Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
A |
G |
5: 138,560,610 (GRCm39) |
S262P |
probably damaging |
Het |
Abcc2 |
A |
G |
19: 43,825,899 (GRCm39) |
E1512G |
probably damaging |
Het |
Abcg2 |
T |
G |
6: 58,661,325 (GRCm39) |
Y459D |
possibly damaging |
Het |
Amy1 |
T |
C |
3: 113,357,248 (GRCm39) |
Y197C |
probably damaging |
Het |
Bptf |
A |
G |
11: 106,990,541 (GRCm39) |
I516T |
probably damaging |
Het |
Capn12 |
T |
A |
7: 28,582,532 (GRCm39) |
|
probably null |
Het |
Cbln2 |
T |
A |
18: 86,734,797 (GRCm39) |
L190Q |
probably damaging |
Het |
Ccdc157 |
C |
T |
11: 4,098,592 (GRCm39) |
E305K |
possibly damaging |
Het |
Ccdc47 |
A |
G |
11: 106,095,830 (GRCm39) |
S289P |
probably benign |
Het |
Chd3 |
C |
T |
11: 69,239,264 (GRCm39) |
E1756K |
probably null |
Het |
Chrd |
G |
T |
16: 20,553,272 (GRCm39) |
A183S |
possibly damaging |
Het |
Cp |
C |
T |
3: 20,039,822 (GRCm39) |
R880* |
probably null |
Het |
Cyp24a1 |
A |
T |
2: 170,336,063 (GRCm39) |
D191E |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,020,613 (GRCm39) |
Y1252C |
probably damaging |
Het |
Eps8l1 |
A |
G |
7: 4,480,403 (GRCm39) |
D487G |
probably damaging |
Het |
Fam227b |
T |
G |
2: 125,965,948 (GRCm39) |
Q159P |
probably damaging |
Het |
Fat3 |
A |
G |
9: 16,289,481 (GRCm39) |
I14T |
probably benign |
Het |
Fbxl19 |
C |
A |
7: 127,349,217 (GRCm39) |
T129N |
possibly damaging |
Het |
Fuca2 |
T |
C |
10: 13,381,665 (GRCm39) |
F193L |
probably benign |
Het |
H2-Q1 |
T |
C |
17: 35,539,603 (GRCm39) |
|
probably null |
Het |
Hgh1 |
A |
G |
15: 76,254,631 (GRCm39) |
M336V |
probably benign |
Het |
Il12b |
T |
C |
11: 44,298,857 (GRCm39) |
L104P |
probably benign |
Het |
Kcnh2 |
A |
T |
5: 24,537,989 (GRCm39) |
F125I |
probably benign |
Het |
Kcnk7 |
A |
G |
19: 5,756,104 (GRCm39) |
H110R |
probably benign |
Het |
Kdm3a |
G |
A |
6: 71,588,764 (GRCm39) |
P415L |
probably benign |
Het |
Kifc3 |
T |
C |
8: 95,830,077 (GRCm39) |
T610A |
probably benign |
Het |
Krbox5 |
A |
G |
13: 67,991,111 (GRCm39) |
|
probably null |
Het |
Lmbr1l |
C |
A |
15: 98,809,372 (GRCm39) |
|
probably null |
Het |
Lmo7 |
T |
A |
14: 102,157,975 (GRCm39) |
M1436K |
unknown |
Het |
Lrp1 |
C |
T |
10: 127,394,491 (GRCm39) |
C2574Y |
probably damaging |
Het |
Med13l |
A |
G |
5: 118,859,587 (GRCm39) |
E258G |
possibly damaging |
Het |
Mesp1 |
T |
C |
7: 79,442,906 (GRCm39) |
I124V |
probably damaging |
Het |
Mrgpra2a |
A |
T |
7: 47,076,934 (GRCm39) |
I108N |
probably benign |
Het |
Nos1 |
G |
T |
5: 118,033,925 (GRCm39) |
R349L |
possibly damaging |
Het |
Or5k3 |
C |
T |
16: 58,969,327 (GRCm39) |
T38I |
