Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
A |
T |
12: 118,904,359 (GRCm39) |
F144I |
probably damaging |
Het |
Als2cl |
A |
G |
9: 110,719,496 (GRCm39) |
R468G |
possibly damaging |
Het |
Arsk |
C |
A |
13: 76,246,576 (GRCm39) |
|
probably benign |
Het |
Cacna1d |
T |
C |
14: 29,833,039 (GRCm39) |
H912R |
probably damaging |
Het |
Ccr1 |
A |
T |
9: 123,764,371 (GRCm39) |
V53D |
possibly damaging |
Het |
Cfap91 |
G |
A |
16: 38,156,764 (GRCm39) |
S47L |
possibly damaging |
Het |
Clec2d |
G |
A |
6: 129,160,076 (GRCm39) |
R30K |
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,591,535 (GRCm39) |
V975A |
possibly damaging |
Het |
Col4a1 |
AGCCAGGGATGCCAGG |
AGCCAGG |
8: 11,268,014 (GRCm39) |
|
probably benign |
Het |
Cul7 |
T |
C |
17: 46,969,263 (GRCm39) |
S907P |
probably benign |
Het |
Depdc1b |
A |
T |
13: 108,498,794 (GRCm39) |
H159L |
possibly damaging |
Het |
Dhx57 |
T |
C |
17: 80,583,011 (GRCm39) |
H198R |
probably benign |
Het |
Dpp7 |
T |
C |
2: 25,246,311 (GRCm39) |
D10G |
probably damaging |
Het |
Esp18 |
G |
A |
17: 39,719,023 (GRCm39) |
M7I |
possibly damaging |
Het |
Fam120a |
G |
T |
13: 49,039,219 (GRCm39) |
A979E |
possibly damaging |
Het |
Fam167a |
A |
G |
14: 63,689,828 (GRCm39) |
T42A |
probably damaging |
Het |
Gm973 |
A |
G |
1: 59,605,827 (GRCm39) |
R553G |
probably benign |
Het |
Ift140 |
T |
A |
17: 25,254,786 (GRCm39) |
I422N |
probably benign |
Het |
Jag1 |
CTTT |
CTTTT |
2: 136,932,802 (GRCm39) |
|
probably null |
Het |
Limk2 |
A |
G |
11: 3,300,731 (GRCm39) |
F204L |
probably damaging |
Het |
Lmo7 |
A |
G |
14: 102,124,624 (GRCm39) |
D361G |
probably damaging |
Het |
Muc2 |
CGTG |
CGTGTG |
7: 141,699,185 (GRCm38) |
|
probably null |
Het |
Nup98 |
T |
A |
7: 101,809,923 (GRCm39) |
T536S |
probably damaging |
Het |
Or52e2 |
T |
A |
7: 102,804,520 (GRCm39) |
M145L |
probably benign |
Het |
Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
Pcdh18 |
A |
T |
3: 49,711,252 (GRCm39) |
F21Y |
probably benign |
Het |
Pcna-ps2 |
T |
A |
19: 9,261,487 (GRCm39) |
Y249N |
probably damaging |
Het |
Prkce |
A |
T |
17: 86,932,886 (GRCm39) |
D622V |
probably damaging |
Het |
Prss47 |
A |
C |
13: 65,197,208 (GRCm39) |
V176G |
possibly damaging |
Het |
Prss55 |
C |
T |
14: 64,314,627 (GRCm39) |
R181H |
probably benign |
Het |
Prtg |
A |
T |
9: 72,752,225 (GRCm39) |
I204L |
probably benign |
Het |
Pura |
T |
C |
18: 36,420,720 (GRCm39) |
I169T |
probably damaging |
Het |
Rttn |
C |
T |
18: 89,119,815 (GRCm39) |
T1750I |
probably benign |
Het |
Slc25a26 |
T |
A |
6: 94,484,639 (GRCm39) |
S60T |
probably damaging |
Het |
Tktl2 |
G |
A |
8: 66,964,999 (GRCm39) |
V186M |
probably damaging |
Het |
Tmem94 |
T |
A |
11: 115,682,804 (GRCm39) |
C614S |
probably benign |
Het |
Trim12a |
T |
C |
7: 103,953,469 (GRCm39) |
N214S |
probably benign |
Het |
Ube3c |
T |
C |
5: 29,806,344 (GRCm39) |
Y329H |
probably benign |
Het |
Unc80 |
A |
T |
1: 66,710,757 (GRCm39) |
E2675D |
probably benign |
Het |
Usf3 |
C |
T |
16: 44,036,321 (GRCm39) |
P267L |
probably benign |
Het |
Vmn1r129 |
A |
T |
7: 21,094,635 (GRCm39) |
Y194* |
probably null |
Het |
Zfp750 |
T |
C |
11: 121,403,807 (GRCm39) |
E356G |
probably benign |
Het |
|
Other mutations in Ubxn2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00956:Ubxn2a
|
APN |
12 |
4,933,956 (GRCm39) |
missense |
probably benign |
0.00 |
R0611:Ubxn2a
|
UTSW |
12 |
4,930,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R1808:Ubxn2a
|
UTSW |
12 |
4,935,839 (GRCm39) |
missense |
probably benign |
0.00 |
R1883:Ubxn2a
|
UTSW |
12 |
4,944,563 (GRCm39) |
nonsense |
probably null |
|
R2163:Ubxn2a
|
UTSW |
12 |
4,935,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R2404:Ubxn2a
|
UTSW |
12 |
4,933,851 (GRCm39) |
missense |
probably benign |
0.00 |
R3051:Ubxn2a
|
UTSW |
12 |
4,941,322 (GRCm39) |
nonsense |
probably null |
|
R3052:Ubxn2a
|
UTSW |
12 |
4,941,322 (GRCm39) |
nonsense |
probably null |
|
R3053:Ubxn2a
|
UTSW |
12 |
4,941,322 (GRCm39) |
nonsense |
probably null |
|
R4204:Ubxn2a
|
UTSW |
12 |
4,944,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Ubxn2a
|
UTSW |
12 |
4,933,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5182:Ubxn2a
|
UTSW |
12 |
4,930,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R5366:Ubxn2a
|
UTSW |
12 |
4,930,741 (GRCm39) |
missense |
probably benign |
0.04 |
R5518:Ubxn2a
|
UTSW |
12 |
4,952,238 (GRCm39) |
missense |
probably benign |
0.31 |
R7414:Ubxn2a
|
UTSW |
12 |
4,941,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R7613:Ubxn2a
|
UTSW |
12 |
4,933,832 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8914:Ubxn2a
|
UTSW |
12 |
4,930,754 (GRCm39) |
missense |
probably benign |
0.42 |
|