Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
A |
T |
17: 46,635,317 (GRCm39) |
W229R |
probably damaging |
Het |
Adck2 |
T |
C |
6: 39,560,998 (GRCm39) |
|
probably null |
Het |
Ahi1 |
A |
T |
10: 20,930,968 (GRCm39) |
N936I |
probably damaging |
Het |
Ass1 |
T |
C |
2: 31,404,813 (GRCm39) |
S365P |
probably damaging |
Het |
Atp9b |
T |
C |
18: 80,935,072 (GRCm39) |
K208E |
possibly damaging |
Het |
Bag6 |
G |
A |
17: 35,364,898 (GRCm39) |
|
probably null |
Het |
Bptf |
A |
T |
11: 106,945,421 (GRCm39) |
V2491E |
probably damaging |
Het |
Cd300ld2 |
T |
A |
11: 114,904,619 (GRCm39) |
R83W |
probably damaging |
Het |
Chrnd |
T |
C |
1: 87,126,434 (GRCm39) |
F396L |
probably damaging |
Het |
Cyp3a13 |
G |
A |
5: 137,893,546 (GRCm39) |
P439S |
probably damaging |
Het |
Dnhd1 |
C |
A |
7: 105,364,770 (GRCm39) |
H4279N |
probably damaging |
Het |
Fam118a |
T |
C |
15: 84,929,038 (GRCm39) |
|
probably null |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fasn |
T |
A |
11: 120,699,115 (GRCm39) |
D2386V |
probably benign |
Het |
Fat1 |
G |
A |
8: 45,477,532 (GRCm39) |
V2170I |
probably benign |
Het |
Fdps |
T |
C |
3: 89,000,958 (GRCm39) |
R374G |
probably benign |
Het |
Fhl5 |
T |
C |
4: 25,213,681 (GRCm39) |
D85G |
probably benign |
Het |
Flvcr1 |
T |
C |
1: 190,757,861 (GRCm39) |
M144V |
possibly damaging |
Het |
Gask1b |
T |
C |
3: 79,848,769 (GRCm39) |
I505T |
probably damaging |
Het |
Gpr31b |
A |
G |
17: 13,270,765 (GRCm39) |
S135P |
probably damaging |
Het |
Hey2 |
A |
T |
10: 30,710,413 (GRCm39) |
D113E |
probably benign |
Het |
Hoxc5 |
T |
A |
15: 102,923,807 (GRCm39) |
I201N |
probably damaging |
Het |
Ighv1-50 |
A |
T |
12: 115,083,794 (GRCm39) |
W3R |
probably damaging |
Het |
Impa1 |
A |
G |
3: 10,380,348 (GRCm39) |
I208T |
probably benign |
Het |
Iqcj |
T |
C |
3: 67,954,624 (GRCm39) |
L43P |
possibly damaging |
Het |
Itga10 |
T |
C |
3: 96,564,030 (GRCm39) |
F895L |
probably damaging |
Het |
Kdm4b |
T |
C |
17: 56,706,435 (GRCm39) |
C850R |
probably damaging |
Het |
Krt25 |
A |
T |
11: 99,208,205 (GRCm39) |
I341N |
probably damaging |
Het |
L3mbtl3 |
T |
A |
10: 26,168,567 (GRCm39) |
R621* |
probably null |
Het |
Lipm |
T |
C |
19: 34,078,563 (GRCm39) |
|
probably benign |
Het |
Macrod2 |
A |
T |
2: 142,098,441 (GRCm39) |
D286V |
probably damaging |
Het |
Mad2l2 |
T |
A |
4: 148,225,411 (GRCm39) |
V27E |
possibly damaging |
Het |
Map4k4 |
T |
A |
1: 40,050,842 (GRCm39) |
H768Q |
probably benign |
Het |
Mgat4d |
A |
G |
8: 84,081,496 (GRCm39) |
N83S |
probably benign |
Het |
Nucb1 |
C |
T |
7: 45,148,282 (GRCm39) |
R141H |
possibly damaging |
Het |
Or2t46 |
A |
G |
11: 58,472,491 (GRCm39) |
K274E |
possibly damaging |
Het |
Pcdhga2 |
A |
C |
18: 37,803,719 (GRCm39) |
D521A |
probably damaging |
Het |
Pcnx1 |
T |
C |
12: 81,964,586 (GRCm39) |
V251A |
probably benign |
Het |
Pdf |
A |
T |
8: 107,774,833 (GRCm39) |
M133K |
probably damaging |
Het |
Piezo2 |
A |
G |
18: 63,166,057 (GRCm39) |
F2058S |
probably damaging |
Het |
Plekhb2 |
T |
A |
1: 34,915,982 (GRCm39) |
|
probably null |
Het |
Ppp2r3d |
G |
C |
9: 101,052,547 (GRCm39) |
H221D |
probably damaging |
Het |
Prl2c5 |
A |
T |
13: 13,357,503 (GRCm39) |
|
probably null |
Het |
Puf60 |
T |
A |
15: 75,947,663 (GRCm39) |
M49L |
probably benign |
Het |
Rdh16f1 |
T |
C |
10: 127,624,561 (GRCm39) |
V133A |
probably benign |
Het |
Slc22a23 |
G |
T |
13: 34,528,362 (GRCm39) |
A140D |
probably benign |
