Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
T |
C |
2: 151,315,435 (GRCm39) |
K81R |
probably benign |
Het |
Acacb |
T |
C |
5: 114,351,712 (GRCm39) |
F1150L |
probably benign |
Het |
Acat3 |
A |
G |
17: 13,146,273 (GRCm39) |
Y237H |
possibly damaging |
Het |
Arfgap3 |
T |
C |
15: 83,206,869 (GRCm39) |
T240A |
probably benign |
Het |
Arl6ip1 |
AAAATAAATAAATAAATAAATAAATA |
AAAATAAATAAATAAATAAATAAATAAATA |
7: 117,721,122 (GRCm39) |
|
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,590,675 (GRCm39) |
S23G |
possibly damaging |
Het |
Cemip2 |
G |
T |
19: 21,819,479 (GRCm39) |
R1090L |
probably damaging |
Het |
Clasp1 |
A |
G |
1: 118,506,636 (GRCm39) |
N949S |
probably damaging |
Het |
Csrp1 |
T |
G |
1: 135,673,065 (GRCm39) |
C61G |
probably damaging |
Het |
Dgka |
A |
T |
10: 128,557,064 (GRCm39) |
L637Q |
probably damaging |
Het |
Dst |
G |
A |
1: 34,251,328 (GRCm39) |
R1801H |
probably damaging |
Het |
Edil3 |
T |
C |
13: 89,328,397 (GRCm39) |
S284P |
probably damaging |
Het |
Eif2d |
A |
G |
1: 131,082,100 (GRCm39) |
Y64C |
probably damaging |
Het |
Ell2 |
A |
G |
13: 75,910,067 (GRCm39) |
D139G |
probably damaging |
Het |
Fam187a |
A |
G |
11: 102,777,038 (GRCm39) |
R281G |
probably damaging |
Het |
Gin1 |
A |
G |
1: 97,720,145 (GRCm39) |
D380G |
possibly damaging |
Het |
Gpr149 |
T |
G |
3: 62,511,924 (GRCm39) |
D25A |
possibly damaging |
Het |
Gyg1 |
A |
G |
3: 20,206,901 (GRCm39) |
S90P |
probably benign |
Het |
Hpx |
C |
T |
7: 105,244,354 (GRCm39) |
M190I |
probably null |
Het |
Irf2bpl |
C |
T |
12: 86,929,810 (GRCm39) |
V288I |
probably benign |
Het |
Lyst |
A |
G |
13: 13,810,574 (GRCm39) |
H748R |
probably benign |
Het |
Mmrn1 |
G |
A |
6: 60,935,164 (GRCm39) |
G220D |
probably damaging |
Het |
Mpdz |
A |
T |
4: 81,299,999 (GRCm39) |
M333K |
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,370,847 (GRCm39) |
S2556F |
possibly damaging |
Het |
Nfix |
CAAAAA |
CAAAA |
8: 85,442,876 (GRCm39) |
|
probably null |
Het |
Ntsr1 |
A |
G |
2: 180,142,545 (GRCm39) |
D112G |
probably damaging |
Het |
Or56b1 |
T |
A |
7: 104,285,356 (GRCm39) |
N158K |
possibly damaging |
Het |
Or7a42 |
T |
C |
10: 78,791,117 (GRCm39) |
F26S |
probably benign |
Het |
Or9s14 |
A |
C |
1: 92,536,317 (GRCm39) |
T253P |
possibly damaging |
Het |
Parg |
A |
G |
14: 31,976,493 (GRCm39) |
K178R |
probably benign |
Het |
Pde8b |
C |
A |
13: 95,359,053 (GRCm39) |
C90F |
probably benign |
Het |
Pld1 |
G |
A |
3: 28,174,932 (GRCm39) |
V857I |
probably benign |
Het |
Rad54l2 |
A |
C |
9: 106,594,994 (GRCm39) |
V321G |
probably damaging |
Het |
Rcn2 |
A |
G |
9: 55,952,491 (GRCm39) |
Y112C |
possibly damaging |
Het |
Rnf123 |
A |
T |
9: 107,941,162 (GRCm39) |
D639E |
probably benign |
Het |
Rufy2 |
C |
T |
10: 62,840,551 (GRCm39) |
Q441* |
probably null |
Het |
Scgb2b12 |
T |
C |
7: 32,026,063 (GRCm39) |
Y43C |
probably damaging |
Het |
Scrn3 |
T |
A |
2: 73,149,845 (GRCm39) |
|
probably null |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Slc22a8 |
T |
C |
19: 8,585,597 (GRCm39) |
S321P |
probably benign |
Het |
Tex11 |
C |
A |
X: 99,977,021 (GRCm39) |
A487S |
possibly damaging |
Het |
Tex2 |
A |
G |
11: 106,458,398 (GRCm39) |
|
probably benign |
Het |
Trip13 |
A |
G |
13: 74,081,009 (GRCm39) |
I119T |
probably benign |
Het |
Tsku |
C |
T |
7: 98,002,205 (GRCm39) |
R42H |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,602,911 (GRCm39) |
I16691T |
possibly damaging |
Het |
Tyr |
A |
G |
7: 87,078,276 (GRCm39) |
L528P |
possibly damaging |
Het |
Uggt2 |
C |
T |
14: 119,286,674 (GRCm39) |
D221N |
probably damaging |
Het |
Wnt4 |
A |
G |
4: 137,023,654 (GRCm39) |
K207R |
possibly damaging |
Het |
Zfp608 |
T |
C |
18: 55,121,267 (GRCm39) |
R107G |
probably damaging |
Het |
|
Other mutations in Ubxn2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01912:Ubxn2b
|
APN |
4 |
6,203,767 (GRCm39) |
splice site |
probably null |
|
IGL02096:Ubxn2b
|
APN |
4 |
6,214,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02272:Ubxn2b
|
APN |
4 |
6,216,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Ubxn2b
|
UTSW |
4 |
6,203,875 (GRCm39) |
splice site |
probably benign |
|
R0482:Ubxn2b
|
UTSW |
4 |
6,196,404 (GRCm39) |
splice site |
probably null |
|
R1903:Ubxn2b
|
UTSW |
4 |
6,208,889 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5071:Ubxn2b
|
UTSW |
4 |
6,214,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7622:Ubxn2b
|
UTSW |
4 |
6,214,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R8034:Ubxn2b
|
UTSW |
4 |
6,191,167 (GRCm39) |
missense |
probably benign |
0.06 |
R8836:Ubxn2b
|
UTSW |
4 |
6,216,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R9156:Ubxn2b
|
UTSW |
4 |
6,214,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R9413:Ubxn2b
|
UTSW |
4 |
6,204,607 (GRCm39) |
missense |
probably damaging |
1.00 |
|