Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,077,058 (GRCm39) |
D708G |
probably damaging |
Het |
Abca16 |
T |
C |
7: 120,021,024 (GRCm39) |
|
probably benign |
Het |
Abcc5 |
T |
C |
16: 20,197,207 (GRCm39) |
D674G |
probably damaging |
Het |
Abr |
A |
G |
11: 76,355,125 (GRCm39) |
|
probably benign |
Het |
Arfgef3 |
A |
G |
10: 18,619,363 (GRCm39) |
I4T |
possibly damaging |
Het |
Btla |
A |
G |
16: 45,070,911 (GRCm39) |
N290S |
possibly damaging |
Het |
Catip |
C |
A |
1: 74,407,642 (GRCm39) |
R325S |
probably damaging |
Het |
Cep120 |
A |
G |
18: 53,839,902 (GRCm39) |
L786P |
possibly damaging |
Het |
Cnot8 |
A |
G |
11: 58,006,133 (GRCm39) |
I221V |
probably benign |
Het |
Eloc |
A |
T |
1: 16,716,013 (GRCm39) |
D37E |
probably benign |
Het |
Fabp12 |
A |
C |
3: 10,312,754 (GRCm39) |
N89K |
probably benign |
Het |
Frmd3 |
T |
C |
4: 74,106,075 (GRCm39) |
Y574H |
probably damaging |
Het |
Frmd4a |
T |
C |
2: 4,540,047 (GRCm39) |
|
probably benign |
Het |
Gatc |
G |
A |
5: 115,479,076 (GRCm39) |
Q45* |
probably null |
Het |
Gm5414 |
T |
C |
15: 101,535,410 (GRCm39) |
D225G |
probably benign |
Het |
Itpkc |
G |
T |
7: 26,911,795 (GRCm39) |
A592E |
probably benign |
Het |
Kl |
G |
T |
5: 150,911,948 (GRCm39) |
V566L |
probably benign |
Het |
Lpin1 |
T |
A |
12: 16,608,477 (GRCm39) |
D545V |
probably damaging |
Het |
Mtcl1 |
T |
C |
17: 66,692,880 (GRCm39) |
Y483C |
probably damaging |
Het |
Neb |
C |
T |
2: 52,112,982 (GRCm39) |
W67* |
probably null |
Het |
Nrarp |
T |
C |
2: 25,071,298 (GRCm39) |
V59A |
possibly damaging |
Het |
Nuf2 |
G |
A |
1: 169,333,641 (GRCm39) |
T345M |
probably benign |
Het |
Or52n20 |
T |
C |
7: 104,320,149 (GRCm39) |
I80T |
probably benign |
Het |
Pacs2 |
T |
A |
12: 113,020,462 (GRCm39) |
H278Q |
probably benign |
Het |
Pot1a |
T |
C |
6: 25,753,276 (GRCm39) |
K420R |
probably benign |
Het |
Rag2 |
A |
G |
2: 101,460,392 (GRCm39) |
Y234C |
probably damaging |
Het |
Ralgds |
C |
T |
2: 28,440,554 (GRCm39) |
Q88* |
probably null |
Het |
Rictor |
T |
C |
15: 6,799,258 (GRCm39) |
S365P |
probably damaging |
Het |
Slco1a1 |
G |
A |
6: 141,871,339 (GRCm39) |
Q276* |
probably null |
Het |
Tas2r134 |
C |
T |
2: 51,518,160 (GRCm39) |
T213I |
probably benign |
Het |
Tecpr1 |
A |
G |
5: 144,148,358 (GRCm39) |
I349T |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,907,813 (GRCm39) |
S1286P |
probably damaging |
Het |
Trafd1 |
A |
G |
5: 121,513,113 (GRCm39) |
V375A |
possibly damaging |
Het |
Vmn2r110 |
T |
A |
17: 20,803,889 (GRCm39) |
I229L |
probably benign |
Het |
Vnn1 |
T |
C |
10: 23,776,608 (GRCm39) |
Y320H |
probably benign |
Het |
Zfp990 |
T |
C |
4: 145,263,518 (GRCm39) |
V172A |
probably benign |
Het |
|
Other mutations in Ficd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01622:Ficd
|
APN |
5 |
113,876,622 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01899:Ficd
|
APN |
5 |
113,875,158 (GRCm39) |
missense |
probably benign |
|
IGL02237:Ficd
|
APN |
5 |
113,876,373 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02527:Ficd
|
APN |
5 |
113,875,027 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03030:Ficd
|
APN |
5 |
113,874,990 (GRCm39) |
missense |
probably benign |
|
IGL03062:Ficd
|
APN |
5 |
113,876,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03339:Ficd
|
APN |
5 |
113,876,800 (GRCm39) |
missense |
probably benign |
0.00 |
R0145:Ficd
|
UTSW |
5 |
113,876,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R5207:Ficd
|
UTSW |
5 |
113,875,072 (GRCm39) |
missense |
probably benign |
0.15 |
R5530:Ficd
|
UTSW |
5 |
113,876,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R6730:Ficd
|
UTSW |
5 |
113,876,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7256:Ficd
|
UTSW |
5 |
113,876,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R7624:Ficd
|
UTSW |
5 |
113,876,751 (GRCm39) |
missense |
probably benign |
0.03 |
R7960:Ficd
|
UTSW |
5 |
113,877,020 (GRCm39) |
missense |
probably benign |
0.00 |
R8757:Ficd
|
UTSW |
5 |
113,876,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R8759:Ficd
|
UTSW |
5 |
113,876,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R8870:Ficd
|
UTSW |
5 |
113,876,248 (GRCm39) |
missense |
probably damaging |
0.98 |
R9224:Ficd
|
UTSW |
5 |
113,875,196 (GRCm39) |
missense |
probably benign |
|
|