Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
A |
T |
8: 41,207,768 (GRCm39) |
N345Y |
probably benign |
Het |
Ampd3 |
G |
A |
7: 110,387,887 (GRCm39) |
G107S |
probably damaging |
Het |
Bcas3 |
T |
A |
11: 85,448,236 (GRCm39) |
I632N |
probably benign |
Het |
Cald1 |
G |
T |
6: 34,732,577 (GRCm39) |
R83L |
probably damaging |
Het |
Cds2 |
T |
A |
2: 132,147,180 (GRCm39) |
L420Q |
probably damaging |
Het |
Col6a1 |
A |
T |
10: 76,556,800 (GRCm39) |
Y266N |
probably damaging |
Het |
Ctps1 |
A |
G |
4: 120,400,919 (GRCm39) |
|
probably null |
Het |
Enam |
A |
G |
5: 88,651,878 (GRCm39) |
N1129S |
possibly damaging |
Het |
Erc1 |
T |
C |
6: 119,773,887 (GRCm39) |
E356G |
probably damaging |
Het |
Fbxl4 |
T |
A |
4: 22,427,166 (GRCm39) |
V469E |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably null |
Het |
Grm2 |
T |
G |
9: 106,525,356 (GRCm39) |
Y453S |
probably damaging |
Het |
Htt |
A |
G |
5: 35,008,561 (GRCm39) |
|
probably null |
Het |
Jakmip1 |
A |
G |
5: 37,291,593 (GRCm39) |
I681V |
possibly damaging |
Het |
Lair1 |
A |
G |
7: 4,031,784 (GRCm39) |
S108P |
probably damaging |
Het |
Lrp12 |
A |
C |
15: 39,741,377 (GRCm39) |
F446C |
probably damaging |
Het |
Ncoa6 |
C |
T |
2: 155,275,960 (GRCm39) |
R95Q |
probably damaging |
Het |
Nup210 |
T |
C |
6: 91,005,793 (GRCm39) |
T614A |
probably benign |
Het |
Or1b1 |
T |
C |
2: 36,995,476 (GRCm39) |
Y62C |
probably damaging |
Het |
Or52p2 |
A |
T |
7: 102,237,166 (GRCm39) |
Y261* |
probably null |
Het |
Or8b12 |
T |
C |
9: 37,658,131 (GRCm39) |
S234P |
probably damaging |
Het |
Ppp1r12a |
T |
C |
10: 108,098,212 (GRCm39) |
S311P |
probably damaging |
Het |
Rsph3a |
C |
A |
17: 8,164,736 (GRCm39) |
P32Q |
probably benign |
Het |
Sorl1 |
T |
C |
9: 41,902,752 (GRCm39) |
T1602A |
probably benign |
Het |
Svil |
C |
G |
18: 5,056,690 (GRCm39) |
P521R |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,652,509 (GRCm39) |
Y1580C |
probably damaging |
Het |
Vwce |
T |
C |
19: 10,641,463 (GRCm39) |
F730L |
probably benign |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zc2hc1c |
A |
G |
12: 85,343,330 (GRCm39) |
D489G |
probably damaging |
Het |
|
Other mutations in Gm11568 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0483:Gm11568
|
UTSW |
11 |
99,749,209 (GRCm39) |
missense |
unknown |
|
R0558:Gm11568
|
UTSW |
11 |
99,748,872 (GRCm39) |
missense |
unknown |
|
R2273:Gm11568
|
UTSW |
11 |
99,749,070 (GRCm39) |
missense |
unknown |
|
R2274:Gm11568
|
UTSW |
11 |
99,749,070 (GRCm39) |
missense |
unknown |
|
R2275:Gm11568
|
UTSW |
11 |
99,749,070 (GRCm39) |
missense |
unknown |
|
R4436:Gm11568
|
UTSW |
11 |
99,749,421 (GRCm39) |
missense |
unknown |
|
R4985:Gm11568
|
UTSW |
11 |
99,749,274 (GRCm39) |
missense |
unknown |
|
R5078:Gm11568
|
UTSW |
11 |
99,749,181 (GRCm39) |
missense |
unknown |
|
R5083:Gm11568
|
UTSW |
11 |
99,748,798 (GRCm39) |
start codon destroyed |
probably null |
|
R6879:Gm11568
|
UTSW |
11 |
99,749,053 (GRCm39) |
missense |
unknown |
|
R7486:Gm11568
|
UTSW |
11 |
99,749,292 (GRCm39) |
missense |
unknown |
|
R7855:Gm11568
|
UTSW |
11 |
99,749,010 (GRCm39) |
missense |
unknown |
|
R9496:Gm11568
|
UTSW |
11 |
99,749,044 (GRCm39) |
small insertion |
probably benign |
|
R9500:Gm11568
|
UTSW |
11 |
99,749,065 (GRCm39) |
small insertion |
probably benign |
|
R9500:Gm11568
|
UTSW |
11 |
99,749,044 (GRCm39) |
small insertion |
probably benign |
|
|