Het |
Slc25a42 |
A |
G |
8: 70,641,573 (GRCm39) |
L136P |
probably damaging |
Het |
Slc36a3 |
T |
A |
11: 55,020,519 (GRCm39) |
M284L |
probably damaging |
Het |
Tas2r115 |
T |
A |
6: 132,714,895 (GRCm39) |
I19F |
probably damaging |
Het |
Tmc2 |
A |
G |
2: 130,103,300 (GRCm39) |
H812R |
probably benign |
Het |
Vmn2r26 |
A |
G |
6: 124,016,057 (GRCm39) |
S174G |
possibly damaging |
Het |
Vstm4 |
T |
A |
14: 32,585,959 (GRCm39) |
|
probably null |
Het |
Vwc2 |
C |
A |
11: 11,104,250 (GRCm39) |
P261T |
probably damaging |
Het |
Zfhx3 |
C |
G |
8: 109,683,453 (GRCm39) |
H3631D |
unknown |
Het |
Zfp335 |
A |
G |
2: 164,735,640 (GRCm39) |
C1105R |
probably damaging |
Het |
Zfp488 |
A |
G |
14: 33,692,755 (GRCm39) |
L136P |
probably benign |
Het |
Zzef1 |
G |
A |
11: 72,803,983 (GRCm39) |
R2575H |
probably damaging |
Het |
|
Other mutations in Robo2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00666:Robo2
|
APN |
16 |
73,758,588 (GRCm39) |
missense |
probably benign |
|
IGL00849:Robo2
|
APN |
16 |
73,770,665 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL00908:Robo2
|
APN |
16 |
73,782,579 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00944:Robo2
|
APN |
16 |
73,730,585 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00955:Robo2
|
APN |
16 |
73,812,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00970:Robo2
|
APN |
16 |
73,693,934 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01020:Robo2
|
APN |
16 |
73,725,039 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01347:Robo2
|
APN |
16 |
74,149,744 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02280:Robo2
|
APN |
16 |
73,843,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02424:Robo2
|
APN |
16 |
73,770,189 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03376:Robo2
|
APN |
16 |
73,753,380 (GRCm39) |
missense |
probably damaging |
1.00 |
LCD18:Robo2
|
UTSW |
16 |
74,055,954 (GRCm38) |
intron |
probably benign |
|
P0018:Robo2
|
UTSW |
16 |
73,843,694 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0314:Robo2
|
UTSW |
16 |
73,753,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0324:Robo2
|
UTSW |
16 |
73,764,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0539:Robo2
|
UTSW |
16 |
73,782,462 (GRCm39) |
splice site |
probably benign |
|
R0620:Robo2
|
UTSW |
16 |
73,764,690 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0630:Robo2
|
UTSW |
16 |
73,713,093 (GRCm39) |
missense |
probably benign |
0.05 |
R0701:Robo2
|
UTSW |
16 |
73,843,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R1155:Robo2
|
UTSW |
16 |
73,831,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1168:Robo2
|
UTSW |
16 |
73,745,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Robo2
|
UTSW |
16 |
73,713,016 (GRCm39) |
splice site |
probably null |
|
R1195:Robo2
|
UTSW |
16 |
73,713,016 (GRCm39) |
splice site |
probably null |
|
R1195:Robo2
|
UTSW |
16 |
73,713,016 (GRCm39) |
splice site |
probably null |
|
R1317:Robo2
|
UTSW |
16 |
73,831,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R1422:Robo2
|
UTSW |
16 |
73,775,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R1452:Robo2
|
UTSW |
16 |
73,758,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Robo2
|
UTSW |
16 |
73,695,889 (GRCm39) |
missense |
probably benign |
0.36 |
R1709:Robo2
|
UTSW |
16 |
73,753,411 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1751:Robo2
|
UTSW |
16 |
