Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9830107B12Rik |
A |
G |
17: 48,452,681 (GRCm39) |
F86S |
probably damaging |
Het |
Aamdc |
A |
T |
7: 97,224,855 (GRCm39) |
Y2* |
probably null |
Het |
Acta1 |
T |
A |
8: 124,620,360 (GRCm39) |
D26V |
possibly damaging |
Het |
Adra1d |
A |
C |
2: 131,403,502 (GRCm39) |
L196R |
probably damaging |
Het |
Agbl2 |
G |
A |
2: 90,621,909 (GRCm39) |
C132Y |
probably benign |
Het |
Amd1 |
A |
G |
10: 40,170,226 (GRCm39) |
V92A |
probably benign |
Het |
Arid4b |
T |
A |
13: 14,310,844 (GRCm39) |
I149K |
probably benign |
Het |
Atg7 |
A |
G |
6: 114,674,041 (GRCm39) |
M312V |
probably benign |
Het |
Bap1 |
T |
A |
14: 30,978,643 (GRCm39) |
V381E |
probably damaging |
Het |
Cbfa2t3 |
C |
T |
8: 123,369,720 (GRCm39) |
V207I |
possibly damaging |
Het |
Cdh24 |
T |
C |
14: 54,870,030 (GRCm39) |
Q629R |
probably benign |
Het |
Cdhr2 |
G |
T |
13: 54,867,606 (GRCm39) |
V479L |
probably benign |
Het |
Chd2 |
A |
G |
7: 73,101,506 (GRCm39) |
S1407P |
probably benign |
Het |
Clstn2 |
A |
G |
9: 97,681,523 (GRCm39) |
V39A |
possibly damaging |
Het |
Cwh43 |
T |
A |
5: 73,578,806 (GRCm39) |
M357K |
possibly damaging |
Het |
Dcdc2a |
T |
A |
13: 25,386,180 (GRCm39) |
D351E |
probably benign |
Het |
Dennd6b |
T |
C |
15: 89,069,576 (GRCm39) |
I517V |
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,915,497 (GRCm39) |
E4374G |
probably damaging |
Het |
Emsy |
A |
G |
7: 98,275,922 (GRCm39) |
S336P |
possibly damaging |
Het |
Enoph1 |
A |
T |
5: 100,208,841 (GRCm39) |
E65D |
probably benign |
Het |
Fam83f |
T |
A |
15: 80,556,281 (GRCm39) |
L55Q |
probably damaging |
Het |
Fry |
T |
C |
5: 150,401,472 (GRCm39) |
F379L |
|
Het |
Fscb |
A |
T |
12: 64,521,382 (GRCm39) |
M28K |
probably benign |
Het |
Gas7 |
G |
A |
11: 67,574,260 (GRCm39) |
V412M |
probably damaging |
Het |
Gatad1 |
T |
C |
5: 3,693,540 (GRCm39) |
R210G |
probably benign |
Het |
Gcn1 |
T |
A |
5: 115,727,057 (GRCm39) |
V638E |
probably benign |
Het |
Ggt1 |
A |
T |
10: 75,414,733 (GRCm39) |
I184F |
probably damaging |
Het |
Gigyf2 |
A |
G |
1: 87,368,629 (GRCm39) |
N1103S |
probably benign |
Het |
Gm5592 |
G |
A |
7: 40,935,887 (GRCm39) |
A130T |
possibly damaging |
Het |
Gys2 |
T |
C |
6: 142,394,230 (GRCm39) |
|
probably null |
Het |
Hmcn1 |
C |
A |
1: 150,525,743 (GRCm39) |
E3327* |
probably null |
Het |
Ighv1-36 |
C |
T |
12: 114,843,656 (GRCm39) |
G68E |
probably damaging |
Het |
Igkv6-32 |
G |
A |
6: 70,051,089 (GRCm39) |
T89M |
probably damaging |
Het |
Ipo7 |
A |
G |
7: 109,652,014 (GRCm39) |
D931G |
probably benign |
Het |
Jakmip1 |
A |
G |
5: 37,330,631 (GRCm39) |
E437G |
probably benign |
Het |
Lingo3 |
C |
T |
10: 80,671,955 (GRCm39) |
|
probably benign |
Het |
Lnpep |
A |
G |
17: 17,758,900 (GRCm39) |
S815P |
probably damaging |
Het |
Ly6a |
T |
C |
15: 74,869,449 (GRCm39) |
D2G |
probably damaging |
Het |
Madd |
C |
A |
2: 90,988,359 (GRCm39) |
E1223* |
probably null |
Het |
Mapk8ip3 |
A |
T |
17: 25,120,078 (GRCm39) |
|
probably null |
Het |
Mecom |
T |
C |
3: 30,033,987 (GRCm39) |
E239G |
probably damaging |
Het |
Mug1 |
T |
C |
6: 121,852,838 (GRCm39) |
V889A |
probably benign |
Het |
Myo18b |
T |
A |
5: 112,938,986 (GRCm39) |
N1675I |
probably benign |
Het |
Ndrg4 |
T |
C |
8: 96,426,756 (GRCm39) |
F50L |
possibly damaging |
Het |
Ndst4 |
A |
G |
3: 125,508,293 (GRCm39) |
Y286C |
probably damaging |
Het |
Nrp2 |
C |
T |
1: 62,784,567 (GRCm39) |
R239C |
probably damaging |
Het |
Olfm3 |
A |
G |
3: 114,895,604 (GRCm39) |
D195G |
probably damaging |
Het |
Or2y14 |
A |
T |
11: 49,404,941 (GRCm39) |
T159S |
probably damaging |
Het |
Or4p21 |
G |
T |
2: 88,277,003 (GRCm39) |
T93K |
probably benign |
Het |
Pds5a |
A |
G |
