Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4galt |
T |
C |
15: 83,112,468 (GRCm39) |
E105G |
probably damaging |
Het |
Apc |
A |
G |
18: 34,445,429 (GRCm39) |
D757G |
probably damaging |
Het |
Arpc3 |
A |
T |
5: 122,539,781 (GRCm39) |
I45F |
probably damaging |
Het |
C3 |
C |
A |
17: 57,529,249 (GRCm39) |
V597L |
probably damaging |
Het |
Ccdc181 |
A |
G |
1: 164,108,213 (GRCm39) |
N299D |
probably benign |
Het |
Cdr1 |
T |
A |
X: 60,229,154 (GRCm39) |
Q4L |
unknown |
Het |
Cep170 |
G |
A |
1: 176,564,454 (GRCm39) |
S1464F |
probably damaging |
Het |
Cfh |
A |
G |
1: 140,030,557 (GRCm39) |
Y826H |
probably damaging |
Het |
Chic2 |
A |
G |
5: 75,171,954 (GRCm39) |
|
probably benign |
Het |
Chrne |
T |
C |
11: 70,509,338 (GRCm39) |
H81R |
probably benign |
Het |
Clec4e |
A |
G |
6: 123,260,599 (GRCm39) |
I153T |
probably benign |
Het |
Col14a1 |
A |
T |
15: 55,272,300 (GRCm39) |
D699V |
unknown |
Het |
Cul3 |
T |
G |
1: 80,259,144 (GRCm39) |
S379R |
probably damaging |
Het |
Cyp3a11 |
T |
A |
5: 145,797,189 (GRCm39) |
I397F |
possibly damaging |
Het |
Dnah1 |
T |
C |
14: 31,022,906 (GRCm39) |
K1077R |
probably benign |
Het |
Dnajc18 |
A |
G |
18: 35,813,972 (GRCm39) |
S266P |
probably benign |
Het |
Dydc1 |
T |
G |
14: 40,800,647 (GRCm39) |
L74R |
probably damaging |
Het |
Echdc2 |
G |
T |
4: 108,027,067 (GRCm39) |
A71S |
possibly damaging |
Het |
Fer1l4 |
T |
A |
2: 155,886,650 (GRCm39) |
D693V |
probably benign |
Het |
Fscn3 |
T |
C |
6: 28,430,604 (GRCm39) |
V258A |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,869,516 (GRCm39) |
I4255N |
probably damaging |
Het |
Il1rl2 |
A |
G |
1: 40,382,200 (GRCm39) |
I171V |
possibly damaging |
Het |
Ino80d |
G |
T |
1: 63,097,467 (GRCm39) |
T809K |
probably damaging |
Het |
Lama2 |
A |
T |
10: 27,220,566 (GRCm39) |
L433* |
probably null |
Het |
Nlrp9c |
A |
T |
7: 26,084,533 (GRCm39) |
S349T |
probably benign |
Het |
Parp11 |
T |
C |
6: 127,466,981 (GRCm39) |
I124T |
possibly damaging |
Het |
Parp8 |
A |
T |
13: 116,999,605 (GRCm39) |
|
probably benign |
Het |
Pgm1 |
T |
C |
4: 99,827,236 (GRCm39) |
F379L |
probably damaging |
Het |
Phf21b |
T |
C |
15: 84,671,448 (GRCm39) |
H482R |
probably benign |
Het |
Phka1 |
A |
C |
X: 101,584,716 (GRCm39) |
|
probably null |
Het |
Plekhh1 |
T |
C |
12: 79,100,430 (GRCm39) |
W133R |
probably damaging |
Het |
Polr2a |
A |
C |
11: 69,636,516 (GRCm39) |
L405* |
probably null |
Het |
Prrg3 |
T |
A |
X: 71,010,108 (GRCm39) |
V3E |
probably damaging |
Het |
Pth1r |
T |
C |
9: 110,551,648 (GRCm39) |
K484E |
probably damaging |
Het |
Rcbtb1 |
T |
C |
14: 59,460,727 (GRCm39) |
L230P |
probably damaging |
Het |
Slc51a |
G |
A |
16: 32,297,568 (GRCm39) |
R110C |
probably damaging |
Het |
Ssbp2 |
T |
C |
13: 91,672,720 (GRCm39) |
Y27H |
probably damaging |
Het |
Sult2a4 |
A |
G |
7: 13,665,692 (GRCm39) |
V157A |
probably damaging |
Het |
Tbx15 |
G |
A |
3: 99,259,296 (GRCm39) |
S389N |
probably benign |
Het |
Ttn |
T |
G |
2: 76,671,424 (GRCm39) |
|
probably benign |
Het |
Ube2n |
T |
C |
10: 95,378,127 (GRCm39) |
|
probably benign |
Het |
Wdr95 |
G |
A |
5: 149,505,352 (GRCm39) |
|
probably null |
Het |
Wsb2 |
T |
C |
5: 117,514,620 (GRCm39) |
S298P |
possibly damaging |
Het |
Zc3h7a |
T |
C |
16: 10,974,166 (GRCm39) |
|
probably null |
Het |
Zfp747 |
G |
A |
7: 126,973,180 (GRCm39) |
