Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd2 |
T |
C |
15: 91,062,489 (GRCm39) |
N483S |
probably benign |
Het |
Acoxl |
T |
G |
2: 127,820,658 (GRCm39) |
L70R |
probably damaging |
Het |
Ankrd44 |
A |
T |
1: 54,706,576 (GRCm39) |
F627I |
probably benign |
Het |
Ash2l |
A |
T |
8: 26,308,623 (GRCm39) |
I552N |
probably damaging |
Het |
B4galt1 |
A |
G |
4: 40,807,812 (GRCm39) |
S330P |
probably damaging |
Het |
Bnip3 |
T |
C |
7: 138,500,435 (GRCm39) |
S52G |
probably damaging |
Het |
Btd |
A |
G |
14: 31,384,278 (GRCm39) |
Q88R |
probably benign |
Het |
C4bp |
A |
G |
1: 130,566,922 (GRCm39) |
V318A |
probably benign |
Het |
Cacna1e |
G |
A |
1: 154,312,214 (GRCm39) |
Q1530* |
probably null |
Het |
Calm1 |
T |
C |
12: 100,166,485 (GRCm39) |
F23S |
probably benign |
Het |
Cep290 |
T |
G |
10: 100,399,132 (GRCm39) |
I2218R |
probably benign |
Het |
Ces2c |
T |
C |
8: 105,574,672 (GRCm39) |
I43T |
probably benign |
Het |
Cyp2d9 |
T |
C |
15: 82,338,602 (GRCm39) |
L1P |
probably null |
Het |
Dgki |
C |
A |
6: 37,276,748 (GRCm39) |
|
probably benign |
Het |
Dhh |
A |
G |
15: 98,796,023 (GRCm39) |
L44P |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,594,274 (GRCm39) |
I3409V |
probably damaging |
Het |
Dnah7b |
G |
A |
1: 46,246,816 (GRCm39) |
R1664H |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 31,070,721 (GRCm39) |
M4469T |
probably damaging |
Het |
Ehhadh |
T |
C |
16: 21,581,181 (GRCm39) |
I604V |
probably benign |
Het |
Esr1 |
A |
G |
10: 4,951,418 (GRCm39) |
I599V |
probably benign |
Het |
Faf1 |
G |
A |
4: 109,697,564 (GRCm39) |
D297N |
probably damaging |
Het |
Gfra1 |
A |
T |
19: 58,252,386 (GRCm39) |
N380K |
probably damaging |
Het |
Ghitm |
A |
G |
14: 36,855,700 (GRCm39) |
C8R |
probably damaging |
Het |
Ifna4 |
C |
A |
4: 88,760,519 (GRCm39) |
T141K |
probably benign |
Het |
Itsn2 |
A |
G |
12: 4,757,660 (GRCm39) |
Y1424C |
probably damaging |
Het |
Kcnj10 |
A |
G |
1: 172,197,266 (GRCm39) |
D260G |
probably damaging |
Het |
Klf16 |
T |
C |
10: 80,405,020 (GRCm39) |
D164G |
probably damaging |
Het |
Klhdc7b |
T |
A |
15: 89,271,785 (GRCm39) |
L889Q |
probably damaging |
Het |
Lcmt2 |
C |
G |
2: 120,969,911 (GRCm39) |
V171L |
probably benign |
Het |
Lrp11 |
A |
G |
10: 7,466,348 (GRCm39) |
E153G |
probably benign |
Het |
Lsr |
T |
C |
7: 30,665,465 (GRCm39) |
Y163C |
probably damaging |
Het |
Man1a |
A |
T |
10: 53,783,668 (GRCm39) |
|
probably null |
Het |
Mmp24 |
C |
T |
2: 155,657,819 (GRCm39) |
P570S |
possibly damaging |
Het |
Ms4a3 |
A |
G |
19: 11,608,742 (GRCm39) |
M170T |
probably damaging |
Het |
Naip5 |
C |
A |
13: 100,358,378 (GRCm39) |
A953S |
possibly damaging |
Het |
Nfrkb |
T |
C |
9: 31,314,919 (GRCm39) |
S580P |
probably damaging |
Het |
Or51q1c |
T |
G |
7: 103,653,097 (GRCm39) |
V205G |
probably benign |
Het |
Or8b38 |
T |
C |
9: 37,973,389 (GRCm39) |
Y258H |
probably damaging |
Het |
Padi6 |
T |
G |
4: 140,458,506 (GRCm39) |
D462A |
probably damaging |
Het |
Pde6a |
A |
G |
18: 61,364,561 (GRCm39) |
R206G |
probably benign |
Het |
Plk4 |
A |
G |
3: 40,759,589 (GRCm39) |
N162D |
probably benign |
Het |
Ptpn13 |
T |
A |
5: 103,717,721 (GRCm39) |
D1922E |
probably benign |
Het |
Rangap1 |
G |
A |
15: 81,613,956 (GRCm39) |
|
probably benign |
Het |
Rapgef3 |
A |
G |
15: 97,658,481 (GRCm39) |
L175P |
probably damaging |
Het |
Rps6kb1 |
G |
C |
11: 86,435,484 (GRCm39) |
|
probably null |
Het |
Satb1 |
T |
C |
17: 52,111,375 (GRCm39) |
Y161C |
probably damaging |
Het |
Sel1l3 |
C |
A |
5: 53,301,525 (GRCm39) |
|
probably null |
Het |
Slc17a7 |
C |
T |
7: 44,822,358 (GRCm39) |
S398L |
possibly damaging |
Het |
Slc22a4 |
T |
A |
11: 53,918,477 (GRCm39) |
E109V |
possibly damaging |
Het |
Slc26a7 |
C |
T |
