Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl3 |
C |
A |
7: 82,216,232 (GRCm39) |
D878E |
possibly damaging |
Het |
Adipor2 |
A |
C |
6: 119,334,203 (GRCm39) |
F336V |
possibly damaging |
Het |
Akt3 |
A |
T |
1: 176,877,756 (GRCm39) |
Y337* |
probably null |
Het |
Aoc1 |
A |
G |
6: 48,882,871 (GRCm39) |
N249S |
probably benign |
Het |
Ap1b1 |
T |
A |
11: 4,969,427 (GRCm39) |
L261Q |
probably damaging |
Het |
Ap3b1 |
T |
A |
13: 94,599,017 (GRCm39) |
D530E |
probably benign |
Het |
Arid4b |
T |
A |
13: 14,361,900 (GRCm39) |
M788K |
possibly damaging |
Het |
Atp2c2 |
A |
T |
8: 120,479,756 (GRCm39) |
I762F |
probably damaging |
Het |
Bhlhe23 |
C |
A |
2: 180,418,136 (GRCm39) |
R134L |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 28,777,934 (GRCm39) |
D687G |
probably damaging |
Het |
Ccdc136 |
G |
A |
6: 29,405,940 (GRCm39) |
M95I |
probably benign |
Het |
Cdk12 |
T |
A |
11: 98,115,355 (GRCm39) |
I832N |
unknown |
Het |
Clcn2 |
A |
C |
16: 20,526,418 (GRCm39) |
|
probably null |
Het |
Csrnp2 |
C |
T |
15: 100,380,574 (GRCm39) |
R239Q |
probably damaging |
Het |
Dhrs13 |
T |
A |
11: 77,927,965 (GRCm39) |
D270E |
probably benign |
Het |
Dlgap2 |
G |
A |
8: 14,793,284 (GRCm39) |
G426D |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Fam120a |
A |
G |
13: 49,045,440 (GRCm39) |
Y799H |
probably damaging |
Het |
Farp1 |
G |
A |
14: 121,460,066 (GRCm39) |
V112I |
probably benign |
Het |
Fhip2a |
A |
G |
19: 57,367,177 (GRCm39) |
D240G |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,816,776 (GRCm39) |
I4170V |
probably benign |
Het |
Gm12185 |
A |
G |
11: 48,806,531 (GRCm39) |
V220A |
probably benign |
Het |
Gpr37l1 |
T |
C |
1: 135,094,860 (GRCm39) |
Y128C |
probably damaging |
Het |
Gsto2 |
A |
T |
19: 47,860,227 (GRCm39) |
R7* |
probably null |
Het |
Itih3 |
C |
T |
14: 30,631,430 (GRCm39) |
G822D |
probably benign |
Het |
Kcnu1 |
A |
T |
8: 26,403,673 (GRCm39) |
D728V |
probably damaging |
Het |
Khdc4 |
G |
T |
3: 88,593,736 (GRCm39) |
G42W |
probably damaging |
Het |
Lnpep |
G |
A |
17: 17,750,758 (GRCm39) |
T976I |
probably damaging |
Het |
Map1b |
A |
C |
13: 99,562,449 (GRCm39) |
H2420Q |
unknown |
Het |
Mc1r |
A |
G |
8: 124,134,435 (GRCm39) |
K63E |
probably damaging |
Het |
Mpped1 |
G |
A |
15: 83,720,584 (GRCm39) |
V15M |
probably damaging |
Het |
Ncor1 |
T |
C |
11: 62,264,272 (GRCm39) |
T103A |
probably benign |
Het |
Nhsl1 |
A |
T |
10: 18,407,062 (GRCm39) |
T1399S |
probably benign |
Het |
Nlrc5 |
C |
T |
8: 95,216,996 (GRCm39) |
T995M |
probably benign |
Het |
Nrbp1 |
G |
A |
5: 31,403,190 (GRCm39) |
|
probably null |
Het |
Or10g9 |
A |
C |
9: 39,912,493 (GRCm39) |
F10C |
probably damaging |
Het |
Or4c116 |
G |
T |
2: 88,942,640 (GRCm39) |
T72N |
possibly damaging |
Het |
Or8k27 |
T |
C |
2: 86,275,580 (GRCm39) |
T249A |
probably benign |
Het |
Pcdhb13 |
T |
C |
18: 37,576,663 (GRCm39) |
L347P |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,128,563 (GRCm39) |
T4047A |
probably benign |
Het |
Prrt2 |
T |
A |
7: 126,618,769 (GRCm39) |
D232V |
probably damaging |
Het |
Psmd5 |
A |
C |
2: 34,746,545 (GRCm39) |
M344R |
probably benign |
Het |
Qsox1 |
A |
G |
1: 155,666,851 (GRCm39) |
Y213H |
probably benign |
Het |
Rmc1 |
A |
G |
18: 12,309,203 (GRCm39) |
N92D |
possibly damaging |
Het |
Sclt1 |
T |
C |
3: 41,685,337 (GRCm39) |
R39G |
unknown |
Het |
Syne1 |
A |
T |
10: 5,093,285 (GRCm39) |
|
probably null |
Het |
Tmem163 |
G |
T |
1: 127,479,078 (GRCm39) |
A147E |
probably damaging |
Het |
Trav13n-4 |
A |
T |
14: 53,601,557 (GRCm39) |
M109L |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,039,790 (GRCm39) |
