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 |
Yars2 |
C |
T |
16: 16,124,406 (GRCm39) |
R338* |
probably null |
Het |
Zfp668 |
A |
T |
7: 127,465,454 (GRCm39) |
C577S |
probably damaging |
Het |
|
Other mutations in Trim56 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02604:Trim56
|
APN |
5 |
137,141,930 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02653:Trim56
|
APN |
5 |
137,141,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Trim56
|
APN |
5 |
137,142,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R0711:Trim56
|
UTSW |
5 |
137,141,846 (GRCm39) |
missense |
probably benign |
0.00 |
R1167:Trim56
|
UTSW |
5 |
137,141,374 (GRCm39) |
missense |
probably damaging |
0.98 |
R1470:Trim56
|
UTSW |
5 |
137,142,017 (GRCm39) |
missense |
probably damaging |
0.99 |
R1470:Trim56
|
UTSW |
5 |
137,142,017 (GRCm39) |
missense |
probably damaging |
0.99 |
R1508:Trim56
|
UTSW |
5 |
137,142,791 (GRCm39) |
missense |
probably benign |
0.00 |
R1791:Trim56
|
UTSW |
5 |
137,143,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Trim56
|
UTSW |
5 |
137,141,528 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4274:Trim56
|
UTSW |
5 |
137,142,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Trim56
|
UTSW |
5 |
137,142,918 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4766:Trim56
|
UTSW |
5 |
137,141,579 (GRCm39) |
missense |
probably benign |
0.07 |
R4932:Trim56
|
UTSW |
5 |
137,143,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R5117:Trim56
|
UTSW |
5 |
137,142,832 (GRCm39) |
missense |
probably benign |
0.13 |
R6444:Trim56
|
UTSW |
5 |
137,141,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R6747:Trim56
|
UTSW |
5 |
137,143,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6962:Trim56
|
UTSW |
5 |
137,141,501 (GRCm39) |
missense |
probably damaging |
0.97 |
R7115:Trim56
|
UTSW |
5 |
137,142,514 (GRCm39) |
missense |
probably damaging |
0.98 |
R7266:Trim56
|
UTSW |
5 |
137,143,097 (GRCm39) |
missense |
probably damaging |
0.98 |
R7706:Trim56
|
UTSW |
5 |
137,143,510 (GRCm39) |
missense |
probably benign |
0.00 |
R8347:Trim56
|
UTSW |
5 |
137,141,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Trim56
|
UTSW |
5 |
137,141,783 (GRCm39) |
missense |
probably benign |
|
R8695:Trim56
|
UTSW |
5 |
137,143,429 (GRCm39) |
missense |
probably benign |
0.15 |
R9152:Trim56
|
UTSW |
5 |
137,143,387 (GRCm39) |
missense |
probably benign |
0.06 |
R9166:Trim56
|
UTSW |
5 |
137,142,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Trim56
|
UTSW |
5 |
137,141,632 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Trim56
|
UTSW |
5 |
137,143,064 (GRCm39) |
missense |
probably damaging |
1.00 |
|