Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy5 |
A |
G |
16: 35,099,607 (GRCm39) |
E719G |
probably damaging |
Het |
Ankdd1a |
A |
G |
9: 65,424,220 (GRCm39) |
M31T |
possibly damaging |
Het |
Atp13a5 |
T |
C |
16: 29,070,154 (GRCm39) |
K911E |
possibly damaging |
Het |
Bpifb3 |
G |
T |
2: 153,766,728 (GRCm39) |
L210F |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,728,334 (GRCm39) |
Y211C |
probably damaging |
Het |
Carm1 |
C |
A |
9: 21,494,373 (GRCm39) |
P297T |
probably damaging |
Het |
Cdh19 |
A |
T |
1: 110,852,787 (GRCm39) |
Y383N |
probably benign |
Het |
Cfap221 |
T |
C |
1: 119,860,583 (GRCm39) |
H681R |
probably damaging |
Het |
Cmya5 |
A |
C |
13: 93,210,972 (GRCm39) |
S3274A |
possibly damaging |
Het |
Cndp2 |
T |
A |
18: 84,693,203 (GRCm39) |
K186* |
probably null |
Het |
Ctdp1 |
G |
T |
18: 80,494,470 (GRCm39) |
F310L |
probably damaging |
Het |
Cyp2c55 |
A |
T |
19: 39,019,853 (GRCm39) |
I264F |
probably damaging |
Het |
Dhx40 |
A |
T |
11: 86,664,649 (GRCm39) |
F628I |
probably damaging |
Het |
Disc1 |
T |
A |
8: 125,862,128 (GRCm39) |
M500K |
possibly damaging |
Het |
Dnah5 |
A |
C |
15: 28,349,970 (GRCm39) |
D2551A |
possibly damaging |
Het |
Esyt1 |
A |
G |
10: 128,352,543 (GRCm39) |
|
probably null |
Het |
Fam78a |
T |
C |
2: 31,972,843 (GRCm39) |
S26G |
probably damaging |
Het |
Fn1 |
G |
A |
1: 71,687,003 (GRCm39) |
|
probably null |
Het |
Gbx1 |
T |
C |
5: 24,709,916 (GRCm39) |
T310A |
probably benign |
Het |
Ggh |
T |
A |
4: 20,042,219 (GRCm39) |
C16S |
unknown |
Het |
Gm11595 |
T |
A |
11: 99,663,600 (GRCm39) |
T27S |
unknown |
Het |
Gm17334 |
T |
A |
11: 53,663,564 (GRCm39) |
|
probably benign |
Het |
Gsk3b |
A |
G |
16: 38,014,311 (GRCm39) |
I256M |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,620,711 (GRCm39) |
S1166R |
probably benign |
Het |
Hyou1 |
T |
C |
9: 44,293,322 (GRCm39) |
|
probably null |
Het |
Jup |
G |
T |
11: 100,265,167 (GRCm39) |
R637S |
probably benign |
Het |
Lama2 |
T |
A |
10: 26,929,027 (GRCm39) |
I2087F |
possibly damaging |
Het |
Lamc1 |
T |
G |
1: 153,097,417 (GRCm39) |
K1542N |
probably benign |
Het |
Lgals4 |
G |
T |
7: 28,540,117 (GRCm39) |
|
|
Het |
Lrrc8d |
A |
G |
5: 105,959,626 (GRCm39) |
D12G |
probably damaging |
Het |
Lrwd1 |
C |
T |
5: 136,161,888 (GRCm39) |
V207M |
possibly damaging |
Het |
Mbd1 |
T |
A |
18: 74,406,762 (GRCm39) |
|
probably null |
Het |
Msi1 |
T |
A |
5: 115,588,984 (GRCm39) |
I333N |
probably damaging |
Het |
Neo1 |
C |
T |
9: 58,814,354 (GRCm39) |
V871I |
probably benign |
Het |
Nr2c1 |
T |
C |
10: 94,024,078 (GRCm39) |
C428R |
probably damaging |
Het |
Ntm |
A |
G |
9: 29,322,978 (GRCm39) |
L14P |
probably damaging |
Het |
Nxpe4 |
