Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
A |
T |
17: 84,972,257 (GRCm39) |
|
silent |
Het |
Ackr2 |
T |
A |
9: 121,737,729 (GRCm39) |
C35S |
probably damaging |
Het |
Adcy8 |
T |
A |
15: 64,573,940 (GRCm39) |
K1054N |
probably damaging |
Het |
Adgrf1 |
A |
T |
17: 43,601,879 (GRCm39) |
|
probably benign |
Het |
Akap9 |
T |
A |
5: 4,127,959 (GRCm39) |
I3765K |
probably benign |
Het |
Brwd1 |
A |
T |
16: 95,824,610 (GRCm39) |
F1219I |
|
Het |
Btc |
A |
T |
5: 91,508,603 (GRCm39) |
|
probably null |
Het |
Cd163 |
C |
T |
6: 124,285,947 (GRCm39) |
R166* |
probably null |
Het |
Cfap52 |
G |
A |
11: 67,822,656 (GRCm39) |
S405L |
probably benign |
Het |
Clcn2 |
A |
G |
16: 20,531,414 (GRCm39) |
L210P |
possibly damaging |
Het |
Creb3l3 |
T |
A |
10: 80,924,452 (GRCm39) |
|
probably null |
Het |
Csn1s2a |
A |
T |
5: 87,934,458 (GRCm39) |
I144F |
probably benign |
Het |
Dedd |
G |
T |
1: 171,167,888 (GRCm39) |
|
probably benign |
Het |
Eef2k |
C |
T |
7: 120,491,124 (GRCm39) |
R537C |
probably damaging |
Het |
Epas1 |
A |
T |
17: 87,135,267 (GRCm39) |
R633S |
probably benign |
Het |
Fmn2 |
C |
A |
1: 174,436,198 (GRCm39) |
T723N |
unknown |
Het |
Frmd4a |
G |
T |
2: 4,608,765 (GRCm39) |
G878W |
probably damaging |
Het |
Ggcx |
T |
G |
6: 72,402,924 (GRCm39) |
F294C |
probably damaging |
Het |
Ghr |
G |
A |
15: 3,370,470 (GRCm39) |
P132S |
possibly damaging |
Het |
Gm15446 |
A |
T |
5: 110,091,299 (GRCm39) |
H517L |
probably damaging |
Het |
Gm5862 |
T |
C |
5: 26,226,624 (GRCm39) |
T93A |
probably damaging |
Het |
Gnb1l |
T |
A |
16: 18,359,745 (GRCm39) |
I50N |
probably damaging |
Het |
Greb1l |
A |
G |
18: 10,532,797 (GRCm39) |
Y897C |
probably damaging |
Het |
Greb1l |
T |
C |
18: 10,558,795 (GRCm39) |
C1817R |
probably damaging |
Het |
Ier5 |
C |
A |
1: 154,974,275 (GRCm39) |
W301L |
probably damaging |
Het |
Irf2bp2 |
A |
G |
8: 127,318,456 (GRCm39) |
L370P |
probably benign |
Het |
Itga9 |
T |
A |
9: 118,636,344 (GRCm39) |
N677K |
probably damaging |
Het |
Itgb7 |
G |
T |
15: 102,132,797 (GRCm39) |
R172S |
|
Het |
Kdm6b |
A |
T |
11: 69,292,977 (GRCm39) |
C1266* |
probably null |
Het |
Kmt2c |
A |
T |
5: 25,489,343 (GRCm39) |
V4532E |
probably damaging |
Het |
Kprp |
A |
C |
3: 92,732,226 (GRCm39) |
F275V |
probably damaging |
Het |
Map3k21 |
G |
A |
8: 126,664,050 (GRCm39) |
R537H |
probably damaging |
Het |
Mchr1 |
T |
G |
15: 81,119,980 (GRCm39) |
D2E |
probably benign |
Het |
Mixl1 |
T |
C |
1: 180,522,245 (GRCm39) |
D212G |
probably damaging |
Het |
Mup2 |
T |
C |
4: 60,139,717 (GRCm39) |
T24A |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,291,459 (GRCm39) |
D1160N |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,291,468 (GRCm39) |
S1157G |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,358,264 (GRCm39) |
K991E |
possibly damaging |
Het |
Ndufb11b |
T |
A |
15: 81,865,011 (GRCm39) |
M84K |
probably damaging |
Het |
Nfe2l1 |
G |
A |
11: 96,710,573 (GRCm39) |
A552V |
possibly damaging |
Het |
Or2p2 |
C |
T |
13: 21,256,784 (GRCm39) |
R229H |
possibly damaging |
Het |
Or51r1 |
T |
G |
7: 102,228,433 (GRCm39) |
S244A |
probably damaging |
Het |
Or56b1 |
C |
T |
7: 104,285,291 (GRCm39) |
R137C |
probably benign |
Het |
Pds5a |
A |
G |
5: 65,804,479 (GRCm39) |
S527P |
possibly damaging |
Het |
Peg10 |
T |
TCCC |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pgc |
T |
A |
17: 48,043,351 (GRCm39) |
V233E |
probably damaging |
Het |
Pias1 |
T |
C |
9: 62,888,164 (GRCm39) |
|
probably benign |
Het |
Pign |
A |
T |
1: 105,556,246 (GRCm39) |
W72R |
unknown |
Het |
Pmm1 |
C |
