Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519G04Rik |
A |
G |
5: 115,012,384 (GRCm39) |
|
probably null |
Het |
Abca4 |
C |
T |
3: 121,838,139 (GRCm39) |
|
probably benign |
Het |
Ackr2 |
A |
G |
9: 121,738,374 (GRCm39) |
M250V |
probably benign |
Het |
Actn4 |
A |
G |
7: 28,615,632 (GRCm39) |
I147T |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,647,261 (GRCm39) |
S3093N |
probably damaging |
Het |
Arid5b |
C |
T |
10: 67,934,417 (GRCm39) |
G495E |
probably benign |
Het |
Armh1 |
C |
A |
4: 117,070,938 (GRCm39) |
A396S |
probably benign |
Het |
Brwd1 |
G |
A |
16: 95,842,543 (GRCm39) |
T798M |
probably benign |
Het |
Cdk13 |
G |
A |
13: 17,947,138 (GRCm39) |
T540I |
possibly damaging |
Het |
Cdkn1c |
A |
G |
7: 143,014,371 (GRCm39) |
V25A |
possibly damaging |
Het |
Col2a1 |
T |
C |
15: 97,874,581 (GRCm39) |
E1420G |
unknown |
Het |
Dbf4 |
G |
A |
5: 8,447,867 (GRCm39) |
P448S |
probably damaging |
Het |
Dnajb7 |
T |
C |
15: 81,291,620 (GRCm39) |
N239S |
probably benign |
Het |
Dnttip1 |
A |
G |
2: 164,596,061 (GRCm39) |
D102G |
probably damaging |
Het |
Dpp8 |
T |
A |
9: 64,986,000 (GRCm39) |
V830D |
probably damaging |
Het |
Eddm13 |
G |
A |
7: 6,272,891 (GRCm39) |
|
probably null |
Het |
Eef1g |
T |
C |
19: 8,945,653 (GRCm39) |
V29A |
probably benign |
Het |
Enpp2 |
T |
A |
15: 54,702,790 (GRCm39) |
Y906F |
probably damaging |
Het |
Epb41l4a |
A |
G |
18: 34,139,069 (GRCm39) |
L23P |
possibly damaging |
Het |
Exoc1 |
T |
A |
5: 76,691,420 (GRCm39) |
M248K |
probably benign |
Het |
Fam83b |
T |
C |
9: 76,398,157 (GRCm39) |
Y982C |
probably damaging |
Het |
Fat4 |
C |
T |
3: 38,943,327 (GRCm39) |
A740V |
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,812,149 (GRCm39) |
S2823T |
probably benign |
Het |
Gckr |
T |
C |
5: 31,454,899 (GRCm39) |
|
|
Het |
Gpr150 |
A |
T |
13: 76,204,093 (GRCm39) |
V284E |
probably damaging |
Het |
Grtp1 |
T |
G |
8: 13,227,103 (GRCm39) |
I344L |
probably benign |
Het |
Heatr5a |
T |
A |
12: 52,008,313 (GRCm39) |
N10I |
probably damaging |
Het |
Herc2 |
C |
A |
7: 55,802,903 (GRCm39) |
L2109I |
probably damaging |
Het |
Hs1bp3 |
T |
A |
12: 8,367,935 (GRCm39) |
D61E |
probably damaging |
Het |
Ifit1bl1 |
T |
A |
19: 34,572,283 (GRCm39) |
Y58F |
probably benign |
Het |
Itfg1 |
A |
G |
8: 86,490,979 (GRCm39) |
F317L |
probably benign |
Het |
Itsn1 |
T |
C |
16: 91,638,491 (GRCm39) |
I764T |
unknown |
Het |
Med8 |
A |
C |
4: 118,268,853 (GRCm39) |
|
probably null |
Het |
Mpeg1 |
C |
A |
19: 12,440,458 (GRCm39) |
P639T |
probably damaging |
Het |
Mtcl3 |
T |
A |
10: 29,072,393 (GRCm39) |
Y562N |
probably damaging |
Het |
Nedd9 |
A |
G |
13: 41,469,785 (GRCm39) |
L456P |
probably benign |
Het |
Neo1 |
A |
G |
9: 58,833,078 (GRCm39) |
S556P |
probably damaging |
Het |
Nphp3 |
T |
A |
9: 103,882,592 (GRCm39) |
|
probably null |
Het |
Nup205 |
T |
C |
6: 35,154,555 (GRCm39) |
V53A |
possibly damaging |
Het |
Nvl |
A |
T |
1: 180,962,509 (GRCm39) |
S154T |
probably benign |
Het |
Or10h1 |
G |
T |
17: 33,418,603 (GRCm39) |
G194* |
probably null |
Het |
Or1e31 |
A |
T |
11: 73,689,787 (GRCm39) |
N265K |
probably benign |
Het |
Or2ag2 |
A |
T |
7: 106,485,880 (GRCm39) |
V48D |
possibly damaging |
Het |
Or2h2c |
A |
G |
17: 37,422,283 (GRCm39) |
