Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Aarsd1 |
A |
C |
11: 101,301,597 (GRCm39) |
S262A |
probably benign |
Het |
Abhd17c |
A |
G |
7: 83,763,637 (GRCm39) |
Y189H |
probably damaging |
Het |
Adam33 |
T |
C |
2: 130,895,606 (GRCm39) |
R570G |
possibly damaging |
Het |
Alpk2 |
G |
A |
18: 65,424,464 (GRCm39) |
R1441W |
probably damaging |
Het |
Arhgap21 |
A |
G |
2: 20,885,464 (GRCm39) |
V581A |
probably benign |
Het |
Bcat2 |
T |
C |
7: 45,234,980 (GRCm39) |
V226A |
possibly damaging |
Het |
Cdh10 |
A |
G |
15: 19,013,521 (GRCm39) |
N707S |
possibly damaging |
Het |
Chd9 |
T |
C |
8: 91,659,174 (GRCm39) |
F45L |
unknown |
Het |
Clec1a |
T |
C |
6: 129,428,606 (GRCm39) |
T25A |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,259,671 (GRCm39) |
F1338L |
probably damaging |
Het |
Cthrc1 |
A |
G |
15: 38,947,868 (GRCm39) |
T196A |
probably benign |
Het |
Ctsm |
A |
T |
13: 61,686,299 (GRCm39) |
V228D |
probably damaging |
Het |
Dennd3 |
A |
T |
15: 73,429,477 (GRCm39) |
D920V |
probably damaging |
Het |
Dnah17 |
A |
G |
11: 117,987,452 (GRCm39) |
I1286T |
probably benign |
Het |
Dnah3 |
T |
A |
7: 119,551,473 (GRCm39) |
T2949S |
probably benign |
Het |
Dram1 |
C |
T |
10: 88,192,703 (GRCm39) |
V28M |
probably benign |
Het |
Eml5 |
A |
G |
12: 98,827,554 (GRCm39) |
Y559H |
probably damaging |
Het |
Ermard |
C |
T |
17: 15,273,554 (GRCm39) |
R380C |
possibly damaging |
Het |
Fam181a |
A |
G |
12: 103,282,107 (GRCm39) |
D4G |
probably damaging |
Het |
Gabrd |
C |
A |
4: 155,472,803 (GRCm39) |
V127L |
probably damaging |
Het |
Galnt12 |
T |
A |
4: 47,104,163 (GRCm39) |
Y140* |
probably null |
Het |
Gpr161 |
A |
T |
1: 165,146,389 (GRCm39) |
K442* |
probably null |
Het |
Haus6 |
A |
T |
4: 86,513,665 (GRCm39) |
N332K |
probably benign |
Het |
Igsf3 |
T |
A |
3: 101,358,322 (GRCm39) |
Y738N |
probably damaging |
Het |
Itsn1 |
T |
A |
16: 91,625,264 (GRCm39) |
*622R |
probably null |
Het |
Kcna2 |
T |
A |
3: 107,012,887 (GRCm39) |
Y489* |
probably null |
Het |
Limk1 |
A |
G |
5: 134,701,864 (GRCm39) |
|
probably null |
Het |
Manba |
A |
T |
3: 135,255,079 (GRCm39) |
D479V |
probably benign |
Het |
Myh6 |
A |
T |
14: 55,189,779 (GRCm39) |
I1089N |
possibly damaging |
Het |
Npas4 |
T |
A |
19: 5,038,492 (GRCm39) |
D142V |
probably damaging |
Het |
Nr4a1 |
T |
C |
15: 101,168,053 (GRCm39) |
F30L |
probably benign |
Het |
Numbl |
C |
T |
7: 26,976,327 (GRCm39) |
R336C |
|
Het |
Or10x4 |
G |
A |
1: 174,218,742 (GRCm39) |
A36T |
probably benign |
Het |
Or5p4 |
T |
C |
7: 107,680,040 (GRCm39) |
I13T |
|
Het |
Pcdha11 |
A |
G |
18: 37,145,484 (GRCm39) |
E525G |
probably damaging |
Het |
Pdia2 |
T |
C |
17: 26,416,174 (GRCm39) |
T298A |
probably benign |
Het |
Per3 |
G |
A |
4: 151,094,945 (GRCm39) |
T946I |
probably benign |
Het |
Pla2r1 |
A |
T |
2: 60,258,902 (GRCm39) |
V1162D |
probably damaging |
Het |
Plxnd1 |
T |
A |
6: 115,932,730 (GRCm39) |
N1917Y |
probably damaging |
Het |
Pole3 |
A |
T |
4: 62,442,277 (GRCm39) |
D114E |
unknown |
Het |
Ppil3 |
T |
C |
1: 58,470,397 (GRCm39) |
D151G |
probably benign |
Het |
Psd3 |
A |
T |
8: 68,165,833 (GRCm39) |
M365K |
unknown |
Het |
Psme2b |
T |
G |
11: 48,836,566 (GRCm39) |
H127P |
probably damaging |
Het |
Ric8a |
C |
G |
7: 140,437,393 (GRCm39) |
R4G |
probably benign |
Het |
Rock2 |
A |
T |
12: 17,027,763 (GRCm39) |
D1360V |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,674,192 (GRCm39) |
T847A |
probably benign |
Het |
Slc12a1 |
T |
A |
2: 125,028,144 (GRCm39) |
V480E |
probably damaging |
Het |
Slc32a1 |
T |
C |
2: 158,456,241 (GRCm39) |
F299L |
probably benign |
Het |
Slc44a2 |
A |
G |
9: 21,258,333 (GRCm39) |
Y500C |
|
Het |
Ssbp2 |
A |
G |
13: 91,823,157 (GRCm39) |
D192G |
probably benign |
Het |
Stat5b |
T |
C |
11: 100,681,674 (GRCm39) |
K527E |
probably benign |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Usp50 |
