Het |
Chrnb2 |
G |
A |
3: 89,670,681 (GRCm39) |
|
probably benign |
Het |
Col24a1 |
G |
A |
3: 145,029,162 (GRCm39) |
G550D |
probably damaging |
Het |
Cryl1 |
T |
C |
14: 57,550,534 (GRCm39) |
D110G |
probably damaging |
Het |
Deaf1 |
A |
G |
7: 140,902,874 (GRCm39) |
I150T |
probably damaging |
Het |
Eif3a |
A |
T |
19: 60,770,747 (GRCm39) |
D33E |
possibly damaging |
Het |
Fabp12 |
C |
A |
3: 10,315,114 (GRCm39) |
G78C |
probably benign |
Het |
Fat1 |
A |
G |
8: 45,476,651 (GRCm39) |
D1899G |
probably damaging |
Het |
Galnt13 |
G |
A |
2: 54,744,660 (GRCm39) |
V120I |
probably benign |
Het |
Ganab |
G |
A |
19: 8,889,840 (GRCm39) |
A635T |
probably damaging |
Het |
Gm17509 |
G |
A |
13: 117,357,380 (GRCm39) |
|
probably benign |
Het |
Hfm1 |
T |
A |
5: 107,043,800 (GRCm39) |
|
probably benign |
Het |
Hoxd13 |
A |
C |
2: 74,500,440 (GRCm39) |
D327A |
probably damaging |
Het |
Ints4 |
G |
T |
7: 97,140,137 (GRCm39) |
|
probably null |
Het |
Kcna10 |
A |
T |
3: 107,102,259 (GRCm39) |
T297S |
probably benign |
Het |
Ldb2 |
G |
A |
5: 44,699,057 (GRCm39) |
T127I |
probably damaging |
Het |
Mapk7 |
T |
C |
11: 61,382,498 (GRCm39) |
D68G |
probably damaging |
Het |
Msh3 |
A |
T |
13: 92,357,596 (GRCm39) |
|
probably benign |
Het |
Muc6 |
A |
G |
7: 141,217,402 (GRCm39) |
S2359P |
possibly damaging |
Het |
Mup6 |
A |
T |
4: 60,005,990 (GRCm39) |
I161F |
possibly damaging |
Het |
Nup160 |
G |
A |
2: 90,534,169 (GRCm39) |
V665I |
probably benign |
Het |
Or13a22 |
A |
G |
7: 140,073,034 (GRCm39) |
N161S |
possibly damaging |
Het |
Or14a258 |
T |
C |
7: 86,034,929 (GRCm39) |
Y313C |
possibly damaging |
Het |
Or4e5 |
T |
A |
14: 52,727,533 (GRCm39) |
D296V |
probably damaging |
Het |
Otog |
G |
A |
7: 45,900,762 (GRCm39) |
V352I |
probably damaging |
Het |
Oxct1 |
T |
A |
15: 4,064,764 (GRCm39) |
V34D |
probably benign |
Het |
Pcdhb21 |
T |
A |
18: 37,648,944 (GRCm39) |
|
probably null |
Het |
Pcdhb8 |
T |
G |
18: 37,490,299 (GRCm39) |
V659G |
probably damaging |
Het |
Plxnb2 |
T |
C |
15: 89,042,234 (GRCm39) |
N1590S |
probably benign |
Het |
Rnf168 |
G |
T |
16: 32,097,099 (GRCm39) |
R56L |
possibly damaging |
Het |
Scn8a |
C |
T |
15: 100,872,496 (GRCm39) |
P362S |
probably benign |
Het |
Slc1a3 |
T |
A |
15: 8,668,562 (GRCm39) |
I468F |
probably damaging |
Het |
Slc39a14 |
G |
A |
14: 70,556,368 (GRCm39) |
R3W |
probably damaging |
Het |
Slc7a6 |
T |
A |
8: 106,921,149 (GRCm39) |
N373K |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,080,087 (GRCm39) |
S1955P |
possibly damaging |
Het |
Stat5a |
T |
A |
11: 100,753,965 (GRCm39) |
Y98* |
probably null |
Het |
Thsd7b |
G |
T |
1: 130,138,013 (GRCm39) |
G1564C |
probably damaging |
Het |
Zc3h13 |
T |
C |
14: 75,569,206 (GRCm39) |
V1351A |
possibly damaging |
Het |
|
Other mutations in Gstm3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01585:Gstm3
|
APN |
3 |
107,873,474 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01637:Gstm3
|
APN |
3 |
107,874,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01937:Gstm3
|
APN |
3 |
107,874,973 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01945:Gstm3
|
APN |
3 |
107,874,973 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02307:Gstm3
|
APN |
3 |
107,874,929 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02820:Gstm3
|
APN |
3 |
107,876,074 (GRCm39) |
splice site |
probably benign |
|
IGL03038:Gstm3
|
APN |
3 |
107,873,485 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03271:Gstm3
|
APN |
3 |
107,873,513 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03097:Gstm3
|
UTSW |
3 |
107,876,117 (GRCm39) |
missense |
probably benign |
|
R0009:Gstm3
|
UTSW |
3 |
107,875,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Gstm3
|
UTSW |
3 |
107,873,586 (GRCm39) |
splice site |
probably benign |
|
R1623:Gstm3
|
UTSW |
3 |
107,875,151 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2108:Gstm3
|
UTSW |
3 |
107,873,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R3005:Gstm3
|
UTSW |
3 |
107,874,923 (GRCm39) |
missense |
probably benign |
0.03 |
R3802:Gstm3
|
UTSW |
3 |
107,871,551 (GRCm39) |
missense |
probably benign |
0.03 |
R3803:Gstm3
|
UTSW |
3 |
107,871,551 (GRCm39) |
missense |
probably benign |
0.03 |
R3804:Gstm3
|
UTSW |
3 |
107,871,551 (GRCm39) |
missense |
probably benign |
0.03 |
R4604:Gstm3
|
UTSW |
3 |
107,875,513 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4837:Gstm3
|
UTSW |
3 |
107,871,531 (GRCm39) |
missense |
probably benign |
|
R6593:Gstm3
|
UTSW |
3 |
107,875,511 (GRCm39) |
missense |
probably benign |
0.01 |
R6963:Gstm3
|
UTSW |
3 |
107,874,940 (GRCm39) |
missense |
probably benign |
0.01 |
R7790:Gstm3
|
UTSW |
3 |
107,876,555 (GRCm39) |
start gained |
probably benign |
|
R9245:Gstm3
|
UTSW |
3 |
107,874,956 (GRCm39) |
missense |
probably benign |
0.01 |
R9465:Gstm3
|
UTSW |
3 |
107,873,431 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9753:Gstm3
|
UTSW |
3 |
107,875,493 (GRCm39) |
missense |
probably damaging |
1.00 |
|