Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406C07Rik |
A |
T |
9: 15,203,326 (GRCm39) |
N159K |
probably damaging |
Het |
Arhgef10l |
T |
C |
4: 140,245,058 (GRCm39) |
|
probably benign |
Het |
Atosa |
A |
G |
9: 74,861,107 (GRCm39) |
D4G |
possibly damaging |
Het |
Avil |
A |
G |
10: 126,843,618 (GRCm39) |
S153G |
possibly damaging |
Het |
C2cd3 |
G |
A |
7: 100,067,747 (GRCm39) |
D877N |
probably damaging |
Het |
Clca3a2 |
G |
A |
3: 144,519,405 (GRCm39) |
A257V |
probably benign |
Het |
Cramp1 |
T |
A |
17: 25,202,931 (GRCm39) |
H366L |
probably benign |
Het |
Cyp2c37 |
C |
T |
19: 39,998,287 (GRCm39) |
S393L |
probably damaging |
Het |
Defb8 |
T |
A |
8: 19,495,950 (GRCm39) |
I37L |
probably benign |
Het |
Dennd4b |
C |
A |
3: 90,185,039 (GRCm39) |
|
probably null |
Het |
Eps8l2 |
G |
A |
7: 140,936,115 (GRCm39) |
R223H |
probably damaging |
Het |
Erbin |
A |
G |
13: 103,961,400 (GRCm39) |
L1302P |
probably benign |
Het |
Exoc3l |
A |
G |
8: 106,021,993 (GRCm39) |
W37R |
probably damaging |
Het |
Fap |
T |
C |
2: 62,333,725 (GRCm39) |
N668S |
probably damaging |
Het |
Gas7 |
A |
G |
11: 67,565,107 (GRCm39) |
N250S |
probably damaging |
Het |
H2bc12 |
T |
A |
13: 22,220,391 (GRCm39) |
V112E |
probably damaging |
Het |
Hivep1 |
C |
A |
13: 42,309,956 (GRCm39) |
P732Q |
probably damaging |
Het |
Irx4 |
G |
T |
13: 73,416,545 (GRCm39) |
A314S |
probably benign |
Het |
Itgb8 |
A |
T |
12: 119,144,712 (GRCm39) |
L332* |
probably null |
Het |
Kctd19 |
A |
G |
8: 106,111,960 (GRCm39) |
|
probably null |
Het |
Kif14 |
G |
A |
1: 136,443,697 (GRCm39) |
S1290N |
probably benign |
Het |
Klk1b3 |
C |
T |
7: 43,850,888 (GRCm39) |
T140I |
probably benign |
Het |
Lama1 |
A |
G |
17: 68,081,477 (GRCm39) |
N1305D |
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,410,201 (GRCm39) |
V1515E |
probably damaging |
Het |
Man2b1 |
A |
G |
8: 85,813,440 (GRCm39) |
|
probably null |
Het |
Mocos |
A |
G |
18: 24,832,988 (GRCm39) |
T818A |
probably benign |
Het |
Mpc2 |
G |
T |
1: 165,307,081 (GRCm39) |
W94L |
probably benign |
Het |
Mrc1 |
G |
A |
2: 14,243,296 (GRCm39) |
V141I |
probably benign |
Het |
Nalcn |
T |
C |
14: 123,697,663 (GRCm39) |
T538A |
probably benign |
Het |
Ndufs3 |
G |
A |
2: 90,732,744 (GRCm39) |
T114M |
probably damaging |
Het |
Noct |
T |
C |
3: 51,157,621 (GRCm39) |
C320R |
probably damaging |
Het |
Or5b117 |
T |
A |
19: 13,431,185 (GRCm39) |
Q232L |
probably benign |
Het |
Pcdha11 |
G |
T |
18: 37,138,844 (GRCm39) |
A158S |
probably damaging |
Het |
Pcdhga8 |
T |
A |
18: 37,860,109 (GRCm39) |
D388E |
probably benign |
Het |
Peg3 |
T |
C |
7: 6,712,069 (GRCm39) |
E1051G |
possibly damaging |
Het |
Phlda2 |
T |
A |
7: 143,055,918 (GRCm39) |
I104F |
probably damaging |
Het |
Polr2a |
A |
G |
11: 69,626,339 (GRCm39) |
S1604P |
possibly damaging |
Het |
Pomt2 |
C |
T |
12: 87,186,417 (GRCm39) |
|
probably null |
Het |
Ppp6r2 |
G |
A |
15: 89,137,458 (GRCm39) |
|
probably null |
Het |
Prdm2 |
T |
G |
4: 142,861,454 (GRCm39) |
Q612P |
probably benign |
Het |
Prr5 |
C |
A |
15: 84,586,978 (GRCm39) |
R243S |
probably damaging |
Het |
Ptgdr2 |
T |
C |
19: 10,918,233 (GRCm39) |
I250T |
probably benign |
Het |
Rad54l2 |
A |
T |
9: 106,590,739 (GRCm39) |
C462* |
probably null |
Het |
Sec16a |
T |
A |
2: 26,329,969 (GRCm39) |
E682V |
probably damaging |
Het |
Serpina3i |
A |
G |
12: 104,232,725 (GRCm39) |
D210G |
probably damaging |
Het |
Slain2 |
T |
A |
5: 73,114,748 (GRCm39) |
D326E |
probably benign |
Het |
Sned1 |
A |
G |
1: 93,209,374 (GRCm39) |
E829G |
probably damaging |
Het |
Steap4 |
G |
A |
5: 8,026,995 (GRCm39) |
W319* |
probably null |
Het |
Taar8c |
A |
G |
10: 23,977,701 (GRCm39) |
V37A |
probably benign |
Het |
Tdrd12 |
T |
A |
7: 35,184,654 (GRCm39) |
Y753F |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,937,222 (GRCm39) |
S3770G |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,708,460 (GRCm39) |
N48S |
possibly damaging |
Het |
|
Other mutations in Zfp558 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00532:Zfp558
|
APN |
9 |
18,367,883 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL00722:Zfp558
|
APN |
9 |
18,367,817 (GRCm39) |
missense |
probably damaging |
0.97 |
R0270:Zfp558
|
UTSW |
9 |
18,379,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R0708:Zfp558
|
UTSW |
9 |
18,368,123 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1521:Zfp558
|
UTSW |
9 |
18,367,859 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1618:Zfp558
|
UTSW |
9 |
18,380,579 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2323:Zfp558
|
UTSW |
9 |
18,380,573 (GRCm39) |
critical splice donor site |
probably null |
|
R2939:Zfp558
|
UTSW |
9 |
18,367,924 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4537:Zfp558
|
UTSW |
9 |
18,368,798 (GRCm39) |
missense |
probably null |
0.72 |
R4569:Zfp558
|
UTSW |
9 |
18,367,799 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4570:Zfp558
|
UTSW |
9 |
18,367,799 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4571:Zfp558
|
UTSW |
9 |
18,367,799 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4619:Zfp558
|
UTSW |
9 |
18,367,577 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5207:Zfp558
|
UTSW |
9 |
18,368,296 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5530:Zfp558
|
UTSW |
9 |
18,367,669 (GRCm39) |
missense |
probably benign |
0.05 |
R7892:Zfp558
|
UTSW |
9 |
18,379,993 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8309:Zfp558
|
UTSW |
9 |
18,368,213 (GRCm39) |
missense |
probably benign |
0.02 |
R9006:Zfp558
|
UTSW |
9 |
18,367,776 (GRCm39) |
missense |
possibly damaging |
0.86 |
|