5: 65,809,741 (GRCm39) |
L407P |
possibly damaging |
Het |
Pgm2 |
A |
G |
5: 64,269,425 (GRCm39) |
N504S |
probably benign |
Het |
Plce1 |
A |
G |
19: 38,690,283 (GRCm39) |
M656V |
probably damaging |
Het |
Pou6f2 |
T |
C |
13: 18,414,209 (GRCm39) |
T189A |
unknown |
Het |
Ppp1r12b |
T |
C |
1: 134,803,807 (GRCm39) |
S451G |
probably benign |
Het |
Prox1 |
T |
G |
1: 189,893,107 (GRCm39) |
N446T |
probably damaging |
Het |
Ralgapa2 |
T |
A |
2: 146,195,199 (GRCm39) |
R1195S |
probably damaging |
Het |
Rere |
A |
G |
4: 150,701,832 (GRCm39) |
D37G |
probably damaging |
Het |
Tfip11 |
T |
A |
5: 112,482,796 (GRCm39) |
M560K |
possibly damaging |
Het |
Thop1 |
T |
C |
10: 80,915,320 (GRCm39) |
V260A |
probably damaging |
Het |
Tle6 |
A |
G |
10: 81,434,476 (GRCm39) |
M41T |
possibly damaging |
Het |
Trav13d-4 |
T |
C |
14: 53,995,249 (GRCm39) |
S68P |
possibly damaging |
Het |
Trim24 |
A |
G |
6: 37,934,661 (GRCm39) |
N826S |
probably damaging |
Het |
Tuba3a |
T |
C |
6: 125,255,433 (GRCm39) |
E414G |
probably damaging |
Het |
Vmn2r78 |
A |
G |
7: 86,571,695 (GRCm39) |
I502V |
probably benign |
Het |
Vmn2r79 |
A |
T |
7: 86,651,336 (GRCm39) |
Y245F |
probably benign |
Het |
|
Other mutations in 0610040J01Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01621:0610040J01Rik
|
APN |
5 |
64,055,726 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02229:0610040J01Rik
|
APN |
5 |
64,055,696 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02389:0610040J01Rik
|
APN |
5 |
64,053,826 (GRCm39) |
missense |
probably null |
1.00 |
IGL02411:0610040J01Rik
|
APN |
5 |
64,055,459 (GRCm39) |
missense |
probably benign |
0.31 |
R0243:0610040J01Rik
|
UTSW |
5 |
64,055,806 (GRCm39) |
missense |
probably benign |
0.10 |
R0411:0610040J01Rik
|
UTSW |
5 |
64,053,834 (GRCm39) |
splice site |
probably benign |
|
R1978:0610040J01Rik
|
UTSW |
5 |
64,055,880 (GRCm39) |
nonsense |
probably null |
|
R2072:0610040J01Rik
|
UTSW |
5 |
64,056,080 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2202:0610040J01Rik
|
UTSW |
5 |
64,056,011 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3161:0610040J01Rik
|
UTSW |
5 |
64,053,833 (GRCm39) |
splice site |
probably benign |
|
R3162:0610040J01Rik
|
UTSW |
5 |
64,053,833 (GRCm39) |
splice site |
probably benign |
|
R4428:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4429:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4430:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4431:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4464:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4465:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4467:0610040J01Rik
|
UTSW |
5 |
64,056,182 (GRCm39) |
unclassified |
probably benign |
|
R4491:0610040J01Rik
|
UTSW |
5 |
64,055,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R5161:0610040J01Rik
|
UTSW |
5 |
64,055,344 (GRCm39) |
nonsense |
probably null |
|
R6115:0610040J01Rik
|
UTSW |
5 |
64,055,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6273:0610040J01Rik
|
UTSW |
5 |
64,055,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R7445:0610040J01Rik
|
UTSW |
5 |
64,055,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R7593:0610040J01Rik
|
UTSW |
5 |
64,055,774 (GRCm39) |
missense |
probably damaging |
0.97 |
R8140:0610040J01Rik
|
UTSW |
5 |
64,055,954 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8165:0610040J01Rik
|
UTSW |
5 |
64,055,289 (GRCm39) |
splice site |
probably null |
|
R8557:0610040J01Rik
|
UTSW |
5 |
64,055,954 (GRCm39) |
missense |
probably benign |
0.04 |
R9671:0610040J01Rik
|
UTSW |
5 |
64,055,948 (GRCm39) |
nonsense |
probably null |
|
R9782:0610040J01Rik
|
UTSW |
5 |
64,053,796 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|