Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aurka |
T |
C |
2: 172,199,117 (GRCm39) |
M318V |
probably benign |
Het |
Cacna2d1 |
T |
A |
5: 16,531,342 (GRCm39) |
D560E |
probably damaging |
Het |
Ccdc148 |
T |
A |
2: 58,872,988 (GRCm39) |
T202S |
probably benign |
Het |
Cdc42bpb |
T |
C |
12: 111,271,412 (GRCm39) |
D1149G |
probably damaging |
Het |
Clasp1 |
T |
A |
1: 118,390,285 (GRCm39) |
N156K |
probably damaging |
Het |
Cox18 |
G |
A |
5: 90,365,434 (GRCm39) |
T255I |
possibly damaging |
Het |
Cse1l |
A |
G |
2: 166,783,394 (GRCm39) |
T783A |
probably damaging |
Het |
Dnajc16 |
T |
C |
4: 141,491,996 (GRCm39) |
Y609C |
probably damaging |
Het |
Doc2g |
A |
G |
19: 4,056,630 (GRCm39) |
T339A |
probably benign |
Het |
Eif5a |
T |
C |
11: 69,808,896 (GRCm39) |
|
probably benign |
Het |
Epha3 |
A |
G |
16: 63,386,940 (GRCm39) |
|
probably null |
Het |
Esco1 |
A |
T |
18: 10,594,355 (GRCm39) |
C310* |
probably null |
Het |
Fam222a |
A |
G |
5: 114,749,101 (GRCm39) |
Y99C |
probably damaging |
Het |
Fzd2 |
T |
C |
11: 102,496,573 (GRCm39) |
L339P |
probably damaging |
Het |
Gfral |
A |
T |
9: 76,104,576 (GRCm39) |
N145K |
probably damaging |
Het |
Gga1 |
T |
A |
15: 78,777,990 (GRCm39) |
N618K |
probably benign |
Het |
Gpatch3 |
T |
A |
4: 133,310,397 (GRCm39) |
H447Q |
probably damaging |
Het |
Gpn1 |
A |
T |
5: 31,666,747 (GRCm39) |
R346* |
probably null |
Het |
Gsg1 |
T |
C |
6: 135,214,558 (GRCm39) |
E317G |
probably benign |
Het |
Gsk3b |
A |
G |
16: 38,004,816 (GRCm39) |
N129S |
probably damaging |
Het |
Hmg20b |
G |
T |
10: 81,184,789 (GRCm39) |
D94E |
possibly damaging |
Het |
Kash5 |
C |
T |
7: 44,849,695 (GRCm39) |
G76D |
probably benign |
Het |
Klhdc9 |
T |
A |
1: 171,187,386 (GRCm39) |
H204L |
possibly damaging |
Het |
Klhl24 |
A |
G |
16: 19,925,638 (GRCm39) |
I55M |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,520,104 (GRCm39) |
D2002G |
probably benign |
Het |
Lama4 |
A |
G |
10: 38,950,742 (GRCm39) |
N1015S |
probably damaging |
Het |
Lpp |
T |
C |
16: 24,580,697 (GRCm39) |
C263R |
probably benign |
Het |
Lrp1b |
T |
C |
2: 41,159,216 (GRCm39) |
I1689V |
|
Het |
Mipep |
C |
A |
14: 61,022,284 (GRCm39) |
Q50K |
probably benign |
Het |
Mx1 |
T |
C |
16: 97,257,454 (GRCm39) |
D101G |
probably benign |
Het |
Nabp2 |
C |
G |
10: 128,244,676 (GRCm39) |
E37Q |
possibly damaging |
Het |
Nme6 |
A |
G |
9: 109,671,104 (GRCm39) |
I115V |
possibly damaging |
Het |
Nup93 |
A |
T |
8: 94,970,355 (GRCm39) |
T85S |
probably benign |
Het |
Oit3 |
T |
A |
10: 59,266,835 (GRCm39) |
I224F |
possibly damaging |
Het |
Parp14 |
T |
C |
16: 35,678,975 (GRCm39) |
K331R |
probably benign |
Het |
Pls1 |
T |
A |
9: 95,643,443 (GRCm39) |
T519S |
probably benign |
Het |
Rcn3 |
A |
G |
7: 44,736,118 (GRCm39) |
F197L |
probably benign |
Het |
Rnf213 |
C |
T |
11: 119,349,218 (GRCm39) |
T3773I |
|
Het |
Rprd1b |
A |
T |
2: 157,889,877 (GRCm39) |
I153L |
probably benign |
Het |
Scel |
A |
G |
14: 103,829,804 (GRCm39) |
D462G |
possibly damaging |
Het |
Sh3bp1 |
C |
T |
15: 78,794,276 (GRCm39) |
S548L |
possibly damaging |
Het |
Sim1 |
T |
A |
10: 50,860,284 (GRCm39) |
Y715* |
probably null |
Het |
Slc18a2 |
A |
T |
19: 59,282,293 (GRCm39) |
Q500L |
possibly damaging |
Het |
Slc5a8 |
T |
G |
10: 88,722,365 (GRCm39) |
M66R |
probably damaging |
Het |
Slco1a6 |
T |
C |
6: 142,055,246 (GRCm39) |
T233A |
probably damaging |
Het |