73,831,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R1761:Robo2
|
UTSW |
16 |
73,831,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Robo2
|
UTSW |
16 |
73,713,033 (GRCm39) |
missense |
probably benign |
0.00 |
R1911:Robo2
|
UTSW |
16 |
73,755,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Robo2
|
UTSW |
16 |
73,696,042 (GRCm39) |
missense |
probably benign |
|
R2005:Robo2
|
UTSW |
16 |
73,730,003 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2851:Robo2
|
UTSW |
16 |
73,758,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Robo2
|
UTSW |
16 |
73,717,635 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3732:Robo2
|
UTSW |
16 |
73,717,635 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3733:Robo2
|
UTSW |
16 |
73,717,635 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3734:Robo2
|
UTSW |
16 |
73,717,635 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3913:Robo2
|
UTSW |
16 |
73,831,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R3956:Robo2
|
UTSW |
16 |
73,758,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R4394:Robo2
|
UTSW |
16 |
73,745,267 (GRCm39) |
missense |
probably benign |
0.13 |
R4426:Robo2
|
UTSW |
16 |
73,745,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Robo2
|
UTSW |
16 |
73,770,132 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4454:Robo2
|
UTSW |
16 |
74,149,407 (GRCm39) |
intron |
probably benign |
|
R4478:Robo2
|
UTSW |
16 |
73,812,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R4586:Robo2
|
UTSW |
16 |
73,758,761 (GRCm39) |
missense |
probably damaging |
0.96 |
R4621:Robo2
|
UTSW |
16 |
73,782,821 (GRCm39) |
missense |
probably benign |
0.00 |
R4673:Robo2
|
UTSW |
16 |
73,701,266 (GRCm39) |
splice site |
probably null |
|
R4798:Robo2
|
UTSW |
16 |
74,149,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R4812:Robo2
|
UTSW |
16 |
73,713,176 (GRCm39) |
missense |
probably benign |
0.00 |
R4855:Robo2
|
UTSW |
16 |
73,768,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R4910:Robo2
|
UTSW |
16 |
73,730,666 (GRCm39) |
missense |
probably damaging |
0.99 |
R4916:Robo2
|
UTSW |
16 |
73,695,803 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4948:Robo2
|
UTSW |
16 |
74,149,726 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5325:Robo2
|
UTSW |
16 |
73,770,673 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5326:Robo2
|
UTSW |
16 |
73,695,853 (GRCm39) |
missense |
probably benign |
0.20 |
R5447:Robo2
|
UTSW |
16 |
73,770,654 (GRCm39) |
nonsense |
probably null |
|
R5542:Robo2
|
UTSW |
16 |
73,695,853 (GRCm39) |
missense |
probably benign |
0.20 |
R5545:Robo2
|
UTSW |
16 |
73,758,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Robo2
|
UTSW |
16 |
73,758,707 (GRCm39) |
missense |
probably damaging |
0.99 |
R5734:Robo2
|
UTSW |
16 |
74,149,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Robo2
|
UTSW |
16 |
73,692,668 (GRCm39) |
utr 3 prime |
probably benign |
|
R5960:Robo2
|
UTSW |
16 |
73,730,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R6126:Robo2
|
UTSW |
16 |
73,717,570 (GRCm39) |
missense |
probably benign |
0.00 |
R6130:Robo2
|
UTSW |
16 |
73,717,570 (GRCm39) |
missense |
probably benign |
0.00 |
R6153:Robo2
|
UTSW |
16 |
73,717,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6240:Robo2
|
UTSW |
16 |
73,779,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Robo2
|
UTSW |
16 |
73,764,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R6304:Robo2
|