4: 14,590,477 (GRCm39) |
A105T |
probably damaging |
Het |
Slc47a1 |
T |
C |
11: 61,254,277 (GRCm39) |
N145S |
possibly damaging |
Het |
Tank |
A |
G |
2: 61,483,876 (GRCm39) |
T441A |
probably benign |
Het |
Tefm |
T |
C |
11: 80,031,279 (GRCm39) |
|
probably benign |
Het |
Ttbk2 |
T |
C |
2: 120,575,851 (GRCm39) |
Y1042C |
probably benign |
Het |
Wdfy3 |
T |
C |
5: 102,077,894 (GRCm39) |
Q892R |
probably damaging |
Het |
Wdr33 |
T |
A |
18: 32,021,500 (GRCm39) |
H683Q |
unknown |
Het |
Zfp36l2 |
T |
A |
17: 84,495,089 (GRCm39) |
I12F |
probably benign |
Het |
Zfyve26 |
A |
T |
12: 79,291,170 (GRCm39) |
M2145K |
probably benign |
Het |
|
Other mutations in Lrrc43 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02123:Lrrc43
|
APN |
5 |
123,632,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02364:Lrrc43
|
APN |
5 |
123,639,275 (GRCm39) |
missense |
possibly damaging |
0.77 |
PIT4520001:Lrrc43
|
UTSW |
5 |
123,630,530 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0019:Lrrc43
|
UTSW |
5 |
123,639,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0279:Lrrc43
|
UTSW |
5 |
123,635,085 (GRCm39) |
splice site |
probably null |
|
R0523:Lrrc43
|
UTSW |
5 |
123,639,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R1723:Lrrc43
|
UTSW |
5 |
123,630,276 (GRCm39) |
unclassified |
probably benign |
|
R2104:Lrrc43
|
UTSW |
5 |
123,639,177 (GRCm39) |
missense |
probably benign |
0.00 |
R2213:Lrrc43
|
UTSW |
5 |
123,641,640 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2269:Lrrc43
|
UTSW |
5 |
123,641,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Lrrc43
|
UTSW |
5 |
123,639,227 (GRCm39) |
missense |
probably benign |
0.00 |
R4629:Lrrc43
|
UTSW |
5 |
123,637,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R4941:Lrrc43
|
UTSW |
5 |
123,639,126 (GRCm39) |
missense |
probably benign |
0.01 |
R4960:Lrrc43
|
UTSW |
5 |
123,637,675 (GRCm39) |
missense |
probably benign |
0.19 |
R5028:Lrrc43
|
UTSW |
5 |
123,646,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R5387:Lrrc43
|
UTSW |
5 |
123,637,734 (GRCm39) |
splice site |
probably null |
|
R5653:Lrrc43
|
UTSW |
5 |
123,637,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R6266:Lrrc43
|
UTSW |
5 |
123,641,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R6323:Lrrc43
|
UTSW |
5 |
123,641,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6703:Lrrc43
|
UTSW |
5 |
123,637,532 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6869:Lrrc43
|
UTSW |
5 |
123,642,339 (GRCm39) |
critical splice donor site |
probably null |
|
R6909:Lrrc43
|
UTSW |
5 |
123,638,482 (GRCm39) |
missense |
probably benign |
0.14 |
R7023:Lrrc43
|
UTSW |
5 |
123,641,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R7910:Lrrc43
|
UTSW |
5 |
123,639,084 (GRCm39) |
missense |
probably benign |
0.27 |
R7910:Lrrc43
|
UTSW |
5 |
123,630,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R8093:Lrrc43
|
UTSW |
5 |
123,639,192 (GRCm39) |
missense |
probably benign |
0.41 |
R8127:Lrrc43
|
UTSW |
5 |
123,630,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R8351:Lrrc43
|
UTSW |
5 |
123,632,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R8722:Lrrc43
|
UTSW |
5 |
123,646,142 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8920:Lrrc43
|
UTSW |
5 |
123,639,194 (GRCm39) |
missense |
probably benign |
0.00 |
R9189:Lrrc43
|
UTSW |
5 |
123,646,109 (GRCm39) |
missense |
probably benign |
0.00 |
R9305:Lrrc43
|
UTSW |
5 |
123,646,219 (GRCm39) |
missense |
unknown |
|
R9544:Lrrc43
|
UTSW |
5 |
123,641,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Lrrc43
|
UTSW |
5 |
123,641,307 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Lrrc43
|
UTSW |
5 |
123,639,381 (GRCm39) |
missense |
probably benign |
0.04 |
|