Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
C |
T |
16: 56,471,088 (GRCm39) |
R578* |
probably null |
Het |
Adam8 |
T |
A |
7: 139,563,851 (GRCm39) |
D717V |
probably benign |
Het |
Aknad1 |
T |
C |
3: 108,682,417 (GRCm39) |
|
probably null |
Het |
Alk |
A |
T |
17: 72,512,937 (GRCm39) |
W341R |
probably damaging |
Het |
Ankdd1b |
G |
A |
13: 96,591,091 (GRCm39) |
Q101* |
probably null |
Het |
Anpep |
A |
C |
7: 79,476,380 (GRCm39) |
S829A |
probably benign |
Het |
Armh3 |
A |
G |
19: 45,948,781 (GRCm39) |
S233P |
probably damaging |
Het |
Ate1 |
A |
T |
7: 130,115,511 (GRCm39) |
C72S |
probably damaging |
Het |
Atp6v0a4 |
G |
A |
6: 38,037,999 (GRCm39) |
L533F |
probably damaging |
Het |
Bach1 |
T |
C |
16: 87,512,267 (GRCm39) |
|
probably benign |
Het |
Baz2b |
T |
C |
2: 59,799,599 (GRCm39) |
D240G |
probably benign |
Het |
Cdc14b |
C |
T |
13: 64,357,014 (GRCm39) |
S21N |
probably damaging |
Het |
Cdh3 |
A |
G |
8: 107,270,520 (GRCm39) |
I466V |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,452,224 (GRCm39) |
D180G |
probably damaging |
Het |
Cyp2c40 |
A |
T |
19: 39,791,105 (GRCm39) |
|
probably null |
Het |
Dclk2 |
C |
T |
3: 86,827,188 (GRCm39) |
R97H |
probably damaging |
Het |
Ddx52 |
T |
C |
11: 83,846,031 (GRCm39) |
|
probably null |
Het |
Dhx58 |
C |
T |
11: 100,587,797 (GRCm39) |
|
probably null |
Het |
Dmp1 |
T |
A |
5: 104,360,427 (GRCm39) |
S368T |
probably damaging |
Het |
Dnah17 |
C |
A |
11: 117,964,474 (GRCm39) |
V2435L |
probably benign |
Het |
Dnajc7 |
A |
G |
11: 100,510,402 (GRCm39) |
V10A |
probably benign |
Het |
Dscam |
G |
T |
16: 96,420,771 (GRCm39) |
T1705K |
possibly damaging |
Het |
Dscaml1 |
G |
A |
9: 45,361,890 (GRCm39) |
V217M |
probably damaging |
Het |
Dync2h1 |
A |
G |
9: 7,142,648 (GRCm39) |
|
probably null |
Het |
F5 |
A |
G |
1: 164,021,488 (GRCm39) |
D1321G |
probably damaging |
Het |
Fam174a |
C |
T |
1: 95,241,770 (GRCm39) |
P77S |
probably benign |
Het |
Fars2 |
G |
A |
13: 36,389,051 (GRCm39) |
R180H |
probably damaging |
Het |
Fnbp1 |
T |
C |
2: 30,945,532 (GRCm39) |
T154A |
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,805,203 (GRCm39) |
N507K |
probably damaging |
Het |
Glg1 |
G |
T |
8: 111,887,407 (GRCm39) |
Y449* |
probably null |
Het |
Gm15130 |
A |
T |
2: 110,964,560 (GRCm39) |
Y187* |
probably null |
Het |
Gm973 |
A |
T |
1: 59,591,713 (GRCm39) |
K366* |
probably null |
Het |
H2bc11 |
T |
A |
13: 22,227,533 (GRCm39) |
V45E |
possibly damaging |
Het |
Hao1 |
A |
G |
2: 134,347,540 (GRCm39) |
I255T |
probably damaging |
Het |
Herc6 |
T |
A |
6: 57,575,423 (GRCm39) |
V148E |
probably damaging |
Het |
Insm2 |
T |
A |
12: 55,647,677 (GRCm39) |
C474S |
possibly damaging |
Het |
Itch |
T |
C |
2: 155,052,502 (GRCm39) |
|
probably null |
Het |
Itga2 |
A |
G |
13: 114,993,909 (GRCm39) |
V748A |
probably damaging |
Het |
Itga9 |
T |
A |
9: 118,510,826 (GRCm39) |
S452T |
probably damaging |
Het |
Kdm4b |
C |
A |
17: 56,693,178 (GRCm39) |
D338E |
probably benign |
Het |
Krt40 |
G |
A |
11: 99,431,045 (GRCm39) |
R155C |
probably damaging |
Het |
Krtap16-1 |
A |
G |
11: 99,876,000 (GRCm39) |
V468A |
