Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
B4galnt2 |
A |
G |
11: 95,764,757 (GRCm39) |
S237P |
probably damaging |
Het |
Btla |
A |
G |
16: 45,059,509 (GRCm39) |
H71R |
possibly damaging |
Het |
Calml3 |
T |
A |
13: 3,853,759 (GRCm39) |
K149* |
probably null |
Het |
Cyp2c29 |
T |
C |
19: 39,275,619 (GRCm39) |
W20R |
probably damaging |
Het |
Dnah8 |
G |
A |
17: 30,892,894 (GRCm39) |
|
probably null |
Het |
Elf3 |
T |
C |
1: 135,182,691 (GRCm39) |
T345A |
probably damaging |
Het |
Erc2 |
T |
C |
14: 28,197,606 (GRCm39) |
|
probably benign |
Het |
Gm10375 |
C |
T |
14: 43,842,289 (GRCm39) |
C147Y |
probably damaging |
Het |
Gsdma2 |
A |
G |
11: 98,539,916 (GRCm39) |
R13G |
probably damaging |
Het |
H3c1 |
G |
A |
13: 23,945,943 (GRCm39) |
|
probably null |
Het |
L3mbtl3 |
A |
G |
10: 26,207,710 (GRCm39) |
|
probably benign |
Het |
Micall2 |
T |
C |
5: 139,702,481 (GRCm39) |
N254S |
probably benign |
Het |
Myh4 |
A |
T |
11: 67,143,042 (GRCm39) |
D990V |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,962,745 (GRCm39) |
F394I |
probably damaging |
Het |
Nek1 |
C |
T |
8: 61,525,364 (GRCm39) |
Q601* |
probably null |
Het |
Or4k37 |
T |
A |
2: 111,159,125 (GRCm39) |
Y120* |
probably null |
Het |
Or52n2c |
C |
T |
7: 104,574,594 (GRCm39) |
V126I |
probably benign |
Het |
Plcb1 |
C |
T |
2: 135,212,348 (GRCm39) |
P980S |
probably benign |
Het |
Puf60 |
T |
C |
15: 75,943,699 (GRCm39) |
D224G |
probably damaging |
Het |
Pus7l |
T |
A |
15: 94,423,691 (GRCm39) |
H586L |
probably benign |
Het |
Rims2 |
T |
C |
15: 39,315,748 (GRCm39) |
S585P |
probably benign |
Het |
Rxfp1 |
T |
A |
3: 79,574,990 (GRCm39) |
D207V |
probably benign |
Het |
Scgb2b7 |
A |
T |
7: 31,404,506 (GRCm39) |
C65S |
probably damaging |
Het |
Sptlc2 |
A |
G |
12: 87,402,431 (GRCm39) |
I165T |
probably benign |
Het |
Sult2a3 |
A |
G |
7: 13,801,559 (GRCm39) |
V260A |
probably damaging |
Het |
Tas2r125 |
A |
G |
6: 132,887,553 (GRCm39) |
|
probably null |
Het |
Tbx18 |
T |
A |
9: 87,587,633 (GRCm39) |
I495F |
probably damaging |
Het |
Top2b |
A |
T |
14: 16,393,163 (GRCm38) |
N274I |
possibly damaging |
Het |
Vmn2r53 |
T |
G |
7: 12,340,318 (GRCm39) |
T52P |
probably damaging |
Het |
|
Other mutations in Ighg3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Ighg3
|
APN |
12 |
113,323,457 (GRCm39) |
missense |
unknown |
|
IGL02641:Ighg3
|
APN |
12 |
113,323,818 (GRCm39) |
missense |
unknown |
|
R0630:Ighg3
|
UTSW |
12 |
113,323,714 (GRCm39) |
splice site |
probably benign |
|
R4957:Ighg3
|
UTSW |
12 |
113,324,750 (GRCm39) |
missense |
unknown |
|
R6407:Ighg3
|
UTSW |
12 |
113,323,770 (GRCm39) |
missense |
unknown |
|
R6745:Ighg3
|
UTSW |
12 |
113,323,890 (GRCm39) |
missense |
unknown |
|
R7801:Ighg3
|
UTSW |
12 |
113,323,436 (GRCm39) |
missense |
|
|
R7824:Ighg3
|
UTSW |
12 |
113,323,426 (GRCm39) |
missense |
|
|
R8075:Ighg3
|
UTSW |
12 |
113,321,097 (GRCm39) |
missense |
|
|
R8076:Ighg3
|
UTSW |
12 |
113,324,158 (GRCm39) |
missense |
probably benign |
|
R8887:Ighg3
|
UTSW |
12 |
113,323,845 (GRCm39) |
missense |
|
|
R9314:Ighg3
|
UTSW |
12 |
113,323,946 (GRCm39) |
missense |
|
|
|