Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl4 |
C |
T |
4: 111,514,620 (GRCm39) |
|
probably benign |
Het |
Cit |
T |
C |
5: 116,011,904 (GRCm39) |
|
probably benign |
Het |
Clmp |
A |
G |
9: 40,685,737 (GRCm39) |
N211S |
probably damaging |
Het |
Cnot2 |
A |
G |
10: 116,330,722 (GRCm39) |
|
probably benign |
Het |
Cntn6 |
A |
G |
6: 104,753,418 (GRCm39) |
|
probably benign |
Het |
Dnajb9 |
C |
T |
12: 44,255,096 (GRCm39) |
|
probably benign |
Het |
Ece2 |
T |
A |
16: 20,451,847 (GRCm39) |
N411K |
possibly damaging |
Het |
Fshr |
A |
G |
17: 89,354,127 (GRCm39) |
I77T |
possibly damaging |
Het |
Fshr |
A |
G |
17: 89,293,121 (GRCm39) |
M519T |
probably damaging |
Het |
Gm10654 |
G |
A |
8: 71,384,775 (GRCm39) |
|
noncoding transcript |
Het |
Gm5093 |
A |
G |
17: 46,750,517 (GRCm39) |
I170T |
probably benign |
Het |
Meis3 |
A |
G |
7: 15,917,744 (GRCm39) |
K299R |
probably damaging |
Het |
Nxf1 |
T |
C |
19: 8,741,061 (GRCm39) |
F15L |
probably damaging |
Het |
Nxpe3 |
T |
C |
16: 55,670,076 (GRCm39) |
D343G |
probably benign |
Het |
Or4a73 |
A |
T |
2: 89,420,656 (GRCm39) |
Y268N |
probably benign |
Het |
Polr3k |
A |
G |
2: 181,507,820 (GRCm39) |
T65A |
probably damaging |
Het |
Preb |
A |
T |
5: 31,115,665 (GRCm39) |
W222R |
probably damaging |
Het |
Psmd11 |
T |
C |
11: 80,360,671 (GRCm39) |
I56T |
probably damaging |
Het |
Rtkn2 |
A |
G |
10: 67,853,667 (GRCm39) |
T232A |
probably damaging |
Het |
Scaf11 |
T |
C |
15: 96,318,064 (GRCm39) |
|
probably null |
Het |
Slc4a10 |
A |
T |
2: 62,097,780 (GRCm39) |
K493M |
probably damaging |
Het |
Stard10 |
A |
G |
7: 100,991,777 (GRCm39) |
K112E |
probably damaging |
Het |
Sugp1 |
A |
T |
8: 70,522,217 (GRCm39) |
|
probably benign |
Het |
Tasor |
A |
G |
14: 27,163,918 (GRCm39) |
I235V |
possibly damaging |
Het |
Tmem156 |
T |
C |
5: 65,233,040 (GRCm39) |
E139G |
probably damaging |
Het |
Tubd1 |
C |
T |
11: 86,439,834 (GRCm39) |
|
probably benign |
Het |
Uap1 |
G |
A |
1: 169,986,460 (GRCm39) |
T174M |
probably damaging |
Het |
Vmn2r13 |
T |
C |
5: 109,304,398 (GRCm39) |
T678A |
probably damaging |
Het |
Vmn2r84 |
A |
T |
10: 130,222,556 (GRCm39) |
C555S |
probably damaging |
Het |
Vps13d |
T |
C |
4: 144,894,889 (GRCm39) |
|
probably null |
Het |
Vps8 |
T |
C |
16: 21,254,573 (GRCm39) |
|
probably null |
Het |
Wee1 |
A |
G |
7: 109,738,899 (GRCm39) |
N590S |
probably damaging |
Het |
Zfp112 |
C |
A |
7: 23,825,103 (GRCm39) |
S357Y |
probably damaging |
Het |
Zscan4d |
A |
G |
7: 10,896,692 (GRCm39) |
V226A |
probably benign |
Het |
|
Other mutations in Zfp423 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Zfp423
|
APN |
8 |
88,508,239 (GRCm39) |
splice site |
probably null |
|
IGL01359:Zfp423
|
APN |
8 |
88,507,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01780:Zfp423
|
APN |
8 |
88,508,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02250:Zfp423
|
APN |
8 |
88,509,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02301:Zfp423
|
APN |
8 |
88,508,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02320:Zfp423
|
APN |
8 |
88,508,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02804:Zfp423
|
APN |
8 |
88,509,285 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03090:Zfp423
|
APN |
8 |
88,508,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03198:Zfp423
