Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810064F22Rik |
T |
A |
9: 22,119,333 (GRCm39) |
|
noncoding transcript |
Het |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Abl1 |
T |
C |
2: 31,669,022 (GRCm39) |
Y110H |
probably damaging |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Agbl3 |
G |
A |
6: 34,762,219 (GRCm39) |
R73Q |
probably damaging |
Het |
Agl |
C |
T |
3: 116,572,267 (GRCm39) |
|
probably null |
Het |
Amotl1 |
G |
A |
9: 14,504,747 (GRCm39) |
Q191* |
probably null |
Het |
Apbb1ip |
A |
G |
2: 22,743,214 (GRCm39) |
K349E |
possibly damaging |
Het |
Arhgap10 |
G |
A |
8: 78,146,718 (GRCm39) |
Q229* |
probably null |
Het |
Aspm |
C |
T |
1: 139,405,810 (GRCm39) |
Q1566* |
probably null |
Het |
B3gnt3 |
G |
A |
8: 72,145,517 (GRCm39) |
R284C |
probably damaging |
Het |
Bltp3b |
T |
G |
10: 89,630,346 (GRCm39) |
V382G |
probably damaging |
Het |
Brd4 |
A |
G |
17: 32,439,211 (GRCm39) |
V423A |
probably damaging |
Het |
Btbd9 |
A |
T |
17: 30,743,839 (GRCm39) |
I221N |
probably damaging |
Het |
Camp |
A |
G |
9: 109,676,519 (GRCm39) |
V168A |
probably benign |
Het |
Cd1d2 |
T |
A |
3: 86,896,556 (GRCm39) |
|
probably null |
Het |
Cdkn2d |
A |
T |
9: 21,202,223 (GRCm39) |
V8D |
probably benign |
Het |
Cimap1a |
A |
G |
7: 140,429,375 (GRCm39) |
Y168C |
probably damaging |
Het |
Clec4g |
T |
C |
8: 3,766,534 (GRCm39) |
N256D |
probably damaging |
Het |
Clspn |
A |
G |
4: 126,469,743 (GRCm39) |
I771V |
probably benign |
Het |
Cntn6 |
A |
G |
6: 104,836,436 (GRCm39) |
E862G |
possibly damaging |
Het |
Col6a5 |
T |
C |
9: 105,775,950 (GRCm39) |
T1702A |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,745,888 (GRCm39) |
|
probably benign |
Het |
Dubr |
T |
C |
16: 50,552,886 (GRCm39) |
|
noncoding transcript |
Het |
Dusp26 |
G |
A |
8: 31,584,165 (GRCm39) |
V91M |
probably damaging |
Het |
Edc4 |
A |
T |
8: 106,614,557 (GRCm39) |
|
probably benign |
Het |
F5 |
C |
T |
1: 164,019,715 (GRCm39) |
A730V |
probably damaging |
Het |
Foxf1 |
A |
G |
8: 121,813,553 (GRCm39) |
T358A |
probably benign |
Het |
Frem1 |
A |
T |
4: 82,834,995 (GRCm39) |
N1810K |
possibly damaging |
Het |
Galc |
A |
T |
12: 98,223,136 (GRCm39) |
F87I |
probably damaging |
Het |
Gars1 |
A |
G |
6: 55,023,403 (GRCm39) |
D66G |
probably damaging |
Het |
Gbp11 |
G |
A |
5: 105,473,374 (GRCm39) |
L460F |
probably damaging |
Het |
Gdf7 |
T |
C |
12: 8,348,014 (GRCm39) |
I436V |
probably damaging |
Het |
Gigyf2 |
C |
T |
1: 87,282,135 (GRCm39) |
|
probably benign |
Het |
Gm12239 |
T |
C |
11: 55,906,779 (GRCm39) |
|
noncoding transcript |
Het |
Gm5592 |
A |
C |
7: 40,866,895 (GRCm39) |
|
probably benign |
Het |
Gphn |
G |
A |
12: 78,673,984 (GRCm39) |
V526M |
probably damaging |
Het |
Grid1 |
A |
G |
14: 35,043,598 (GRCm39) |
I318V |
probably benign |
Het |
Grm2 |
C |
A |
9: 106,531,331 (GRCm39) |
V53F |
possibly damaging |
Het |
Gtpbp1 |
T |
C |
15: 79,603,406 (GRCm39) |
S632P |
probably benign |
Het |
H2-M1 |
A |
G |
17: 36,980,950 (GRCm39) |
F329L |
probably benign |
Het |
Hecw1 |
T |
A |
13: 14,491,477 (GRCm39) |
D92V |
probably benign |
Het |
Hgh1 |
T |
C |
15: 76,253,382 (GRCm39) |
L76P |
probably damaging |
Het |
Idi2 |
C |
A |
13: 9,007,879 (GRCm39) |
N63K |
probably benign |
Het |
Ift122 |
A |
G |
6: 115,839,707 (GRCm39) |
T25A |
possibly damaging |
Het |
Itgb2l |
A |
T |
16: 96,227,317 (GRCm39) |
C575* |
probably null |
Het |
Jup |
A |
G |
11: 100,273,867 (GRCm39) |
S225P |
possibly damaging |
Het |
Kcng3 |
A |
T |
17: 83,895,735 (GRCm39) |
C244S |
probably damaging |
Het |
Klhl2 |
T |
A |
8: 65,287,111 (GRCm39) |
M46L |
possibly damaging |
Het |
Ksr1 |
A |
T |
11: 78,918,528 (GRCm39) |
I460N |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,544,599 (GRCm39) |