A |
G |
2: 126,619,817 (GRCm39) |
|
probably null |
Het |
Vegfc |
A |
T |
8: 54,610,053 (GRCm39) |
M70L |
probably benign |
Het |
Vmn1r40 |
A |
G |
6: 89,691,854 (GRCm39) |
T224A |
probably benign |
Het |
Vmn2r116 |
A |
G |
17: 23,605,919 (GRCm39) |
D277G |
probably benign |
Het |
Vti1a |
T |
A |
19: 55,612,278 (GRCm39) |
I197N |
possibly damaging |
Het |
Zfyve9 |
C |
A |
4: 108,576,435 (GRCm39) |
L215F |
probably damaging |
Het |
Znrf3 |
A |
T |
11: 5,288,710 (GRCm39) |
Y19* |
probably null |
Het |
|
Other mutations in Parp9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01160:Parp9
|
APN |
16 |
35,768,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01365:Parp9
|
APN |
16 |
35,768,324 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01628:Parp9
|
APN |
16 |
35,777,285 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02274:Parp9
|
APN |
16 |
35,768,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02693:Parp9
|
APN |
16 |
35,777,340 (GRCm39) |
missense |
probably benign |
0.01 |
R0109:Parp9
|
UTSW |
16 |
35,768,711 (GRCm39) |
missense |
probably damaging |
0.97 |
R0109:Parp9
|
UTSW |
16 |
35,768,711 (GRCm39) |
missense |
probably damaging |
0.97 |
R0559:Parp9
|
UTSW |
16 |
35,768,362 (GRCm39) |
missense |
probably benign |
0.00 |
R1126:Parp9
|
UTSW |
16 |
35,768,110 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1346:Parp9
|
UTSW |
16 |
35,777,267 (GRCm39) |
missense |
probably benign |
0.00 |
R1472:Parp9
|
UTSW |
16 |
35,774,050 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1642:Parp9
|
UTSW |
16 |
35,788,067 (GRCm39) |
missense |
probably benign |
0.37 |
R1900:Parp9
|
UTSW |
16 |
35,792,591 (GRCm39) |
missense |
probably benign |
0.00 |
R2055:Parp9
|
UTSW |
16 |
35,773,984 (GRCm39) |
missense |
probably damaging |
0.97 |
R3177:Parp9
|
UTSW |
16 |
35,768,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R3277:Parp9
|
UTSW |
16 |
35,768,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R4039:Parp9
|
UTSW |
16 |
35,780,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R4869:Parp9
|
UTSW |
16 |
35,777,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R4950:Parp9
|
UTSW |
16 |
35,768,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Parp9
|
UTSW |
16 |
35,784,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R5117:Parp9
|
UTSW |
16 |
35,792,202 (GRCm39) |
splice site |
probably null |
|
R5180:Parp9
|
UTSW |
16 |
35,774,106 (GRCm39) |
nonsense |
probably null |
|
R5415:Parp9
|
UTSW |
16 |
35,763,752 (GRCm39) |
missense |
probably damaging |
0.97 |
R5535:Parp9
|
UTSW |
16 |
35,777,195 (GRCm39) |
missense |
probably damaging |
0.98 |
R5727:Parp9
|
UTSW |
16 |
35,784,467 (GRCm39) |
nonsense |
probably null |
|
R5842:Parp9
|
UTSW |
16 |
35,763,778 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5942:Parp9
|
UTSW |
16 |
35,792,259 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6110:Parp9
|
UTSW |
16 |
35,773,996 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6193:Parp9
|
UTSW |
16 |
35,767,921 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6707:Parp9
|
UTSW |
16 |
35,768,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R6957:Parp9
|
UTSW |
16 |
35,768,716 (GRCm39) |
missense |
probably benign |
0.00 |
R7014:Parp9
|
UTSW |
16 |
35,780,433 (GRCm39) |
critical splice donor site |
probably null |
|
R7064:Parp9
|
UTSW |
16 |
35,774,042 (GRCm39) |
missense |
probably benign |
0.07 |
R7205:Parp9
|
UTSW |
16 |
35,777,360 (GRCm39) |
missense |
probably benign |
0.00 |
R7221:Parp9
|
UTSW |
16 |
35,774,071 (GRCm39) |
missense |
probably benign |
0.00 |
R7693:Parp9
|
UTSW |
16 |
35,777,282 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8810:Parp9
|
UTSW |
16 |
35,773,981 (GRCm39) |
nonsense |
probably null |
|
R9154:Parp9
|
UTSW |
16 |
35,768,543 (GRCm39) |
missense |
probably damaging |
0.99 |
|