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 |
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 |
Zfp558 |
C |
A |
9: 18,368,219 (GRCm39) |
G190* |
probably null |
Het |
|
Other mutations in Slain2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01589:Slain2
|
APN |
5 |
73,098,789 (GRCm39) |
splice site |
probably benign |
|
IGL02177:Slain2
|
APN |
5 |
73,072,008 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02225:Slain2
|
APN |
5 |
73,098,733 (GRCm39) |
missense |
probably damaging |
0.99 |
R1630:Slain2
|
UTSW |
5 |
73,133,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Slain2
|
UTSW |
5 |
73,114,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Slain2
|
UTSW |
5 |
73,114,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Slain2
|
UTSW |
5 |
73,114,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R4743:Slain2
|
UTSW |
5 |
73,114,927 (GRCm39) |
nonsense |
probably null |
|
R4839:Slain2
|
UTSW |
5 |
73,106,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4853:Slain2
|
UTSW |
5 |
73,105,941 (GRCm39) |
missense |
probably benign |
0.01 |
R4914:Slain2
|
UTSW |
5 |
73,115,609 (GRCm39) |
missense |
probably benign |
0.26 |
R5859:Slain2
|
UTSW |
5 |
73,105,888 (GRCm39) |
intron |
probably benign |
|
R7251:Slain2
|
UTSW |
5 |
73,131,891 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7327:Slain2
|
UTSW |
5 |
73,132,002 (GRCm39) |
missense |
probably benign |
0.00 |
R7528:Slain2
|
UTSW |
5 |
73,072,143 (GRCm39) |
nonsense |
probably null |
|
R7586:Slain2
|
UTSW |
5 |
73,123,165 (GRCm39) |
missense |
probably benign |
|
R7763:Slain2
|
UTSW |
5 |
73,105,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R7973:Slain2
|
UTSW |
5 |
73,112,779 (GRCm39) |
nonsense |
probably null |
|
R8994:Slain2
|
UTSW |
5 |
73,114,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Slain2
|
UTSW |
5 |
73,114,969 (GRCm39) |
nonsense |
probably null |
|
|