Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
G |
3: 121,921,828 (GRCm39) |
D1128G |
probably damaging |
Het |
Acsm3 |
A |
T |
7: 119,368,131 (GRCm39) |
R116* |
probably null |
Het |
Acte1 |
G |
T |
7: 143,434,902 (GRCm39) |
|
probably null |
Het |
Ahnak |
T |
A |
19: 8,989,943 (GRCm39) |
D3742E |
probably damaging |
Het |
Arhgef17 |
A |
G |
7: 100,528,818 (GRCm39) |
S598P |
possibly damaging |
Het |
Asxl2 |
T |
C |
12: 3,552,310 (GRCm39) |
F1351L |
probably damaging |
Het |
Atg7 |
C |
T |
6: 114,672,588 (GRCm39) |
T267I |
possibly damaging |
Het |
Bace2 |
A |
G |
16: 97,209,692 (GRCm39) |
K202R |
probably benign |
Het |
Bccip |
G |
T |
7: 133,311,249 (GRCm39) |
V55L |
probably benign |
Het |
Bpifa1 |
T |
A |
2: 153,988,052 (GRCm39) |
H198Q |
possibly damaging |
Het |
Btbd7 |
A |
G |
12: 102,777,430 (GRCm39) |
Y466H |
probably damaging |
Het |
Cdc45 |
A |
C |
16: 18,605,521 (GRCm39) |
S480A |
probably benign |
Het |
Cenpe |
T |
C |
3: 134,935,839 (GRCm39) |
Y425H |
possibly damaging |
Het |
Cep76 |
A |
C |
18: 67,767,977 (GRCm39) |
M185R |
probably damaging |
Het |
Chd5 |
G |
T |
4: 152,456,122 (GRCm39) |
M930I |
probably damaging |
Het |
Clstn2 |
G |
T |
9: 97,343,395 (GRCm39) |
T684K |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,491,943 (GRCm39) |
N1270S |
possibly damaging |
Het |
Crxos |
A |
G |
7: 15,636,850 (GRCm39) |
H141R |
probably benign |
Het |
Dcc |
A |
G |
18: 71,553,433 (GRCm39) |
I741T |
possibly damaging |
Het |
Ddx20 |
A |
T |
3: 105,587,685 (GRCm39) |
C430* |
probably null |
Het |
Dgki |
G |
A |
6: 37,273,615 (GRCm39) |
T12M |
probably benign |
Het |
Dock6 |
T |
C |
9: 21,721,153 (GRCm39) |
N1676S |
possibly damaging |
Het |
Exosc6 |
G |
A |
8: 111,783,028 (GRCm39) |
R9H |
probably damaging |
Het |
Fstl5 |
A |
G |
3: 76,569,114 (GRCm39) |
Q589R |
probably damaging |
Het |
Gm4846 |
T |
A |
1: 166,324,959 (GRCm39) |
Y44F |
probably benign |
Het |
Gpr15lg |
A |
G |
14: 36,829,352 (GRCm39) |
S44P |
probably damaging |
Het |
Gtf3c2 |
A |
C |
5: 31,326,401 (GRCm39) |
I370R |
probably damaging |
Het |
Hjurp |
CTCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCT |
C |
1: 88,193,999 (GRCm39) |
|
probably benign |
Het |
Hspg2 |
A |
G |
4: 137,287,726 (GRCm39) |
M3696V |
possibly damaging |
Het |
Itga1 |
A |
T |
13: 115,166,695 (GRCm39) |
C167* |
probably null |
Het |
Khdc4 |
T |
C |
3: 88,593,853 (GRCm39) |
S81P |
probably benign |
Het |
Kpna2 |
A |
G |
11: 106,880,158 (GRCm39) |
S497P |
probably damaging |
Het |
Krt77 |
T |
A |
15: 101,774,064 (GRCm39) |
T197S |
probably damaging |
Het |
Krtap6-5 |
T |
C |
16: 88,844,655 (GRCm39) |
Y26C |
unknown |
Het |
Lhfpl5 |
A |
T |
17: 28,799,133 (GRCm39) |
D214V |
possibly damaging |
Het |
Lrrtm1 |
A |
G |
6: 77,221,596 (GRCm39) |
E351G |
probably damaging |
Het |
Mphosph9 |
A |
G |
5: 124,403,427 (GRCm39) |
V867A |
probably benign |
Het |
Mtcl1 |
T |
A |
17: 66,650,879 (GRCm39) |
M1529L |
probably benign |
Het |
Mthfr |
A |
T |
4: 148,132,626 (GRCm39) |
Q268L |
probably damaging |
Het |
Myo1d |
A |
T |
11: 80,565,744 (GRCm39) |
N360K |
probably damaging |
Het |
Nbea |
AC |
A |
3: 55,998,393 (GRCm39) |
|
probably null |
Het |
Or1e33 |
A |
T |
11: 73,738,108 (GRCm39) |
V281E |
probably damaging |
Het |
Or4p8 |
T |
C |
2: 88,727,255 (GRCm39) |
S229G |
probably benign |
Het |
Or5an1b |
A |
T |
19: 12,299,336 (GRCm39) |
M285K |
