Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm2 |
C |
T |
4: 144,285,224 (GRCm39) |
A138T |
probably damaging |
Het |
Acot10 |
T |
C |
15: 20,666,348 (GRCm39) |
N131S |
probably benign |
Het |
Agbl5 |
A |
G |
5: 31,049,177 (GRCm39) |
Y220C |
probably damaging |
Het |
Ankdd1a |
C |
T |
9: 65,415,343 (GRCm39) |
A227T |
possibly damaging |
Het |
Ap3b1 |
A |
T |
13: 94,664,803 (GRCm39) |
Q914L |
unknown |
Het |
Arhgef25 |
T |
C |
10: 127,021,751 (GRCm39) |
D216G |
possibly damaging |
Het |
Bcas2 |
T |
A |
3: 103,079,187 (GRCm39) |
|
probably benign |
Het |
Bpifb5 |
A |
C |
2: 154,072,139 (GRCm39) |
H282P |
possibly damaging |
Het |
Ccdc121rt2 |
A |
T |
5: 112,598,334 (GRCm39) |
I294F |
possibly damaging |
Het |
Ccdc167 |
A |
G |
17: 29,924,556 (GRCm39) |
I15T |
probably damaging |
Het |
Cd248 |
A |
G |
19: 5,120,009 (GRCm39) |
N619S |
probably benign |
Het |
Chrna1 |
A |
G |
2: 73,400,828 (GRCm39) |
F234S |
possibly damaging |
Het |
Clcc1 |
T |
G |
3: 108,580,682 (GRCm39) |
M332R |
probably damaging |
Het |
Cmklr1 |
T |
A |
5: 113,752,999 (GRCm39) |
M1L |
possibly damaging |
Het |
Cntnap5c |
A |
G |
17: 58,199,032 (GRCm39) |
M109V |
probably benign |
Het |
Coq2 |
A |
G |
5: 100,809,729 (GRCm39) |
I18T |
possibly damaging |
Het |
Crybg3 |
T |
C |
16: 59,350,701 (GRCm39) |
S880G |
probably damaging |
Het |
Cubn |
A |
G |
2: 13,482,889 (GRCm39) |
C286R |
probably damaging |
Het |
Defa24 |
T |
C |
8: 22,225,299 (GRCm39) |
V63A |
probably benign |
Het |
Dnah6 |
C |
T |
6: 73,063,200 (GRCm39) |
R2634H |
probably damaging |
Het |
Dusp8 |
T |
A |
7: 141,636,756 (GRCm39) |
|
probably null |
Het |
Elac1 |
T |
C |
18: 73,871,939 (GRCm39) |
D352G |
probably damaging |
Het |
Ermap |
A |
T |
4: 119,042,800 (GRCm39) |
V241E |
probably damaging |
Het |
Fgf10 |
T |
A |
13: 118,852,047 (GRCm39) |
M43K |
probably benign |
Het |
Gabrd |
A |
G |
4: 155,471,724 (GRCm39) |
V193A |
probably damaging |
Het |
Hectd4 |
T |
G |
5: 121,392,283 (GRCm39) |
C182W |
possibly damaging |
Het |
Hook3 |
C |
T |
8: 26,524,968 (GRCm39) |
W26* |
probably null |
Het |
Kif1a |
C |
A |
1: 92,982,663 (GRCm39) |
E714* |
probably null |
Het |
Krt6b |
T |
C |
15: 101,587,386 (GRCm39) |
E236G |
probably damaging |
Het |
Large2 |
A |
G |
2: 92,199,861 (GRCm39) |
L209P |
probably damaging |
Het |
Lats1 |
A |
G |
10: 7,578,871 (GRCm39) |
N665S |
probably benign |
Het |
Lrrc37 |
A |
T |
11: 103,509,756 (GRCm39) |
|
probably benign |
Het |
Lrrtm3 |
T |
C |
10: 63,925,001 (GRCm39) |
I55M |
probably benign |
Het |
Ltk |
A |
G |
2: 119,582,238 (GRCm39) |
S838P |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,217,194 (GRCm39) |
I348V |
probably benign |
Het |
Mag |
T |
A |
7: 30,600,104 (GRCm39) |
S559C |
probably damaging |
Het |
Mink1 |
A |
G |
11: 70,503,120 (GRCm39) |
H1072R |
possibly damaging |
Het |
Mycbp2 |
T |
A |
14: 103,392,862 (GRCm39) |
Q833L |
probably damaging |
Het |
Myh4 |
G |
A |
11: 67,146,159 (GRCm39) |
E1406K |
possibly damaging |
Het |
Npc1 |
C |
T |
18: 12,330,302 (GRCm39) |
V950I |
probably benign |
Het |
Npl |
A |
G |
1: 153,394,627 (GRCm39) |
|
probably null |
Het |
Or10w3 |
A |
G |
19: 13,703,753 (GRCm39) |
I43V |
probably benign |
Het |
Or11g27 |
T |
A |
14: 50,771,711 (GRCm39) |
F281I |
probably benign |
Het |
Or2m13 |
A |
T |
16: 19,226,167 (GRCm39) |
F200I |
possibly damaging |
Het |
Or8b36 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 37,937,836 (GRCm39) |
|
probably null |
Het |
Oxsm |
A |
T |
14: 16,242,220 (GRCm38) |
I183N |
probably damaging |
Het |
Pde7a |
T |
C |
3: 19,297,327 (GRCm39) |
I108V |
probably benign |
Het |
Pgghg |
A |
T |
7: 140,526,289 (GRCm39) |
T585S |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,452,921 (GRCm39) |
D3949N |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,169,331 (GRCm39) |
H1777Q |
possibly damaging |
Het |
Rela |
G |
A |
19: 5,695,438 (GRCm39) |
|
probably null |
Het |
Rilpl1 |
C |
A |
5: 124,652,602 (GRCm39) |
G41W |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,417,477 (GRCm39) |
