Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankhd1 |
T |
C |
18: 36,694,103 (GRCm39) |
S105P |
probably damaging |
Het |
Ano5 |
G |
A |
7: 51,233,562 (GRCm39) |
R658H |
possibly damaging |
Het |
Ap3b2 |
T |
A |
7: 81,126,500 (GRCm39) |
I367F |
probably damaging |
Het |
Apaf1 |
A |
T |
10: 90,898,015 (GRCm39) |
C247* |
probably null |
Het |
Aqp8 |
G |
A |
7: 123,065,889 (GRCm39) |
W228* |
probably null |
Het |
Arhgap32 |
T |
A |
9: 32,093,256 (GRCm39) |
V178D |
probably damaging |
Het |
Atp10b |
T |
A |
11: 43,136,252 (GRCm39) |
W1127R |
probably damaging |
Het |
Bcl6 |
A |
T |
16: 23,787,159 (GRCm39) |
C580* |
probably null |
Het |
Brd1 |
T |
C |
15: 88,597,584 (GRCm39) |
T568A |
probably benign |
Het |
Brsk1 |
C |
T |
7: 4,718,371 (GRCm39) |
P665L |
possibly damaging |
Het |
Cblc |
A |
G |
7: 19,526,857 (GRCm39) |
L125P |
probably damaging |
Het |
Ccdc87 |
T |
C |
19: 4,890,878 (GRCm39) |
S457P |
probably damaging |
Het |
Cxcr5 |
C |
T |
9: 44,424,690 (GRCm39) |
M322I |
probably benign |
Het |
Cyb5r4 |
T |
A |
9: 86,937,881 (GRCm39) |
F300Y |
probably benign |
Het |
Cyp3a25 |
T |
C |
5: 145,928,356 (GRCm39) |
T230A |
possibly damaging |
Het |
Dhx9 |
A |
G |
1: 153,347,481 (GRCm39) |
V409A |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,392,009 (GRCm39) |
D3790G |
probably damaging |
Het |
Gin1 |
A |
G |
1: 97,703,257 (GRCm39) |
T27A |
possibly damaging |
Het |
Gipc1 |
A |
T |
8: 84,390,755 (GRCm39) |
M287L |
probably benign |
Het |
Kat6a |
T |
A |
8: 23,428,176 (GRCm39) |
L1177* |
probably null |
Het |
Klhl20 |
A |
G |
1: 160,918,040 (GRCm39) |
V82A |
probably damaging |
Het |
Kmt2e |
T |
C |
5: 23,702,805 (GRCm39) |
I995T |
probably damaging |
Het |
Lpin1 |
A |
T |
12: 16,590,990 (GRCm39) |
V814E |
probably damaging |
Het |
Luzp1 |
T |
A |
4: 136,269,787 (GRCm39) |
V670D |
probably damaging |
Het |
Lyst |
C |
A |
13: 13,809,212 (GRCm39) |
A294E |
possibly damaging |
Het |
Olr1 |
T |
A |
6: 129,476,992 (GRCm39) |
E91V |
probably damaging |
Het |
Or1j1 |
A |
T |
2: 36,702,966 (GRCm39) |
I46N |
probably damaging |
Het |
Or2k2 |
A |
T |
4: 58,785,672 (GRCm39) |
F17I |
probably damaging |
Het |
Or8b55 |
C |
T |
9: 38,727,072 (GRCm39) |
T91I |
probably benign |
Het |
Pam |
T |
C |
1: 97,770,024 (GRCm39) |
Y476C |
probably damaging |
Het |
Pcdhac1 |
T |
C |
18: 37,225,470 (GRCm39) |
L761P |
probably damaging |
Het |
Phf21b |
C |
T |
15: 84,678,101 (GRCm39) |
W300* |
probably null |
Het |
Pld2 |
T |
C |
11: 70,448,387 (GRCm39) |
*945Q |
probably null |
Het |
Ppp1r37 |
C |
T |
7: 19,269,448 (GRCm39) |
V145M |
probably damaging |
Het |
Rasgrf1 |
T |
A |
9: 89,866,342 (GRCm39) |
N593K |
probably damaging |
Het |
Rhot1 |
T |
G |
11: 80,141,181 (GRCm39) |
|
probably null |
Het |
Rmnd1 |
A |
T |
10: 4,377,382 (GRCm39) |
M99K |
probably benign |
Het |
Ros1 |
G |
A |
10: 52,019,482 (GRCm39) |
T697I |
possibly damaging |
Het |
Scgb1b10 |
G |
T |
7: 31,800,303 (GRCm39) |
A4S |
probably benign |
Het |
Shc3 |
T |
C |
13: 51,670,630 (GRCm39) |
Y39C |
probably damaging |
Het |
Slc25a23 |
A |
G |
17: 57,352,500 (GRCm39) |
|
probably benign |
Het |
Slc5a8 |
C |
T |
10: 88,755,290 (GRCm39) |
L466F |
possibly damaging |
Het |
Sqor |
G |
A |
2: 122,629,523 (GRCm39) |
C127Y |
probably benign |
Het |
Sv2a |
G |
C |
3: 96,097,619 (GRCm39) |
W467S |
possibly damaging |
Het |
Togaram2 |
G |
T |
17: 71,994,667 (GRCm39) |
D39Y |
probably damaging |
Het |
Tspan11 |
T |
A |
6: 127,915,240 (GRCm39) |
|
probably null |
Het |
Usp32 |
A |
G |
11: 84,968,240 (GRCm39) |
V141A |
possibly damaging |
Het |
Zbtb38 |
T |
C |
9: 96,569,473 (GRCm39) |
H537R |
probably damaging |
Het |
Zfp637 |
G |
A |
6: 117,820,291 (GRCm39) |
G3E |
probably damaging |
Het |
Zfp788 |
T |
A |
7: 41,299,540 (GRCm39) |
Y673* |
probably null |
Het |
Zhx2 |
T |
C |
15: 57,685,704 (GRCm39) |
S358P |
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 |
IGL03201:Zfat
|
APN |
15 |
68,037,758 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|