E1283G |
probably damaging |
Het |
Trpm6 |
T |
A |
19: 18,855,129 (GRCm39) |
D1929E |
probably damaging |
Het |
Upb1 |
A |
T |
10: 75,273,978 (GRCm39) |
D335V |
probably damaging |
Het |
Vps26b |
T |
C |
9: 26,924,104 (GRCm39) |
E213G |
probably damaging |
Het |
Vwc2 |
C |
T |
11: 11,104,215 (GRCm39) |
T249I |
probably benign |
Het |
Wwc2 |
A |
G |
8: 48,353,826 (GRCm39) |
Y103H |
possibly damaging |
Het |
Zan |
A |
G |
5: 137,391,409 (GRCm39) |
C4692R |
unknown |
Het |
Zfp106 |
T |
C |
2: 120,369,935 (GRCm39) |
E29G |
probably damaging |
Het |
Zfp551 |
G |
A |
7: 12,150,767 (GRCm39) |
A214V |
possibly damaging |
Het |
Zfp981 |
T |
A |
4: 146,622,363 (GRCm39) |
H429Q |
probably benign |
Het |
|
Other mutations in Pwp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00707:Pwp1
|
APN |
10 |
85,714,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00778:Pwp1
|
APN |
10 |
85,715,752 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01086:Pwp1
|
APN |
10 |
85,715,757 (GRCm39) |
splice site |
probably null |
|
IGL02526:Pwp1
|
APN |
10 |
85,717,967 (GRCm39) |
splice site |
probably null |
|
IGL02596:Pwp1
|
APN |
10 |
85,707,882 (GRCm39) |
splice site |
probably null |
|
IGL03164:Pwp1
|
APN |
10 |
85,714,367 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03269:Pwp1
|
APN |
10 |
85,718,768 (GRCm39) |
missense |
probably damaging |
0.98 |
Annuals
|
UTSW |
10 |
85,712,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0031:Pwp1
|
UTSW |
10 |
85,721,760 (GRCm39) |
missense |
probably benign |
0.20 |
R0049:Pwp1
|
UTSW |
10 |
85,721,480 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0049:Pwp1
|
UTSW |
10 |
85,721,480 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0766:Pwp1
|
UTSW |
10 |
85,715,173 (GRCm39) |
missense |
probably damaging |
0.98 |
R0926:Pwp1
|
UTSW |
10 |
85,712,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1238:Pwp1
|
UTSW |
10 |
85,721,726 (GRCm39) |
missense |
probably benign |
0.02 |
R1312:Pwp1
|
UTSW |
10 |
85,715,173 (GRCm39) |
missense |
probably damaging |
0.98 |
R1420:Pwp1
|
UTSW |
10 |
85,712,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Pwp1
|
UTSW |
10 |
85,717,943 (GRCm39) |
missense |
probably benign |
0.45 |
R3277:Pwp1
|
UTSW |
10 |
85,717,943 (GRCm39) |
missense |
probably benign |
0.45 |
R3818:Pwp1
|
UTSW |
10 |
85,723,993 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4008:Pwp1
|
UTSW |
10 |
85,717,898 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5964:Pwp1
|
UTSW |
10 |
85,718,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R6252:Pwp1
|
UTSW |
10 |
85,710,373 (GRCm39) |
missense |
probably benign |
0.00 |
R6280:Pwp1
|
UTSW |
10 |
85,710,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R7168:Pwp1
|
UTSW |
10 |
85,720,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R7213:Pwp1
|
UTSW |
10 |
85,712,173 (GRCm39) |
missense |
probably benign |
|
R7236:Pwp1
|
UTSW |
10 |
85,715,147 (GRCm39) |
missense |
probably benign |
0.00 |
R7840:Pwp1
|
UTSW |
10 |
85,723,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R9025:Pwp1
|
UTSW |
10 |
85,718,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R9063:Pwp1
|
UTSW |
10 |
85,720,431 (GRCm39) |
missense |
probably benign |
0.00 |
R9366:Pwp1
|
UTSW |
10 |
85,717,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R9451:Pwp1
|
UTSW |
10 |
85,714,428 (GRCm39) |
missense |
probably damaging |
0.99 |
R9535:Pwp1
|
UTSW |
10 |
85,723,958 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9563:Pwp1
|
UTSW |
10 |
85,712,370 (GRCm39) |
missense |
probably damaging |
0.99 |
|