Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
C |
17: 24,616,474 (GRCm39) |
V972A |
probably benign |
Het |
Adamts14 |
T |
G |
10: 61,106,998 (GRCm39) |
T41P |
probably damaging |
Het |
Adamtsl3 |
C |
T |
7: 82,077,621 (GRCm39) |
T102I |
probably damaging |
Het |
Ago3 |
T |
C |
4: 126,264,109 (GRCm39) |
I366V |
probably null |
Het |
Aldh1a7 |
A |
G |
19: 20,692,067 (GRCm39) |
V242A |
possibly damaging |
Het |
Asxl3 |
T |
C |
18: 22,655,829 (GRCm39) |
S1280P |
probably benign |
Het |
Caprin1 |
G |
T |
2: 103,599,862 (GRCm39) |
N604K |
probably damaging |
Het |
Catsperb |
T |
C |
12: 101,412,305 (GRCm39) |
W131R |
probably damaging |
Het |
Ccdc18 |
A |
G |
5: 108,345,725 (GRCm39) |
E957G |
probably damaging |
Het |
Ccn6 |
T |
A |
10: 39,027,194 (GRCm39) |
D346V |
probably damaging |
Het |
Cd28 |
G |
A |
1: 60,785,681 (GRCm39) |
V17I |
probably benign |
Het |
Cfl2 |
A |
T |
12: 54,908,398 (GRCm39) |
L75* |
probably null |
Het |
Clspn |
T |
A |
4: 126,455,609 (GRCm39) |
L45H |
probably damaging |
Het |
Col4a2 |
A |
G |
8: 11,479,305 (GRCm39) |
|
probably null |
Het |
Cracd |
GCGCGAGGCCGAGAGGCAGGAGGAGGAAGCAAGACAACGCGAGGCCGAGAGGCAGG |
GCGCGAGGCCGAGAGGCAGG |
5: 77,004,801 (GRCm39) |
|
probably benign |
Het |
Dgka |
A |
T |
10: 128,556,881 (GRCm39) |
I663N |
probably damaging |
Het |
Eppk1 |
C |
T |
15: 75,993,249 (GRCm39) |
V1211I |
probably benign |
Het |
Fam193b |
A |
G |
13: 55,698,117 (GRCm39) |
S280P |
probably damaging |
Het |
Fgd2 |
C |
T |
17: 29,583,934 (GRCm39) |
A116V |
probably damaging |
Het |
Fmo5 |
C |
A |
3: 97,558,811 (GRCm39) |
Q424K |
probably benign |
Het |
Fn3k |
T |
C |
11: 121,340,987 (GRCm39) |
L214P |
probably damaging |
Het |
Gm3404 |
A |
T |
5: 146,465,108 (GRCm39) |
R283W |
possibly damaging |
Het |
Gtdc1 |
A |
G |
2: 44,678,993 (GRCm39) |
|
probably benign |
Het |
Hepacam |
T |
C |
9: 37,279,049 (GRCm39) |
I26T |
probably benign |
Het |
Hltf |
T |
C |
3: 20,152,291 (GRCm39) |
F596L |
probably damaging |
Het |
Ipo7 |
T |
G |
7: 109,652,000 (GRCm39) |
D926E |
probably benign |
Het |
Krt16 |
G |
A |
11: 100,137,083 (GRCm39) |
Q463* |
probably null |
Het |
Lats1 |
T |
C |
10: 7,588,613 (GRCm39) |
F1077L |
probably damaging |
Het |
Lrrc69 |
T |
C |
4: 14,704,014 (GRCm39) |
I269V |
probably benign |
Het |
Mcm6 |
C |
T |
1: 128,273,685 (GRCm39) |
E382K |
possibly damaging |
Het |
Npbwr1 |
A |
T |
1: 5,987,446 (GRCm39) |
C23S |
possibly damaging |
Het |
Nsd3 |
T |
C |
8: 26,184,811 (GRCm39) |
C962R |
probably damaging |
Het |
Nufip2 |
T |
C |
11: 77,583,391 (GRCm39) |
L435P |
probably damaging |
Het |
Or10d4c |
C |
T |
9: 39,558,798 (GRCm39) |
Q259* |
probably null |
Het |
Or1e23 |
T |
C |
11: 73,407,440 (GRCm39) |
N195S |
probably damaging |
Het |
Psen1 |
T |
C |
12: 83,761,630 (GRCm39) |
V144A |
possibly damaging |
Het |
Psmg2 |
T |
A |
18: 67,779,077 (GRCm39) |
S82T |
possibly damaging |
Het |
Ptcd2 |
A |
C |
13: 99,469,462 (GRCm39) |
F154V |
probably damaging |
Het |
Ptchd4 |
A |
C |
17: 42,813,512 (GRCm39) |
