Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agpat5 |
A |
G |
8: 18,929,621 (GRCm39) |
E250G |
probably benign |
Het |
Aox4 |
A |
T |
1: 58,294,670 (GRCm39) |
T960S |
probably damaging |
Het |
Bach2 |
T |
A |
4: 32,563,150 (GRCm39) |
L539H |
probably damaging |
Het |
Capn1 |
A |
T |
19: 6,044,877 (GRCm39) |
L465Q |
probably damaging |
Het |
Cd300c |
A |
G |
11: 114,850,453 (GRCm39) |
F117L |
probably benign |
Het |
Cep104 |
T |
G |
4: 154,069,400 (GRCm39) |
M207R |
probably damaging |
Het |
Chd2 |
A |
G |
7: 73,141,163 (GRCm39) |
Y577H |
possibly damaging |
Het |
Col4a1 |
C |
A |
8: 11,259,650 (GRCm39) |
G1341V |
probably damaging |
Het |
Cplane2 |
C |
T |
4: 140,945,900 (GRCm39) |
R148C |
probably damaging |
Het |
Cspg4 |
T |
G |
9: 56,804,905 (GRCm39) |
D1905E |
probably damaging |
Het |
Dhx37 |
T |
C |
5: 125,508,677 (GRCm39) |
K86R |
probably benign |
Het |
Drd2 |
T |
A |
9: 49,313,443 (GRCm39) |
V204D |
probably damaging |
Het |
Gclc |
A |
T |
9: 77,699,242 (GRCm39) |
I520L |
probably benign |
Het |
Gpat3 |
A |
G |
5: 101,032,252 (GRCm39) |
D183G |
probably benign |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Gprin3 |
T |
C |
6: 59,330,618 (GRCm39) |
E563G |
probably benign |
Het |
Grm8 |
A |
T |
6: 27,761,228 (GRCm39) |
L332* |
probably null |
Het |
Grpel1 |
T |
A |
5: 36,626,827 (GRCm39) |
N36K |
probably benign |
Het |
Hecw1 |
C |
T |
13: 14,520,643 (GRCm39) |
S198N |
probably benign |
Het |
Kcna2 |
T |
C |
3: 107,012,112 (GRCm39) |
I231T |
probably benign |
Het |
Lpcat1 |
T |
C |
13: 73,637,212 (GRCm39) |
I114T |
possibly damaging |
Het |
Mast4 |
G |
T |
13: 102,875,319 (GRCm39) |
H1350N |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,195,756 (GRCm39) |
|
probably benign |
Het |
Ntn1 |
C |
G |
11: 68,276,619 (GRCm39) |
D110H |
probably damaging |
Het |
Or2b11 |
G |
T |
11: 59,462,427 (GRCm39) |
N46K |
probably damaging |
Het |
Pigb |
T |
C |
9: 72,924,755 (GRCm39) |
N468S |
probably benign |
Het |
Pik3r2 |
G |
A |
8: 71,223,065 (GRCm39) |
R452C |
probably benign |
Het |
Plekhg1 |
A |
G |
10: 3,823,400 (GRCm39) |
T123A |
probably damaging |
Het |
Ptges3l |
T |
C |
11: 101,312,443 (GRCm39) |
*67W |
probably null |
Het |
Rgs12 |
G |
A |
5: 35,123,359 (GRCm39) |
V381M |
possibly damaging |
Het |
Rrm2 |
G |
T |
12: 24,758,598 (GRCm39) |
A47S |
probably benign |
Het |
Six2 |
G |
T |
17: 85,992,615 (GRCm39) |
S296Y |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,463,081 (GRCm39) |
C392* |
probably null |
Het |
Snx5 |
A |
T |
2: 144,096,821 (GRCm39) |
|
probably null |
Het |
Svep1 |
A |
G |
4: 58,096,177 (GRCm39) |
L1481P |
probably damaging |
Het |
Ube3b |
C |
A |
5: 114,538,012 (GRCm39) |
Q368K |
probably damaging |
Het |
Zfhx4 |
A |
T |
3: 5,466,269 (GRCm39) |
K2142N |
probably damaging |
Het |
Zfp729a |
A |
T |
13: 67,767,997 (GRCm39) |
F744Y |
probably damaging |
Het |
|
Other mutations in Tspan18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01539:Tspan18
|
APN |
2 |
93,041,198 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02897:Tspan18
|
APN |
2 |
93,050,518 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2513:Tspan18
|
UTSW |
2 |
93,050,440 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3826:Tspan18
|
UTSW |
2 |
93,050,453 (GRCm39) |
missense |
probably benign |
0.00 |
R3827:Tspan18
|
UTSW |
2 |
93,050,453 (GRCm39) |
missense |
probably benign |
0.00 |
R4114:Tspan18
|
UTSW |
2 |
93,142,291 (GRCm39) |
critical splice donor site |
probably null |
|
R4697:Tspan18
|
UTSW |
2 |
93,142,375 (GRCm39) |
splice site |
probably null |
|
R5468:Tspan18
|
UTSW |
2 |
93,040,207 (GRCm39) |
missense |
probably benign |
|
R6358:Tspan18
|
UTSW |
2 |
93,040,219 (GRCm39) |
missense |
probably benign |
0.17 |
R6707:Tspan18
|
UTSW |
2 |
93,040,302 (GRCm39) |
missense |
probably benign |
0.27 |
R7389:Tspan18
|
UTSW |
2 |
93,040,272 (GRCm39) |
missense |
probably benign |
0.05 |
R7942:Tspan18
|
UTSW |
2 |
93,041,203 (GRCm39) |
missense |
probably benign |
0.01 |
R7955:Tspan18
|
UTSW |
2 |
93,040,305 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8155:Tspan18
|
UTSW |
2 |
93,040,357 (GRCm39) |
splice site |
probably null |
|
R9255:Tspan18
|
UTSW |
2 |
93,040,200 (GRCm39) |
missense |
probably benign |
|
R9328:Tspan18
|
UTSW |
2 |
93,036,065 (GRCm39) |
missense |
probably benign |
0.12 |
R9510:Tspan18
|
UTSW |
2 |
93,050,462 (GRCm39) |
missense |
probably damaging |
1.00 |
|