|
APN |
8 |
88,508,304 (GRCm39) |
missense |
possibly damaging |
0.73 |
swell
|
UTSW |
8 |
88,413,187 (GRCm39) |
splice site |
probably null |
|
Temptation
|
UTSW |
8 |
88,508,381 (GRCm39) |
missense |
probably benign |
0.25 |
trials
|
UTSW |
8 |
88,507,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Zfp423
|
UTSW |
8 |
88,508,887 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0142:Zfp423
|
UTSW |
8 |
88,506,968 (GRCm39) |
nonsense |
probably null |
|
R0256:Zfp423
|
UTSW |
8 |
88,500,262 (GRCm39) |
nonsense |
probably null |
|
R0538:Zfp423
|
UTSW |
8 |
88,508,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R0542:Zfp423
|
UTSW |
8 |
88,507,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Zfp423
|
UTSW |
8 |
88,508,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R1179:Zfp423
|
UTSW |
8 |
88,414,700 (GRCm39) |
missense |
probably damaging |
0.97 |
R1417:Zfp423
|
UTSW |
8 |
88,500,284 (GRCm39) |
splice site |
probably null |
|
R1429:Zfp423
|
UTSW |
8 |
88,413,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R1570:Zfp423
|
UTSW |
8 |
88,509,186 (GRCm39) |
missense |
probably benign |
0.37 |
R2013:Zfp423
|
UTSW |
8 |
88,509,025 (GRCm39) |
missense |
probably benign |
0.43 |
R2043:Zfp423
|
UTSW |
8 |
88,509,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Zfp423
|
UTSW |
8 |
88,507,986 (GRCm39) |
missense |
probably benign |
0.04 |
R2108:Zfp423
|
UTSW |
8 |
88,507,806 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2358:Zfp423
|
UTSW |
8 |
88,507,179 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3177:Zfp423
|
UTSW |
8 |
88,508,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R3277:Zfp423
|
UTSW |
8 |
88,508,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R3738:Zfp423
|
UTSW |
8 |
88,507,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R3739:Zfp423
|
UTSW |
8 |
88,507,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Zfp423
|
UTSW |
8 |
88,507,140 (GRCm39) |
missense |
probably benign |
0.03 |
R4034:Zfp423
|
UTSW |
8 |
88,507,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R4425:Zfp423
|
UTSW |
8 |
88,509,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Zfp423
|
UTSW |
8 |
88,414,709 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4700:Zfp423
|
UTSW |
8 |
88,508,338 (GRCm39) |
splice site |
probably null |
|
R4753:Zfp423
|
UTSW |
8 |
88,508,074 (GRCm39) |
missense |
probably benign |
0.00 |
R4818:Zfp423
|
UTSW |
8 |
88,631,128 (GRCm39) |
missense |
probably benign |
0.00 |
R5026:Zfp423
|
UTSW |
8 |
88,507,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R5190:Zfp423
|
UTSW |
8 |
88,509,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R5243:Zfp423
|
UTSW |
8 |
88,500,275 (GRCm39) |
missense |
probably benign |
0.03 |
R5284:Zfp423
|
UTSW |
8 |
88,508,305 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5586:Zfp423
|
UTSW |
8 |
88,585,968 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5601:Zfp423
|
UTSW |
8 |
88,508,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Zfp423
|
UTSW |
8 |
88,508,955 (GRCm39) |
missense |
probably damaging |
0.99 |
R5717:Zfp423
|
UTSW |
8 |
88,413,187 (GRCm39) |
splice site |
probably null |
|
R5801:Zfp423
|
UTSW |
8 |
88,585,990 (GRCm39) |
missense |
probably damaging |