probably damaging |
Het |
Or5m11 |
T |
A |
2: 85,782,185 (GRCm39) |
Y259* |
probably null |
Het |
P2rx5 |
A |
T |
11: 73,062,655 (GRCm39) |
T455S |
probably damaging |
Het |
Palld |
A |
T |
8: 61,969,591 (GRCm39) |
F1244L |
unknown |
Het |
Pbld1 |
A |
G |
10: 62,907,829 (GRCm39) |
T125A |
|
Het |
Pde3b |
G |
A |
7: 114,014,697 (GRCm39) |
|
probably benign |
Het |
Pfkm |
T |
C |
15: 98,019,188 (GRCm39) |
S180P |
probably damaging |
Het |
Pla2g4d |
T |
A |
2: 120,100,453 (GRCm39) |
R626S |
possibly damaging |
Het |
Postn |
A |
G |
3: 54,282,515 (GRCm39) |
E492G |
possibly damaging |
Het |
Prph2 |
A |
G |
17: 47,230,818 (GRCm39) |
D237G |
probably damaging |
Het |
Psmd4 |
T |
C |
3: 94,942,604 (GRCm39) |
H105R |
probably damaging |
Het |
Pygl |
T |
C |
12: 70,242,401 (GRCm39) |
N685S |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,315,266 (GRCm39) |
F502S |
unknown |
Het |
Sik1 |
T |
C |
17: 32,066,167 (GRCm39) |
I607V |
probably benign |
Het |
Slc26a3 |
T |
A |
12: 31,513,470 (GRCm39) |
I464N |
possibly damaging |
Het |
Slc38a9 |
A |
G |
13: 112,825,910 (GRCm39) |
N116S |
probably damaging |
Het |
Sorcs2 |
C |
A |
5: 36,181,910 (GRCm39) |
|
probably null |
Het |
Spink5 |
T |
C |
18: 44,119,367 (GRCm39) |
L226P |
probably damaging |
Het |
Tab1 |
G |
A |
15: 80,034,754 (GRCm39) |
V180I |
probably benign |
Het |
Tacc2 |
T |
G |
7: 130,226,058 (GRCm39) |
S914R |
probably damaging |
Het |
Tacc2 |
C |
T |
7: 130,226,209 (GRCm39) |
R965C |
probably benign |
Het |
Tlr9 |
A |
G |
9: 106,101,972 (GRCm39) |
D421G |
probably damaging |
Het |
Tmem181a |
T |
C |
17: 6,307,265 (GRCm39) |
L16P |
probably damaging |
Het |
Trim58 |
A |
T |
11: 58,542,075 (GRCm39) |
H345L |
probably damaging |
Het |
Ttc13 |
G |
A |
8: 125,400,290 (GRCm39) |
R688C |
probably benign |
Het |
Uso1 |
A |
G |
5: 92,335,173 (GRCm39) |
H511R |
probably benign |
Het |
Vmn2r5 |
A |
T |
3: 64,411,721 (GRCm39) |
Y282* |
probably null |
Het |
|
Other mutations in Ube2o |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Ube2o
|
APN |
11 |
116,435,580 (GRCm39) |
missense |
probably benign |
|
IGL00973:Ube2o
|
APN |
11 |
116,432,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01291:Ube2o
|
APN |
11 |
116,430,960 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01804:Ube2o
|
APN |
11 |
116,435,199 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02138:Ube2o
|
APN |
11 |
116,434,226 (GRCm39) |
splice site |
probably benign |
|
IGL02317:Ube2o
|
APN |
11 |
116,432,389 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02515:Ube2o
|
APN |
11 |
116,434,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:Ube2o
|
APN |
11 |
116,432,591 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03062:Ube2o
|
APN |
11 |
116,432,468 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03145:Ube2o
|
APN |
11 |
116,434,835 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03190:Ube2o
|
APN |
11 |
116,435,954 (GRCm39) |
missense |
probably damaging |
1.00 |
Delay
|
UTSW |
11 |
116,430,898 (GRCm39) |
missense |
probably damaging |
1.00 |
Tarry
|
UTSW |
11 |
116,432,194 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU05:Ube2o
|
UTSW |
11 |
116,430,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R0519:Ube2o
|
UTSW |
11 |
116,437,285 (GRCm39) |
critical splice donor site |
probably null |
|
R0666:Ube2o
|
UTSW |
11 |
