| Other mutations in this stock |
Total: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110038F14Rik |
G |
A |
15: 76,834,475 (GRCm39) |
V124I |
probably damaging |
Het |
| 4930444P10Rik |
A |
T |
1: 16,148,870 (GRCm39) |
L61* |
probably null |
Het |
| Abca7 |
T |
C |
10: 79,847,131 (GRCm39) |
I1705T |
probably damaging |
Het |
| Ablim1 |
T |
A |
19: 57,049,760 (GRCm39) |
I393F |
probably damaging |
Het |
| Adamts5 |
A |
G |
16: 85,696,722 (GRCm39) |
L145P |
probably damaging |
Het |
| Ano6 |
T |
C |
15: 95,846,310 (GRCm39) |
I537T |
probably damaging |
Het |
| AU018091 |
T |
C |
7: 3,212,153 (GRCm39) |
I190V |
possibly damaging |
Het |
| Camk1 |
T |
A |
6: 113,315,333 (GRCm39) |
D155V |
probably damaging |
Het |
| Cdh6 |
A |
C |
15: 13,064,581 (GRCm39) |
I103S |
probably damaging |
Het |
| Cntnap1 |
A |
G |
11: 101,072,614 (GRCm39) |
D537G |
probably benign |
Het |
| Col6a3 |
T |
C |
1: 90,730,054 (GRCm39) |
K1144E |
probably damaging |
Het |
| Cpeb1 |
T |
A |
7: 81,021,929 (GRCm39) |
E71D |
probably benign |
Het |
| Cps1 |
T |
C |
1: 67,234,325 (GRCm39) |
L904P |
possibly damaging |
Het |
| Cyfip1 |
T |
A |
7: 55,553,958 (GRCm39) |
F700I |
probably damaging |
Het |
| Dmp1 |
G |
A |
5: 104,354,965 (GRCm39) |
M1I |
probably null |
Het |
| Efcab6 |
A |
T |
15: 83,938,713 (GRCm39) |
M1K |
probably null |
Het |
| Extl2 |
A |
T |
3: 115,821,131 (GRCm39) |
H312L |
possibly damaging |
Het |
| Fat4 |
C |
A |
3: 38,944,728 (GRCm39) |
A1207D |
possibly damaging |
Het |
| Flnb |
T |
C |
14: 7,926,518 (GRCm38) |
|
probably benign |
Het |
| Hdac10 |
G |
T |
15: 89,008,071 (GRCm39) |
A593E |
possibly damaging |
Het |
| Hdhd2 |
T |
C |
18: 77,052,969 (GRCm39) |
|
probably null |
Het |
| Kcnq2 |
A |
G |
2: 180,751,582 (GRCm39) |
|
probably benign |
Het |
| Kdm7a |
A |
G |
6: 39,142,064 (GRCm39) |
F405L |
probably damaging |
Het |
| Lypd6b |
C |
A |
2: 49,833,642 (GRCm39) |
|
probably benign |
Het |
| Mki67 |
A |
T |
7: 135,296,651 (GRCm39) |
D2794E |
possibly damaging |
Het |
| Mtmr14 |
T |
A |
6: 113,243,287 (GRCm39) |
F40I |
probably damaging |
Het |
| Or2y3 |
G |
T |
17: 38,393,544 (GRCm39) |
S108R |
possibly damaging |
Het |
| Or5p55 |
A |
T |
7: 107,566,741 (GRCm39) |
I46F |
probably damaging |
Het |
| Or6d13 |
T |
A |
6: 116,517,968 (GRCm39) |
C185S |
probably damaging |
Het |
| Or6x1 |
A |
T |
9: 40,099,052 (GRCm39) |
I214F |
probably benign |
Het |
| Ppargc1a |
C |
A |
5: 51,631,664 (GRCm39) |
V322L |
probably benign |
Het |
| Ppfibp1 |
T |
A |
6: 146,931,195 (GRCm39) |
M917K |
probably benign |
Het |
| Prkg2 |
C |
T |
5: 99,117,795 (GRCm39) |
|
probably null |
Het |
| Rfx4 |
A |
G |
10: 84,704,246 (GRCm39) |
E296G |
possibly damaging |
Het |
| Rfx8 |
T |
A |
1: 39,722,110 (GRCm39) |
K292* |
probably null |
Het |
| Scamp3 |
C |
A |
3: 89,084,973 (GRCm39) |
|
probably benign |
Het |
| Scn4a |
A |
T |
11: 106,221,190 (GRCm39) |
I823N |
possibly damaging |