probably damaging |
Het |
Lactb2 |
G |
A |
1: 13,708,619 (GRCm39) |
P143L |
probably damaging |
Het |
Lrba |
C |
A |
3: 86,550,021 (GRCm39) |
T2330K |
probably damaging |
Het |
Lrp2bp |
A |
T |
8: 46,466,208 (GRCm39) |
I106F |
probably benign |
Het |
Luzp2 |
A |
G |
7: 54,485,710 (GRCm39) |
K2E |
probably damaging |
Het |
Lypd6 |
T |
C |
2: 50,078,855 (GRCm39) |
|
probably null |
Het |
Maml1 |
A |
T |
11: 50,148,694 (GRCm39) |
D1015E |
probably benign |
Het |
Mdfi |
T |
G |
17: 48,131,906 (GRCm39) |
D106A |
possibly damaging |
Het |
Olfm3 |
T |
C |
3: 114,874,755 (GRCm39) |
M17T |
probably benign |
Het |
Or2n1d |
A |
C |
17: 38,646,731 (GRCm39) |
I228L |
possibly damaging |
Het |
Or2o1 |
A |
G |
11: 49,051,717 (GRCm39) |
Y292C |
probably damaging |
Het |
Or8c16 |
T |
A |
9: 38,130,714 (GRCm39) |
N198K |
probably damaging |
Het |
Or8g30 |
A |
G |
9: 39,230,725 (GRCm39) |
F62L |
probably benign |
Het |
Otud7b |
T |
G |
3: 96,058,227 (GRCm39) |
L261V |
probably damaging |
Het |
P2ry1 |
A |
G |
3: 60,910,893 (GRCm39) |
N11D |
probably damaging |
Het |
Pate2 |
T |
C |
9: 35,596,978 (GRCm39) |
|
probably benign |
Het |
Pcdhb16 |
A |
T |
18: 37,612,458 (GRCm39) |
T473S |
probably benign |
Het |
Per1 |
A |
G |
11: 68,992,057 (GRCm39) |
E137G |
probably damaging |
Het |
Phf11d |
T |
C |
14: 59,590,791 (GRCm39) |
T189A |
probably benign |
Het |
Pik3r5 |
C |
A |
11: 68,386,030 (GRCm39) |
S738R |
possibly damaging |
Het |
Pikfyve |
A |
G |
1: 65,285,635 (GRCm39) |
Y913C |
possibly damaging |
Het |
Pkd1 |
T |
G |
17: 24,795,107 (GRCm39) |
S2265A |
probably damaging |
Het |
Pkhd1l1 |
C |
A |
15: 44,419,428 (GRCm39) |
N2964K |
probably damaging |
Het |
Plch1 |
T |
G |
3: 63,688,967 (GRCm39) |
D79A |
probably damaging |
Het |
Pnliprp1 |
A |
C |
19: 58,728,901 (GRCm39) |
T363P |
possibly damaging |
Het |
Ppp1r10 |
T |
A |
17: 36,240,352 (GRCm39) |
D547E |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,628,701 (GRCm39) |
I3482K |
probably benign |
Het |
Ptpn4 |
A |
G |
1: 119,649,598 (GRCm39) |
Y333H |
probably damaging |
Het |
Ptpru |
T |
A |
4: 131,548,279 (GRCm39) |
M73L |
probably benign |
Het |
Rrp12 |
A |
G |
19: 41,865,867 (GRCm39) |
Y698H |
probably damaging |
Het |
Scaf8 |
T |
C |
17: 3,227,398 (GRCm39) |
F338L |
unknown |
Het |
Slc17a1 |
G |
T |
13: 24,064,576 (GRCm39) |
V347L |
probably benign |
Het |
Slc1a2 |
T |
A |
2: 102,578,883 (GRCm39) |
V263E |
probably damaging |
Het |
Slc29a4 |
T |
C |
5: 142,704,327 (GRCm39) |
V327A |
probably benign |
Het |
Slc6a3 |
A |
C |
13: 73,705,195 (GRCm39) |
I229L |
probably benign |
Het |
Sos2 |
T |
C |
12: 69,654,145 (GRCm39) |
I703V |
probably benign |
Het |
Srpk1 |
T |
C |
17: 28,840,982 (GRCm39) |
T15A |
probably benign |
Het |
St6gal2 |
A |
T |
17: 55,817,367 (GRCm39) |
Q510L |
probably benign |
Het |
Stk24 |
T |
C |
14: 121,532,130 (GRCm39) |
D289G |
possibly damaging |
Het |
Taf2 |
T |
G |
15: 54,929,364 (GRCm39) |
K64T |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,813,735 (GRCm39) |
E257G |
possibly damaging |
Het |
Tmem102 |
A |
T |
11: 69,695,022 (GRCm39) |
F317I |
probably damaging |
Het |
Trav10 |
A |
