Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam32 |
T |
C |
8: 25,374,471 (GRCm39) |
E507G |
probably damaging |
Het |
Adam39 |
C |
T |
8: 41,277,768 (GRCm39) |
T53I |
probably benign |
Het |
Adam4 |
A |
T |
12: 81,468,535 (GRCm39) |
S29T |
possibly damaging |
Het |
Adamdec1 |
C |
A |
14: 68,815,353 (GRCm39) |
E104* |
probably null |
Het |
Alas1 |
G |
T |
9: 106,113,676 (GRCm39) |
P523Q |
probably damaging |
Het |
Aldh3a1 |
A |
G |
11: 61,104,320 (GRCm39) |
D69G |
probably benign |
Het |
Arhgap29 |
T |
A |
3: 121,808,620 (GRCm39) |
V1266E |
probably damaging |
Het |
Bcdin3d |
T |
C |
15: 99,368,719 (GRCm39) |
D160G |
probably damaging |
Het |
Btaf1 |
T |
A |
19: 36,955,772 (GRCm39) |
F569I |
probably benign |
Het |
Cacna1b |
A |
G |
2: 24,521,956 (GRCm39) |
L1718S |
probably damaging |
Het |
Casd1 |
A |
G |
6: 4,629,975 (GRCm39) |
Y457C |
probably damaging |
Het |
Creb3 |
T |
C |
4: 43,563,192 (GRCm39) |
V97A |
probably benign |
Het |
Cux2 |
G |
T |
5: 122,025,539 (GRCm39) |
S43* |
probably null |
Het |
Fhip1a |
A |
T |
3: 85,638,020 (GRCm39) |
V93D |
probably damaging |
Het |
Fsbp |
T |
G |
4: 11,579,841 (GRCm39) |
N36K |
probably benign |
Het |
Gm11565 |
A |
G |
11: 99,806,040 (GRCm39) |
D144G |
probably benign |
Het |
Gpn3 |
A |
G |
5: 122,511,981 (GRCm39) |
Y19C |
probably damaging |
Het |
Gstz1 |
A |
T |
12: 87,208,837 (GRCm39) |
T148S |
probably benign |
Het |
Gtf3c5 |
A |
G |
2: 28,462,236 (GRCm39) |
I282T |
probably benign |
Het |
Hspa2 |
T |
A |
12: 76,452,514 (GRCm39) |
S403T |
possibly damaging |
Het |
Il27 |
G |
A |
7: 126,190,251 (GRCm39) |
T121I |
possibly damaging |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Kctd1 |
T |
A |
18: 15,196,284 (GRCm39) |
|
probably benign |
Het |
Kynu |
A |
G |
2: 43,569,815 (GRCm39) |
T366A |
probably damaging |
Het |
Lama5 |
G |
A |
2: 179,841,059 (GRCm39) |
T507I |
probably damaging |
Het |
Myh11 |
C |
T |
16: 14,087,105 (GRCm39) |
V124M |
probably damaging |
Het |
Myh14 |
T |
A |
7: 44,273,754 (GRCm39) |
H1331L |
probably damaging |
Het |
Myh2 |
T |
A |
11: 67,079,303 (GRCm39) |
L957Q |
probably damaging |
Het |
Myh4 |
T |
C |
11: 67,137,227 (GRCm39) |
F483L |
probably benign |
Het |
Nbeal1 |
A |
C |
1: 60,368,549 (GRCm39) |
K2631N |
probably damaging |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Ogg1 |
T |
C |
6: 113,304,268 (GRCm39) |
C28R |
probably damaging |
Het |
Or13c7c |
T |
C |
4: 43,836,430 (GRCm39) |
H20R |
probably benign |
Het |
Or5b24 |
G |
A |
19: 12,912,461 (GRCm39) |
A120T |
probably damaging |
Het |
Or5k17 |
C |
T |
16: 58,746,053 (GRCm39) |
V294I |
possibly damaging |
Het |
Or6e1 |
C |
T |
14: 54,519,789 (GRCm39) |
A188T |
possibly damaging |
Het |
Or7g35 |
A |
G |
9: 19,496,726 (GRCm39) |
K298E |
possibly damaging |
Het |
Parp6 |
G |
C |
9: 59,547,393 (GRCm39) |
R460P |
probably damaging |
Het |
Phf14 |
A |
G |
6: 11,992,056 (GRCm39) |
H744R |
probably damaging |
Het |
Pibf1 |
A |
G |
14: 99,370,787 (GRCm39) |
N263S |
possibly damaging |
Het |
Plcb4 |
A |
G |
2: 135,774,191 (GRCm39) |
T158A |
possibly damaging |
Het |
Plce1 |
T |
C |
19: 38,737,840 (GRCm39) |
S1615P |
possibly damaging |
Het |
Plxna3 |
T |
G |
X: 73,382,554 (GRCm39) |
|
probably null |
Het |
Rad54b |
T |
A |
4: 11,609,449 (GRCm39) |
H633Q |
probably benign |
Het |
Rgs22 |
T |
A |
15: 36,100,079 (GRCm39) |
Y212F |
probably benign |
Het |
Rnd3 |
G |
A |
2: 51,022,553 (GRCm39) |
A163V |
probably benign |
Het |
Rnf10 |
A |
T |
5: 115,389,148 (GRCm39) |
V315E |
probably damaging |
Het |
Rp1l1 |
T |
G |
14: 64,268,719 (GRCm39) |
V1435G |
probably damaging |
Het |
Scaf8 |
T |
A |
17: 3,248,260 (GRCm39) |
D1194E |
probably benign |
Het |
Septin12 |
T |
C |
16: 4,809,807 (GRCm39) |
T198A |
probably damaging |
Het |
Shisa2 |
A |
G |
14: 59,867,629 (GRCm39) |
T294A |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,018,628 (GRCm39) |
|
probably null |
Het |
Strbp |
A |
T |
2: 37,535,691 (GRCm39) |
S6T |
probably damaging |
Het |
Syf2 |
A |
G |
4: 134,661,804 (GRCm39) |
E56G |
probably damaging |
Het |
Thap4 |
T |
C |
1: 93,642,588 (GRCm39) |
|
probably benign |
Het |
Tnfaip3 |
T |
C |
10: 18,887,580 (GRCm39) |
|
probably benign |
Het |
Tnxb |
A |
G |
17: 34,891,514 (GRCm39) |
E619G |
probably damaging |
Het |
Tpr |
G |
A |
1: 150,299,318 (GRCm39) |
A1173T |
probably benign |
Het |
Tspan3 |
G |
A |
9: 56,043,980 (GRCm39) |
R240W |
probably damaging |
Het |
Tut7 |
G |
T |
13: 59,944,659 (GRCm39) |
T658K |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,138,027 (GRCm39) |
S1128L |
probably damaging |
Het |
Ucp1 |
T |
C |
8: 84,021,876 (GRCm39) |
V236A |
probably damaging |
Het |
Usp34 |
TCACCACCACCACCACCACCACCACCAC |
TCACCACCACCACCACCACCACCAC |
11: 23,314,480 (GRCm39) |
|
probably benign |
Het |
Zfp940 |
T |
C |
7: 29,544,863 (GRCm39) |
D348G |
probably benign |
Het |
Zpld2 |
G |
A |
4: 133,927,658 (GRCm39) |
A365V |
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 |
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 |
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 |
|
|