Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933416I08Rik |
TCC |
TCCC |
X: 52,692,862 (GRCm39) |
|
noncoding transcript |
Het |
Ankrd2 |
G |
A |
19: 42,028,533 (GRCm39) |
R63H |
probably damaging |
Het |
Bbs2 |
C |
A |
8: 94,801,041 (GRCm39) |
|
probably benign |
Het |
Btbd7 |
G |
T |
12: 102,779,065 (GRCm39) |
D400E |
probably benign |
Het |
Col17a1 |
C |
T |
19: 47,636,537 (GRCm39) |
|
probably null |
Het |
Col3a1 |
A |
G |
1: 45,368,085 (GRCm39) |
|
probably null |
Het |
Crb1 |
CG |
C |
1: 139,164,824 (GRCm39) |
|
probably null |
Het |
Dpp8 |
C |
G |
9: 64,962,118 (GRCm39) |
S386C |
probably benign |
Het |
Dscaml1 |
A |
C |
9: 45,654,297 (GRCm39) |
D1443A |
probably damaging |
Het |
Dsp |
T |
C |
13: 38,372,421 (GRCm39) |
|
probably benign |
Het |
Elf2 |
C |
T |
3: 51,165,038 (GRCm39) |
R262Q |
probably benign |
Het |
Fat3 |
G |
A |
9: 15,907,896 (GRCm39) |
S2702F |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Gabrb1 |
T |
A |
5: 72,279,497 (GRCm39) |
S347R |
probably benign |
Het |
Hivep1 |
T |
C |
13: 42,309,604 (GRCm39) |
S615P |
probably benign |
Het |
Kcnq3 |
T |
C |
15: 65,897,027 (GRCm39) |
D291G |
possibly damaging |
Het |
Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
Mirt1 |
A |
G |
19: 53,433,710 (GRCm39) |
|
noncoding transcript |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mug1 |
T |
A |
6: 121,857,530 (GRCm39) |
S1085T |
possibly damaging |
Het |
Myo18a |
A |
T |
11: 77,709,596 (GRCm39) |
T190S |
probably benign |
Het |
Myo5a |
G |
A |
9: 75,054,191 (GRCm39) |
|
probably null |
Het |
Or1ak2 |
T |
A |
2: 36,827,635 (GRCm39) |
F168Y |
probably damaging |
Het |
Or1l8 |
A |
T |
2: 36,817,820 (GRCm39) |
M102K |
probably damaging |
Het |
Or1m1 |
A |
T |
9: 18,666,750 (GRCm39) |
Y60* |
probably null |
Het |
Or5an1 |
G |
T |
19: 12,260,876 (GRCm39) |
V155L |
probably benign |
Het |
Or9g3 |
A |
G |
2: 85,589,785 (GRCm39) |
*312Q |
probably null |
Het |
Relch |
T |
A |
1: 105,654,106 (GRCm39) |
V825E |
probably damaging |
Het |
Rgma |
G |
A |
7: 73,067,263 (GRCm39) |
V173M |
probably damaging |
Het |
Rgsl1 |
G |
A |
1: 153,701,422 (GRCm39) |
S379F |
possibly damaging |
Het |
Sec16a |
T |
A |
2: 26,305,759 (GRCm39) |
D2215V |
probably damaging |
Het |
Speer4c1 |
A |
C |
5: 15,919,214 (GRCm39) |
|
probably benign |
Het |
Thrap3 |
G |
A |
4: 126,059,335 (GRCm39) |
|
probably null |
Het |
Ttyh2 |
T |
A |
11: 114,599,680 (GRCm39) |
L370Q |
probably damaging |
Het |
Ugt8a |
T |
C |
3: 125,669,139 (GRCm39) |
R322G |
possibly damaging |
Het |
Vmn2r97 |
T |
C |
17: 19,167,900 (GRCm39) |
M718T |
possibly damaging |
Het |
Zhx2 |
T |
C |
15: 57,686,229 (GRCm39) |
F533L |
possibly damaging |
Het |
|
Other mutations in Cilp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01291:Cilp
|
APN |
9 |
65,186,265 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01340:Cilp
|
APN |
9 |
65,183,256 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02330:Cilp
|
APN |
9 |
65,181,804 (GRCm39) |
splice site |
probably benign |
|
IGL02729:Cilp
|
APN |
9 |
65,185,372 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02833:Cilp
|
APN |
9 |
65,185,206 (GRCm39) |
missense |
probably benign |
|
IGL02961:Cilp
|
APN |
9 |
65,185,891 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03137:Cilp
|
APN |
9 |
65,185,450 (GRCm39) |
missense |
probably benign |
|
IGL03211:Cilp
|
APN |
9 |
65,187,457 (GRCm39) |
missense |
probably benign |
|
IGL03301:Cilp
|
APN |
9 |
65,187,499 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03341:Cilp
|
APN |
9 |
65,185,284 (GRCm39) |
missense |
probably benign |
0.07 |
ANU05:Cilp
|
UTSW |
9 |
65,186,265 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02984:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL02988:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL02991:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL03014:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL03054:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL03055:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL03097:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL03098:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL03134:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL03138:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
