Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
G |
19: 8,989,221 (GRCm39) |
N3502D |
possibly damaging |
Het |
Ambn |
T |
A |
5: 88,609,574 (GRCm39) |
I94K |
possibly damaging |
Het |
Ank3 |
A |
G |
10: 69,660,179 (GRCm39) |
H227R |
probably damaging |
Het |
Arhgap42 |
G |
T |
9: 9,006,446 (GRCm39) |
P650Q |
probably damaging |
Het |
Bahcc1 |
A |
G |
11: 120,162,422 (GRCm39) |
E240G |
possibly damaging |
Het |
Cd19 |
T |
C |
7: 126,010,025 (GRCm39) |
E408G |
probably benign |
Het |
Cdh11 |
G |
A |
8: 103,391,276 (GRCm39) |
T320I |
probably damaging |
Het |
Cep131 |
G |
A |
11: 119,956,517 (GRCm39) |
R944W |
probably damaging |
Het |
Dgkd |
T |
G |
1: 87,853,413 (GRCm39) |
|
probably null |
Het |
Dnaaf1 |
T |
A |
8: 120,309,401 (GRCm39) |
L163Q |
probably damaging |
Het |
Ecpas |
A |
G |
4: 58,814,081 (GRCm39) |
C1342R |
possibly damaging |
Het |
Etl4 |
T |
A |
2: 20,748,919 (GRCm39) |
L550Q |
possibly damaging |
Het |
Evpl |
T |
C |
11: 116,114,633 (GRCm39) |
E1019G |
probably damaging |
Het |
Fam120b |
T |
C |
17: 15,635,091 (GRCm39) |
L601P |
probably damaging |
Het |
Fhit |
C |
A |
14: 9,763,762 (GRCm38) |
R172L |
possibly damaging |
Het |
Hoxa6 |
T |
C |
6: 52,183,523 (GRCm39) |
H174R |
possibly damaging |
Het |
Htra4 |
A |
G |
8: 25,520,561 (GRCm39) |
F367L |
probably damaging |
Het |
Iws1 |
T |
C |
18: 32,219,326 (GRCm39) |
|
probably benign |
Het |
Lats2 |
A |
G |
14: 57,933,591 (GRCm39) |
V842A |
probably damaging |
Het |
Limd2 |
C |
T |
11: 106,050,213 (GRCm39) |
M1I |
probably null |
Het |
Lrp2 |
T |
A |
2: 69,348,787 (GRCm39) |
Q728L |
probably damaging |
Het |
Mcc |
T |
A |
18: 44,606,707 (GRCm39) |
T400S |
possibly damaging |
Het |
Mthfd1l |
A |
G |
10: 3,997,898 (GRCm39) |
D623G |
probably damaging |
Het |
Myocos |
T |
C |
1: 162,484,665 (GRCm39) |
|
probably benign |
Het |
Nat1 |
G |
T |
8: 67,943,995 (GRCm39) |
A124S |
probably benign |
Het |
Nfya |
A |
T |
17: 48,702,715 (GRCm39) |
M62K |
probably benign |
Het |
Nlgn1 |
A |
G |
3: 25,490,506 (GRCm39) |
V378A |
probably damaging |
Het |
Or52r1c |
T |
A |
7: 102,735,265 (GRCm39) |
I175N |
possibly damaging |
Het |
Or5ak22 |
A |
T |
2: 85,230,861 (GRCm39) |
N5K |
probably damaging |
Het |
Pitpnm2 |
T |
C |
5: 124,269,234 (GRCm39) |
S463G |
probably benign |
Het |
Serpinb3b |
T |
C |
1: 107,082,403 (GRCm39) |
E287G |
probably benign |
Het |
Slc16a13 |
T |
C |
11: 70,108,661 (GRCm39) |
T390A |
probably benign |
Het |
Slc7a14 |
A |
G |
3: 31,278,372 (GRCm39) |
M411T |
probably damaging |
Het |
Strn |
A |
G |
17: 79,043,886 (GRCm39) |
F11L |
probably damaging |
Het |
Swap70 |
T |
A |
7: 109,854,956 (GRCm39) |
F85L |
possibly damaging |
Het |
Tanc2 |
T |
A |
11: 105,689,479 (GRCm39) |
W214R |
probably benign |
Het |
Tenm3 |
T |
C |
8: 48,729,773 (GRCm39) |
K1411R |
probably benign |
Het |
Tmem176a |
G |
T |
6: 48,820,759 (GRCm39) |
R116L |
probably damaging |
Het |
Trim71 |
G |
T |
9: 114,354,115 (GRCm39) |
H296Q |
probably damaging |
Het |
Vmn1r67 |
A |
T |
7: 10,180,840 (GRCm39) |
I35L |
probably benign |
Het |
Vnn3 |
A |
G |
10: 23,727,620 (GRCm39) |
T47A |
probably benign |
Het |
Zscan10 |
A |
T |
17: 23,824,581 (GRCm39) |
Q12H |
probably damaging |
Het |
|
Other mutations in Ighg2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02087:Ighg2c
|
APN |
12 |
113,248,986 (GRCm39) |
unclassified |
probably benign |
|
IGL02560:Ighg2c
|
APN |
12 |
113,251,504 (GRCm39) |
missense |
unknown |
|
IGL03339:Ighg2c
|
APN |
12 |
113,251,614 (GRCm39) |
missense |
unknown |
|
R0047:Ighg2c
|
UTSW |
12 |
113,251,788 (GRCm39) |
splice site |
probably benign |
|
R0047:Ighg2c
|
UTSW |
12 |
113,251,788 (GRCm39) |
splice site |
probably benign |
|
R0415:Ighg2c
|
UTSW |
12 |
113,251,530 (GRCm39) |
missense |
unknown |
|
R0571:Ighg2c
|
UTSW |
12 |
113,252,382 (GRCm39) |
nonsense |
probably null |
|
R0634:Ighg2c
|
UTSW |
12 |
113,251,584 (GRCm39) |
missense |
unknown |
|
R0893:Ighg2c
|
UTSW |
12 |
113,251,053 (GRCm39) |
missense |
unknown |
|
R1169:Ighg2c
|
UTSW |
12 |
113,249,572 (GRCm39) |
unclassified |
probably benign |
|
R3895:Ighg2c
|
UTSW |
12 |
113,251,278 (GRCm39) |
missense |
unknown |
|
R5065:Ighg2c
|
UTSW |
12 |
113,251,708 (GRCm39) |
missense |
unknown |
|
R6407:Ighg2c
|
UTSW |
12 |
113,252,271 (GRCm39) |
missense |
unknown |
|
R7052:Ighg2c
|
UTSW |
12 |
113,252,343 (GRCm39) |
missense |
|
|
R7231:Ighg2c
|
UTSW |
12 |
113,251,636 (GRCm39) |
missense |
|
|
R7513:Ighg2c
|
UTSW |
12 |
113,252,471 (GRCm39) |
missense |
|
|
R8783:Ighg2c
|
UTSW |
12 |
113,252,412 (GRCm39) |
missense |
|
|
R9175:Ighg2c
|
UTSW |
12 |
113,252,499 (GRCm39) |
missense |
|
|
R9419:Ighg2c
|
UTSW |
12 |
113,251,015 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1177:Ighg2c
|
UTSW |
12 |
113,251,300 (GRCm39) |
missense |
|
|
|