Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accs |
T |
A |
2: 93,678,448 (GRCm39) |
E12D |
probably damaging |
Het |
Ahnak2 |
C |
A |
12: 112,748,998 (GRCm39) |
R283L |
probably benign |
Het |
BC005624 |
T |
C |
2: 30,864,020 (GRCm39) |
E191G |
probably damaging |
Het |
C1galt1 |
A |
G |
6: 7,871,217 (GRCm39) |
N351S |
probably benign |
Het |
Ccdc162 |
T |
C |
10: 41,415,427 (GRCm39) |
R2179G |
probably benign |
Het |
Ccdc88c |
G |
A |
12: 100,905,284 (GRCm39) |
T1108M |
probably benign |
Het |
Cd47 |
T |
C |
16: 49,714,543 (GRCm39) |
L184P |
probably damaging |
Het |
Cdc40 |
T |
C |
10: 40,717,372 (GRCm39) |
K440E |
probably damaging |
Het |
Cenpe |
G |
A |
3: 134,971,694 (GRCm39) |
V2262I |
probably damaging |
Het |
Cep290 |
A |
G |
10: 100,390,361 (GRCm39) |
K2035E |
probably benign |
Het |
Cks1brt |
G |
T |
8: 85,898,172 (GRCm39) |
L8F |
probably benign |
Het |
Col17a1 |
T |
C |
19: 47,637,442 (GRCm39) |
|
probably benign |
Het |
Coro6 |
A |
T |
11: 77,360,293 (GRCm39) |
N421I |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,269,440 (GRCm39) |
S1480P |
probably damaging |
Het |
Csrnp3 |
G |
T |
2: 65,832,826 (GRCm39) |
A110S |
probably damaging |
Het |
Cyp2d10 |
G |
T |
15: 82,287,240 (GRCm39) |
T461K |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,308,769 (GRCm39) |
V1994A |
probably benign |
Het |
Dnah11 |
T |
A |
12: 118,160,379 (GRCm39) |
N117I |
probably benign |
Het |
Dnajc3 |
A |
G |
14: 119,195,307 (GRCm39) |
Y74C |
probably damaging |
Het |
Fam13c |
T |
A |
10: 70,390,403 (GRCm39) |
F555I |
possibly damaging |
Het |
Fbn1 |
T |
A |
2: 125,188,354 (GRCm39) |
D1495V |
probably damaging |
Het |
Fbrsl1 |
T |
C |
5: 110,595,862 (GRCm39) |
T58A |
probably benign |
Het |
Gjd3 |
A |
G |
11: 102,691,706 (GRCm39) |
I99T |
possibly damaging |
Het |
Glce |
T |
C |
9: 61,977,857 (GRCm39) |
N9S |
probably damaging |
Het |
Gosr1 |
T |
C |
11: 76,641,704 (GRCm39) |
T125A |
possibly damaging |
Het |
Ifi27l2a |
T |
A |
12: 103,406,202 (GRCm39) |
|
probably null |
Het |
Jph1 |
C |
T |
1: 17,167,456 (GRCm39) |
D125N |
possibly damaging |
Het |
Kbtbd12 |
A |
T |
6: 88,595,676 (GRCm39) |
S51R |
probably damaging |
Het |
Klra9 |
A |
T |
6: 130,166,659 (GRCm39) |
|
probably null |
Het |
Kmo |
A |
T |
1: 175,484,289 (GRCm39) |
M340L |
probably benign |
Het |
Lama1 |
T |
C |
17: 68,024,181 (GRCm39) |
I93T |
possibly damaging |
Het |
Limk2 |
A |
T |
11: 3,308,104 (GRCm39) |
|
probably null |
Het |
Mgat5 |
C |
A |
1: 127,248,375 (GRCm39) |
N92K |
probably benign |
Het |
Mib2 |
T |
A |
4: 155,739,256 (GRCm39) |
I908F |
probably damaging |
Het |
Mical1 |
T |
G |
10: 41,356,359 (GRCm39) |
L304R |
probably damaging |
Het |
Mtbp |
G |
T |
15: 55,434,690 (GRCm39) |
|
probably null |
Het |
Myo3a |
T |
C |
2: 22,455,004 (GRCm39) |
Y70H |
probably damaging |
Het |
Neb |
T |
C |
2: 52,133,401 (GRCm39) |
Y3379C |
probably damaging |
Het |
Neurod2 |
G |
T |
11: 98,218,029 (GRCm39) |
N378K |
