Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
G |
A |
11: 58,771,601 (GRCm39) |
R361H |
probably benign |
Het |
Abcd2 |
G |
T |
15: 91,035,876 (GRCm39) |
T663K |
probably damaging |
Het |
Btbd8 |
A |
T |
5: 107,651,742 (GRCm39) |
T212S |
probably benign |
Het |
Bud23 |
C |
T |
5: 135,092,741 (GRCm39) |
R28H |
probably benign |
Het |
Celsr2 |
T |
C |
3: 108,320,256 (GRCm39) |
Y852C |
probably damaging |
Het |
Dll1 |
C |
A |
17: 15,593,866 (GRCm39) |
R167L |
probably benign |
Het |
Hmgxb4 |
A |
G |
8: 75,750,790 (GRCm39) |
T538A |
probably damaging |
Het |
Hrh4 |
T |
C |
18: 13,155,526 (GRCm39) |
V355A |
possibly damaging |
Het |
Hrnr |
A |
T |
3: 93,230,158 (GRCm39) |
E132V |
probably benign |
Het |
Kcnu1 |
A |
T |
8: 26,382,105 (GRCm39) |
Q485L |
probably null |
Het |
Lrp1b |
T |
A |
2: 40,615,526 (GRCm39) |
M3626L |
probably benign |
Het |
Magea6 |
G |
T |
X: 153,707,623 (GRCm39) |
C144* |
probably null |
Het |
Map1a |
G |
T |
2: 121,135,541 (GRCm39) |
R1881L |
probably damaging |
Het |
Naip2 |
T |
A |
13: 100,298,128 (GRCm39) |
Y636F |
probably damaging |
Het |
Or12j5 |
T |
A |
7: 140,083,713 (GRCm39) |
I220F |
probably damaging |
Het |
Or6c2 |
T |
A |
10: 129,362,272 (GRCm39) |
F59I |
probably benign |
Het |
Prg4 |
A |
G |
1: 150,325,839 (GRCm39) |
|
probably benign |
Het |
Ptpn4 |
T |
G |
1: 119,587,642 (GRCm39) |
Q900H |
probably damaging |
Het |
Ralgps1 |
A |
G |
2: 33,062,428 (GRCm39) |
|
probably null |
Het |
Rasgrp4 |
C |
T |
7: 28,845,450 (GRCm39) |
A381V |
possibly damaging |
Het |
Selenbp1 |
A |
T |
3: 94,844,621 (GRCm39) |
K93* |
probably null |
Het |
Skint5 |
T |
A |
4: 113,524,415 (GRCm39) |
K855N |
unknown |
Het |
Tssk4 |
T |
C |
14: 55,887,885 (GRCm39) |
V27A |
possibly damaging |
Het |
Ttc39a |
C |
A |
4: 109,290,219 (GRCm39) |
Q310K |
possibly damaging |
Het |
Utp18 |
C |
T |
11: 93,766,784 (GRCm39) |
V276I |
probably damaging |
Het |
Vmn2r45 |
C |
A |
7: 8,486,603 (GRCm39) |
L228F |
probably damaging |
Het |
|
Other mutations in Ighv7-1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01637:Ighv7-1
|
APN |
12 |
113,860,123 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03006:Ighv7-1
|
APN |
12 |
113,860,145 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03051:Ighv7-1
|
APN |
12 |
113,860,576 (GRCm39) |
unclassified |
probably benign |
|
R3008:Ighv7-1
|
UTSW |
12 |
113,860,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Ighv7-1
|
UTSW |
12 |
113,860,239 (GRCm39) |
missense |
probably damaging |
0.99 |
R6172:Ighv7-1
|
UTSW |
12 |
113,860,183 (GRCm39) |
missense |
probably damaging |
0.99 |
R6213:Ighv7-1
|
UTSW |
12 |
113,860,141 (GRCm39) |
missense |
probably damaging |
0.99 |
R7324:Ighv7-1
|
UTSW |
12 |
113,860,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R8399:Ighv7-1
|
UTSW |
12 |
113,860,532 (GRCm39) |
missense |
unknown |
|
R9193:Ighv7-1
|
UTSW |
12 |
113,860,110 (GRCm39) |
missense |
probably damaging |
1.00 |
|