Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
C |
17: 24,627,671 (GRCm39) |
F1372L |
probably damaging |
Het |
Alcam |
T |
A |
16: 52,073,531 (GRCm39) |
N339I |
probably benign |
Het |
Ankrd35 |
A |
C |
3: 96,587,982 (GRCm39) |
D141A |
probably damaging |
Het |
Apc2 |
A |
G |
10: 80,150,492 (GRCm39) |
I1820V |
probably benign |
Het |
Ccp110 |
T |
A |
7: 118,324,684 (GRCm39) |
|
probably null |
Het |
Copa |
T |
A |
1: 171,946,419 (GRCm39) |
D954E |
probably benign |
Het |
Csmd2 |
A |
T |
4: 128,313,363 (GRCm39) |
I1347F |
possibly damaging |
Het |
Ddx10 |
A |
G |
9: 53,140,498 (GRCm39) |
I301T |
probably benign |
Het |
Defb23 |
T |
A |
2: 152,301,294 (GRCm39) |
M93L |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,970,565 (GRCm39) |
|
probably null |
Het |
Dok3 |
T |
C |
13: 55,671,383 (GRCm39) |
E396G |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,727,055 (GRCm39) |
M1318L |
probably benign |
Het |
Foxm1 |
T |
A |
6: 128,343,167 (GRCm39) |
|
probably benign |
Het |
Gm11992 |
A |
T |
11: 9,011,266 (GRCm39) |
R236W |
probably damaging |
Het |
Greb1 |
T |
C |
12: 16,734,452 (GRCm39) |
I1513V |
probably benign |
Het |
Hivep3 |
A |
G |
4: 119,951,759 (GRCm39) |
E25G |
possibly damaging |
Het |
Itga4 |
T |
C |
2: 79,145,349 (GRCm39) |
S722P |
probably damaging |
Het |
Kirrel3 |
G |
A |
9: 34,946,224 (GRCm39) |
R617H |
probably damaging |
Het |
Mboat1 |
A |
T |
13: 30,425,166 (GRCm39) |
H409L |
possibly damaging |
Het |
Naa15 |
A |
T |
3: 51,351,369 (GRCm39) |
K180* |
probably null |
Het |
Nccrp1 |
A |
G |
7: 28,246,191 (GRCm39) |
S124P |
probably damaging |
Het |
Nphp4 |
T |
C |
4: 152,573,338 (GRCm39) |
I92T |
probably damaging |
Het |
Or13a28 |
G |
A |
7: 140,218,124 (GRCm39) |
C170Y |
probably damaging |
Het |
Or6d14 |
C |
A |
6: 116,533,807 (GRCm39) |
Y140* |
probably null |
Het |
Pkd1l3 |
A |
G |
8: 110,356,798 (GRCm39) |
D741G |
possibly damaging |
Het |
Plcb2 |
C |
T |
2: 118,542,407 (GRCm39) |
|
probably null |
Het |
Pramel19 |
A |
G |
4: 101,798,650 (GRCm39) |
E207G |
probably damaging |
Het |
Prm2 |
G |
A |
16: 10,609,775 (GRCm39) |
|
probably null |
Het |
R3hdm1 |
C |
T |
1: 128,114,497 (GRCm39) |
Q184* |
probably null |
Het |
Rgl1 |
A |
T |
1: 152,424,901 (GRCm39) |
N359K |
probably damaging |
Het |
Rnf44 |
A |
G |
13: 54,829,966 (GRCm39) |
Y366H |
probably damaging |
Het |
Rpap2 |
G |
A |
5: 107,773,835 (GRCm39) |
|
probably null |
Het |
Ryr3 |
T |
C |
2: 112,631,665 (GRCm39) |
N2120S |
probably damaging |
Het |
Samd8 |
A |
G |
14: 21,825,027 (GRCm39) |
|
probably benign |
Het |