T330I |
probably damaging |
Het |
Zfp949 |
A |
G |
9: 88,450,717 (GRCm39) |
R96G |
probably benign |
Het |
|
Other mutations in Zfat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00542:Zfat
|
APN |
15 |
68,042,071 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00862:Zfat
|
APN |
15 |
68,130,512 (GRCm39) |
splice site |
probably null |
|
IGL01021:Zfat
|
APN |
15 |
68,042,015 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01152:Zfat
|
APN |
15 |
67,982,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01733:Zfat
|
APN |
15 |
68,052,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01873:Zfat
|
APN |
15 |
68,096,744 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01990:Zfat
|
APN |
15 |
68,096,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Zfat
|
APN |
15 |
68,052,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Zfat
|
APN |
15 |
68,052,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02955:Zfat
|
APN |
15 |
68,052,963 (GRCm39) |
missense |
probably damaging |
0.98 |
R0145:Zfat
|
UTSW |
15 |
68,058,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0408:Zfat
|
UTSW |
15 |
68,052,141 (GRCm39) |
missense |
probably benign |
0.10 |
R0633:Zfat
|
UTSW |
15 |
68,052,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Zfat
|
UTSW |
15 |
68,084,432 (GRCm39) |
splice site |
probably benign |
|
R1508:Zfat
|
UTSW |
15 |
68,050,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Zfat
|
UTSW |
15 |
68,084,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R1641:Zfat
|
UTSW |
15 |
68,051,959 (GRCm39) |
missense |
probably benign |
0.19 |
R1889:Zfat
|
UTSW |
15 |
67,973,388 (GRCm39) |
missense |
probably benign |
0.00 |
R1959:Zfat
|
UTSW |
15 |
68,018,392 (GRCm39) |
missense |
probably benign |
0.32 |
R2030:Zfat
|
UTSW |
15 |
67,990,783 (GRCm39) |
critical splice donor site |
probably null |
|
R2202:Zfat
|
UTSW |
15 |
68,051,709 (GRCm39) |
missense |
probably benign |
0.36 |
R2340:Zfat
|
UTSW |
15 |
67,973,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R3440:Zfat
|
UTSW |
15 |
67,956,402 (GRCm39) |
missense |
probably benign |
0.00 |
R3442:Zfat
|
UTSW |
15 |
67,973,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R3442:Zfat
|
UTSW |
15 |
67,956,402 (GRCm39) |
missense |
probably benign |
0.00 |
R4406:Zfat
|
UTSW |
15 |
68,052,040 (GRCm39) |
missense |
probably benign |
0.00 |
R4649:Zfat
|
UTSW |
15 |
68,056,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Zfat
|
UTSW |
15 |
68,052,131 (GRCm39) |
missense |
probably benign |
|
R4712:Zfat
|
UTSW |
15 |
67,982,324 (GRCm39) |
critical splice donor site |
probably null |
|
R4745:Zfat
|
UTSW |
15 |
68,052,223 (GRCm39) |
missense |
probably benign |
0.09 |
R4862:Zfat
|
UTSW |
15 |
68,051,959 (GRCm39) |
missense |
probably benign |
0.02 |
R5015:Zfat
|
UTSW |
15 |
68,050,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Zfat
|
UTSW |
15 |
68,052,079 (GRCm39) |
missense |
probably benign |
|
R5208:Zfat
|
UTSW |
15 |
68,052,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Zfat
|
UTSW |
15 |
68,037,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Zfat
|
UTSW |
15 |
67,982,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Zfat
|
UTSW |
15 |
68,051,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R5642:Zfat
|
UTSW |
15 |
68,052,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R5659:Zfat