probably damaging |
Het |
Or2g25 |
A |
G |
17: 37,970,799 (GRCm39) |
S142P |
probably benign |
Het |
Or4k40 |
T |
A |
2: 111,251,003 (GRCm39) |
M98L |
probably benign |
Het |
Or6x1 |
A |
G |
9: 40,099,161 (GRCm39) |
Y250C |
probably damaging |
Het |
Or8k20 |
T |
A |
2: 86,106,337 (GRCm39) |
T165S |
probably damaging |
Het |
Pfdn6 |
T |
C |
17: 34,158,528 (GRCm39) |
Y82C |
probably damaging |
Het |
Pla2g4d |
C |
A |
2: 120,107,971 (GRCm39) |
A313S |
possibly damaging |
Het |
Ptcd3 |
C |
A |
6: 71,885,637 (GRCm39) |
E30* |
probably null |
Het |
Rai1 |
A |
G |
11: 60,078,428 (GRCm39) |
T831A |
probably benign |
Het |
Rims1 |
G |
A |
1: 22,367,172 (GRCm39) |
T1176M |
probably damaging |
Het |
Rin1 |
A |
C |
19: 5,105,171 (GRCm39) |
I744L |
probably benign |
Het |
Rora |
T |
A |
9: 69,282,771 (GRCm39) |
S430T |
probably benign |
Het |
Rsph10b |
T |
A |
5: 143,873,967 (GRCm39) |
S23T |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,746,928 (GRCm39) |
N3773S |
probably benign |
Het |
Scn4a |
A |
G |
11: 106,230,180 (GRCm39) |
Y543H |
probably damaging |
Het |
Scn4a |
C |
A |
11: 106,236,373 (GRCm39) |
G296C |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,535,447 (GRCm39) |
T435A |
probably benign |
Het |
Shank2 |
G |
T |
7: 143,964,890 (GRCm39) |
D833Y |
probably damaging |
Het |
Slc9a2 |
T |
C |
1: 40,802,770 (GRCm39) |
S607P |
possibly damaging |
Het |
Slx4 |
G |
A |
16: 3,809,458 (GRCm39) |
R346W |
probably damaging |
Het |
Spata20 |
A |
T |
11: 94,371,340 (GRCm39) |
C675S |
probably benign |
Het |
Suclg2 |
A |
T |
6: 95,563,997 (GRCm39) |
I196N |
probably damaging |
Het |
Sv2b |
G |
A |
7: 74,798,807 (GRCm39) |
H272Y |
possibly damaging |
Het |
Svep1 |
T |
C |
4: 58,070,629 (GRCm39) |
I2386V |
probably benign |
Het |
Taf13 |
A |
T |
3: 108,488,445 (GRCm39) |
E109D |
possibly damaging |
Het |
Tanc2 |
A |
G |
11: 105,790,606 (GRCm39) |
T976A |
probably benign |
Het |
Tax1bp1 |
A |
G |
6: 52,706,311 (GRCm39) |
Y104C |
probably damaging |
Het |
Tfeb |
T |
C |
17: 48,099,911 (GRCm39) |
|
probably null |
Het |
Tlr9 |
T |
C |
9: 106,101,248 (GRCm39) |
Y180H |
probably damaging |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Ttc12 |
T |
A |
9: 49,356,499 (GRCm39) |
T510S |
probably benign |
Het |
Ubqln1 |
T |
C |
13: 58,339,895 (GRCm39) |
E280G |
probably damaging |
Het |
Urm1 |
T |
C |
2: 29,731,437 (GRCm39) |
W44R |
probably damaging |
Het |
Usp32 |
A |
T |
11: 84,933,406 (GRCm39) |
I34N |
probably benign |
Het |
Vars1 |
T |
C |
17: 35,233,728 (GRCm39) |
L1018P |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,869,894 (GRCm39) |
V206D |
probably damaging |
Het |
Vim |
T |
C |
2: 13,583,270 (GRCm39) |
V224A |
probably damaging |
Het |
Vmn2r106 |
G |
T |
17: 20,498,997 (GRCm39) |
H305N |
probably benign |
Het |
Vmn2r78 |
A |
G |
7: 86,604,132 (GRCm39) |
N770S |
probably damaging |
Het |
Wdr33 |
T |
A |
18: 32,029,684 (GRCm39) |
L961Q |
unknown |
Het |
Xylt2 |
A |
G |
