Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
C |
6: 23,107,709 (GRCm39) |
D358G |
possibly damaging |
Het |
Adam26a |
A |
T |
8: 44,022,178 (GRCm39) |
C437* |
probably null |
Het |
Arhgap10 |
A |
T |
8: 78,037,468 (GRCm39) |
C587S |
probably benign |
Het |
Bank1 |
G |
A |
3: 135,948,721 (GRCm39) |
T285I |
probably benign |
Het |
Bhlha15 |
C |
T |
5: 144,128,257 (GRCm39) |
S123L |
probably damaging |
Het |
Cacul1 |
T |
C |
19: 60,517,475 (GRCm39) |
*305W |
probably null |
Het |
Cep112 |
A |
C |
11: 108,393,977 (GRCm39) |
K365T |
probably damaging |
Het |
Chrm1 |
T |
A |
19: 8,656,453 (GRCm39) |
L386Q |
probably damaging |
Het |
Cnbp |
C |
A |
6: 87,822,194 (GRCm39) |
R110L |
probably damaging |
Het |
Cntnap5a |
A |
T |
1: 116,116,140 (GRCm39) |
I541F |
possibly damaging |
Het |
Dscaml1 |
T |
G |
9: 45,658,438 (GRCm39) |
|
probably benign |
Het |
Enpp3 |
C |
T |
10: 24,653,824 (GRCm39) |
S711N |
probably damaging |
Het |
Eps8 |
G |
T |
6: 137,459,252 (GRCm39) |
N750K |
probably benign |
Het |
Fan1 |
G |
T |
7: 64,023,054 (GRCm39) |
N66K |
probably benign |
Het |
Fbf1 |
G |
A |
11: 116,044,845 (GRCm39) |
T323I |
probably benign |
Het |
Flg2 |
A |
T |
3: 93,127,517 (GRCm39) |
N2143I |
unknown |
Het |
Fn3k |
A |
C |
11: 121,339,744 (GRCm39) |
T169P |
probably benign |
Het |
Fubp1 |
T |
G |
3: 151,926,356 (GRCm39) |
I320R |
probably damaging |
Het |
Gfpt2 |
A |
T |
11: 49,714,607 (GRCm39) |
E335D |
probably benign |
Het |
Gm17472 |
T |
C |
6: 42,957,968 (GRCm39) |
I79T |
probably benign |
Het |
Gpr179 |
G |
A |
11: 97,226,983 (GRCm39) |
S1724L |
probably benign |
Het |
Gtf2h3 |
C |
A |
5: 124,728,967 (GRCm39) |
Y175* |
probably null |
Het |
Hal |
T |
A |
10: 93,328,369 (GRCm39) |
I215N |
probably damaging |
Het |
Htt |
A |
G |
5: 35,053,304 (GRCm39) |
T2546A |
probably benign |
Het |
Ighv1-11 |
T |
C |
12: 114,576,077 (GRCm39) |
Y46C |
probably damaging |
Het |
Lcn4 |
T |
C |
2: 26,558,375 (GRCm39) |
D170G |
probably benign |
Het |
Lrch1 |
T |
A |
14: 75,055,935 (GRCm39) |
D306V |
probably damaging |
Het |
Mtcl1 |
A |
C |
17: 66,650,653 (GRCm39) |
V1604G |
probably damaging |
Het |
Or10g3b |
T |
C |
14: 52,586,625 (GRCm39) |
N293D |
probably damaging |
Het |
Or3a10 |
A |
G |
11: 73,935,926 (GRCm39) |
L58P |
probably damaging |
Het |
Or4c108 |
T |
G |
2: 88,803,552 (GRCm39) |
S228R |
probably damaging |
Het |
Or4k49 |
T |
G |
2: 111,494,587 (GRCm39) |
N5K |
possibly damaging |
Het |
Or9i1b |
G |
A |
19: 13,897,226 (GRCm39) |
V281I |
probably benign |
Het |
Ormdl2 |
A |
G |
10: 128,654,837 (GRCm39) |
L125P |
possibly damaging |
Het |
Pcnx3 |
C |
T |
19: 5,715,412 (GRCm39) |
G1946E |
probably damaging |
Het |
Pde3a |
T |
A |
6: 141,433,527 (GRCm39) |
F803Y |
possibly damaging |
Het |
Pnpla7 |
C |
T |
2: 24,873,635 (GRCm39) |
R214W |
probably damaging |
Het |
Prtg |
T |
C |
