Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
G |
6: 121,647,957 (GRCm39) |
L1150V |
probably damaging |
Het |
AB124611 |
A |
G |
9: 21,455,989 (GRCm39) |
D194G |
possibly damaging |
Het |
Adgrv1 |
A |
G |
13: 81,669,302 (GRCm39) |
L2418P |
probably benign |
Het |
Ap3m1 |
A |
G |
14: 21,090,152 (GRCm39) |
S213P |
probably damaging |
Het |
Apobec2 |
A |
T |
17: 48,739,531 (GRCm39) |
L36H |
|
Het |
Arrb1 |
A |
G |
7: 99,237,280 (GRCm39) |
D78G |
|
Het |
Astn1 |
A |
G |
1: 158,338,555 (GRCm39) |
Q434R |
probably damaging |
Het |
Cadps |
C |
G |
14: 12,705,676 (GRCm38) |
D240H |
probably damaging |
Het |
Cfhr4 |
A |
G |
1: 139,660,085 (GRCm39) |
I680T |
probably damaging |
Het |
Cmya5 |
A |
C |
13: 93,233,878 (GRCm39) |
D403E |
unknown |
Het |
Crxos |
A |
C |
7: 15,631,436 (GRCm39) |
I45L |
probably benign |
Het |
Dmxl1 |
C |
G |
18: 50,072,639 (GRCm39) |
N2744K |
probably damaging |
Het |
Dnah2 |
A |
G |
11: 69,313,687 (GRCm39) |
I4204T |
|
Het |
Ei24 |
A |
G |
9: 36,697,327 (GRCm39) |
S134P |
probably damaging |
Het |
Eif2ak3 |
G |
T |
6: 70,860,614 (GRCm39) |
V397F |
probably damaging |
Het |
Eif4g2 |
T |
C |
7: 110,672,969 (GRCm39) |
I134V |
|
Het |
Fam186a |
A |
G |
15: 99,841,159 (GRCm39) |
I1695T |
possibly damaging |
Het |
Gcnt3 |
T |
C |
9: 69,941,939 (GRCm39) |
M210V |
probably damaging |
Het |
Gpatch8 |
A |
G |
11: 102,370,299 (GRCm39) |
S1080P |
probably benign |
Het |
Gtf3c1 |
A |
G |
7: 125,244,949 (GRCm39) |
L1695P |
possibly damaging |
Het |
Haus3 |
A |
G |
5: 34,324,994 (GRCm39) |
F222L |
probably damaging |
Het |
Kbtbd8 |
C |
T |
6: 95,099,825 (GRCm39) |
Q445* |
probably null |
Het |
Kcnc3 |
A |
G |
7: 44,240,592 (GRCm39) |
N95D |
probably damaging |
Het |
Krt40 |
C |
T |
11: 99,430,693 (GRCm39) |
|
probably null |
Het |
Lgi1 |
A |
G |
19: 38,289,746 (GRCm39) |
T271A |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Map3k21 |
A |
G |
8: 126,665,463 (GRCm39) |
T551A |
possibly damaging |
Het |
Muc5ac |
T |
C |
7: 141,363,529 (GRCm39) |
I2280T |
unknown |
Het |
Mug1 |
C |
A |
6: 121,851,390 (GRCm39) |
D762E |
probably damaging |
Het |
Myo1e |
A |
T |
9: 70,266,605 (GRCm39) |
N615I |
probably damaging |
Het |
Or4k36 |
T |
C |
2: 111,145,827 (GRCm39) |
M1T |
probably null |
Het |
Or51f23 |
T |
C |
7: 102,453,339 (GRCm39) |
L218P |
probably damaging |
Het |
Pld5 |
T |
C |
1: 175,803,104 (GRCm39) |
E387G |
possibly damaging |
Het |
Pld5 |
A |
G |
1: 175,902,003 (GRCm39) |
V195A |
probably benign |
Het |
Rad54l |
T |
C |
4: 115,980,349 (GRCm39) |
|
probably benign |
Het |
Rnf123 |
A |
T |
9: 107,940,227 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,331,574 (GRCm39) |
E2262G |
|
Het |
Rp1 |
C |
A |
1: 4,234,161 (GRCm39) |
V910L |
unknown |
Het |
Rpp21 |
A |
T |
17: 36,568,407 (GRCm39) |
C23S |
probably benign |
Het |
Scn11a |
T |
C |
9: 119,588,989 (GRCm39) |
M1306V |
possibly damaging |
Het |
Scn2b |
C |
T |
9: 45,036,734 (GRCm39) |
L81F |
possibly damaging |
Het |
Sco2 |
T |
C |
15: 89,256,363 (GRCm39) |
D97G |
probably damaging |
Het |
Slc25a54 |
T |
C |
3: 109,001,548 (GRCm39) |
V112A |
probably benign |
Het |
Slc5a11 |
A |
T |
7: 122,864,492 (GRCm39) |
K363* |
probably null |
Het |
Smg1 |
G |
T |
7: 117,753,884 (GRCm39) |
T2563K |
unknown |
Het |
Snap47 |
A |
T |
11: 59,319,290 (GRCm39) |
S283T |
probably damaging |
Het |
Speer4a3 |
CTTT |
C |
5: 26,155,857 (GRCm39) |
|
probably benign |
Het |
Stat1 |
G |
T |
1: 52,178,388 (GRCm39) |
R274L |
probably damaging |
Het |
Stoml1 |
A |
G |
9: 58,164,409 (GRCm39) |
T166A |
|
Het |
Svs5 |
G |
T |
2: 164,079,509 (GRCm39) |
Q133K |
probably benign |
Het |
Tas2r107 |
T |
A |
6: 131,636,422 (GRCm39) |
H209L |
probably benign |
Het |
Tmco3 |
T |
A |
8: 13,360,228 (GRCm39) |
V477D |
possibly damaging |
Het |
Tmem131 |
A |
T |
1: 36,880,767 (GRCm39) |
S168T |
possibly damaging |
Het |
Tmem41a |
T |
C |
16: 21,755,859 (GRCm39) |
N149S |
probably damaging |
Het |
Ttll4 |
T |
C |
1: 74,719,225 (GRCm39) |
F359L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,785,162 (GRCm39) |
M784L |
unknown |
Het |
Ubr1 |
A |
G |
2: 120,703,603 (GRCm39) |
|
probably null |
Het |
Upb1 |
C |
T |
10: 75,265,961 (GRCm39) |
L263F |
probably benign |
Het |
Usp15 |
T |
A |
10: 122,949,553 (GRCm39) |
T935S |
probably benign |
Het |
Zscan4-ps3 |
G |
A |
7: 11,347,164 (GRCm39) |
C400Y |
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 |
R4206:Ubxn2b
|
UTSW |
4 |
6,204,565 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
R9413:Ubxn2b
|
UTSW |
4 |
6,204,607 (GRCm39) |
missense |
probably damaging |
1.00 |
|