Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg3 |
A |
G |
17: 57,187,494 (GRCm39) |
N136S |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,659,303 (GRCm39) |
S496P |
probably damaging |
Het |
Agbl3 |
T |
A |
6: 34,762,242 (GRCm39) |
S81T |
possibly damaging |
Het |
Apobec1 |
A |
T |
6: 122,558,531 (GRCm39) |
Y75N |
probably benign |
Het |
Asic2 |
A |
G |
11: 80,772,479 (GRCm39) |
L517P |
probably benign |
Het |
Atp8a1 |
A |
G |
5: 67,840,126 (GRCm39) |
S752P |
probably damaging |
Het |
Blm |
T |
C |
7: 80,145,754 (GRCm39) |
Y775C |
probably damaging |
Het |
C1qtnf5 |
T |
C |
9: 44,019,901 (GRCm39) |
I175T |
probably benign |
Het |
Ccdc81 |
G |
A |
7: 89,524,946 (GRCm39) |
T545I |
probably benign |
Het |
Ccdc88b |
T |
C |
19: 6,834,317 (GRCm39) |
E174G |
probably damaging |
Het |
Chl1 |
G |
A |
6: 103,692,330 (GRCm39) |
V1066M |
probably damaging |
Het |
Cntn6 |
T |
A |
6: 104,823,103 (GRCm39) |
|
probably null |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cyren |
T |
C |
6: 34,851,404 (GRCm39) |
Y150C |
probably damaging |
Het |
Cysrt1 |
T |
C |
2: 25,129,360 (GRCm39) |
I51V |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,725,702 (GRCm39) |
N69S |
probably benign |
Het |
Gm9631 |
G |
A |
11: 121,834,478 (GRCm39) |
|
|
Het |
Hmcn1 |
T |
C |
1: 150,598,175 (GRCm39) |
Y1709C |
probably damaging |
Het |
Inppl1 |
G |
A |
7: 101,481,526 (GRCm39) |
|
probably benign |
Het |
Iqcc |
T |
C |
4: 129,510,748 (GRCm39) |
T256A |
probably benign |
Het |
Itprid2 |
T |
C |
2: 79,465,986 (GRCm39) |
S35P |
probably damaging |
Het |
Lyst |
G |
A |
13: 13,835,541 (GRCm39) |
C1741Y |
probably benign |
Het |
Lyz1 |
A |
T |
10: 117,124,535 (GRCm39) |
C134S |
probably damaging |
Het |
Mpzl3 |
T |
C |
9: 44,977,815 (GRCm39) |
I141T |
possibly damaging |
Het |
Mterf1a |
T |
C |
5: 3,941,047 (GRCm39) |
N274D |
probably damaging |
Het |
Myo18a |
T |
A |
11: 77,709,519 (GRCm39) |
V543D |
possibly damaging |
Het |
Myo18b |
A |
T |
5: 112,975,852 (GRCm39) |
D1332E |
possibly damaging |
Het |
Or2r11 |
A |
G |
6: 42,437,110 (GRCm39) |
V281A |
probably benign |
Het |
Pcdh15 |
A |
T |
10: 74,138,938 (GRCm39) |
D333V |
probably damaging |
Het |
Plekha7 |
A |
G |
7: 115,757,469 (GRCm39) |
Y494H |
probably damaging |
Het |
Plekhg1 |
A |
G |
10: 3,914,106 (GRCm39) |
N1276S |
probably damaging |
Het |
Ppig |
T |
C |
2: 69,562,571 (GRCm39) |
V5A |
probably benign |
Het |
Prag1 |
A |
T |
8: 36,614,580 (GRCm39) |
|
probably benign |
Het |
Prom1 |
T |
C |
5: 44,220,496 (GRCm39) |
N84S |
probably benign |
Het |
Ptprh |
T |
A |
7: 4,583,929 (GRCm39) |
Y221F |
probably damaging |
Het |
Qsox2 |
A |
G |
2: 26,110,731 (GRCm39) |
Y162H |
probably benign |
Het |
Rab2a |
C |
T |
4: 8,572,553 (GRCm39) |
T49M |
possibly damaging |
Het |
Ring1 |
A |
G |
17: 34,242,122 (GRCm39) |
S96P |
possibly damaging |
Het |
Ripk3 |
A |
G |
14: 56,022,691 (GRCm39) |
F411S |
probably benign |
Het |
Rock1 |
T |
C |
18: 10,070,619 (GRCm39) |
|
probably null |
Het |
Rtn4rl1 |
A |
G |
11: 75,156,645 (GRCm39) |
N359S |
probably damaging |
Het |
Sufu |
A |
G |
19: 46,413,481 (GRCm39) |
T76A |
probably damaging |
Het |
Sugct |
C |
A |
13: 17,627,053 (GRCm39) |
V267F |
probably damaging |
Het |
Tcf4 |
A |
T |
18: 69,697,210 (GRCm39) |
R29W |
probably damaging |
Het |
Tnfsf18 |
A |
T |
1: 161,331,158 (GRCm39) |
I103L |
probably benign |
Het |
Vwf |
A |
G |
6: 125,654,879 (GRCm39) |
E2525G |
probably benign |
Het |
|
Other mutations in Fam83d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02066:Fam83d
|
APN |
2 |
158,627,793 (GRCm39) |
missense |
probably benign |
0.37 |
R0277:Fam83d
|
UTSW |
2 |
158,627,467 (GRCm39) |
missense |
probably benign |
0.05 |
R0323:Fam83d
|
UTSW |
2 |
158,627,467 (GRCm39) |
missense |
probably benign |
0.05 |
R0349:Fam83d
|
UTSW |
2 |
158,621,768 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0571:Fam83d
|
UTSW |
2 |
158,627,611 (GRCm39) |
nonsense |
probably null |
|
R0799:Fam83d
|
UTSW |
2 |
158,621,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R1164:Fam83d
|
UTSW |
2 |
158,625,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1168:Fam83d
|
UTSW |
2 |
158,610,443 (GRCm39) |
missense |
probably benign |
0.01 |
R1186:Fam83d
|
UTSW |
2 |
158,627,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Fam83d
|
UTSW |
2 |
158,610,070 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2896:Fam83d
|
UTSW |
2 |
158,627,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4500:Fam83d
|
UTSW |
2 |
158,627,187 (GRCm39) |
missense |
probably benign |
0.10 |
R4597:Fam83d
|
UTSW |
2 |
158,627,142 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5416:Fam83d
|
UTSW |
2 |
158,627,552 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5866:Fam83d
|
UTSW |
2 |
158,621,750 (GRCm39) |
splice site |
probably null |
|
R6328:Fam83d
|
UTSW |
2 |
158,627,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R6364:Fam83d
|
UTSW |
2 |
158,625,179 (GRCm39) |
critical splice donor site |
probably null |
|
R7031:Fam83d
|
UTSW |
2 |
158,627,227 (GRCm39) |
missense |
probably benign |
0.01 |
R8721:Fam83d
|
UTSW |
2 |
158,627,522 (GRCm39) |
missense |
probably benign |
0.33 |
R9208:Fam83d
|
UTSW |
2 |
158,610,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:Fam83d
|
UTSW |
2 |
158,610,310 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fam83d
|
UTSW |
2 |
158,627,108 (GRCm39) |
missense |
probably damaging |
1.00 |
|