A |
T |
9: 48,304,145 (GRCm39) |
K77N |
probably damaging |
Het |
Or1p1c |
A |
C |
11: 74,160,235 (GRCm39) |
T7P |
possibly damaging |
Het |
Or4c119 |
T |
A |
2: 88,987,505 (GRCm39) |
S5C |
probably damaging |
Het |
Or4f17-ps1 |
T |
A |
2: 111,358,001 (GRCm39) |
M132K |
probably damaging |
Het |
Or8g30 |
T |
C |
9: 39,230,074 (GRCm39) |
T279A |
possibly damaging |
Het |
Or8k18 |
G |
A |
2: 86,085,702 (GRCm39) |
L112F |
probably benign |
Het |
Pappa |
T |
A |
4: 65,074,701 (GRCm39) |
D418E |
probably damaging |
Het |
Pde4d |
G |
A |
13: 109,738,320 (GRCm39) |
|
probably null |
Het |
Pip |
A |
G |
6: 41,828,391 (GRCm39) |
N75S |
possibly damaging |
Het |
Plcl1 |
G |
C |
1: 55,736,411 (GRCm39) |
R584P |
probably benign |
Het |
Pnp |
A |
T |
14: 51,188,471 (GRCm39) |
D237V |
probably damaging |
Het |
Ppp1r12a |
T |
C |
10: 108,098,281 (GRCm39) |
W857R |
probably damaging |
Het |
Pramel13 |
T |
C |
4: 144,119,653 (GRCm39) |
T305A |
possibly damaging |
Het |
Ptchd3 |
A |
T |
11: 121,727,229 (GRCm39) |
M368L |
probably benign |
Het |
Pum1 |
T |
A |
4: 130,501,816 (GRCm39) |
S868R |
probably damaging |
Het |
R3hdml |
A |
T |
2: 163,344,324 (GRCm39) |
S238C |
probably damaging |
Het |
Sall3 |
A |
G |
18: 81,016,402 (GRCm39) |
S509P |
possibly damaging |
Het |
Sap130 |
T |
G |
18: 31,799,418 (GRCm39) |
H298Q |
possibly damaging |
Het |
Selenov |
C |
A |
7: 27,987,458 (GRCm39) |
G307C |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,379,453 (GRCm39) |
H1089Q |
possibly damaging |
Het |
Setdb2 |
T |
C |
14: 59,656,505 (GRCm39) |
N287D |
probably damaging |
Het |
Sis |
C |
T |
3: 72,865,507 (GRCm39) |
V182I |
probably benign |
Het |
Slc32a1 |
A |
C |
2: 158,453,457 (GRCm39) |
D99A |
probably benign |
Het |
Slk |
A |
G |
19: 47,609,327 (GRCm39) |
D760G |
probably damaging |
Het |
Smg5 |
T |
A |
3: 88,258,527 (GRCm39) |
D499E |
probably benign |
Het |
Spata31e2 |
T |
A |
1: 26,723,111 (GRCm39) |
N690Y |
probably benign |
Het |
Stat3 |
T |
C |
11: 100,780,400 (GRCm39) |
T720A |
possibly damaging |
Het |
Trdn |
T |
G |
10: 33,015,110 (GRCm39) |
N21K |
probably damaging |
Het |
Trpm4 |
A |
T |
7: 44,975,992 (GRCm39) |
V118E |
possibly damaging |
Het |
Vgll3 |
A |
G |
16: 65,612,640 (GRCm39) |
Q41R |
probably damaging |
Het |
Vmn1r189 |
A |
G |
13: 22,286,525 (GRCm39) |
V104A |
probably damaging |
Het |
Vmn1r46 |
A |
T |
6: 89,953,389 (GRCm39) |
R79S |
probably benign |
Het |
Zscan4c |
T |
C |
7: 10,740,856 (GRCm39) |
M125T |
probably benign |
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 |
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 |
R6927:Robo2
|
UTSW |
16 |
73,778,946 (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 |
|
|