probably damaging |
Het |
Or7c70 |
T |
C |
10: 78,683,615 (GRCm39) |
I45V |
probably benign |
Het |
Osgin1 |
T |
A |
8: 120,168,176 (GRCm39) |
M1K |
probably null |
Het |
Pde4dip |
C |
T |
3: 97,601,379 (GRCm39) |
S2346N |
probably benign |
Het |
Pde7a |
T |
C |
3: 19,285,258 (GRCm39) |
M310V |
probably benign |
Het |
Pigw |
G |
A |
11: 84,768,585 (GRCm39) |
T248M |
probably damaging |
Het |
Pink1 |
T |
C |
4: 138,044,769 (GRCm39) |
T323A |
probably damaging |
Het |
Polr3a |
C |
T |
14: 24,511,883 (GRCm39) |
R891Q |
probably damaging |
Het |
Prkar1b |
C |
A |
5: 139,094,363 (GRCm39) |
C75F |
probably benign |
Het |
Prss58 |
C |
T |
6: 40,876,987 (GRCm39) |
|
probably null |
Het |
Ptk2 |
G |
A |
15: 73,093,658 (GRCm39) |
P854S |
possibly damaging |
Het |
Pttg1ip2 |
A |
T |
5: 5,516,631 (GRCm39) |
D63E |
possibly damaging |
Het |
Qars1 |
T |
C |
9: 108,389,971 (GRCm39) |
I350T |
probably damaging |
Het |
Qprt |
T |
C |
7: 126,707,984 (GRCm39) |
K149R |
probably damaging |
Het |
Rasgrf1 |
T |
A |
9: 89,873,651 (GRCm39) |
D653E |
probably damaging |
Het |
Rbm26 |
T |
C |
14: 105,381,703 (GRCm39) |
M481V |
possibly damaging |
Het |
Rdx |
C |
T |
9: 51,997,745 (GRCm39) |
T573M |
probably damaging |
Het |
Rgs14 |
A |
G |
13: 55,527,508 (GRCm39) |
|
probably null |
Het |
Rrbp1 |
A |
T |
2: 143,791,600 (GRCm39) |
F1369I |
probably benign |
Het |
Sh2d4b |
T |
A |
14: 40,562,209 (GRCm39) |
T319S |
probably benign |
Het |
Slc7a15 |
G |
T |
12: 8,588,895 (GRCm39) |
N217K |
probably damaging |
Het |
Stmn1 |
A |
G |
4: 134,198,088 (GRCm39) |
K42E |
probably damaging |
Het |
Tbl2 |
T |
G |
5: 135,178,682 (GRCm39) |
W31G |
probably benign |
Het |
Tmem8b |
T |
C |
4: 43,669,845 (GRCm39) |
C114R |
possibly damaging |
Het |
Tsc2 |
T |
C |
17: 24,832,254 (GRCm39) |
S711G |
probably benign |
Het |
Ttn |
T |
C |
2: 76,666,904 (GRCm39) |
R11531G |
unknown |
Het |
Ube2e3 |
T |
C |
2: 78,744,085 (GRCm39) |
Y105H |
probably benign |
Het |
Usp16 |
G |
T |
16: 87,280,059 (GRCm39) |
C753F |
probably benign |
Het |
Vmn1r13 |
T |
C |
6: 57,187,239 (GRCm39) |
S133P |
possibly damaging |
Het |
Vmn2r76 |
T |
A |
7: 85,877,975 (GRCm39) |
Q474L |
probably benign |
Het |
Vps52 |
T |
C |
17: 34,184,262 (GRCm39) |
I601T |
probably benign |
Het |
Wasf1 |
A |
T |
10: 40,802,587 (GRCm39) |
T81S |
possibly damaging |
Het |
Wdr82 |
A |
G |
9: 106,048,532 (GRCm39) |
S39G |
probably benign |
Het |
Zdhhc13 |
A |
G |
7: 48,451,080 (GRCm39) |
I108V |
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 |
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 |
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 |
|
|