Sipa1 |
G |
T |
19: 5,702,099 (GRCm39) |
T937K |
probably damaging |
Het |
Sos1 |
A |
T |
17: 80,730,157 (GRCm39) |
D707E |
probably damaging |
Het |
Tas2r109 |
T |
C |
6: 132,957,477 (GRCm39) |
N151S |
probably benign |
Het |
Try5 |
T |
C |
6: 41,290,358 (GRCm39) |
N42S |
probably benign |
Het |
Ttn |
G |
T |
2: 76,732,338 (GRCm39) |
|
probably benign |
Het |
Utp14b |
A |
G |
1: 78,642,636 (GRCm39) |
E178G |
probably damaging |
Het |
|
Other mutations in Ighg2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01366:Ighg2b
|
APN |
12 |
113,270,656 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01973:Ighg2b
|
APN |
12 |
113,271,305 (GRCm39) |
missense |
unknown |
|
IGL01998:Ighg2b
|
APN |
12 |
113,270,709 (GRCm39) |
missense |
unknown |
|
IGL02147:Ighg2b
|
APN |
12 |
113,270,011 (GRCm39) |
makesense |
probably null |
|
IGL02183:Ighg2b
|
APN |
12 |
113,271,449 (GRCm39) |
missense |
unknown |
|
IGL03089:Ighg2b
|
APN |
12 |
113,270,298 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4453001:Ighg2b
|
UTSW |
12 |
113,270,492 (GRCm39) |
missense |
unknown |
|
R4199:Ighg2b
|
UTSW |
12 |
113,270,907 (GRCm39) |
missense |
probably damaging |
0.96 |
R4459:Ighg2b
|
UTSW |
12 |
113,270,578 (GRCm39) |
missense |
unknown |
|
R4577:Ighg2b
|
UTSW |
12 |
113,270,512 (GRCm39) |
missense |
unknown |
|
R4589:Ighg2b
|
UTSW |
12 |
113,270,104 (GRCm39) |
missense |
unknown |
|
R4807:Ighg2b
|
UTSW |
12 |
113,267,965 (GRCm39) |
unclassified |
probably benign |
|
R4822:Ighg2b
|
UTSW |
12 |
113,270,011 (GRCm39) |
makesense |
probably null |
|
R5424:Ighg2b
|
UTSW |
12 |
113,271,550 (GRCm39) |
missense |
unknown |
|
R5641:Ighg2b
|
UTSW |
12 |
113,270,767 (GRCm39) |
missense |
unknown |
|
R6297:Ighg2b
|
UTSW |
12 |
113,270,512 (GRCm39) |
missense |
unknown |
|
R6701:Ighg2b
|
UTSW |
12 |
113,270,699 (GRCm39) |
missense |
unknown |
|
R6703:Ighg2b
|
UTSW |
12 |
113,268,653 (GRCm39) |
unclassified |
probably benign |
|
R6880:Ighg2b
|
UTSW |
12 |
113,270,726 (GRCm39) |
missense |
|
|
R7342:Ighg2b
|
UTSW |
12 |
113,270,050 (GRCm39) |
missense |
|
|
R7505:Ighg2b
|
UTSW |
12 |
113,268,600 (GRCm39) |
missense |
|
|
R7908:Ighg2b
|
UTSW |
12 |
113,270,074 (GRCm39) |
missense |
|
|
R8543:Ighg2b
|
UTSW |
12 |
113,270,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R8951:Ighg2b
|
UTSW |
12 |
113,270,926 (GRCm39) |
missense |
probably benign |
|
R9237:Ighg2b
|
UTSW |
12 |
113,270,217 (GRCm39) |
missense |
|
|
R9539:Ighg2b
|
UTSW |
12 |
113,270,498 (GRCm39) |
missense |
|
|
R9789:Ighg2b
|
UTSW |
12 |
113,270,304 (GRCm39) |
missense |
|
|
|