M197T |
probably benign |
Het |
Or51ah3 |
A |
T |
7: 103,210,523 (GRCm39) |
I280F |
probably benign |
Het |
Or9k7 |
T |
A |
10: 130,047,130 (GRCm39) |
|
probably null |
Het |
Parvg |
T |
C |
15: 84,222,002 (GRCm39) |
I243T |
probably damaging |
Het |
Paxip1 |
T |
A |
5: 27,970,736 (GRCm39) |
M538L |
unknown |
Het |
Pgghg |
G |
T |
7: 140,525,382 (GRCm39) |
D428Y |
probably damaging |
Het |
Pik3cd |
C |
T |
4: 149,738,507 (GRCm39) |
V777M |
possibly damaging |
Het |
Plcl2 |
A |
C |
17: 50,914,185 (GRCm39) |
K398T |
probably benign |
Het |
Plxna1 |
A |
T |
6: 89,301,520 (GRCm39) |
|
probably null |
Het |
Rbbp6 |
T |
A |
7: 122,589,255 (GRCm39) |
|
probably null |
Het |
Rbbp6 |
T |
C |
7: 122,593,909 (GRCm39) |
Y514H |
possibly damaging |
Het |
Scin |
T |
A |
12: 40,119,414 (GRCm39) |
N538I |
probably damaging |
Het |
Sdcbp |
A |
G |
4: 6,385,144 (GRCm39) |
D121G |
probably benign |
Het |
Sgk1 |
T |
C |
10: 21,872,561 (GRCm39) |
I311T |
probably damaging |
Het |
Shq1 |
A |
C |
6: 100,550,717 (GRCm39) |
L407W |
probably damaging |
Het |
Sipa1 |
A |
T |
19: 5,701,699 (GRCm39) |
S979T |
probably benign |
Het |
Slc25a37 |
G |
T |
14: 69,487,028 (GRCm39) |
T85K |
probably benign |
Het |
Spag9 |
A |
T |
11: 93,904,480 (GRCm39) |
Q112L |
probably damaging |
Het |
Spg11 |
A |
T |
2: 121,896,748 (GRCm39) |
V1686E |
probably damaging |
Het |
Stap2 |
A |
G |
17: 56,304,909 (GRCm39) |
V291A |
probably benign |
Het |
Tnk2 |
C |
T |
16: 32,499,344 (GRCm39) |
R886C |
probably damaging |
Het |
Tnrc6c |
T |
A |
11: 117,611,777 (GRCm39) |
D138E |
possibly damaging |
Het |
Unc13c |
A |
G |
9: 73,587,756 (GRCm39) |
S1426P |
probably benign |
Het |
Vav1 |
G |
A |
17: 57,604,086 (GRCm39) |
V163M |
probably damaging |
Het |
Vmn2r67 |
T |
A |
7: 84,801,196 (GRCm39) |
K247* |
probably null |
Het |
Zc2hc1c |
T |
C |
12: 85,343,336 (GRCm39) |
V491A |
possibly damaging |
Het |
Zfp51 |
A |
G |
17: 21,683,843 (GRCm39) |
T153A |
probably benign |
Het |
Zyx |
A |
G |
6: 42,333,096 (GRCm39) |
E374G |
probably damaging |
Het |
|
Other mutations in A830018L16Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00426:A830018L16Rik
|
APN |
1 |
11,818,278 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01916:A830018L16Rik
|
APN |
1 |
11,818,331 (GRCm39) |
splice site |
probably benign |
|
IGL02040:A830018L16Rik
|
APN |
1 |
12,003,822 (GRCm39) |
intron |
probably benign |
|
IGL02432:A830018L16Rik
|
APN |
1 |
11,818,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02693:A830018L16Rik
|
APN |
1 |
11,666,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02736:A830018L16Rik
|
APN |
1 |
12,042,275 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03293:A830018L16Rik
|
APN |
1 |
11,615,375 (GRCm39) |
splice site |
probably null |
|
IGL02835:A830018L16Rik
|
UTSW |
1 |
12,042,279 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1203:A830018L16Rik
|
UTSW |
1 |
11,588,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:A830018L16Rik
|
UTSW |
1 |
11,868,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R1548:A830018L16Rik
|
UTSW |
1 |
11,588,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R1644:A830018L16Rik
|
UTSW |
1 |
11,484,814 (GRCm39) |
nonsense |
probably null |
|
R1855:A830018L16Rik
|
