Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
A |
G |
4: 103,092,865 (GRCm39) |
I152T |
probably damaging |
Het |
A2m |
C |
T |
6: 121,644,149 (GRCm39) |
T949I |
possibly damaging |
Het |
Begain |
T |
A |
12: 108,999,571 (GRCm39) |
Y605F |
probably benign |
Het |
Cavin2 |
A |
G |
1: 51,328,570 (GRCm39) |
E9G |
possibly damaging |
Het |
Cdh16 |
A |
G |
8: 105,344,323 (GRCm39) |
V72A |
probably damaging |
Het |
Dgkd |
T |
C |
1: 87,844,638 (GRCm39) |
L268P |
probably damaging |
Het |
Eps8 |
T |
A |
6: 137,514,669 (GRCm39) |
Y28F |
possibly damaging |
Het |
Erap1 |
T |
C |
13: 74,823,414 (GRCm39) |
I816T |
probably damaging |
Het |
Fli1 |
A |
T |
9: 32,372,660 (GRCm39) |
F126Y |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm21957 |
A |
T |
7: 124,819,004 (GRCm39) |
|
noncoding transcript |
Het |
Gm5862 |
A |
C |
5: 26,227,769 (GRCm39) |
W41G |
probably benign |
Het |
Hectd1 |
T |
A |
12: 51,841,280 (GRCm39) |
R618* |
probably null |
Het |
Homez |
T |
C |
14: 55,095,633 (GRCm39) |
E25G |
probably damaging |
Het |
Ifngr1 |
C |
A |
10: 19,485,202 (GRCm39) |
N400K |
possibly damaging |
Het |
Lin7a |
G |
A |
10: 107,247,886 (GRCm39) |
V186I |
possibly damaging |
Het |
Lpcat2 |
G |
T |
8: 93,644,675 (GRCm39) |
S448I |
probably damaging |
Het |
Lrp10 |
C |
A |
14: 54,706,119 (GRCm39) |
Y436* |
probably null |
Het |
Myef2l |
G |
A |
3: 10,154,118 (GRCm39) |
V296M |
probably damaging |
Het |
Myo1f |
A |
G |
17: 33,816,991 (GRCm39) |
H707R |
possibly damaging |
Het |
Neurl4 |
A |
G |
11: 69,800,449 (GRCm39) |
N1147D |
probably damaging |
Het |
Or4b1b |
G |
T |
2: 90,112,351 (GRCm39) |
D189E |
probably damaging |
Het |
Or6b3 |
T |
C |
1: 92,438,853 (GRCm39) |
D299G |
probably null |
Het |
Pak6 |
T |
C |
2: 118,523,741 (GRCm39) |
S299P |
probably benign |
Het |
Panx2 |
A |
G |
15: 88,952,970 (GRCm39) |
D487G |
probably damaging |
Het |
Sbspon |
T |
C |
1: 15,929,158 (GRCm39) |
N211S |
probably benign |
Het |
Sgsm1 |
T |
A |
5: 113,434,633 (GRCm39) |
|
probably benign |
Het |
Slc38a4 |
T |
C |
15: 96,917,644 (GRCm39) |
Y27C |
probably benign |
Het |
Sorbs1 |
A |
G |
19: 40,306,460 (GRCm39) |
|
probably benign |
Het |
Sp140l2 |
A |
G |
1: 85,231,907 (GRCm39) |
|
probably benign |
Het |
Ssh1 |
A |
T |
5: 114,104,308 (GRCm39) |
Y35N |
possibly damaging |
Het |
Stx2 |
A |
T |
5: 129,069,329 (GRCm39) |
F127L |
probably damaging |
Het |
Synm |
A |
T |
7: 67,388,885 (GRCm39) |
I325N |
probably damaging |
Het |
Szt2 |
A |
G |
4: 118,233,690 (GRCm39) |
|
probably benign |
Het |
Tbc1d23 |
A |
G |
16: 57,007,048 (GRCm39) |
|
probably benign |
Het |
Tmem50a |
T |
C |
4: 134,625,739 (GRCm39) |
|
probably benign |
Het |
Tpx2 |
T |
G |
2: 152,726,096 (GRCm39) |
L354V |
probably benign |
Het |
Trafd1 |
G |
A |
5: 121,512,094 (GRCm39) |
R399C |
possibly damaging |
Het |
Trem3 |
C |
T |
17: 48,556,903 (GRCm39) |
R125W |
probably damaging |
Het |
Wnk1 |
T |
A |
6: 119,940,446 (GRCm39) |
T62S |
probably damaging |
Het |
Zbtb6 |
T |
C |
2: 37,319,343 (GRCm39) |
E195G |
probably benign |
Het |
Zc3h15 |
A |
G |
2: 83,491,829 (GRCm39) |
D306G |
probably damaging |
Het |
|
Other mutations in Ubp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01941:Ubp1
|
APN |
9 |
113,785,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R0097:Ubp1
|
UTSW |
9 |
113,802,575 (GRCm39) |
splice site |
probably benign |
|
R0097:Ubp1
|
UTSW |
9 |
113,802,575 (GRCm39) |
splice site |
probably benign |
|
R0241:Ubp1
|
UTSW |
9 |
113,795,655 (GRCm39) |
critical splice donor site |
probably null |
|
R0669:Ubp1
|
UTSW |
9 |
113,793,736 (GRCm39) |
splice site |
probably benign |
|
R0709:Ubp1
|
UTSW |
9 |
113,773,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R1416:Ubp1
|
UTSW |
9 |
113,799,239 (GRCm39) |
missense |
probably benign |
0.02 |
R1466:Ubp1
|
UTSW |
9 |
113,773,903 (GRCm39) |
splice site |
probably benign |
|
R1753:Ubp1
|
UTSW |
9 |
113,785,037 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1780:Ubp1
|
UTSW |
9 |
113,793,647 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2235:Ubp1
|
UTSW |
9 |
113,793,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R3418:Ubp1
|
UTSW |
9 |
113,780,754 (GRCm39) |
critical splice donor site |
probably null |
|
R3978:Ubp1
|
UTSW |
9 |
113,785,773 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4024:Ubp1
|
UTSW |
9 |
113,773,951 (GRCm39) |
missense |
probably benign |
0.03 |
R4469:Ubp1
|
UTSW |
9 |
113,787,775 (GRCm39) |
missense |
probably benign |
0.11 |
R4797:Ubp1
|
UTSW |
9 |
113,785,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R4984:Ubp1
|
UTSW |
9 |
113,788,460 (GRCm39) |
missense |
probably damaging |
0.97 |
R5914:Ubp1
|
UTSW |
9 |
113,785,807 (GRCm39) |
missense |
probably benign |
0.00 |
R6971:Ubp1
|
UTSW |
9 |
113,801,831 (GRCm39) |
missense |
probably damaging |
0.97 |
R7718:Ubp1
|
UTSW |
9 |
113,802,597 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8129:Ubp1
|
UTSW |
9 |
113,804,417 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8772:Ubp1
|
UTSW |
9 |
113,801,897 (GRCm39) |
missense |
probably benign |
0.23 |
R9106:Ubp1
|
UTSW |
9 |
113,799,319 (GRCm39) |
missense |
probably benign |
|
|