Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610028H24Rik |
C |
T |
10: 76,290,551 (GRCm39) |
P118S |
probably damaging |
Het |
Adgrl1 |
T |
A |
8: 84,656,343 (GRCm39) |
D215E |
probably damaging |
Het |
Afap1l2 |
T |
C |
19: 56,902,914 (GRCm39) |
D755G |
probably damaging |
Het |
Akr1c18 |
T |
A |
13: 4,194,332 (GRCm39) |
D109V |
possibly damaging |
Het |
Brdt |
G |
A |
5: 107,506,752 (GRCm39) |
R445H |
probably benign |
Het |
Capn2 |
C |
A |
1: 182,307,288 (GRCm39) |
E517* |
probably null |
Het |
Celsr1 |
A |
T |
15: 85,863,303 (GRCm39) |
V1243E |
possibly damaging |
Het |
Cenpe |
C |
G |
3: 134,953,096 (GRCm39) |
|
probably null |
Het |
Cep135 |
A |
G |
5: 76,778,817 (GRCm39) |
E748G |
probably damaging |
Het |
Cfap119 |
C |
A |
7: 127,187,159 (GRCm39) |
V35L |
probably benign |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Col6a1 |
C |
A |
10: 76,545,743 (GRCm39) |
A910S |
unknown |
Het |
Cyp4a14 |
T |
A |
4: 115,347,156 (GRCm39) |
|
probably null |
Het |
Dot1l |
C |
T |
10: 80,619,378 (GRCm39) |
R412W |
probably damaging |
Het |
Dyrk2 |
T |
C |
10: 118,695,594 (GRCm39) |
T555A |
probably benign |
Het |
Foxn3 |
T |
C |
12: 99,162,587 (GRCm39) |
N438S |
probably damaging |
Het |
Gdpd5 |
T |
C |
7: 99,103,001 (GRCm39) |
F320S |
probably damaging |
Het |
Grn |
A |
G |
11: 102,326,560 (GRCm39) |
H413R |
probably damaging |
Het |
Gstm7 |
A |
T |
3: 107,838,963 (GRCm39) |
M3K |
possibly damaging |
Het |
Il17rd |
A |
G |
14: 26,822,293 (GRCm39) |
E673G |
probably damaging |
Het |
Klhl29 |
T |
C |
12: 5,187,500 (GRCm39) |
D288G |
possibly damaging |
Het |
Klk1b11 |
G |
A |
7: 43,426,421 (GRCm39) |
A79T |
probably benign |
Het |
Kmt2a |
A |
G |
9: 44,719,359 (GRCm39) |
V3914A |
unknown |
Het |
Map2k2 |
T |
C |
10: 80,956,877 (GRCm39) |
V307A |
probably benign |
Het |
Mst1r |
G |
T |
9: 107,784,319 (GRCm39) |
|
probably benign |
Het |
Nr3c2 |
A |
G |
8: 77,937,275 (GRCm39) |
E834G |
probably damaging |
Het |
Oga |
A |
T |
19: 45,764,501 (GRCm39) |
L213H |
probably damaging |
Het |
Or5b102 |
A |
T |
19: 13,041,423 (GRCm39) |
Y216F |
probably damaging |
Het |
Or8d2 |
T |
C |
9: 38,759,614 (GRCm39) |
L68P |
probably damaging |
Het |
Plscr4 |
A |
T |
9: 92,364,693 (GRCm39) |
|
probably null |
Het |
Pou2f1 |
A |
G |
1: 165,703,444 (GRCm39) |
S749P |
probably damaging |
Het |
Ppp4r3b |
T |
G |
11: 29,155,701 (GRCm39) |
L556V |
possibly damaging |
Het |
Psd4 |
T |
G |
2: 24,291,108 (GRCm39) |
|
probably null |
Het |
Rbbp4 |
T |
C |
4: 129,228,356 (GRCm39) |
D33G |
probably damaging |
Het |
Rif1 |
T |
A |
2: 51,975,153 (GRCm39) |
M354K |
probably damaging |
Het |
Rmi1 |
A |
G |
13: 58,557,067 (GRCm39) |
K439E |
probably benign |
Het |
Scgb2b7 |
A |
G |
7: 31,404,454 (GRCm39) |
|
probably null |
Het |
Sdc1 |
A |
G |
12: 8,841,370 (GRCm39) |