UTSW |
1 |
11,818,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:A830018L16Rik
|
UTSW |
1 |
12,045,177 (GRCm39) |
missense |
unknown |
|
R2265:A830018L16Rik
|
UTSW |
1 |
12,042,328 (GRCm39) |
critical splice donor site |
probably null |
|
R2296:A830018L16Rik
|
UTSW |
1 |
11,582,275 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2484:A830018L16Rik
|
UTSW |
1 |
11,666,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R3730:A830018L16Rik
|
UTSW |
1 |
11,615,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R3752:A830018L16Rik
|
UTSW |
1 |
11,588,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R3861:A830018L16Rik
|
UTSW |
1 |
11,658,778 (GRCm39) |
splice site |
probably benign |
|
R4305:A830018L16Rik
|
UTSW |
1 |
12,042,300 (GRCm39) |
nonsense |
probably null |
|
R4306:A830018L16Rik
|
UTSW |
1 |
12,042,300 (GRCm39) |
nonsense |
probably null |
|
R4307:A830018L16Rik
|
UTSW |
1 |
12,042,300 (GRCm39) |
nonsense |
probably null |
|
R4558:A830018L16Rik
|
UTSW |
1 |
12,042,300 (GRCm39) |
nonsense |
probably null |
|
R4598:A830018L16Rik
|
UTSW |
1 |
11,818,188 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4652:A830018L16Rik
|
UTSW |
1 |
11,607,566 (GRCm39) |
intron |
probably benign |
|
R5492:A830018L16Rik
|
UTSW |
1 |
11,615,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R5493:A830018L16Rik
|
UTSW |
1 |
11,615,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R5802:A830018L16Rik
|
UTSW |
1 |
12,021,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R6007:A830018L16Rik
|
UTSW |
1 |
11,582,140 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6082:A830018L16Rik
|
UTSW |
1 |
11,868,752 (GRCm39) |
missense |
probably benign |
0.04 |
R6376:A830018L16Rik
|
UTSW |
1 |
11,868,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R6453:A830018L16Rik
|
UTSW |
1 |
11,868,782 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6757:A830018L16Rik
|
UTSW |
1 |
11,666,558 (GRCm39) |
makesense |
probably null |
|
R6833:A830018L16Rik
|
UTSW |
1 |
11,658,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7163:A830018L16Rik
|
UTSW |
1 |
11,484,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R7272:A830018L16Rik
|
UTSW |
1 |
11,658,695 (GRCm39) |
missense |
probably damaging |
0.97 |
R7566:A830018L16Rik
|
UTSW |
1 |
12,021,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R8004:A830018L16Rik
|
UTSW |
1 |
12,021,286 (GRCm39) |
splice site |
probably benign |
|
R8754:A830018L16Rik
|
UTSW |
1 |
11,615,472 (GRCm39) |
missense |
probably benign |
0.33 |
R8944:A830018L16Rik
|
UTSW |
1 |
11,484,706 (GRCm39) |
unclassified |
probably benign |
|
R8993:A830018L16Rik
|
UTSW |
1 |
11,615,491 (GRCm39) |
nonsense |
probably null |
|
R8997:A830018L16Rik
|
UTSW |
1 |
11,615,491 (GRCm39) |
nonsense |
probably null |
|
R9098:A830018L16Rik
|
UTSW |
1 |
11,633,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R9640:A830018L16Rik
|
UTSW |
1 |
12,021,200 (GRCm39) |
missense |
probably damaging |
0.98 |
R9704:A830018L16Rik
|
UTSW |
1 |
11,588,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R9705:A830018L16Rik
|
UTSW |
1 |
11,588,913 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:A830018L16Rik
|
UTSW |
1 |
11,588,849 (GRCm39) |
missense |
probably damaging |
0.96 |
|