F314Y |
probably benign |
Het |
Lbp |
T |
C |
2: 158,169,438 (GRCm39) |
V421A |
possibly damaging |
Het |
Lcp1 |
G |
A |
14: 75,437,929 (GRCm39) |
G113D |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,001,089 (GRCm39) |
L2045H |
probably damaging |
Het |
Mbd2 |
G |
T |
18: 70,701,806 (GRCm39) |
D107Y |
unknown |
Het |
Ms4a14 |
C |
T |
19: 11,287,733 (GRCm39) |
V96I |
possibly damaging |
Het |
N4bp2l2 |
C |
T |
5: 150,585,516 (GRCm39) |
E155K |
probably benign |
Het |
Nbeal2 |
T |
G |
9: 110,460,464 (GRCm39) |
H1790P |
probably damaging |
Het |
Nsg2 |
G |
A |
11: 31,981,806 (GRCm39) |
G84R |
probably benign |
Het |
Or10ad1b |
A |
C |
15: 98,125,425 (GRCm39) |
F34V |
possibly damaging |
Het |
Or12e10 |
A |
G |
2: 87,640,934 (GRCm39) |
T257A |
probably damaging |
Het |
P2rx2 |
T |
C |
5: 110,488,793 (GRCm39) |
N224D |
probably damaging |
Het |
P2rx5 |
A |
T |
11: 73,062,605 (GRCm39) |
E438V |
probably benign |
Het |
Paip1 |
C |
A |
13: 119,586,425 (GRCm39) |
|
probably benign |
Het |
Pik3c2g |
T |
A |
6: 139,714,505 (GRCm39) |
V219E |
probably damaging |
Het |
Ppp1r12b |
T |
C |
1: 134,801,689 (GRCm39) |
E509G |
probably damaging |
Het |
Ppp1r15a |
T |
C |
7: 45,174,797 (GRCm39) |
S4G |
probably benign |
Het |
Ppp5c |
T |
C |
7: 16,742,947 (GRCm39) |
S224G |
probably benign |
Het |
Prr30 |
T |
G |
14: 101,435,879 (GRCm39) |
I228L |
probably benign |
Het |
Purg |
A |
G |
8: 33,877,342 (GRCm39) |
I327V |
possibly damaging |
Het |
Ralb |
T |
C |
1: 119,403,645 (GRCm39) |
T161A |
probably benign |
Het |
Ripor3 |
T |
C |
2: 167,834,733 (GRCm39) |
R253G |
probably benign |
Het |
Scgb2b6 |
T |
C |
7: 31,317,257 (GRCm39) |
|
noncoding transcript |
Het |
Setd5 |
G |
T |
6: 113,128,360 (GRCm39) |
G1438W |
probably damaging |
Het |
Sh3rf3 |
T |
A |
10: 58,649,545 (GRCm39) |
L50Q |
possibly damaging |
Het |
Sipa1l2 |
G |
T |
8: 126,200,340 (GRCm39) |
T662K |
probably damaging |
Het |
Skint5 |
A |
G |
4: 113,437,725 (GRCm39) |
L1021S |
unknown |
Het |
Slc22a23 |
T |
C |
13: 34,387,924 (GRCm39) |
S391G |
probably benign |
Het |
Slc4a5 |
G |
A |
6: 83,247,999 (GRCm39) |
V402I |
probably benign |
Het |
Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
Spink5 |
A |
T |
18: 44,153,908 (GRCm39) |
*1018C |
probably null |
Het |
Stag3 |
T |
A |
5: 138,294,956 (GRCm39) |
|
probably null |
Het |
Tmem117 |
T |
C |
15: 94,992,569 (GRCm39) |
F410L |
probably damaging |
Het |
Tmod1 |
A |
G |
4: 46,090,920 (GRCm39) |
K158E |
possibly damaging |
Het |
Tpsb2 |
GGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTG |
17: 25,585,536 (GRCm39) |
|
probably benign |
Het |
Traf4 |
G |
A |
11: 78,052,346 (GRCm39) |
Q100* |
probably null |
Het |
Trpc4 |
A |
G |
3: 54,209,639 (GRCm39) |
Y668C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,597,927 (GRCm39) |
N11335I |
possibly damaging |
Het |
Usp39 |
A |
T |
6: 72,302,665 (GRCm39) |
V463E |
probably benign |
Het |
Vmn1r6 |
A |
C |
6: 56,979,683 (GRCm39) |
Y115S |
probably benign |
Het |
Vmn2r44 |
A |
G |
7: 8,383,300 (GRCm39) |
I98T |
possibly damaging |
Het |
Zfp462 |
A |
G |
4: 55,010,668 (GRCm39) |
Y878C |
probably damaging |
Het |
Zfp474 |
T |
C |
18: 52,771,503 (GRCm39) |
I52T |
possibly damaging |
Het |
|
Other mutations in Gp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00338:Gp2
|
APN |
7 |
119,053,613 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00818:Gp2
|
APN |
7 |
119,049,350 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01830:Gp2
|
APN |
7 |
119,050,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Gp2
|
APN |
7 |
119,053,692 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02284:Gp2
|
APN |
7 |
119,049,406 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02812:Gp2
