Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arih2 |
T |
C |
9: 108,485,878 (GRCm39) |
N345D |
probably damaging |
Het |
Ascc3 |
C |
T |
10: 50,514,095 (GRCm39) |
S298L |
possibly damaging |
Het |
Cacna1e |
A |
G |
1: 154,317,997 (GRCm39) |
Y1462H |
probably damaging |
Het |
Car9 |
T |
C |
4: 43,509,212 (GRCm39) |
|
probably null |
Het |
Cenpc1 |
A |
T |
5: 86,185,230 (GRCm39) |
M427K |
probably benign |
Het |
Chl1 |
T |
A |
6: 103,624,262 (GRCm39) |
C57S |
probably damaging |
Het |
Cntn3 |
T |
C |
6: 102,397,342 (GRCm39) |
Y77C |
probably damaging |
Het |
Cobll1 |
T |
C |
2: 64,919,865 (GRCm39) |
K1187E |
possibly damaging |
Het |
Fkbpl |
C |
T |
17: 34,865,026 (GRCm39) |
H265Y |
possibly damaging |
Het |
Fmo1 |
T |
G |
1: 162,687,031 (GRCm39) |
E32A |
probably damaging |
Het |
Fnip2 |
G |
A |
3: 79,388,496 (GRCm39) |
T715I |
probably damaging |
Het |
Fzd6 |
T |
A |
15: 38,889,128 (GRCm39) |
I82K |
possibly damaging |
Het |
Grm5 |
T |
C |
7: 87,252,163 (GRCm39) |
S138P |
probably damaging |
Het |
Klra5 |
T |
C |
6: 129,880,553 (GRCm39) |
Y115C |
probably damaging |
Het |
Lgr4 |
T |
C |
2: 109,821,438 (GRCm39) |
|
probably benign |
Het |
Limd1 |
T |
G |
9: 123,345,892 (GRCm39) |
I557S |
probably benign |
Het |
Mpv17l |
A |
T |
16: 13,758,863 (GRCm39) |
I96L |
probably benign |
Het |
Neb |
A |
T |
2: 52,133,343 (GRCm39) |
D3398E |
probably benign |
Het |
Nup155 |
T |
C |
15: 8,176,736 (GRCm39) |
S1005P |
probably benign |
Het |
Or2v2 |
A |
T |
11: 49,004,519 (GRCm39) |
D11E |
possibly damaging |
Het |
Or52a5b |
T |
C |
7: 103,417,388 (GRCm39) |
D72G |
probably damaging |
Het |
Pebp4 |
G |
T |
14: 70,297,103 (GRCm39) |
S214I |
possibly damaging |
Het |
Pex26 |
T |
C |
6: 121,161,443 (GRCm39) |
|
probably null |
Het |
Rbbp8 |
A |
T |
18: 11,848,875 (GRCm39) |
Q230L |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Robo2 |
G |
A |
16: 73,753,525 (GRCm39) |
T784M |
probably damaging |
Het |
Slc5a1 |
T |
C |
5: 33,303,995 (GRCm39) |
I270T |
probably benign |
Het |
Spag4 |
C |
T |
2: 155,909,229 (GRCm39) |
|
probably benign |
Het |
Stt3a |
T |
C |
9: 36,660,841 (GRCm39) |
|
probably benign |
Het |
Svep1 |
C |
T |
4: 58,096,331 (GRCm39) |
E1430K |
possibly damaging |
Het |
Timd5 |
G |
A |
11: 46,419,364 (GRCm39) |
C60Y |
probably damaging |
Het |
Uba6 |
A |
T |
5: 86,265,946 (GRCm39) |
V956E |
probably damaging |
Het |
Ube2j1 |
T |
A |
4: 33,043,991 (GRCm39) |
|
probably benign |
Het |
Ubr5 |
A |
G |
15: 37,997,431 (GRCm39) |
S1741P |
probably damaging |
Het |
Vmn2r1 |
A |
G |
3: 63,993,980 (GRCm39) |
T109A |
probably damaging |
Het |
Vmn2r60 |
T |
C |
7: 41,784,985 (GRCm39) |
|
probably benign |
Het |
Vstm2a |
A |
G |
11: 16,318,388 (GRCm39) |
|
probably benign |
Het |
Zdhhc20 |
T |
A |
14: 58,094,076 (GRCm39) |
K195N |
probably damaging |
Het |
Zzz3 |
T |
C |
3: 152,133,085 (GRCm39) |
S48P |
probably benign |
Het |
|
Other mutations in Zfp683 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02868:Zfp683
|
APN |
4 |
133,783,177 (GRCm39) |
missense |
probably benign |
0.00 |
FR4976:Zfp683
|
UTSW |
4 |
133,786,190 (GRCm39) |
unclassified |
probably benign |
|
R0924:Zfp683
|
UTSW |
4 |
133,783,138 (GRCm39) |
missense |
probably benign |
0.00 |
R1679:Zfp683
|
UTSW |
4 |
133,785,956 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1984:Zfp683
|
UTSW |
4 |
133,784,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Zfp683
|
UTSW |
4 |
133,783,106 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2288:Zfp683
|
UTSW |
4 |
133,783,381 (GRCm39) |
unclassified |
probably benign |
|
R3736:Zfp683
|
UTSW |
4 |
133,784,742 (GRCm39) |
missense |
probably benign |
0.28 |
R5412:Zfp683
|
UTSW |
4 |
133,781,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R6058:Zfp683
|
UTSW |
4 |
133,786,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R6072:Zfp683
|
UTSW |
4 |
133,783,057 (GRCm39) |
missense |
probably benign |
0.00 |
R7174:Zfp683
|
UTSW |
4 |
133,783,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R7419:Zfp683
|
UTSW |
4 |
133,786,211 (GRCm39) |
missense |
probably benign |
0.02 |
R8867:Zfp683
|
UTSW |
4 |
133,785,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R8978:Zfp683
|
UTSW |
4 |
133,781,239 (GRCm39) |
missense |
probably benign |
0.43 |
R9618:Zfp683
|
UTSW |
4 |
133,782,965 (GRCm39) |
missense |
probably benign |
0.00 |
RF004:Zfp683
|
UTSW |
4 |
133,786,185 (GRCm39) |
unclassified |
probably benign |
|
RF044:Zfp683
|
UTSW |
4 |
133,786,185 (GRCm39) |
unclassified |
probably benign |
|
Z1177:Zfp683
|
UTSW |
4 |
133,783,382 (GRCm39) |
missense |
possibly damaging |
0.51 |
|