Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519G04Rik |
C |
T |
5: 115,017,645 (GRCm39) |
A178V |
possibly damaging |
Het |
Acad11 |
A |
G |
9: 103,992,544 (GRCm39) |
I495M |
probably damaging |
Het |
Adgrd1 |
T |
C |
5: 129,192,202 (GRCm39) |
S91P |
probably benign |
Het |
Agk |
A |
G |
6: 40,353,160 (GRCm39) |
I175V |
probably damaging |
Het |
Ascc3 |
A |
T |
10: 50,566,235 (GRCm39) |
N727Y |
probably damaging |
Het |
Atrnl1 |
A |
T |
19: 57,680,195 (GRCm39) |
|
probably benign |
Het |
B4galt3 |
G |
A |
1: 171,099,362 (GRCm39) |
G42D |
probably damaging |
Het |
Brd10 |
A |
T |
19: 29,694,463 (GRCm39) |
S976T |
probably benign |
Het |
Brip1 |
C |
T |
11: 86,088,775 (GRCm39) |
C42Y |
possibly damaging |
Het |
Camkk1 |
T |
C |
11: 72,928,027 (GRCm39) |
F233L |
probably damaging |
Het |
Cdv3 |
A |
G |
9: 103,237,224 (GRCm39) |
|
probably benign |
Het |
Cog3 |
G |
T |
14: 75,968,044 (GRCm39) |
Q430K |
possibly damaging |
Het |
D6Wsu163e |
G |
A |
6: 126,932,184 (GRCm39) |
G308S |
probably damaging |
Het |
Dnah2 |
A |
G |
11: 69,365,111 (GRCm39) |
M1951T |
probably damaging |
Het |
Elavl3 |
G |
A |
9: 21,948,014 (GRCm39) |
T51I |
probably damaging |
Het |
Eri2 |
A |
T |
7: 119,385,303 (GRCm39) |
C399* |
probably null |
Het |
Ezh2 |
A |
T |
6: 47,528,835 (GRCm39) |
|
probably null |
Het |
Fgd6 |
C |
A |
10: 93,969,216 (GRCm39) |
T1161K |
probably damaging |
Het |
Gbf1 |
A |
T |
19: 46,267,731 (GRCm39) |
H1193L |
possibly damaging |
Het |
Gbp2b |
T |
A |
3: 142,312,751 (GRCm39) |
F378Y |
possibly damaging |
Het |
Hectd2 |
G |
A |
19: 36,592,916 (GRCm39) |
V694M |
possibly damaging |
Het |
Hook1 |
T |
A |
4: 95,910,434 (GRCm39) |
S683T |
probably benign |
Het |
Ifi202b |
G |
A |
1: 173,802,550 (GRCm39) |
R95C |
possibly damaging |
Het |
Kdm8 |
G |
T |
7: 125,051,658 (GRCm39) |
V84L |
probably damaging |
Het |
Kifc3 |
G |
A |
8: 95,834,168 (GRCm39) |
|
probably benign |
Het |
Krt26 |
C |
T |
11: 99,224,471 (GRCm39) |
R349Q |
probably benign |
Het |
Lrig1 |
G |
T |
6: 94,593,410 (GRCm39) |
Q424K |
probably damaging |
Het |
Lrriq1 |
A |
T |
10: 103,014,661 (GRCm39) |
M1049K |
probably benign |
Het |
Mcidas |
A |
G |
13: 113,133,377 (GRCm39) |
N103D |
probably benign |
Het |
Mdn1 |
T |
C |
4: 32,749,948 (GRCm39) |
L4377S |
possibly damaging |
Het |
Mrpl41 |
T |
C |
2: 24,864,429 (GRCm39) |
D81G |
possibly damaging |
Het |
Mug2 |
G |
A |
6: 122,024,394 (GRCm39) |
V489I |
probably benign |
Het |
P2rx5 |
G |
T |
11: 73,058,803 (GRCm39) |
|
probably benign |
Het |
Pfas |
A |
T |
11: 68,884,289 (GRCm39) |
|
probably benign |
Het |
Pknox2 |
A |
G |
9: 36,834,929 (GRCm39) |
L180P |
probably damaging |
Het |
Psmd5 |
C |
A |
2: 34,744,286 (GRCm39) |
C412F |
probably benign |
Het |
Rbks |
T |
A |
5: 31,817,361 (GRCm39) |
D136V |
probably damaging |
Het |
Rgl1 |
A |
G |
1: 152,404,220 (GRCm39) |
|
probably benign |
Het |
Scube3 |
A |
G |
17: 28,386,658 (GRCm39) |
D721G |
probably damaging |
Het |
Snrnp200 |
T |
A |
2: 127,074,825 (GRCm39) |
V1466D |
possibly damaging |
Het |
Stambp |
A |
T |
6: 83,529,013 (GRCm39) |
L344Q |
probably damaging |
Het |
Tctn1 |
A |
T |
5: 122,396,912 (GRCm39) |
I157N |
probably damaging |
Het |
Top2b |
T |
A |
14: 16,409,965 (GRCm38) |
D877E |
probably benign |
Het |
Vmn1r78 |
G |
A |
7: 11,886,634 (GRCm39) |
G82S |
probably damaging |
Het |
Vnn1 |
T |
C |
10: 23,779,449 (GRCm39) |
F453L |
possibly damaging |
Het |
Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
|
Other mutations in Cd300ld |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01628:Cd300ld
|
APN |
11 |
114,876,999 (GRCm39) |
missense |
probably benign |
|
IGL01976:Cd300ld
|
APN |
11 |
114,878,270 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02738:Cd300ld
|
APN |
11 |
114,875,076 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03386:Cd300ld
|
APN |
11 |
114,874,998 (GRCm39) |
missense |
probably benign |
|
R2001:Cd300ld
|
UTSW |
11 |
114,878,156 (GRCm39) |
missense |
probably benign |
0.44 |
R2197:Cd300ld
|
UTSW |
11 |
114,875,058 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3039:Cd300ld
|
UTSW |
11 |
114,877,003 (GRCm39) |
missense |
probably benign |
|
R5540:Cd300ld
|
UTSW |
11 |
114,878,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7096:Cd300ld
|
UTSW |
11 |
114,878,321 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7371:Cd300ld
|
UTSW |
11 |
114,878,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7548:Cd300ld
|
UTSW |
11 |
114,878,248 (GRCm39) |
missense |
probably benign |
0.02 |
R7710:Cd300ld
|
UTSW |
11 |
114,875,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Cd300ld
|
UTSW |
11 |
114,878,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9396:Cd300ld
|
UTSW |
11 |
114,878,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|