Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
T |
A |
2: 25,334,406 (GRCm39) |
S1868T |
possibly damaging |
Het |
Abca3 |
G |
A |
17: 24,616,327 (GRCm39) |
W923* |
probably null |
Het |
Abca8b |
A |
G |
11: 109,827,580 (GRCm39) |
M1476T |
probably damaging |
Het |
Abi3bp |
T |
C |
16: 56,498,163 (GRCm39) |
F729S |
probably damaging |
Het |
Acacb |
T |
C |
5: 114,356,919 (GRCm39) |
|
probably benign |
Het |
Aldh3a2 |
A |
G |
11: 61,139,731 (GRCm39) |
L467P |
probably benign |
Het |
Appl1 |
T |
C |
14: 26,684,795 (GRCm39) |
T85A |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,408,574 (GRCm39) |
I2487N |
possibly damaging |
Het |
Bcl2a1c |
G |
A |
9: 114,159,290 (GRCm39) |
V23I |
probably benign |
Het |
C2cd2 |
T |
A |
16: 97,676,323 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
A |
T |
14: 55,731,684 (GRCm39) |
H170L |
possibly damaging |
Het |
Ccdc141 |
C |
T |
2: 76,919,593 (GRCm39) |
V305I |
probably benign |
Het |
Ccdc174 |
G |
A |
6: 91,857,343 (GRCm39) |
|
probably null |
Het |
Cep126 |
T |
G |
9: 8,103,320 (GRCm39) |
Q230P |
possibly damaging |
Het |
Chrm1 |
T |
C |
19: 8,655,859 (GRCm39) |
I188T |
probably benign |
Het |
Depdc5 |
T |
C |
5: 33,081,544 (GRCm39) |
S569P |
probably damaging |
Het |
Drc1 |
G |
A |
5: 30,503,007 (GRCm39) |
E177K |
probably damaging |
Het |
Duox1 |
A |
G |
2: 122,164,279 (GRCm39) |
E913G |
probably benign |
Het |
Fbxw9 |
T |
C |
8: 85,791,055 (GRCm39) |
S241P |
probably damaging |
Het |
Fga |
G |
T |
3: 82,937,606 (GRCm39) |
R161L |
possibly damaging |
Het |
Fn3krp |
G |
T |
11: 121,320,533 (GRCm39) |
G293* |
probably null |
Het |
Gfra1 |
C |
T |
19: 58,255,479 (GRCm39) |
E318K |
probably benign |
Het |
Gli3 |
C |
T |
13: 15,823,219 (GRCm39) |
P314S |
probably damaging |
Het |
Gm5114 |
A |
T |
7: 39,057,490 (GRCm39) |
S710T |
probably benign |
Het |
Gpr141 |
T |
C |
13: 19,936,769 (GRCm39) |
D2G |
probably benign |
Het |
Inppl1 |
G |
A |
7: 101,483,041 (GRCm39) |
Q63* |
probably null |
Het |
Lrrc73 |
T |
A |
17: 46,566,657 (GRCm39) |
V169E |
possibly damaging |
Het |
Lsm11 |
C |
T |
11: 45,824,615 (GRCm39) |
R304Q |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,395,964 (GRCm39) |
D788G |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,533,898 (GRCm39) |
D1844E |
probably damaging |
Het |
Nt5c |
A |
G |
11: 115,382,161 (GRCm39) |
F73L |
probably damaging |
Het |
Osmr |
A |
T |
15: 6,854,085 (GRCm39) |
I541N |
probably damaging |
Het |
Phrf1 |
A |
G |
7: 140,840,413 (GRCm39) |
I1203V |
probably benign |
Het |
Pram1 |
C |
A |
17: 33,861,109 (GRCm39) |
P510Q |
possibly damaging |
Het |
Prepl |
A |
G |
17: 85,379,444 (GRCm39) |
Y415H |
probably benign |
Het |
Prss27 |
A |
T |
17: 24,264,650 (GRCm39) |
H271L |
probably damaging |
Het |
Ptpn18 |
A |
G |
1: 34,510,989 (GRCm39) |
S287G |
probably benign |
Het |
Ptprq |
T |
C |
10: 107,535,584 (GRCm39) |
|
probably benign |
Het |
Sars2 |
A |
G |
7: 28,446,974 (GRCm39) |
K218E |
probably benign |
Het |
Senp6 |
G |
T |
9: 79,999,676 (GRCm39) |
S31I |
probably damaging |
Het |
Shld2 |
G |
T |
14: 33,971,136 (GRCm39) |
T31K |
probably damaging |
Het |
Skint6 |
C |
A |
4: 113,095,246 (GRCm39) |
V138F |
probably damaging |
Het |
Slc4a8 |
C |
A |
15: 100,685,128 (GRCm39) |
H168N |
probably damaging |
Het |
Tbx15 |
T |
G |
3: 99,220,358 (GRCm39) |
I150S |
probably damaging |
Het |
Tbxas1 |
A |
G |
6: 38,959,125 (GRCm39) |
N103D |
probably benign |
Het |
Tmc5 |
A |
G |
7: 118,222,809 (GRCm39) |
N170D |
probably damaging |
Het |
Tmem108 |
A |
T |
9: 103,361,950 (GRCm39) |
N545K |
probably benign |
Het |
Trub1 |
A |
G |
19: 57,441,616 (GRCm39) |
K80E |
possibly damaging |
Het |
Tulp3 |
A |
T |
6: 128,302,923 (GRCm39) |
Y299N |
probably damaging |
Het |
|
Other mutations in Fez2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01307:Fez2
|
APN |
17 |
78,689,029 (GRCm39) |
splice site |
probably benign |
|
IGL02043:Fez2
|
APN |
17 |
78,689,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02898:Fez2
|
APN |
17 |
78,692,184 (GRCm39) |
missense |
probably benign |
0.03 |
R0433:Fez2
|
UTSW |
17 |
78,725,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R0472:Fez2
|
UTSW |
17 |
78,692,261 (GRCm39) |
splice site |
probably benign |
|
R0753:Fez2
|
UTSW |
17 |
78,708,115 (GRCm39) |
small deletion |
probably benign |
|
R4629:Fez2
|
UTSW |
17 |
78,710,183 (GRCm39) |
missense |
probably benign |
0.00 |
R4646:Fez2
|
UTSW |
17 |
78,720,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R5955:Fez2
|
UTSW |
17 |
78,694,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R8048:Fez2
|
UTSW |
17 |
78,694,482 (GRCm39) |
missense |
probably benign |
0.22 |
R8491:Fez2
|
UTSW |
17 |
78,692,200 (GRCm39) |
missense |
probably benign |
0.13 |
R8881:Fez2
|
UTSW |
17 |
78,689,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R9675:Fez2
|
UTSW |
17 |
78,686,169 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9775:Fez2
|
UTSW |
17 |
78,708,183 (GRCm39) |
missense |
probably damaging |
1.00 |
|