|
UTSW |
15 |
67,990,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Zfat
|
UTSW |
15 |
68,051,806 (GRCm39) |
missense |
probably benign |
|
R6046:Zfat
|
UTSW |
15 |
68,052,626 (GRCm39) |
missense |
probably damaging |
0.99 |
R6315:Zfat
|
UTSW |
15 |
67,956,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R6342:Zfat
|
UTSW |
15 |
68,052,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Zfat
|
UTSW |
15 |
68,037,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R6789:Zfat
|
UTSW |
15 |
67,956,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7028:Zfat
|
UTSW |
15 |
68,052,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Zfat
|
UTSW |
15 |
68,052,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Zfat
|
UTSW |
15 |
68,052,211 (GRCm39) |
missense |
probably benign |
|
R7065:Zfat
|
UTSW |
15 |
68,052,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Zfat
|
UTSW |
15 |
68,050,631 (GRCm39) |
missense |
probably benign |
0.12 |
R7208:Zfat
|
UTSW |
15 |
68,051,856 (GRCm39) |
missense |
probably benign |
0.39 |
R7330:Zfat
|
UTSW |
15 |
68,084,600 (GRCm39) |
missense |
probably benign |
0.00 |
R7345:Zfat
|
UTSW |
15 |
67,976,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Zfat
|
UTSW |
15 |
68,052,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7405:Zfat
|
UTSW |
15 |
68,056,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Zfat
|
UTSW |
15 |
68,050,715 (GRCm39) |
nonsense |
probably null |
|
R7672:Zfat
|
UTSW |
15 |
68,130,535 (GRCm39) |
start codon destroyed |
probably null |
0.39 |
R7676:Zfat
|
UTSW |
15 |
68,096,693 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7701:Zfat
|
UTSW |
15 |
68,052,757 (GRCm39) |
nonsense |
probably null |
|
R7825:Zfat
|
UTSW |
15 |
68,051,769 (GRCm39) |
missense |
probably benign |
0.01 |
R8152:Zfat
|
UTSW |
15 |
67,973,355 (GRCm39) |
missense |
probably benign |
0.23 |
R8404:Zfat
|
UTSW |
15 |
67,976,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8405:Zfat
|
UTSW |
15 |
68,018,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8502:Zfat
|
UTSW |
15 |
67,976,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8534:Zfat
|
UTSW |
15 |
68,037,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Zfat
|
UTSW |
15 |
67,956,278 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8887:Zfat
|
UTSW |
15 |
68,056,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Zfat
|
UTSW |
15 |
68,052,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Zfat
|
UTSW |
15 |
67,956,404 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9117:Zfat
|
UTSW |
15 |
68,058,918 (GRCm39) |
missense |
probably damaging |
0.98 |
R9137:Zfat
|
UTSW |
15 |
68,051,794 (GRCm39) |
missense |
probably benign |
0.00 |
R9310:Zfat
|
UTSW |
15 |
67,956,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R9482:Zfat
|
UTSW |
15 |
68,084,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Zfat
|
UTSW |
15 |
68,051,655 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9611:Zfat
|
UTSW |
15 |
68,051,655 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9630:Zfat
|
UTSW |
15 |
67,990,793 (GRCm39) |
missense |
probably benign |
0.37 |
Z1088:Zfat
|
UTSW |
15 |
68,058,950 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Zfat
|
UTSW |
15 |
68,051,677 (GRCm39) |
missense |
probably damaging |
0.99 |
|