Smu1 |
T |
C |
4: 40,739,623 (GRCm39) |
T396A |
probably benign |
Het |
Tas2r104 |
T |
C |
6: 131,662,521 (GRCm39) |
T63A |
possibly damaging |
Het |
Tasor2 |
G |
A |
13: 3,624,979 (GRCm39) |
A1657V |
possibly damaging |
Het |
Top2a |
C |
T |
11: 98,892,199 (GRCm39) |
A1088T |
probably benign |
Het |
Unc13b |
T |
A |
4: 43,091,298 (GRCm39) |
D41E |
probably benign |
Het |
Usp10 |
T |
G |
8: 120,681,631 (GRCm39) |
V696G |
probably benign |
Het |
Xylt2 |
C |
T |
11: 94,557,066 (GRCm39) |
V745M |
probably damaging |
Het |
Zbtb49 |
A |
T |
5: 38,373,820 (GRCm39) |
N41K |
probably damaging |
Het |
Zfp109 |
T |
A |
7: 23,928,779 (GRCm39) |
D218V |
probably benign |
Het |
Zfp420 |
G |
A |
7: 29,575,430 (GRCm39) |
R550Q |
probably benign |
Het |
|
Other mutations in Ucp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0050:Ucp1
|
UTSW |
8 |
84,020,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Ucp1
|
UTSW |
8 |
84,017,233 (GRCm39) |
nonsense |
probably null |
|
R0055:Ucp1
|
UTSW |
8 |
84,017,233 (GRCm39) |
nonsense |
probably null |
|
R0505:Ucp1
|
UTSW |
8 |
84,021,936 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0590:Ucp1
|
UTSW |
8 |
84,018,232 (GRCm39) |
splice site |
probably benign |
|
R0681:Ucp1
|
UTSW |
8 |
84,021,936 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0731:Ucp1
|
UTSW |
8 |
84,024,476 (GRCm39) |
splice site |
probably benign |
|
R1606:Ucp1
|
UTSW |
8 |
84,021,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R1722:Ucp1
|
UTSW |
8 |
84,017,317 (GRCm39) |
missense |
probably benign |
0.25 |
R1809:Ucp1
|
UTSW |
8 |
84,024,496 (GRCm39) |
missense |
probably damaging |
0.99 |
R1823:Ucp1
|
UTSW |
8 |
84,020,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R3809:Ucp1
|
UTSW |
8 |
84,017,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R4085:Ucp1
|
UTSW |
8 |
84,020,580 (GRCm39) |
missense |
probably benign |
0.43 |
R4673:Ucp1
|
UTSW |
8 |
84,021,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Ucp1
|
UTSW |
8 |
84,024,484 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5163:Ucp1
|
UTSW |
8 |
84,020,832 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5421:Ucp1
|
UTSW |
8 |
84,017,320 (GRCm39) |
missense |
probably benign |
0.12 |
R5790:Ucp1
|
UTSW |
8 |
84,024,520 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5994:Ucp1
|
UTSW |
8 |
84,020,567 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6574:Ucp1
|
UTSW |
8 |
84,020,718 (GRCm39) |
critical splice donor site |
probably null |
|
R6732:Ucp1
|
UTSW |
8 |
84,018,106 (GRCm39) |
missense |
probably benign |
0.08 |
R7282:Ucp1
|
UTSW |
8 |
84,020,531 (GRCm39) |
missense |
probably benign |
0.03 |
R7343:Ucp1
|
UTSW |
8 |
84,021,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R7878:Ucp1
|
UTSW |
8 |
84,024,521 (GRCm39) |
missense |
probably benign |
0.19 |
R8008:Ucp1
|
UTSW |
8 |
84,020,640 (GRCm39) |
missense |
probably benign |
0.32 |
R8365:Ucp1
|
UTSW |
8 |
84,020,628 (GRCm39) |
missense |
probably damaging |
0.97 |
R8899:Ucp1
|
UTSW |
8 |
84,017,216 (GRCm39) |
missense |
probably benign |
0.35 |
R9186:Ucp1
|
UTSW |
8 |
84,017,272 (GRCm39) |
nonsense |
probably null |
|
R9499:Ucp1
|
UTSW |
8 |
84,024,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9551:Ucp1
|
UTSW |
8 |
84,024,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9552:Ucp1
|
UTSW |
8 |
84,024,509 (GRCm39) |
missense |
probably damaging |
1.00 |
|