UTSW |
16 |
73,755,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Robo2
|
UTSW |
16 |
73,725,039 (GRCm39) |
missense |
probably benign |
0.06 |
R6431:Robo2
|
UTSW |
16 |
73,843,697 (GRCm39) |
nonsense |
probably null |
|
R6440:Robo2
|
UTSW |
16 |
73,713,010 (GRCm39) |
missense |
probably benign |
0.31 |
R6596:Robo2
|
UTSW |
16 |
73,767,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R6919:Robo2
|
UTSW |
16 |
73,758,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R7029:Robo2
|
UTSW |
16 |
73,745,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Robo2
|
UTSW |
16 |
74,149,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7092:Robo2
|
UTSW |
16 |
73,753,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R7136:Robo2
|
UTSW |
16 |
73,753,438 (GRCm39) |
missense |
probably damaging |
0.99 |
R7192:Robo2
|
UTSW |
16 |
73,717,638 (GRCm39) |
missense |
probably benign |
0.19 |
R7569:Robo2
|
UTSW |
16 |
73,832,003 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7686:Robo2
|
UTSW |
16 |
73,755,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R7720:Robo2
|
UTSW |
16 |
73,693,903 (GRCm39) |
missense |
probably benign |
0.00 |
R7772:Robo2
|
UTSW |
16 |
73,758,777 (GRCm39) |
missense |
probably benign |
0.24 |
R7822:Robo2
|
UTSW |
16 |
73,770,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Robo2
|
UTSW |
16 |
73,770,132 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7881:Robo2
|
UTSW |
16 |
73,717,585 (GRCm39) |
missense |
probably benign |
0.00 |
R7897:Robo2
|
UTSW |
16 |
73,695,838 (GRCm39) |
missense |
probably benign |
|
R8135:Robo2
|
UTSW |
16 |
73,730,048 (GRCm39) |
missense |
probably benign |
0.04 |
R8297:Robo2
|
UTSW |
16 |
73,812,814 (GRCm39) |
nonsense |
probably null |
|
R8307:Robo2
|
UTSW |
16 |
73,753,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R8379:Robo2
|
UTSW |
16 |
73,730,588 (GRCm39) |
missense |
probably damaging |
0.99 |
R8393:Robo2
|
UTSW |
16 |
73,775,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8474:Robo2
|
UTSW |
16 |
73,745,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R8500:Robo2
|
UTSW |
16 |
73,745,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R8721:Robo2
|
UTSW |
16 |
73,703,798 (GRCm39) |
missense |
|
|
R8734:Robo2
|
UTSW |
16 |
73,764,651 (GRCm39) |
splice site |
probably benign |
|
R8735:Robo2
|
UTSW |
16 |
73,755,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R8840:Robo2
|
UTSW |
16 |
73,782,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R8937:Robo2
|
UTSW |
16 |
73,770,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R8937:Robo2
|
UTSW |
16 |
73,770,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Robo2
|
UTSW |
16 |
73,767,941 (GRCm39) |
critical splice donor site |
probably null |
|
R9134:Robo2
|
UTSW |
16 |
73,703,738 (GRCm39) |
missense |
|
|
R9622:Robo2
|
UTSW |
16 |
73,729,952 (GRCm39) |
missense |
probably benign |
0.02 |
R9662:Robo2
|
UTSW |
16 |
73,758,566 (GRCm39) |
critical splice donor site |
probably null |
|
R9708:Robo2
|
UTSW |
16 |
73,770,197 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9779:Robo2
|
UTSW |
16 |
73,767,965 (GRCm39) |
missense |
probably damaging |
0.97 |
X0063:Robo2
|
UTSW |
16 |
73,842,716 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Robo2
|
UTSW |
16 |
73,730,479 (GRCm39) |
missense |
probably benign |
0.35 |
Z1177:Robo2
|
UTSW |
16 |
73,737,187 (GRCm39) |
critical splice acceptor site |
probably null |
|
|