9: 72,813,520 (GRCm39) |
V960A |
probably benign |
Het |
Ptgdr |
T |
C |
14: 45,090,858 (GRCm39) |
E300G |
probably benign |
Het |
Ptpru |
G |
T |
4: 131,522,274 (GRCm39) |
Y710* |
probably null |
Het |
Pxdn |
T |
A |
12: 30,049,195 (GRCm39) |
Y620* |
probably null |
Het |
Pycard |
T |
C |
7: 127,592,797 (GRCm39) |
D10G |
possibly damaging |
Het |
Sh3d21 |
G |
T |
4: 126,055,775 (GRCm39) |
Q160K |
probably benign |
Het |
Slc26a7 |
G |
A |
4: 14,621,269 (GRCm39) |
P39L |
probably benign |
Het |
Snrnp200 |
T |
A |
2: 127,068,928 (GRCm39) |
Y936N |
probably damaging |
Het |
Sox8 |
T |
C |
17: 25,786,617 (GRCm39) |
D362G |
possibly damaging |
Het |
Tcp11 |
T |
G |
17: 28,286,001 (GRCm39) |
N538T |
probably damaging |
Het |
Tent2 |
T |
C |
13: 93,310,997 (GRCm39) |
|
probably benign |
Het |
Tmem132e |
A |
C |
11: 82,325,666 (GRCm39) |
E222A |
probably benign |
Het |
Trpc7 |
T |
C |
13: 56,937,602 (GRCm39) |
E618G |
probably benign |
Het |
Tsc2 |
G |
T |
17: 24,833,340 (GRCm39) |
Q695K |
probably benign |
Het |
Txlnb |
C |
A |
10: 17,718,752 (GRCm39) |
L528M |
possibly damaging |
Het |
Vmn1r176 |
A |
G |
7: 23,534,878 (GRCm39) |
Y92H |
probably benign |
Het |
Vmn2r85 |
T |
A |
10: 130,254,738 (GRCm39) |
I649F |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,171,272 (GRCm39) |
|
probably null |
Het |
Wrn |
A |
T |
8: 33,814,274 (GRCm39) |
I390N |
probably benign |
Het |
Zfp493 |
T |
A |
13: 67,934,976 (GRCm39) |
C310S |
probably damaging |
Het |
|
Other mutations in Gpr151 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02631:Gpr151
|
APN |
18 |
42,711,835 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03167:Gpr151
|
APN |
18 |
42,711,439 (GRCm39) |
missense |
probably benign |
0.06 |
R1561:Gpr151
|
UTSW |
18 |
42,712,221 (GRCm39) |
missense |
probably benign |
0.42 |
R3875:Gpr151
|
UTSW |
18 |
42,711,661 (GRCm39) |
missense |
probably benign |
0.02 |
R4294:Gpr151
|
UTSW |
18 |
42,711,602 (GRCm39) |
missense |
probably benign |
0.00 |
R5188:Gpr151
|
UTSW |
18 |
42,711,820 (GRCm39) |
missense |
probably benign |
|
R5431:Gpr151
|
UTSW |
18 |
42,711,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R5815:Gpr151
|
UTSW |
18 |
42,712,450 (GRCm39) |
missense |
probably benign |
0.00 |
R6199:Gpr151
|
UTSW |
18 |
42,711,619 (GRCm39) |
missense |
probably benign |
0.31 |
R6302:Gpr151
|
UTSW |
18 |
42,712,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R6891:Gpr151
|
UTSW |
18 |
42,711,985 (GRCm39) |
missense |
probably benign |
0.15 |
R7180:Gpr151
|
UTSW |
18 |
42,712,021 (GRCm39) |
nonsense |
probably null |
|
R9328:Gpr151
|
UTSW |
18 |
42,712,270 (GRCm39) |
missense |
probably damaging |
0.98 |
R9421:Gpr151
|
UTSW |
18 |
42,712,220 (GRCm39) |
missense |
probably benign |
0.00 |
R9524:Gpr151
|
UTSW |
18 |
42,712,710 (GRCm39) |
unclassified |
probably benign |
|
|