Het |
| Sdk2 |
A |
G |
11: 113,721,668 (GRCm39) |
V1316A |
probably damaging |
Het |
| Setd2 |
T |
C |
9: 110,402,741 (GRCm39) |
V1794A |
probably damaging |
Het |
| Stard8 |
G |
T |
X: 98,116,694 (GRCm39) |
R983L |
probably damaging |
Het |
| Tbc1d23 |
A |
T |
16: 57,013,038 (GRCm39) |
D311E |
probably benign |
Het |
| Tex21 |
T |
C |
12: 76,245,592 (GRCm39) |
H568R |
probably benign |
Het |
| Tex35 |
T |
C |
1: 156,932,667 (GRCm39) |
|
probably benign |
Het |
| Tgs1 |
T |
A |
4: 3,591,292 (GRCm39) |
F442I |
possibly damaging |
Het |
| Traf2 |
C |
A |
2: 25,414,931 (GRCm39) |
C303F |
probably benign |
Het |
| Trim56 |
A |
T |
5: 137,143,354 (GRCm39) |
V54D |
possibly damaging |
Het |
| Yars2 |
C |
T |
16: 16,124,406 (GRCm39) |
R338* |
probably null |
Het |
|
| Other mutations in Zfp668 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00944:Zfp668
|
APN |
7 |
127,467,079 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01909:Zfp668
|
APN |
7 |
127,465,994 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02404:Zfp668
|
APN |
7 |
127,465,532 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02543:Zfp668
|
APN |
7 |
127,467,494 (GRCm39) |
nonsense |
probably null |
|
|
IGL02946:Zfp668
|
APN |
7 |
127,465,690 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R0078:Zfp668
|
UTSW |
7 |
127,467,210 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1521:Zfp668
|
UTSW |
7 |
127,466,252 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1775:Zfp668
|
UTSW |
7 |
127,465,778 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R1873:Zfp668
|
UTSW |
7 |
127,465,654 (GRCm39) |
splice site |
probably null |
|
|
R1875:Zfp668
|
UTSW |
7 |
127,465,654 (GRCm39) |
splice site |
probably null |
|
|
R2066:Zfp668
|
UTSW |
7 |
127,466,203 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2068:Zfp668
|
UTSW |
7 |
127,465,837 (GRCm39) |
missense |
probably benign |
0.06 |
|
R2278:Zfp668
|
UTSW |
7 |
127,465,998 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5516:Zfp668
|
UTSW |
7 |
127,466,318 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5569:Zfp668
|
UTSW |
7 |
127,466,995 (GRCm39) |
nonsense |
probably null |
|
|
R5875:Zfp668
|
UTSW |
7 |
127,465,474 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R6663:Zfp668
|
UTSW |
7 |
127,466,941 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8543:Zfp668
|
UTSW |
7 |
127,466,392 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8822:Zfp668
|
UTSW |
7 |
127,466,315 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8905:Zfp668
|
UTSW |
7 |
127,465,598 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9191:Zfp668
|
UTSW |
7 |
127,465,658 (GRCm39) |
missense |
probably benign |
|
|
R9217:Zfp668
|
UTSW |
7 |
127,465,804 (GRCm39) |
nonsense |
probably null |
|
|
R9655:Zfp668
|
UTSW |
7 |
127,466,113 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
Incidental Mutation