Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
A |
T |
16: 14,289,877 (GRCm39) |
M1398L |
probably benign |
Het |
Acad12 |
A |
G |
5: 121,742,084 (GRCm39) |
|
probably benign |
Het |
Aldh1a7 |
T |
C |
19: 20,693,293 (GRCm39) |
I209V |
probably benign |
Het |
Alkal2 |
G |
A |
12: 30,937,264 (GRCm39) |
|
probably null |
Het |
Aqr |
A |
G |
2: 113,979,515 (GRCm39) |
F307L |
probably damaging |
Het |
Atp2a2 |
A |
G |
5: 122,595,639 (GRCm39) |
L932P |
probably damaging |
Het |
Atxn7 |
T |
C |
14: 14,013,638 (GRCm38) |
M113T |
probably damaging |
Het |
Blzf1 |
T |
A |
1: 164,134,038 (GRCm39) |
M4L |
probably benign |
Het |
Brca2 |
C |
A |
5: 150,480,364 (GRCm39) |
S2711R |
probably damaging |
Het |
Bzw1 |
A |
T |
1: 58,436,883 (GRCm39) |
Q70L |
probably damaging |
Het |
Cd34 |
T |
A |
1: 194,630,276 (GRCm39) |
I70N |
probably benign |
Het |
Chac1 |
A |
G |
2: 119,181,999 (GRCm39) |
Y39C |
probably damaging |
Het |
Col6a2 |
G |
C |
10: 76,449,112 (GRCm39) |
P275A |
probably damaging |
Het |
Crb1 |
T |
A |
1: 139,176,627 (GRCm39) |
N452I |
probably damaging |
Het |
Ctrc |
T |
C |
4: 141,566,094 (GRCm39) |
N188S |
probably damaging |
Het |
Dnah7b |
G |
A |
1: 46,307,924 (GRCm39) |
|
probably null |
Het |
Etl4 |
GGGGAAGAACCGG |
GGG |
2: 20,811,273 (GRCm39) |
|
probably null |
Het |
Exoc6 |
T |
A |
19: 37,576,081 (GRCm39) |
|
probably null |
Het |
Gm5616 |
T |
A |
9: 48,361,716 (GRCm39) |
|
noncoding transcript |
Het |
Gm7535 |
T |
C |
17: 18,131,788 (GRCm39) |
|
probably benign |
Het |
Hnrnpr |
T |
C |
4: 136,059,798 (GRCm39) |
S200P |
probably damaging |
Het |
Il21 |
T |
A |
3: 37,281,917 (GRCm39) |
K76* |
probably null |
Het |
Jup |
T |
A |
11: 100,267,632 (GRCm39) |
T564S |
possibly damaging |
Het |
Kcns2 |
G |
C |
15: 34,839,199 (GRCm39) |
R187S |
possibly damaging |
Het |
Klhl18 |
G |
A |
9: 110,275,896 (GRCm39) |
T84M |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,630,882 (GRCm39) |
L2280M |
probably damaging |
Het |
Ncoa6 |
A |
G |
2: 155,263,756 (GRCm39) |
I226T |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,396,196 (GRCm39) |
Y126N |
possibly damaging |
Het |
Nlrp4a |
T |
A |
7: 26,149,589 (GRCm39) |
C399S |
probably damaging |
Het |
Nphp3 |
A |
G |
9: 103,913,352 (GRCm39) |
K54E |
probably damaging |
Het |
Nsun2 |
T |
A |
13: 69,771,368 (GRCm39) |
V326E |
probably benign |
Het |
Oosp3 |
T |
C |
19: 11,674,537 (GRCm39) |
|
probably null |
Het |
Or4k15b |
A |
G |
14: 50,272,746 (GRCm39) |
I38T |
probably benign |
Het |
Pcdhga9 |
T |
C |
18: 37,871,301 (GRCm39) |
S377P |
probably damaging |
Het |
Pdlim3 |
A |
G |
8: 46,368,300 (GRCm39) |
|
probably null |
Het |
Pla2r1 |
A |
T |
2: 60,345,328 (GRCm39) |
W343R |
probably damaging |
Het |
Prox2 |
A |
G |
12: 85,134,721 (GRCm39) |
V520A |
probably benign |
Het |
Rfx3 |
T |
C |
19: 27,771,008 (GRCm39) |
|
probably null |
Het |
Rif1 |
A |
C |
2: 52,011,170 (GRCm39) |
R2412S |
possibly damaging |
Het |
Rreb1 |
T |
C |
13: 38,131,397 (GRCm39) |
L1517P |
probably benign |
Het |
Rxfp1 |
T |
C |
3: 79,594,199 (GRCm39) |
N65S |
probably damaging |
Het |
Sbf2 |
T |
C |
7: 110,038,108 (GRCm39) |
E399G |
probably damaging |
Het |
Slc36a4 |
A |
C |
9: 15,640,098 (GRCm39) |
|
probably null |
Het |
Slco1a1 |
A |
T |
6: 141,885,695 (GRCm39) |
M110K |
probably damaging |
Het |
Stat5a |
T |
A |
11: 100,767,634 (GRCm39) |
C401S |
probably benign |
Het |
Ticam1 |
TCACACA |
TCACA |
17: 56,577,629 (GRCm39) |
|
probably null |
Het |
Tmem150c |
T |
C |
5: 100,231,523 (GRCm39) |
T151A |
probably damaging |
Het |
Ube4a |
A |
T |
9: 44,862,179 (GRCm39) |
M173K |
probably damaging |
Het |
Vmn1r188 |
A |
T |
13: 22,272,342 (GRCm39) |
S99C |
probably damaging |
Het |
Vmn2r70 |
C |
T |
7: 85,208,572 (GRCm39) |
C635Y |
probably damaging |
Het |
Zfp644 |
T |
C |
5: 106,767,461 (GRCm39) |
K24E |
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 |
IGL01837:Ighg2b
|
APN |
12 |
113,270,065 (GRCm39) |
missense |
unknown |
|
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 |
|
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 |
|
|
|