Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001O22Rik |
A |
T |
2: 30,686,458 (GRCm39) |
V278D |
possibly damaging |
Het |
Acacb |
A |
G |
5: 114,322,167 (GRCm39) |
D227G |
possibly damaging |
Het |
Akap9 |
A |
G |
5: 4,096,064 (GRCm39) |
E2313G |
probably benign |
Het |
Cchcr1 |
A |
T |
17: 35,839,745 (GRCm39) |
E564D |
probably damaging |
Het |
Cers2 |
G |
A |
3: 95,229,008 (GRCm39) |
|
probably benign |
Het |
Ciita |
A |
T |
16: 10,329,669 (GRCm39) |
E648V |
possibly damaging |
Het |
Cir1 |
C |
T |
2: 73,142,804 (GRCm39) |
C10Y |
probably damaging |
Het |
Clasp1 |
T |
A |
1: 118,518,214 (GRCm39) |
F1087I |
probably damaging |
Het |
Cped1 |
C |
A |
6: 22,138,681 (GRCm39) |
F415L |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,181,292 (GRCm39) |
T1060A |
possibly damaging |
Het |
Epha5 |
G |
T |
5: 84,232,587 (GRCm39) |
P809H |
probably damaging |
Het |
Fuca1 |
T |
A |
4: 135,650,273 (GRCm39) |
|
probably null |
Het |
Galnt2l |
A |
T |
8: 123,627,372 (GRCm39) |
*98R |
probably null |
Het |
Gm26796 |
G |
A |
12: 80,805,564 (GRCm39) |
R237C |
unknown |
Het |
Idua |
A |
G |
5: 108,827,600 (GRCm39) |
Y138C |
probably benign |
Het |
Ighd |
A |
T |
12: 113,373,253 (GRCm39) |
L240H |
probably benign |
Het |
Ing2 |
C |
G |
8: 48,121,861 (GRCm39) |
C229S |
probably benign |
Het |
Kat8 |
G |
A |
7: 127,523,988 (GRCm39) |
E343K |
probably damaging |
Het |
Kctd8 |
A |
T |
5: 69,267,828 (GRCm39) |
N427K |
probably benign |
Het |
Kif16b |
T |
C |
2: 142,544,586 (GRCm39) |
E1147G |
probably damaging |
Het |
Kif18a |
G |
A |
2: 109,120,190 (GRCm39) |
|
probably benign |
Het |
Krt82 |
T |
A |
15: 101,456,820 (GRCm39) |
R187* |
probably null |
Het |
Lrrk2 |
T |
C |
15: 91,593,593 (GRCm39) |
|
probably null |
Het |
M1ap |
T |
C |
6: 82,945,083 (GRCm39) |
Y126H |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,970,044 (GRCm39) |
N226D |
possibly damaging |
Het |
Mtmr11 |
A |
G |
3: 96,075,185 (GRCm39) |
D353G |
possibly damaging |
Het |
Nfkbia |
A |
T |
12: 55,538,005 (GRCm39) |
H149Q |
probably damaging |
Het |
Nr5a1 |
A |
T |
2: 38,598,511 (GRCm39) |
F95L |
probably damaging |
Het |
Nutm2 |
A |
G |
13: 50,623,891 (GRCm39) |
Y196C |
probably benign |
Het |
Oxtr |
A |
G |
6: 112,466,457 (GRCm39) |
I101T |
probably damaging |
Het |
Pcsk2 |
T |
A |
2: 143,591,035 (GRCm39) |
|
probably null |
Het |
Pde5a |
T |
C |
3: 122,611,604 (GRCm39) |
I514T |
probably benign |
Het |
Pign |
A |
G |
1: 105,516,788 (GRCm39) |
W585R |
possibly damaging |
Het |
Pomgnt1 |
A |
G |
4: 116,012,933 (GRCm39) |
S407G |
probably benign |
Het |
Ppfia3 |
G |
A |
7: 45,003,040 (GRCm39) |
T372I |
probably damaging |
Het |
Prrc2b |
A |
T |
2: 32,102,144 (GRCm39) |
E739V |
probably damaging |
Het |
Ro60 |
A |
G |
1: 143,642,503 (GRCm39) |
V209A |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,574,047 (GRCm39) |
E192G |
probably damaging |
Het |
Slmap |
T |
C |
14: 26,183,435 (GRCm39) |
D316G |
probably damaging |
Het |
Smim8 |
GGTTTAATGAAGAG |
GG |
4: 34,771,259 (GRCm39) |
|
probably benign |
Het |
Smim8 |
TTTAATGAAGAGCT |
TT |
4: 34,771,261 (GRCm39) |
|
probably benign |
Het |
Tgm2 |
T |
A |
2: 157,984,974 (GRCm39) |
Y44F |
possibly damaging |
Het |
Tmc8 |
C |
A |
11: 117,683,455 (GRCm39) |
S670* |
probably null |
Het |
Tmem145 |
A |
G |
7: 25,014,946 (GRCm39) |
D523G |
probably benign |
Het |
Vmn2r115 |
G |
A |
17: 23,566,937 (GRCm39) |
G483E |
probably damaging |
Het |
|
Other mutations in Cfap161 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01827:Cfap161
|
APN |
7 |
83,442,648 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01999:Cfap161
|
APN |
7 |
83,440,899 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02291:Cfap161
|
APN |
7 |
83,440,847 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02444:Cfap161
|
APN |
7 |
83,425,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Cfap161
|
UTSW |
7 |
83,443,245 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0652:Cfap161
|
UTSW |
7 |
83,442,484 (GRCm39) |
missense |
probably null |
0.01 |
R1599:Cfap161
|
UTSW |
7 |
83,425,287 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1828:Cfap161
|
UTSW |
7 |
83,440,932 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2117:Cfap161
|
UTSW |
7 |
83,425,184 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2262:Cfap161
|
UTSW |
7 |
83,442,580 (GRCm39) |
missense |
probably benign |
0.37 |
R3618:Cfap161
|
UTSW |
7 |
83,429,390 (GRCm39) |
nonsense |
probably null |
|
R4015:Cfap161
|
UTSW |
7 |
83,429,479 (GRCm39) |
missense |
probably benign |
0.01 |
R6477:Cfap161
|
UTSW |
7 |
83,443,230 (GRCm39) |
nonsense |
probably null |
|
R6478:Cfap161
|
UTSW |
7 |
83,442,484 (GRCm39) |
missense |
probably benign |
0.00 |
R7108:Cfap161
|
UTSW |
7 |
83,442,518 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7203:Cfap161
|
UTSW |
7 |
83,425,258 (GRCm39) |
missense |
probably damaging |
0.97 |
R7582:Cfap161
|
UTSW |
7 |
83,426,290 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8714:Cfap161
|
UTSW |
7 |
83,442,482 (GRCm39) |
missense |
probably benign |
0.11 |
R8762:Cfap161
|
UTSW |
7 |
83,443,282 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9587:Cfap161
|
UTSW |
7 |
83,440,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Cfap161
|
UTSW |
7 |
83,442,579 (GRCm39) |
missense |
probably benign |
0.00 |
R9702:Cfap161
|
UTSW |
7 |
83,442,652 (GRCm39) |
missense |
probably benign |
0.00 |
|