|
APN |
7 |
119,051,452 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03049:Gp2
|
APN |
7 |
119,049,517 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03368:Gp2
|
APN |
7 |
119,052,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03369:Gp2
|
APN |
7 |
119,050,783 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4687001:Gp2
|
UTSW |
7 |
119,050,801 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0179:Gp2
|
UTSW |
7 |
119,051,540 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0367:Gp2
|
UTSW |
7 |
119,053,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R0544:Gp2
|
UTSW |
7 |
119,053,719 (GRCm39) |
missense |
probably benign |
0.00 |
R0973:Gp2
|
UTSW |
7 |
119,053,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Gp2
|
UTSW |
7 |
119,053,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Gp2
|
UTSW |
7 |
119,053,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R1413:Gp2
|
UTSW |
7 |
119,050,853 (GRCm39) |
missense |
probably benign |
0.15 |
R1557:Gp2
|
UTSW |
7 |
119,049,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1638:Gp2
|
UTSW |
7 |
119,050,721 (GRCm39) |
critical splice donor site |
probably null |
|
R1709:Gp2
|
UTSW |
7 |
119,050,808 (GRCm39) |
missense |
probably null |
1.00 |
R1932:Gp2
|
UTSW |
7 |
119,053,455 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2109:Gp2
|
UTSW |
7 |
119,052,155 (GRCm39) |
missense |
probably benign |
|
R2159:Gp2
|
UTSW |
7 |
119,051,507 (GRCm39) |
missense |
probably benign |
0.06 |
R2285:Gp2
|
UTSW |
7 |
119,049,308 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4657:Gp2
|
UTSW |
7 |
119,056,391 (GRCm39) |
missense |
probably benign |
0.38 |
R4829:Gp2
|
UTSW |
7 |
119,056,407 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4927:Gp2
|
UTSW |
7 |
119,052,118 (GRCm39) |
missense |
probably benign |
0.00 |
R5022:Gp2
|
UTSW |
7 |
119,048,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Gp2
|
UTSW |
7 |
119,053,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R5443:Gp2
|
UTSW |
7 |
119,053,821 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5444:Gp2
|
UTSW |
7 |
119,053,821 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5681:Gp2
|
UTSW |
7 |
119,051,517 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5732:Gp2
|
UTSW |
7 |
119,048,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Gp2
|
UTSW |
7 |
119,048,352 (GRCm39) |
missense |
probably benign |
0.02 |
R6963:Gp2
|
UTSW |
7 |
119,052,120 (GRCm39) |
missense |
probably benign |
0.03 |
R7014:Gp2
|
UTSW |
7 |
119,050,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R7087:Gp2
|
UTSW |
7 |
119,049,455 (GRCm39) |
missense |
probably damaging |
0.99 |
R7223:Gp2
|
UTSW |
7 |
119,050,721 (GRCm39) |
critical splice donor site |
probably null |
|
R7497:Gp2
|
UTSW |
7 |
119,053,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8165:Gp2
|
UTSW |
7 |
119,049,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R8343:Gp2
|
UTSW |
7 |
119,042,010 (GRCm39) |
missense |
probably benign |
0.01 |
R8344:Gp2
|
UTSW |
7 |
119,042,010 (GRCm39) |
missense |
probably benign |
0.01 |
R8345:Gp2
|
UTSW |
7 |
119,042,010 (GRCm39) |
missense |
probably benign |
0.01 |
R8431:Gp2
|
UTSW |
7 |
119,042,010 (GRCm39) |
missense |
probably benign |
0.01 |
R8432:Gp2
|
UTSW |
7 |
119,042,010 (GRCm39) |
missense |
probably benign |
0.01 |
R8463:Gp2
|
UTSW |
7 |
119,053,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R9169:Gp2
|
UTSW |
7 |
119,041,929 (GRCm39) |
missense |
probably benign |
|
R9439:Gp2
|
UTSW |
7 |
119,053,433 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Gp2
|
UTSW |
7 |
119,042,042 (GRCm39) |
missense |
probably benign |
0.01 |
|