Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,774,419 (GRCm39) |
S1203P |
probably benign |
Het |
Adamts1 |
A |
G |
16: 85,594,936 (GRCm39) |
V341A |
possibly damaging |
Het |
Arf2 |
G |
A |
11: 103,874,459 (GRCm39) |
G144S |
probably benign |
Het |
Atr |
A |
G |
9: 95,756,455 (GRCm39) |
N862D |
probably benign |
Het |
Chd6 |
C |
T |
2: 160,825,682 (GRCm39) |
V1141I |
possibly damaging |
Het |
Chst5 |
C |
A |
8: 112,616,842 (GRCm39) |
K259N |
probably benign |
Het |
Dchs1 |
T |
A |
7: 105,413,383 (GRCm39) |
D1144V |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,282,792 (GRCm39) |
Y2795C |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,316,280 (GRCm39) |
N3131S |
probably damaging |
Het |
Dnah7c |
G |
A |
1: 46,654,527 (GRCm39) |
G1436R |
probably damaging |
Het |
Emp2 |
T |
A |
16: 10,102,374 (GRCm39) |
Y146F |
probably damaging |
Het |
Exoc6 |
C |
T |
19: 37,562,189 (GRCm39) |
Q148* |
probably null |
Het |
Fam13b |
T |
C |
18: 34,630,488 (GRCm39) |
D90G |
probably damaging |
Het |
Fam186b |
T |
G |
15: 99,177,598 (GRCm39) |
Y576S |
probably benign |
Het |
Fras1 |
T |
C |
5: 96,857,775 (GRCm39) |
V2023A |
probably benign |
Het |
Grm5 |
A |
C |
7: 87,675,808 (GRCm39) |
M441L |
probably damaging |
Het |
Hhatl |
A |
G |
9: 121,617,343 (GRCm39) |
Y297H |
probably damaging |
Het |
Ifi30 |
A |
G |
8: 71,219,188 (GRCm39) |
|
probably benign |
Het |
Ing2 |
G |
T |
8: 48,122,040 (GRCm39) |
N169K |
possibly damaging |
Het |
Kat6a |
T |
G |
8: 23,428,028 (GRCm39) |
S1128A |
probably benign |
Het |
Madd |
T |
C |
2: 90,992,420 (GRCm39) |
E1041G |
possibly damaging |
Het |
Mcm3 |
CT |
CTT |
1: 20,878,972 (GRCm39) |
|
probably null |
Het |
Mfsd5 |
G |
A |
15: 102,189,513 (GRCm39) |
G295D |
possibly damaging |
Het |
Minar1 |
A |
T |
9: 89,483,125 (GRCm39) |
N757K |
probably benign |
Het |
Mmp20 |
T |
A |
9: 7,628,378 (GRCm39) |
|
probably null |
Het |
Mybphl |
T |
C |
3: 108,282,070 (GRCm39) |
V100A |
probably benign |
Het |
Ndfip2 |
T |
A |
14: 105,539,750 (GRCm39) |
|
probably null |
Het |
Or7e170 |
A |
G |
9: 19,795,484 (GRCm39) |
V39A |
probably benign |
Het |
Or7e175 |
T |
A |
9: 20,049,228 (GRCm39) |
V272E |
probably benign |
Het |
Or8b1c |
T |
A |
9: 38,384,831 (GRCm39) |
S263T |
possibly damaging |
Het |
Phf19 |
T |
G |
2: 34,787,135 (GRCm39) |
D443A |
probably damaging |
Het |
Piezo1 |
A |
G |
8: 123,234,394 (GRCm39) |
V84A |
probably damaging |
Het |
Septin9 |
A |
G |
11: 117,243,094 (GRCm39) |
I94V |
probably benign |
Het |
Slc35a1 |
C |
A |
4: 34,675,032 (GRCm39) |
V132L |
probably benign |
Het |
Sntg1 |
G |
A |
1: 8,484,494 (GRCm39) |
S442L |
probably benign |
Het |
Tcf25 |
A |
G |
8: 124,108,196 (GRCm39) |
T84A |
probably benign |
Het |
Tchhl1 |
C |
G |
3: 93,378,863 (GRCm39) |
S522R |
probably damaging |
Het |
Tmem106b |
A |
G |
6: 13,075,041 (GRCm39) |
E76G |
probably damaging |
Het |
Tnk2 |
C |
T |
16: 32,499,482 (GRCm39) |
P932S |
probably benign |
Het |
Trib1 |
G |
A |
15: 59,526,350 (GRCm39) |
V307I |
probably benign |
Het |
Trib3 |
A |
T |
2: 152,185,215 (GRCm39) |
D11E |
probably benign |
Het |
Trim34b |
T |
C |
7: 103,980,640 (GRCm39) |
S243P |
possibly damaging |
Het |
Vmn2r50 |
A |
G |
7: 9,781,905 (GRCm39) |
I280T |
probably damaging |
Het |
Zfp1010 |
A |
T |
2: 176,956,765 (GRCm39) |
C244* |
probably null |
Het |
Zfp445 |
G |
T |
9: 122,682,211 (GRCm39) |
Q577K |
probably benign |
Het |
Zfp599 |
T |
C |
9: 22,160,957 (GRCm39) |
K403E |
probably damaging |
Het |
|
Other mutations in Cep295nl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00958:Cep295nl
|
APN |
11 |
118,224,730 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02883:Cep295nl
|
APN |
11 |
118,224,735 (GRCm39) |
missense |
probably benign |
0.01 |
R1724:Cep295nl
|
UTSW |
11 |
118,223,854 (GRCm39) |
missense |
probably benign |
0.03 |
R1815:Cep295nl
|
UTSW |
11 |
118,223,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R1999:Cep295nl
|
UTSW |
11 |
118,223,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R2161:Cep295nl
|
UTSW |
11 |
118,223,335 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2198:Cep295nl
|
UTSW |
11 |
118,223,419 (GRCm39) |
missense |
probably benign |
0.00 |
R4871:Cep295nl
|
UTSW |
11 |
118,224,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R5348:Cep295nl
|
UTSW |
11 |
118,224,425 (GRCm39) |
missense |
probably damaging |
0.98 |
R6379:Cep295nl
|
UTSW |
11 |
118,224,556 (GRCm39) |
missense |
probably benign |
0.04 |
R7038:Cep295nl
|
UTSW |
11 |
118,223,815 (GRCm39) |
missense |
probably benign |
0.27 |
R7254:Cep295nl
|
UTSW |
11 |
118,223,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R7456:Cep295nl
|
UTSW |
11 |
118,224,376 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7494:Cep295nl
|
UTSW |
11 |
118,224,758 (GRCm39) |
missense |
probably benign |
|
R8982:Cep295nl
|
UTSW |
11 |
118,224,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R9303:Cep295nl
|
UTSW |
11 |
118,224,766 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9305:Cep295nl
|
UTSW |
11 |
118,224,766 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9451:Cep295nl
|
UTSW |
11 |
118,224,446 (GRCm39) |
nonsense |
probably null |
|
R9617:Cep295nl
|
UTSW |
11 |
118,224,000 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9621:Cep295nl
|
UTSW |
11 |
118,224,766 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Cep295nl
|
UTSW |
11 |
118,224,699 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cep295nl
|
UTSW |
11 |
118,223,845 (GRCm39) |
missense |
possibly damaging |
0.90 |
|