Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
A |
G |
16: 56,474,418 (GRCm39) |
T448A |
possibly damaging |
Het |
Adamtsl1 |
T |
A |
4: 86,075,110 (GRCm39) |
|
probably null |
Het |
Adgra3 |
A |
G |
5: 50,215,900 (GRCm39) |
V73A |
probably benign |
Het |
Aggf1 |
T |
C |
13: 95,489,358 (GRCm39) |
|
probably benign |
Het |
Aktip |
C |
T |
8: 91,853,520 (GRCm39) |
V96I |
possibly damaging |
Het |
Atm |
A |
G |
9: 53,433,476 (GRCm39) |
I258T |
probably benign |
Het |
Baz1b |
C |
T |
5: 135,273,160 (GRCm39) |
T1428I |
probably damaging |
Het |
C3ar1 |
A |
T |
6: 122,826,934 (GRCm39) |
Y428N |
probably damaging |
Het |
Cadps |
A |
G |
14: 12,597,380 (GRCm38) |
S437P |
probably damaging |
Het |
Car4 |
C |
T |
11: 84,856,593 (GRCm39) |
P294S |
probably damaging |
Het |
Cenpq |
A |
G |
17: 41,235,223 (GRCm39) |
L213P |
probably damaging |
Het |
Cept1 |
A |
G |
3: 106,446,504 (GRCm39) |
|
probably null |
Het |
Cln6 |
A |
G |
9: 62,754,407 (GRCm39) |
I150V |
probably benign |
Het |
Cyp2c67 |
A |
G |
19: 39,605,861 (GRCm39) |
M345T |
probably damaging |
Het |
Dapk2 |
T |
A |
9: 66,153,805 (GRCm39) |
I187N |
probably damaging |
Het |
Dkk2 |
A |
G |
3: 131,883,673 (GRCm39) |
D191G |
probably benign |
Het |
Dnah8 |
T |
A |
17: 30,986,785 (GRCm39) |
F3145I |
probably damaging |
Het |
Dock1 |
A |
C |
7: 134,710,548 (GRCm39) |
D1190A |
possibly damaging |
Het |
Ehhadh |
T |
A |
16: 21,581,620 (GRCm39) |
L457F |
probably damaging |
Het |
Ercc6l2 |
T |
C |
13: 64,001,497 (GRCm39) |
L552P |
probably damaging |
Het |
Ghrhr |
T |
G |
6: 55,361,138 (GRCm39) |
I284S |
probably damaging |
Het |
Gm10288 |
A |
T |
3: 146,544,954 (GRCm39) |
|
noncoding transcript |
Het |
Gp6 |
T |
G |
7: 4,397,507 (GRCm39) |
I19L |
probably benign |
Het |
Gria4 |
G |
A |
9: 4,456,206 (GRCm39) |
S698L |
possibly damaging |
Het |
Ifng |
A |
T |
10: 118,278,410 (GRCm39) |
I53F |
possibly damaging |
Het |
Kazn |
A |
C |
4: 141,874,327 (GRCm39) |
|
probably null |
Het |
Khk |
A |
T |
5: 31,085,848 (GRCm39) |
I136F |
probably damaging |
Het |
Lnx1 |
T |
A |
5: 74,788,027 (GRCm39) |
N98Y |
probably damaging |
Het |
Lsp1 |
T |
C |
7: 142,042,679 (GRCm39) |
|
probably null |
Het |
Lta4h |
A |
T |
10: 93,314,329 (GRCm39) |
N467I |
probably benign |
Het |
Mcmbp |
C |
A |
7: 128,311,505 (GRCm39) |
|
probably null |
Het |
Me2 |
A |
T |
18: 73,931,038 (GRCm39) |
I85K |
probably benign |
Het |
Muc4 |
C |
T |
16: 32,569,804 (GRCm39) |
T288I |
possibly damaging |
Het |
Nadsyn1 |
A |
T |
7: 143,353,649 (GRCm39) |
Y525N |
probably damaging |
Het |
Nt5e |
G |
A |
9: 88,209,946 (GRCm39) |
V70M |
probably damaging |
Het |
Or52e4 |
G |
A |
7: 104,706,182 (GRCm39) |
G243D |
probably damaging |
Het |
Or8b36 |
A |
T |
9: 37,937,332 (GRCm39) |
I77L |
possibly damaging |
