Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef33 |
T |
A |
17: 80,667,802 (GRCm39) |
V289D |
probably damaging |
Het |
Cabp5 |
A |
G |
7: 13,137,271 (GRCm39) |
M93V |
probably damaging |
Het |
Ces1a |
A |
C |
8: 93,762,668 (GRCm39) |
V201G |
probably damaging |
Het |
Cisd1 |
A |
G |
10: 71,172,181 (GRCm39) |
F34L |
probably benign |
Het |
Cyp26a1 |
T |
C |
19: 37,688,426 (GRCm39) |
L316P |
probably damaging |
Het |
Ddx39a |
A |
G |
8: 84,448,386 (GRCm39) |
I213V |
probably benign |
Het |
Ddx59 |
A |
T |
1: 136,367,519 (GRCm39) |
N542I |
probably benign |
Het |
Dytn |
T |
C |
1: 63,703,581 (GRCm39) |
T233A |
probably benign |
Het |
Fbxo7 |
A |
G |
10: 85,860,302 (GRCm39) |
T49A |
possibly damaging |
Het |
Fmnl2 |
C |
A |
2: 52,926,510 (GRCm39) |
|
probably benign |
Het |
Golga2 |
G |
T |
2: 32,194,225 (GRCm39) |
K610N |
probably damaging |
Het |
Hipk4 |
T |
C |
7: 27,228,060 (GRCm39) |
Y269H |
probably damaging |
Het |
Ifi209 |
T |
C |
1: 173,470,267 (GRCm39) |
V285A |
possibly damaging |
Het |
Ifna1 |
A |
G |
4: 88,768,523 (GRCm39) |
D67G |
probably benign |
Het |
Map3k13 |
T |
G |
16: 21,724,005 (GRCm39) |
V329G |
probably damaging |
Het |
Mrm3 |
T |
C |
11: 76,134,683 (GRCm39) |
W29R |
possibly damaging |
Het |
Nherf1 |
T |
C |
11: 115,068,060 (GRCm39) |
V200A |
possibly damaging |
Het |
Nos1ap |
T |
C |
1: 170,156,820 (GRCm39) |
I213V |
possibly damaging |
Het |
Nphp4 |
C |
T |
4: 152,640,732 (GRCm39) |
T1033M |
probably damaging |
Het |
Nr5a2 |
T |
C |
1: 136,868,266 (GRCm39) |
|
probably null |
Het |
Nrcam |
A |
G |
12: 44,620,610 (GRCm39) |
Y885C |
probably damaging |
Het |
Odr4 |
A |
G |
1: 150,262,107 (GRCm39) |
|
probably null |
Het |
Or1e17 |
T |
C |
11: 73,831,756 (GRCm39) |
V228A |
probably benign |
Het |
Or8b57 |
T |
C |
9: 40,004,082 (GRCm39) |
H60R |
probably damaging |
Het |
Ovgp1 |
T |
A |
3: 105,893,829 (GRCm39) |
|
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,376,113 (GRCm39) |
S1341G |
probably benign |
Het |
Pld2 |
T |
G |
11: 70,447,905 (GRCm39) |
L856R |
probably benign |
Het |
Plod1 |
A |
G |
4: 148,003,344 (GRCm39) |
F494L |
possibly damaging |
Het |
Pnkd |
T |
A |
1: 74,389,027 (GRCm39) |
S233T |
possibly damaging |
Het |
Rnf144b |
T |
C |
13: 47,393,255 (GRCm39) |
I198T |
probably damaging |
Het |
Rsc1a1 |
G |
T |
4: 141,412,376 (GRCm39) |
Q179K |
probably benign |
Het |
Slc5a10 |
C |
T |
11: 61,598,632 (GRCm39) |
W249* |
probably null |
Het |
Spata32 |
T |
G |
11: 103,098,973 (GRCm39) |
|
probably benign |
Het |
Stk4 |
T |
A |
2: 163,938,817 (GRCm39) |
H228Q |
probably damaging |
Het |
Szt2 |
T |
A |
4: 118,242,030 (GRCm39) |
Q1592L |
probably benign |
Het |
Tnc |
T |
A |
4: 63,893,493 (GRCm39) |
I1598F |
probably damaging |
Het |
Togaram2 |
A |
T |
17: 72,011,749 (GRCm39) |
D476V |
probably benign |
Het |
Ttll6 |
T |
G |
11: 96,030,601 (GRCm39) |
|
probably benign |
Het |
Vmn2r118 |
A |
G |
17: 55,899,655 (GRCm39) |
S750P |
probably benign |
Het |
Zswim5 |
C |
T |
4: 116,842,892 (GRCm39) |
T879I |
probably damaging |
Het |
|
Other mutations in Angel1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01678:Angel1
|
APN |
12 |
86,763,800 (GRCm39) |
missense |
probably benign |
|
IGL02738:Angel1
|
APN |
12 |
86,752,060 (GRCm39) |
missense |
probably benign |
0.10 |
R0521:Angel1
|
UTSW |
12 |
86,769,681 (GRCm39) |
missense |
probably benign |
0.01 |
R0626:Angel1
|
UTSW |
12 |
86,764,487 (GRCm39) |
critical splice donor site |
probably null |
|
R1929:Angel1
|
UTSW |
12 |
86,749,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Angel1
|
UTSW |
12 |
86,767,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4292:Angel1
|
UTSW |
12 |
86,767,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4295:Angel1
|
UTSW |
12 |
86,767,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4450:Angel1
|
UTSW |
12 |
86,768,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Angel1
|
UTSW |
12 |
86,768,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R7097:Angel1
|
UTSW |
12 |
86,773,158 (GRCm39) |
missense |
probably damaging |
0.98 |
R7284:Angel1
|
UTSW |
12 |
86,767,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R7616:Angel1
|
UTSW |
12 |
86,764,510 (GRCm39) |
missense |
probably benign |
0.00 |
R7984:Angel1
|
UTSW |
12 |
86,767,068 (GRCm39) |
missense |
probably benign |
0.33 |
R9010:Angel1
|
UTSW |
12 |
86,770,153 (GRCm39) |
missense |
possibly damaging |
0.78 |
|