0.99 |
R5917:Zfp423
|
UTSW |
8 |
88,508,860 (GRCm39) |
nonsense |
probably null |
|
R5985:Zfp423
|
UTSW |
8 |
88,508,774 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6111:Zfp423
|
UTSW |
8 |
88,509,315 (GRCm39) |
missense |
probably damaging |
0.99 |
R6306:Zfp423
|
UTSW |
8 |
88,508,662 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6770:Zfp423
|
UTSW |
8 |
88,508,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R6970:Zfp423
|
UTSW |
8 |
88,530,407 (GRCm39) |
missense |
probably benign |
0.00 |
R7029:Zfp423
|
UTSW |
8 |
88,414,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R7060:Zfp423
|
UTSW |
8 |
88,509,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R7074:Zfp423
|
UTSW |
8 |
88,509,060 (GRCm39) |
missense |
probably benign |
0.00 |
R7121:Zfp423
|
UTSW |
8 |
88,507,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7242:Zfp423
|
UTSW |
8 |
88,631,155 (GRCm39) |
missense |
probably benign |
0.07 |
R7359:Zfp423
|
UTSW |
8 |
88,508,871 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7426:Zfp423
|
UTSW |
8 |
88,507,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R7540:Zfp423
|
UTSW |
8 |
88,414,695 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7640:Zfp423
|
UTSW |
8 |
88,507,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7767:Zfp423
|
UTSW |
8 |
88,507,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R7938:Zfp423
|
UTSW |
8 |
88,622,304 (GRCm39) |
missense |
unknown |
|
R7986:Zfp423
|
UTSW |
8 |
88,506,978 (GRCm39) |
missense |
probably benign |
0.04 |
R8347:Zfp423
|
UTSW |
8 |
88,509,784 (GRCm39) |
missense |
probably damaging |
0.99 |
R8356:Zfp423
|
UTSW |
8 |
88,509,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8676:Zfp423
|
UTSW |
8 |
88,509,338 (GRCm39) |
missense |
probably benign |
0.04 |
R8710:Zfp423
|
UTSW |
8 |
88,507,549 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8794:Zfp423
|
UTSW |
8 |
88,507,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R8832:Zfp423
|
UTSW |
8 |
88,507,827 (GRCm39) |
missense |
probably damaging |
0.98 |
R9018:Zfp423
|
UTSW |
8 |
88,508,381 (GRCm39) |
missense |
probably benign |
0.25 |
R9182:Zfp423
|
UTSW |
8 |
88,508,742 (GRCm39) |
missense |
probably damaging |
0.99 |
R9309:Zfp423
|
UTSW |
8 |
88,509,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R9312:Zfp423
|
UTSW |
8 |
88,508,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9453:Zfp423
|
UTSW |
8 |
88,508,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9469:Zfp423
|
UTSW |
8 |
88,509,519 (GRCm39) |
missense |
probably damaging |
0.99 |
R9480:Zfp423
|
UTSW |
8 |
88,631,115 (GRCm39) |
critical splice donor site |
probably null |
|
R9483:Zfp423
|
UTSW |
8 |
88,507,725 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9510:Zfp423
|
UTSW |
8 |
88,510,041 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9521:Zfp423
|
UTSW |
8 |
88,509,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R9606:Zfp423
|
UTSW |
8 |
88,414,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R9789:Zfp423
|
UTSW |
8 |
88,506,877 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Zfp423
|
UTSW |
8 |
88,586,048 (GRCm39) |
missense |
possibly damaging |
0.49 |
Z1177:Zfp423
|
UTSW |
8 |
88,507,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|