116,433,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R1056:Ube2o
|
UTSW |
11 |
116,437,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R1202:Ube2o
|
UTSW |
11 |
116,432,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1424:Ube2o
|
UTSW |
11 |
116,434,558 (GRCm39) |
missense |
probably benign |
|
R1469:Ube2o
|
UTSW |
11 |
116,436,650 (GRCm39) |
splice site |
probably benign |
|
R1720:Ube2o
|
UTSW |
11 |
116,435,433 (GRCm39) |
missense |
probably benign |
|
R1791:Ube2o
|
UTSW |
11 |
116,432,320 (GRCm39) |
missense |
probably benign |
0.01 |
R1893:Ube2o
|
UTSW |
11 |
116,439,661 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1997:Ube2o
|
UTSW |
11 |
116,436,163 (GRCm39) |
missense |
probably damaging |
0.99 |
R2156:Ube2o
|
UTSW |
11 |
116,471,972 (GRCm39) |
missense |
probably damaging |
0.98 |
R2199:Ube2o
|
UTSW |
11 |
116,435,571 (GRCm39) |
missense |
probably benign |
|
R2414:Ube2o
|
UTSW |
11 |
116,439,683 (GRCm39) |
missense |
probably benign |
0.02 |
R3766:Ube2o
|
UTSW |
11 |
116,437,689 (GRCm39) |
splice site |
probably benign |
|
R4749:Ube2o
|
UTSW |
11 |
116,432,734 (GRCm39) |
missense |
probably benign |
0.11 |
R5213:Ube2o
|
UTSW |
11 |
116,432,285 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5403:Ube2o
|
UTSW |
11 |
116,439,633 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5441:Ube2o
|
UTSW |
11 |
116,435,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R5727:Ube2o
|
UTSW |
11 |
116,430,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R6125:Ube2o
|
UTSW |
11 |
116,435,576 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6125:Ube2o
|
UTSW |
11 |
116,432,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R6234:Ube2o
|
UTSW |
11 |
116,430,316 (GRCm39) |
missense |
probably benign |
0.17 |
R6278:Ube2o
|
UTSW |
11 |
116,430,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6324:Ube2o
|
UTSW |
11 |
116,430,185 (GRCm39) |
missense |
probably benign |
0.00 |
R6346:Ube2o
|
UTSW |
11 |
116,432,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R6389:Ube2o
|
UTSW |
11 |
116,439,684 (GRCm39) |
missense |
probably null |
0.72 |
R7040:Ube2o
|
UTSW |
11 |
116,432,686 (GRCm39) |
missense |
probably benign |
0.08 |
R7072:Ube2o
|
UTSW |
11 |
116,432,327 (GRCm39) |
missense |
probably benign |
0.13 |
R7270:Ube2o
|
UTSW |
11 |
116,434,761 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7420:Ube2o
|
UTSW |
11 |
116,430,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Ube2o
|
UTSW |
11 |
116,471,905 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7818:Ube2o
|
UTSW |
11 |
116,434,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R7916:Ube2o
|
UTSW |
11 |
116,471,884 (GRCm39) |
missense |
probably benign |
|
R8212:Ube2o
|
UTSW |
11 |
116,439,624 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8679:Ube2o
|
UTSW |
11 |
116,432,273 (GRCm39) |
nonsense |
probably null |
|
R9085:Ube2o
|
UTSW |
11 |
116,436,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Ube2o
|
UTSW |
11 |
116,471,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Ube2o
|
UTSW |
11 |
116,430,210 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9569:Ube2o
|
UTSW |
11 |
116,434,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R9686:Ube2o
|
UTSW |
11 |
116,434,779 (GRCm39) |
missense |
probably benign |
|
R9689:Ube2o
|
UTSW |
11 |
116,435,639 (GRCm39) |
missense |
possibly damaging |
0.84 |
|