G |
14: 53,743,497 (GRCm39) |
S33G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,745,408 (GRCm39) |
I5214F |
probably damaging |
Het |
Ube2f |
T |
A |
1: 91,182,002 (GRCm39) |
L2Q |
probably damaging |
Het |
Ube4b |
A |
G |
4: 149,429,069 (GRCm39) |
F857L |
probably damaging |
Het |
Vmn2r18 |
T |
A |
5: 151,485,602 (GRCm39) |
I631F |
possibly damaging |
Het |
Zfp280d |
T |
A |
9: 72,219,947 (GRCm39) |
S241T |
possibly damaging |
Het |
Zfp638 |
T |
A |
6: 83,956,544 (GRCm39) |
L1717* |
probably null |
Het |
Zfp719 |
A |
G |
7: 43,240,535 (GRCm39) |
N708D |
possibly damaging |
Het |
|
Other mutations in Cog1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02407:Cog1
|
APN |
11 |
113,544,852 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02631:Cog1
|
APN |
11 |
113,547,304 (GRCm39) |
nonsense |
probably null |
|
IGL03258:Cog1
|
APN |
11 |
113,545,919 (GRCm39) |
nonsense |
probably null |
|
R0243:Cog1
|
UTSW |
11 |
113,547,821 (GRCm39) |
unclassified |
probably benign |
|
R0336:Cog1
|
UTSW |
11 |
113,553,076 (GRCm39) |
missense |
probably benign |
0.28 |
R1061:Cog1
|
UTSW |
11 |
113,542,863 (GRCm39) |
missense |
probably benign |
|
R1539:Cog1
|
UTSW |
11 |
113,543,058 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1757:Cog1
|
UTSW |
11 |
113,543,130 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1782:Cog1
|
UTSW |
11 |
113,544,792 (GRCm39) |
missense |
probably benign |
|
R1924:Cog1
|
UTSW |
11 |
113,547,038 (GRCm39) |
missense |
probably benign |
|
R2120:Cog1
|
UTSW |
11 |
113,540,424 (GRCm39) |
missense |
probably damaging |
0.98 |
R2121:Cog1
|
UTSW |
11 |
113,540,424 (GRCm39) |
missense |
probably damaging |
0.98 |
R2137:Cog1
|
UTSW |
11 |
113,550,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R3809:Cog1
|
UTSW |
11 |
113,545,836 (GRCm39) |
missense |
probably benign |
|
R4042:Cog1
|
UTSW |
11 |
113,551,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4287:Cog1
|
UTSW |
11 |
113,544,853 (GRCm39) |
missense |
probably damaging |
0.99 |
R4679:Cog1
|
UTSW |
11 |
113,543,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R4774:Cog1
|
UTSW |
11 |
113,548,253 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6575:Cog1
|
UTSW |
11 |
113,546,887 (GRCm39) |
missense |
probably benign |
0.36 |
R7026:Cog1
|
UTSW |
11 |
113,540,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R7233:Cog1
|
UTSW |
11 |
113,540,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R8013:Cog1
|
UTSW |
11 |
113,546,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R8014:Cog1
|
UTSW |
11 |
113,546,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R8027:Cog1
|
UTSW |
11 |
113,543,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8865:Cog1
|
UTSW |
11 |
113,549,324 (GRCm39) |
missense |
probably benign |
0.33 |
R9071:Cog1
|
UTSW |
11 |
113,546,939 (GRCm39) |
missense |
probably damaging |
0.99 |
R9110:Cog1
|
UTSW |
11 |
113,544,807 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9255:Cog1
|
UTSW |
11 |
113,547,019 (GRCm39) |
missense |
probably benign |
|
Z1176:Cog1
|
UTSW |
11 |
113,542,808 (GRCm39) |
missense |
probably damaging |
0.98 |
|