Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730480H06Rik |
A |
G |
5: 48,536,699 (GRCm39) |
T132A |
possibly damaging |
Het |
Abcb1b |
T |
G |
5: 8,915,865 (GRCm39) |
V1249G |
probably damaging |
Het |
Cdc5l |
A |
G |
17: 45,737,449 (GRCm39) |
L103P |
probably damaging |
Het |
Clrn2 |
G |
T |
5: 45,617,485 (GRCm39) |
A119S |
possibly damaging |
Het |
Cop1 |
A |
T |
1: 159,077,600 (GRCm39) |
H145L |
probably benign |
Het |
Cyp4f13 |
G |
C |
17: 33,143,833 (GRCm39) |
P497R |
probably damaging |
Het |
Dennd4a |
A |
G |
9: 64,794,161 (GRCm39) |
E660G |
probably damaging |
Het |
Dhx34 |
T |
C |
7: 15,952,472 (GRCm39) |
Y51C |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,409,414 (GRCm39) |
I3611V |
probably damaging |
Het |
Dock2 |
A |
T |
11: 34,181,622 (GRCm39) |
L1647Q |
probably benign |
Het |
Dpy19l4 |
G |
A |
4: 11,267,659 (GRCm39) |
T427M |
probably benign |
Het |
Eef2k |
T |
C |
7: 120,487,103 (GRCm39) |
L417P |
probably benign |
Het |
Eng |
A |
G |
2: 32,568,906 (GRCm39) |
S477G |
probably benign |
Het |
Enox1 |
T |
C |
14: 77,870,012 (GRCm39) |
I424T |
probably benign |
Het |
Faim2 |
A |
G |
15: 99,408,473 (GRCm39) |
V253A |
probably benign |
Het |
Farp2 |
A |
G |
1: 93,531,139 (GRCm39) |
I546V |
possibly damaging |
Het |
Fcgbp |
T |
G |
7: 27,785,978 (GRCm39) |
Y472D |
probably damaging |
Het |
Gm43302 |
A |
T |
5: 105,424,570 (GRCm39) |
C357S |
possibly damaging |
Het |
Gm47189 |
T |
C |
14: 41,492,053 (GRCm39) |
T75A |
probably damaging |
Het |
Mms22l |
A |
G |
4: 24,496,908 (GRCm39) |
M1V |
probably null |
Het |
Myo3a |
A |
T |
2: 22,401,084 (GRCm39) |
I618F |
probably damaging |
Het |
Nqo2 |
T |
C |
13: 34,165,477 (GRCm39) |
F125L |
probably damaging |
Het |
Or10q1 |
T |
A |
19: 13,726,593 (GRCm39) |
M41K |
possibly damaging |
Het |
Pdcd6ip |
G |
A |
9: 113,518,775 (GRCm39) |
H162Y |
probably benign |
Het |
Potefam1 |
C |
T |
2: 111,059,755 (GRCm39) |
M1I |
probably null |
Het |
Potegl |
A |
G |
2: 23,097,852 (GRCm39) |
E10G |
probably benign |
Het |
Robo3 |
A |
G |
9: 37,336,664 (GRCm39) |
F368S |
probably damaging |
Het |
Rsph4a |
G |
A |
10: 33,781,488 (GRCm39) |
A113T |
probably benign |
Het |
Smc2 |
A |
T |
4: 52,450,992 (GRCm39) |
N270I |
probably benign |
Het |
Son |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCAGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,183 (GRCm39) |
|
probably benign |
Het |
Spsb4 |
A |
G |
9: 96,877,622 (GRCm39) |
|
probably null |
Het |
Spta1 |
G |
A |
1: 174,043,051 (GRCm39) |
R1399Q |
probably benign |
Het |
Stab1 |
T |
C |
14: 30,877,790 (GRCm39) |
D749G |
probably damaging |
Het |
Tas2r115 |
A |
T |
6: 132,714,887 (GRCm39) |
N21K |
probably damaging |
Het |
Tbkbp1 |
A |
G |
11: 97,037,429 (GRCm39) |
V221A |
probably benign |
Het |
Tln2 |
G |
T |
9: 67,261,749 (GRCm39) |
N663K |
probably benign |
Het |
Tmprss11g |
A |
T |
5: 86,640,119 (GRCm39) |
I170K |
probably benign |
Het |
Tnfrsf21 |
G |
A |
17: 43,349,128 (GRCm39) |
E247K |
probably benign |
Het |
Trim23 |
T |
C |
13: 104,337,817 (GRCm39) |
Y522H |
probably benign |
Het |
Vmn1r204 |
G |
A |
13: 22,740,879 (GRCm39) |
C170Y |
probably damaging |
Het |
Vwa8 |
G |
T |
14: 79,174,617 (GRCm39) |
E349* |
probably null |
Het |
Xpo7 |
A |
G |
14: 70,907,989 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rad9b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Rad9b
|
APN |
5 |
122,482,310 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02375:Rad9b
|
APN |
5 |
122,471,405 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0027:Rad9b
|
UTSW |
5 |
122,489,786 (GRCm39) |
unclassified |
probably benign |
|
R0027:Rad9b
|
UTSW |
5 |
122,489,786 (GRCm39) |
unclassified |
probably benign |
|
R0103:Rad9b
|
UTSW |
5 |
122,469,590 (GRCm39) |
missense |
probably damaging |
0.99 |
R0103:Rad9b
|
UTSW |
5 |
122,469,590 (GRCm39) |
missense |
probably damaging |
0.99 |
R0975:Rad9b
|
UTSW |
5 |
122,472,320 (GRCm39) |
splice site |
probably null |
|
R2006:Rad9b
|
UTSW |
5 |
122,477,842 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2265:Rad9b
|
UTSW |
5 |
122,489,405 (GRCm39) |
missense |
probably damaging |
0.98 |
R4818:Rad9b
|
UTSW |
5 |
122,477,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5392:Rad9b
|
UTSW |
5 |
122,489,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R6041:Rad9b
|
UTSW |
5 |
122,489,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R6109:Rad9b
|
UTSW |
5 |
122,482,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R6133:Rad9b
|
UTSW |
5 |
122,477,831 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6566:Rad9b
|
UTSW |
5 |
122,490,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R6695:Rad9b
|
UTSW |
5 |
122,489,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R7295:Rad9b
|
UTSW |
5 |
122,472,341 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7299:Rad9b
|
UTSW |
5 |
122,490,677 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7301:Rad9b
|
UTSW |
5 |
122,490,677 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8954:Rad9b
|
UTSW |
5 |
122,482,293 (GRCm39) |
missense |
probably benign |
0.44 |
Z1088:Rad9b
|
UTSW |
5 |
122,471,435 (GRCm39) |
missense |
possibly damaging |
0.90 |
|