K1212E |
probably benign |
Het |
Sgca |
A |
C |
11: 94,863,393 (GRCm39) |
L28V |
probably damaging |
Het |
Ssmem1 |
A |
G |
6: 30,519,758 (GRCm39) |
R148G |
probably damaging |
Het |
St8sia5 |
A |
T |
18: 77,333,836 (GRCm39) |
N165Y |
probably damaging |
Het |
Tbl2 |
A |
T |
5: 135,188,223 (GRCm39) |
H339L |
probably benign |
Het |
Tcof1 |
G |
A |
18: 60,961,897 (GRCm39) |
P718L |
probably damaging |
Het |
Trim72 |
A |
T |
7: 127,603,786 (GRCm39) |
E44V |
possibly damaging |
Het |
Try10 |
T |
A |
6: 41,332,523 (GRCm39) |
S60T |
probably benign |
Het |
Xrn2 |
A |
G |
2: 146,905,262 (GRCm39) |
I856V |
probably benign |
Het |
|
Other mutations in Usp31 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00341:Usp31
|
APN |
7 |
121,305,893 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00421:Usp31
|
APN |
7 |
121,247,873 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00657:Usp31
|
APN |
7 |
121,247,454 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01917:Usp31
|
APN |
7 |
121,278,708 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02444:Usp31
|
APN |
7 |
121,278,718 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03090:Usp31
|
APN |
7 |
121,278,753 (GRCm39) |
splice site |
probably benign |
|
R0334:Usp31
|
UTSW |
7 |
121,258,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R0945:Usp31
|
UTSW |
7 |
121,269,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1326:Usp31
|
UTSW |
7 |
121,247,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R2116:Usp31
|
UTSW |
7 |
121,247,919 (GRCm39) |
missense |
probably benign |
0.39 |
R3113:Usp31
|
UTSW |
7 |
121,278,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R4072:Usp31
|
UTSW |
7 |
121,267,005 (GRCm39) |
splice site |
probably null |
|
R4075:Usp31
|
UTSW |
7 |
121,267,005 (GRCm39) |
splice site |
probably null |
|
R4076:Usp31
|
UTSW |
7 |
121,267,005 (GRCm39) |
splice site |
probably null |
|
R4306:Usp31
|
UTSW |
7 |
121,306,152 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4675:Usp31
|
UTSW |
7 |
121,306,548 (GRCm39) |
unclassified |
probably benign |
|
R4960:Usp31
|
UTSW |
7 |
121,247,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R5368:Usp31
|
UTSW |
7 |
121,260,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R5396:Usp31
|
UTSW |
7 |
121,267,005 (GRCm39) |
splice site |
probably null |
|
R5456:Usp31
|
UTSW |
7 |
121,269,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R5475:Usp31
|
UTSW |
7 |
121,250,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Usp31
|
UTSW |
7 |
121,250,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Usp31
|
UTSW |
7 |
121,248,698 (GRCm39) |
missense |
probably benign |
0.05 |
R6688:Usp31
|
UTSW |
7 |
121,277,553 (GRCm39) |
missense |
probably benign |
0.01 |
R6875:Usp31
|
UTSW |
7 |
121,248,863 (GRCm39) |
nonsense |
probably null |
|
R6895:Usp31
|
UTSW |
7 |
121,252,399 (GRCm39) |
missense |
probably benign |
0.00 |
R7570:Usp31
|
UTSW |
7 |
121,274,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7633:Usp31
|
UTSW |
7 |
121,258,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R7666:Usp31
|
UTSW |
7 |
121,248,404 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7841:Usp31
|
UTSW |
7 |
121,276,535 (GRCm39) |
missense |
probably damaging |
0.96 |
R7841:Usp31
|
UTSW |
7 |
121,247,679 (GRCm39) |
missense |
probably benign |
0.00 |
R8013:Usp31
|
UTSW |
7 |
121,248,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R8014:Usp31
|
UTSW |
7 |
121,248,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R8118:Usp31
|
UTSW |
7 |
121,276,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R8140:Usp31
|
UTSW |
7 |
121,248,249 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9063:Usp31
|
UTSW |
7 |
121,306,466 (GRCm39) |
missense |
probably benign |
|
R9795:Usp31
|
UTSW |
7 |
121,247,499 (GRCm39) |
missense |
probably benign |
0.00 |
X0062:Usp31
|
UTSW |
7 |
121,250,737 (GRCm39) |
missense |
possibly damaging |
0.50 |
|