T |
15: 81,839,896 (GRCm39) |
R143H |
probably damaging |
Het |
Proc |
A |
G |
18: 32,268,950 (GRCm39) |
S12P |
possibly damaging |
Het |
Rida |
T |
A |
15: 34,488,823 (GRCm39) |
Q23L |
probably damaging |
Het |
Slc22a8 |
A |
G |
19: 8,587,025 (GRCm39) |
E406G |
possibly damaging |
Het |
Slc2a7 |
A |
G |
4: 150,242,625 (GRCm39) |
T238A |
probably benign |
Het |
Spata31h1 |
T |
A |
10: 82,123,894 (GRCm39) |
S3039C |
possibly damaging |
Het |
Spp1 |
A |
G |
5: 104,588,167 (GRCm39) |
I190V |
probably benign |
Het |
Srgap1 |
T |
C |
10: 121,628,257 (GRCm39) |
D882G |
probably damaging |
Het |
Ssrp1 |
T |
A |
2: 84,875,811 (GRCm39) |
W557R |
probably damaging |
Het |
Strn |
C |
G |
17: 79,043,790 (GRCm39) |
A43P |
probably benign |
Het |
Taf6 |
A |
C |
5: 138,180,465 (GRCm39) |
Y300D |
probably damaging |
Het |
Tesk2 |
A |
G |
4: 116,658,933 (GRCm39) |
Y270C |
probably damaging |
Het |
Tnnt3 |
T |
A |
7: 142,065,823 (GRCm39) |
D153E |
probably benign |
Het |
Ubl7 |
A |
G |
9: 57,826,637 (GRCm39) |
H117R |
possibly damaging |
Het |
Vcan |
T |
A |
13: 89,839,146 (GRCm39) |
T2133S |
possibly damaging |
Het |
Vrk2 |
T |
A |
11: 26,543,917 (GRCm39) |
|
probably benign |
Het |
Wdr72 |
A |
C |
9: 74,125,902 (GRCm39) |
Q1011P |
possibly damaging |
Het |
Wls |
T |
A |
3: 159,615,403 (GRCm39) |
I306N |
possibly damaging |
Het |
Zfp654 |
A |
G |
16: 64,611,496 (GRCm39) |
S283P |
probably damaging |
Het |
Zfp956 |
C |
T |
6: 47,939,462 (GRCm39) |
T170I |
possibly damaging |
Het |
|
Other mutations in Lrrc4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02230:Lrrc4
|
APN |
6 |
28,830,879 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03223:Lrrc4
|
APN |
6 |
28,831,469 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03410:Lrrc4
|
APN |
6 |
28,830,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Lrrc4
|
UTSW |
6 |
28,829,734 (GRCm39) |
missense |
probably benign |
0.05 |
R0233:Lrrc4
|
UTSW |
6 |
28,829,734 (GRCm39) |
missense |
probably benign |
0.05 |
R0456:Lrrc4
|
UTSW |
6 |
28,831,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R1162:Lrrc4
|
UTSW |
6 |
28,831,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R2001:Lrrc4
|
UTSW |
6 |
28,830,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R2089:Lrrc4
|
UTSW |
6 |
28,830,586 (GRCm39) |
missense |
probably benign |
0.45 |
R2091:Lrrc4
|
UTSW |
6 |
28,830,586 (GRCm39) |
missense |
probably benign |
0.45 |
R2091:Lrrc4
|
UTSW |
6 |
28,830,586 (GRCm39) |
missense |
probably benign |
0.45 |
R2353:Lrrc4
|
UTSW |
6 |
28,831,451 (GRCm39) |
missense |
probably benign |
0.00 |
R5079:Lrrc4
|
UTSW |
6 |
28,830,769 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5197:Lrrc4
|
UTSW |
6 |
28,830,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Lrrc4
|
UTSW |
6 |
28,830,905 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6755:Lrrc4
|
UTSW |
6 |
28,831,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R7660:Lrrc4
|
UTSW |
6 |
28,829,816 (GRCm39) |
missense |
probably benign |
0.00 |
R7661:Lrrc4
|
UTSW |
6 |
28,829,762 (GRCm39) |
missense |
probably benign |
0.00 |
R8113:Lrrc4
|
UTSW |
6 |
28,829,902 (GRCm39) |
missense |
probably damaging |
0.97 |
R8272:Lrrc4
|
UTSW |
6 |
28,662,192 (GRCm39) |
missense |
unknown |
|
R9094:Lrrc4
|
UTSW |
6 |
28,830,206 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9197:Lrrc4
|
UTSW |
6 |
28,831,318 (GRCm39) |
missense |
probably benign |
0.01 |
R9447:Lrrc4
|
UTSW |
6 |
28,830,650 (GRCm39) |
missense |
probably benign |
0.08 |
R9803:Lrrc4
|
UTSW |
6 |
28,662,199 (GRCm39) |
missense |
probably benign |
0.00 |
|