D237G |
probably benign |
Het |
Sel1l3 |
T |
C |
5: 53,357,593 (GRCm39) |
Y133C |
probably damaging |
Het |
Snx31 |
A |
G |
15: 36,523,587 (GRCm39) |
|
probably null |
Het |
Snx7 |
A |
G |
3: 117,632,488 (GRCm39) |
F201S |
probably damaging |
Het |
Tas2r131 |
C |
T |
6: 132,934,438 (GRCm39) |
V124I |
possibly damaging |
Het |
Tbx20 |
A |
T |
9: 24,651,581 (GRCm39) |
|
probably null |
Het |
Topbp1 |
A |
T |
9: 103,197,756 (GRCm39) |
N445I |
probably damaging |
Het |
Tpx2 |
T |
A |
2: 152,709,263 (GRCm39) |
I31K |
possibly damaging |
Het |
Trpv3 |
T |
A |
11: 73,179,088 (GRCm39) |
V499E |
probably damaging |
Het |
Tshr |
G |
A |
12: 91,500,743 (GRCm39) |
W258* |
probably null |
Het |
Usp32 |
G |
T |
11: 84,878,107 (GRCm39) |
D1543E |
probably damaging |
Het |
Usp39 |
A |
G |
6: 72,315,521 (GRCm39) |
|
probably benign |
Het |
Vac14 |
T |
C |
8: 111,361,020 (GRCm39) |
S197P |
probably damaging |
Het |
Vars2 |
A |
G |
17: 35,971,835 (GRCm39) |
S497P |
probably damaging |
Het |
Zfp462 |
C |
A |
4: 55,008,637 (GRCm39) |
P201Q |
probably benign |
Het |
Zkscan5 |
A |
G |
5: 145,157,847 (GRCm39) |
Q783R |
possibly damaging |
Het |
|
Other mutations in Ogfod3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01954:Ogfod3
|
APN |
11 |
121,093,851 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02398:Ogfod3
|
APN |
11 |
121,093,851 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02458:Ogfod3
|
APN |
11 |
121,091,749 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03411:Ogfod3
|
APN |
11 |
121,068,630 (GRCm39) |
makesense |
probably null |
|
PIT4403001:Ogfod3
|
UTSW |
11 |
121,087,561 (GRCm39) |
critical splice donor site |
probably null |
|
R0145:Ogfod3
|
UTSW |
11 |
121,085,896 (GRCm39) |
splice site |
probably benign |
|
R1302:Ogfod3
|
UTSW |
11 |
121,074,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Ogfod3
|
UTSW |
11 |
121,074,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Ogfod3
|
UTSW |
11 |
121,086,027 (GRCm39) |
missense |
probably benign |
0.42 |
R4825:Ogfod3
|
UTSW |
11 |
121,086,027 (GRCm39) |
missense |
probably benign |
0.42 |
R4909:Ogfod3
|
UTSW |
11 |
121,088,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Ogfod3
|
UTSW |
11 |
121,093,761 (GRCm39) |
missense |
probably benign |
0.01 |
R6953:Ogfod3
|
UTSW |
11 |
121,093,824 (GRCm39) |
missense |
probably benign |
|
R7051:Ogfod3
|
UTSW |
11 |
121,086,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R7618:Ogfod3
|
UTSW |
11 |
121,093,804 (GRCm39) |
missense |
probably damaging |
0.96 |
R8112:Ogfod3
|
UTSW |
11 |
121,095,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R8714:Ogfod3
|
UTSW |
11 |
121,087,608 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9769:Ogfod3
|
UTSW |
11 |
121,074,357 (GRCm39) |
missense |
probably damaging |
0.99 |
|