Het |
Or9k7 |
T |
G |
10: 130,046,603 (GRCm39) |
Y132S |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,373,129 (GRCm39) |
|
probably benign |
Het |
Ppm1d |
A |
T |
11: 85,236,541 (GRCm39) |
E440V |
probably damaging |
Het |
Pramel32 |
A |
T |
4: 88,546,127 (GRCm39) |
I405N |
probably damaging |
Het |
Ripor2 |
A |
T |
13: 24,915,572 (GRCm39) |
E1047D |
probably damaging |
Het |
Rwdd2b |
G |
A |
16: 87,234,336 (GRCm39) |
A18V |
probably benign |
Het |
Serpina5 |
G |
T |
12: 104,068,384 (GRCm39) |
K148N |
probably damaging |
Het |
Setx |
A |
G |
2: 29,036,976 (GRCm39) |
K1154E |
probably benign |
Het |
Skap1 |
T |
A |
11: 96,599,382 (GRCm39) |
|
probably null |
Het |
Spcs2 |
T |
C |
7: 99,498,241 (GRCm39) |
K81R |
probably damaging |
Het |
Stt3b |
T |
A |
9: 115,079,975 (GRCm39) |
M646L |
possibly damaging |
Het |
Suco |
T |
C |
1: 161,646,195 (GRCm39) |
T1169A |
probably benign |
Het |
Susd1 |
A |
T |
4: 59,427,985 (GRCm39) |
Y66* |
probably null |
Het |
Trim34a |
T |
A |
7: 103,910,441 (GRCm39) |
C414* |
probably null |
Het |
Trim58 |
G |
A |
11: 58,542,176 (GRCm39) |
G379S |
probably damaging |
Het |
Vmn2r50 |
T |
A |
7: 9,787,002 (GRCm39) |
Q35L |
probably benign |
Het |
Zfp418 |
T |
C |
7: 7,177,690 (GRCm39) |
|
probably benign |
Het |
Zfp57 |
G |
A |
17: 37,320,919 (GRCm39) |
V258I |
probably benign |
Het |
Zng1 |
A |
T |
19: 24,909,026 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cyb5r3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Cyb5r3
|
APN |
15 |
83,044,605 (GRCm39) |
missense |
probably benign |
|
IGL02358:Cyb5r3
|
APN |
15 |
83,045,136 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02666:Cyb5r3
|
APN |
15 |
83,044,554 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4466001:Cyb5r3
|
UTSW |
15 |
83,046,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Cyb5r3
|
UTSW |
15 |
83,046,137 (GRCm39) |
missense |
probably benign |
0.00 |
R0063:Cyb5r3
|
UTSW |
15 |
83,046,137 (GRCm39) |
missense |
probably benign |
0.00 |
R0368:Cyb5r3
|
UTSW |
15 |
83,042,993 (GRCm39) |
missense |
probably benign |
0.01 |
R3976:Cyb5r3
|
UTSW |
15 |
83,044,330 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4953:Cyb5r3
|
UTSW |
15 |
83,042,822 (GRCm39) |
nonsense |
probably null |
|
R5249:Cyb5r3
|
UTSW |
15 |
83,042,836 (GRCm39) |
intron |
probably benign |
|
R5665:Cyb5r3
|
UTSW |
15 |
83,038,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Cyb5r3
|
UTSW |
15 |
83,038,917 (GRCm39) |
missense |
probably benign |
0.10 |
R6368:Cyb5r3
|
UTSW |
15 |
83,044,325 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7255:Cyb5r3
|
UTSW |
15 |
83,044,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9559:Cyb5r3
|
UTSW |
15 |
83,043,123 (GRCm39) |
nonsense |
probably null |
|
|