D471A |
probably benign |
Het |
Robo4 |
C |
T |
9: 37,315,674 (GRCm39) |
T309I |
possibly damaging |
Het |
Runx3 |
T |
C |
4: 134,898,455 (GRCm39) |
F209L |
probably damaging |
Het |
Setd1a |
T |
C |
7: 127,395,676 (GRCm39) |
|
probably benign |
Het |
Slc35g3 |
T |
C |
11: 69,652,446 (GRCm39) |
E22G |
probably benign |
Het |
Spag9 |
T |
A |
11: 94,013,647 (GRCm39) |
M1303K |
possibly damaging |
Het |
Ssh2 |
T |
A |
11: 77,340,533 (GRCm39) |
S562T |
probably benign |
Het |
Tiparp |
T |
C |
3: 65,453,798 (GRCm39) |
|
probably null |
Het |
Topbp1 |
C |
T |
9: 103,213,264 (GRCm39) |
P1028L |
probably benign |
Het |
Unc45a |
A |
T |
7: 79,975,840 (GRCm39) |
L833Q |
possibly damaging |
Het |
Vmn2r85 |
T |
C |
10: 130,261,311 (GRCm39) |
Y342C |
probably damaging |
Het |
Vmn2r95 |
G |
A |
17: 18,664,161 (GRCm39) |
C460Y |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,852,848 (GRCm39) |
I2376N |
probably damaging |
Het |
Zbtb21 |
C |
A |
16: 97,753,315 (GRCm39) |
A351S |
possibly damaging |
Het |
Zzef1 |
T |
G |
11: 72,735,267 (GRCm39) |
Y623D |
probably damaging |
Het |
|
Other mutations in Potegl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00694:Potegl
|
APN |
2 |
23,120,180 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02141:Potegl
|
APN |
2 |
23,120,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Potegl
|
APN |
2 |
23,102,667 (GRCm39) |
intron |
probably benign |
|
IGL03328:Potegl
|
APN |
2 |
23,102,817 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0467:Potegl
|
UTSW |
2 |
23,102,832 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0723:Potegl
|
UTSW |
2 |
23,146,936 (GRCm39) |
splice site |
probably benign |
|
R1169:Potegl
|
UTSW |
2 |
23,146,994 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1507:Potegl
|
UTSW |
2 |
23,098,086 (GRCm39) |
missense |
probably damaging |
0.98 |
R4965:Potegl
|
UTSW |
2 |
23,135,127 (GRCm39) |
missense |
probably benign |
0.40 |
R5198:Potegl
|
UTSW |
2 |
23,102,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R5619:Potegl
|
UTSW |
2 |
23,147,017 (GRCm39) |
critical splice donor site |
probably null |
|
R5677:Potegl
|
UTSW |
2 |
23,102,730 (GRCm39) |
missense |
probably damaging |
0.98 |
R5715:Potegl
|
UTSW |
2 |
23,097,989 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6123:Potegl
|
UTSW |
2 |
23,120,134 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6263:Potegl
|
UTSW |
2 |
23,156,745 (GRCm39) |
unclassified |
probably benign |
|
R6858:Potegl
|
UTSW |
2 |
23,102,676 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7427:Potegl
|
UTSW |
2 |
23,147,006 (GRCm39) |
missense |
probably benign |
|
R7577:Potegl
|
UTSW |
2 |
23,097,837 (GRCm39) |
missense |
probably benign |
|
R8086:Potegl
|
UTSW |
2 |
23,130,934 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8342:Potegl
|
UTSW |
2 |
23,147,017 (GRCm39) |
critical splice donor site |
probably null |
|
R8495:Potegl
|
UTSW |
2 |
23,097,852 (GRCm39) |
missense |
probably benign |
0.26 |
|