11: 94,559,575 (GRCm39) |
S356P |
possibly damaging |
Het |
Zbtb14 |
A |
G |
17: 69,694,575 (GRCm39) |
N91S |
probably damaging |
Het |
Zc3h6 |
T |
C |
2: 128,858,654 (GRCm39) |
L895S |
probably damaging |
Het |
Zc3h7b |
C |
T |
15: 81,661,289 (GRCm39) |
P376L |
probably benign |
Het |
Zfp131 |
T |
C |
13: 120,228,079 (GRCm39) |
T523A |
probably benign |
Het |
|
Other mutations in Oog4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01580:Oog4
|
APN |
4 |
143,165,682 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02207:Oog4
|
APN |
4 |
143,165,510 (GRCm39) |
missense |
probably benign |
0.20 |
R0038:Oog4
|
UTSW |
4 |
143,165,514 (GRCm39) |
missense |
probably benign |
0.20 |
R0038:Oog4
|
UTSW |
4 |
143,165,514 (GRCm39) |
missense |
probably benign |
0.20 |
R0326:Oog4
|
UTSW |
4 |
143,165,773 (GRCm39) |
missense |
probably benign |
0.03 |
R0372:Oog4
|
UTSW |
4 |
143,164,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1056:Oog4
|
UTSW |
4 |
143,164,581 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1598:Oog4
|
UTSW |
4 |
143,164,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R4028:Oog4
|
UTSW |
4 |
143,166,770 (GRCm39) |
missense |
probably benign |
0.02 |
R4029:Oog4
|
UTSW |
4 |
143,166,770 (GRCm39) |
missense |
probably benign |
0.02 |
R4030:Oog4
|
UTSW |
4 |
143,166,770 (GRCm39) |
missense |
probably benign |
0.02 |
R4705:Oog4
|
UTSW |
4 |
143,165,445 (GRCm39) |
missense |
probably benign |
0.00 |
R5260:Oog4
|
UTSW |
4 |
143,164,424 (GRCm39) |
missense |
probably benign |
0.00 |
R5945:Oog4
|
UTSW |
4 |
143,164,293 (GRCm39) |
missense |
probably benign |
0.01 |
R6499:Oog4
|
UTSW |
4 |
143,164,548 (GRCm39) |
missense |
probably damaging |
0.96 |
R6614:Oog4
|
UTSW |
4 |
143,164,445 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6852:Oog4
|
UTSW |
4 |
143,165,679 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7371:Oog4
|
UTSW |
4 |
143,165,346 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7375:Oog4
|
UTSW |
4 |
143,165,544 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7501:Oog4
|
UTSW |
4 |
143,164,022 (GRCm39) |
frame shift |
probably null |
|
R7564:Oog4
|
UTSW |
4 |
143,164,022 (GRCm39) |
frame shift |
probably null |
|
R7678:Oog4
|
UTSW |
4 |
143,164,022 (GRCm39) |
frame shift |
probably null |
|
R7688:Oog4
|
UTSW |
4 |
143,164,022 (GRCm39) |
frame shift |
probably null |
|
R7689:Oog4
|
UTSW |
4 |
143,164,022 (GRCm39) |
frame shift |
probably null |
|
R8219:Oog4
|
UTSW |
4 |
143,166,508 (GRCm39) |
missense |
probably benign |
0.00 |
R8274:Oog4
|
UTSW |
4 |
143,166,459 (GRCm39) |
splice site |
probably benign |
|
R8352:Oog4
|
UTSW |
4 |
143,164,047 (GRCm39) |
missense |
probably benign |
0.22 |
R8452:Oog4
|
UTSW |
4 |
143,164,047 (GRCm39) |
missense |
probably benign |
0.22 |
Z1177:Oog4
|
UTSW |
4 |
143,164,145 (GRCm39) |
missense |
probably benign |
0.06 |
Z1177:Oog4
|
UTSW |
4 |
143,164,144 (GRCm39) |
missense |
possibly damaging |
0.91 |
|