IGL03147:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
R0096:Cilp
|
UTSW |
9 |
65,180,952 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0219:Cilp
|
UTSW |
9 |
65,176,872 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0347:Cilp
|
UTSW |
9 |
65,187,435 (GRCm39) |
missense |
probably benign |
|
R0699:Cilp
|
UTSW |
9 |
65,177,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Cilp
|
UTSW |
9 |
65,187,598 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1148:Cilp
|
UTSW |
9 |
65,187,598 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1155:Cilp
|
UTSW |
9 |
65,176,869 (GRCm39) |
missense |
probably benign |
0.01 |
R1544:Cilp
|
UTSW |
9 |
65,183,127 (GRCm39) |
missense |
probably benign |
0.03 |
R1584:Cilp
|
UTSW |
9 |
65,186,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R1586:Cilp
|
UTSW |
9 |
65,186,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2055:Cilp
|
UTSW |
9 |
65,186,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R2069:Cilp
|
UTSW |
9 |
65,185,372 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2070:Cilp
|
UTSW |
9 |
65,186,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R2414:Cilp
|
UTSW |
9 |
65,181,927 (GRCm39) |
splice site |
probably benign |
|
R4284:Cilp
|
UTSW |
9 |
65,185,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4630:Cilp
|
UTSW |
9 |
65,187,162 (GRCm39) |
missense |
probably benign |
0.17 |
R4632:Cilp
|
UTSW |
9 |
65,187,162 (GRCm39) |
missense |
probably benign |
0.17 |
R4870:Cilp
|
UTSW |
9 |
65,186,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Cilp
|
UTSW |
9 |
65,185,302 (GRCm39) |
missense |
probably benign |
0.17 |
R5568:Cilp
|
UTSW |
9 |
65,187,515 (GRCm39) |
missense |
probably benign |
0.04 |
R5621:Cilp
|
UTSW |
9 |
65,186,073 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5889:Cilp
|
UTSW |
9 |
65,187,625 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6645:Cilp
|
UTSW |
9 |
65,186,587 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6878:Cilp
|
UTSW |
9 |
65,187,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R6982:Cilp
|
UTSW |
9 |
65,187,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R7330:Cilp
|
UTSW |
9 |
65,187,527 (GRCm39) |
missense |
probably benign |
|
R7967:Cilp
|
UTSW |
9 |
65,185,494 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8305:Cilp
|
UTSW |
9 |
65,186,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R8306:Cilp
|
UTSW |
9 |
65,186,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R8307:Cilp
|
UTSW |
9 |
65,186,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R8308:Cilp
|
UTSW |
9 |
65,186,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R8386:Cilp
|
UTSW |
9 |
65,186,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R8407:Cilp
|
UTSW |
9 |
65,181,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R8542:Cilp
|
UTSW |
9 |
65,185,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:Cilp
|
UTSW |
9 |
65,186,535 (GRCm39) |
missense |
probably benign |
0.26 |
R8951:Cilp
|
UTSW |
9 |
65,180,220 (GRCm39) |
missense |
probably benign |
0.01 |
R9060:Cilp
|
UTSW |
9 |
65,186,302 (GRCm39) |
missense |
probably benign |
0.01 |
R9257:Cilp
|
UTSW |
9 |
65,174,451 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9265:Cilp
|
UTSW |
9 |
65,187,333 (GRCm39) |
missense |
probably benign |
|
R9358:Cilp
|
UTSW |
9 |
65,183,269 (GRCm39) |
missense |
probably benign |
|
R9401:Cilp
|
UTSW |
9 |
65,185,381 (GRCm39) |
missense |
probably damaging |
0.98 |
X0024:Cilp
|
UTSW |
9 |
65,186,925 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Cilp
|
UTSW |
9 |
65,186,980 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
Z1176:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
Z1177:Cilp
|
UTSW |
9 |
65,187,412 (GRCm39) |
frame shift |
probably null |
|
|