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 |
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 |
Lrrc43 |
A |
T |
5: 123,632,366 (GRCm39) |
T170S |
probably damaging |
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 Btd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01125:Btd
|
APN |
14 |
31,389,733 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02728:Btd
|
APN |
14 |
31,389,319 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02965:Btd
|
APN |
14 |
31,389,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R1503:Btd
|
UTSW |
14 |
31,389,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Btd
|
UTSW |
14 |
31,388,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R1817:Btd
|
UTSW |
14 |
31,384,246 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1868:Btd
|
UTSW |
14 |
31,389,266 (GRCm39) |
missense |
probably benign |
0.13 |
R2225:Btd
|
UTSW |
14 |
31,389,017 (GRCm39) |
missense |
probably benign |
0.00 |
R2418:Btd
|
UTSW |
14 |
31,363,093 (GRCm39) |
critical splice donor site |
probably null |
|
R4660:Btd
|
UTSW |
14 |
31,389,760 (GRCm39) |
missense |
probably benign |
0.00 |
R4923:Btd
|
UTSW |
14 |
31,384,044 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5703:Btd
|
UTSW |
14 |
31,389,004 (GRCm39) |
nonsense |
probably null |
|
R5806:Btd
|
UTSW |
14 |
31,389,469 (GRCm39) |
missense |
probably benign |
|
R6110:Btd
|
UTSW |
14 |
31,363,065 (GRCm39) |
unclassified |
probably benign |
|
R6119:Btd
|
UTSW |
14 |
31,363,065 (GRCm39) |
unclassified |
probably benign |
|
R6120:Btd
|
UTSW |
14 |
31,363,065 (GRCm39) |
unclassified |
probably benign |
|
R7019:Btd
|
UTSW |
14 |
31,389,063 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7019:Btd
|
UTSW |
14 |
31,389,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R7021:Btd
|
UTSW |
14 |
31,389,788 (GRCm39) |
missense |
probably benign |
|
R7837:Btd
|
UTSW |
14 |
31,388,784 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8176:Btd
|
UTSW |
14 |
31,384,073 (GRCm39) |
missense |
probably benign |
0.14 |
R8249:Btd
|
UTSW |
14 |
31,387,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R8516:Btd
|
UTSW |
14 |
31,388,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R9098:Btd
|
UTSW |
14 |
31,384,233 (GRCm39) |
missense |
probably benign |
0.00 |
R9465:Btd
|
UTSW |
14 |
31,389,643 (GRCm39) |
missense |
probably benign |
0.00 |
|