Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk2 |
T |
C |
18: 65,422,809 (GRCm39) |
Y1963C |
probably benign |
Het |
Bptf |
T |
A |
11: 107,001,952 (GRCm39) |
N387Y |
probably damaging |
Het |
C1ql2 |
T |
C |
1: 120,269,340 (GRCm39) |
L165P |
probably damaging |
Het |
Col5a2 |
C |
A |
1: 45,415,938 (GRCm39) |
C1403F |
probably damaging |
Het |
Gab1 |
C |
A |
8: 81,515,226 (GRCm39) |
R364L |
possibly damaging |
Het |
Htr3a |
G |
T |
9: 48,812,355 (GRCm39) |
Y250* |
probably null |
Het |
Ighg2c |
T |
C |
12: 113,252,271 (GRCm39) |
K94E |
unknown |
Het |
Il36rn |
A |
G |
2: 24,171,365 (GRCm39) |
Y151C |
probably damaging |
Het |
Kif22 |
G |
A |
7: 126,632,375 (GRCm39) |
R312C |
probably damaging |
Het |
Lap3 |
T |
A |
5: 45,669,267 (GRCm39) |
V472E |
probably damaging |
Het |
Mast3 |
T |
C |
8: 71,234,772 (GRCm39) |
T762A |
probably benign |
Het |
Mfsd12 |
T |
C |
10: 81,198,067 (GRCm39) |
|
probably null |
Het |
Mrpl39 |
T |
C |
16: 84,529,273 (GRCm39) |
K123R |
probably benign |
Het |
Mup8 |
T |
A |
4: 60,220,394 (GRCm39) |
T113S |
possibly damaging |
Het |
Nhp2 |
T |
C |
11: 51,510,730 (GRCm39) |
V29A |
probably benign |
Het |
Or14a260 |
T |
C |
7: 85,985,277 (GRCm39) |
E109G |
possibly damaging |
Het |
Pex3 |
T |
C |
10: 13,422,112 (GRCm39) |
R63G |
probably damaging |
Het |
Pfkl |
A |
G |
10: 77,824,507 (GRCm39) |
|
probably null |
Het |
Rims2 |
T |
C |
15: 39,315,724 (GRCm39) |
S617P |
probably damaging |
Het |
Rnf223 |
A |
T |
4: 156,216,816 (GRCm39) |
T64S |
probably damaging |
Het |
Rrp12 |
C |
T |
19: 41,872,181 (GRCm39) |
V432M |
probably damaging |
Het |
Sag |
T |
C |
1: 87,742,528 (GRCm39) |
V100A |
probably benign |
Het |
Slc17a7 |
C |
T |
7: 44,819,350 (GRCm39) |
A167V |
probably benign |
Het |
Slc38a6 |
T |
C |
12: 73,356,949 (GRCm39) |
F115S |
probably damaging |
Het |
Spata31h1 |
A |
G |
10: 82,129,645 (GRCm39) |
S1122P |
probably benign |
Het |
Spdye4a |
T |
C |
5: 143,211,454 (GRCm39) |
T37A |
probably benign |
Het |
Sphk2 |
T |
C |
7: 45,362,024 (GRCm39) |
T138A |
possibly damaging |
Het |
Srgap3 |
T |
C |
6: 112,699,967 (GRCm39) |
S1004G |
probably damaging |
Het |
Sult1a1 |
T |
C |
7: 126,272,356 (GRCm39) |
|
probably null |
Het |
Tmem212 |
A |
G |
3: 27,938,988 (GRCm39) |
V166A |
probably benign |
Het |
Tor4a |
A |
G |
2: 25,084,952 (GRCm39) |
L317P |
probably benign |
Het |
Trim43c |
A |
T |
9: 88,722,467 (GRCm39) |
T38S |
probably benign |
Het |
Tshz1 |
C |
A |
18: 84,034,091 (GRCm39) |
V106F |
possibly damaging |
Het |
Tut4 |
G |
T |
4: 108,415,979 (GRCm39) |
E1648D |
probably damaging |
Het |
Yap1 |
A |
G |
9: 7,962,373 (GRCm39) |
M225T |
possibly damaging |
Het |
Zfp74 |
T |
C |
7: 29,635,048 (GRCm39) |
E220G |
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 |
|
IGL03252:Ighg3
|
APN |
12 |
113,324,184 (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 |
|
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 |
|
|
|