Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap1 |
A |
T |
11: 69,781,729 (GRCm39) |
C64* |
probably null |
Het |
Ccng2 |
G |
A |
5: 93,418,746 (GRCm39) |
D124N |
probably damaging |
Het |
Cttnbp2 |
G |
A |
6: 18,382,817 (GRCm39) |
P1317L |
probably damaging |
Het |
Dsg1a |
T |
A |
18: 20,453,982 (GRCm39) |
V29E |
probably damaging |
Het |
Exoc6b |
T |
C |
6: 84,885,208 (GRCm39) |
K244E |
probably benign |
Het |
Fastkd5 |
A |
G |
2: 130,456,605 (GRCm39) |
F662L |
probably benign |
Het |
Fbxl18 |
T |
C |
5: 142,871,580 (GRCm39) |
M488V |
probably damaging |
Het |
Gas2l3 |
C |
T |
10: 89,249,366 (GRCm39) |
G584D |
probably benign |
Het |
Gm28042 |
T |
C |
2: 119,869,519 (GRCm39) |
F405L |
possibly damaging |
Het |
Gtf3c2 |
T |
C |
5: 31,317,168 (GRCm39) |
K635E |
probably damaging |
Het |
H2-Q2 |
A |
G |
17: 35,561,654 (GRCm39) |
Y48C |
probably damaging |
Het |
Hddc2 |
T |
C |
10: 31,192,330 (GRCm39) |
I78T |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,273,969 (GRCm39) |
M2708K |
probably benign |
Het |
Ift88 |
T |
C |
14: 57,677,189 (GRCm39) |
S119P |
probably benign |
Het |
Mta2 |
T |
C |
19: 8,925,668 (GRCm39) |
C388R |
probably damaging |
Het |
Mymx |
G |
T |
17: 45,912,594 (GRCm39) |
|
probably benign |
Het |
Naga |
A |
G |
15: 82,214,861 (GRCm39) |
Y366H |
possibly damaging |
Het |
Nlrp9a |
A |
G |
7: 26,257,006 (GRCm39) |
E208G |
probably damaging |
Het |
Nr4a2 |
C |
T |
2: 57,001,983 (GRCm39) |
V94M |
probably benign |
Het |
Or4c124 |
G |
T |
2: 89,156,368 (GRCm39) |
T52K |
probably benign |
Het |
Osbpl8 |
G |
T |
10: 111,112,424 (GRCm39) |
|
probably benign |
Het |
Pitpnb |
T |
A |
5: 111,486,222 (GRCm39) |
V42D |
probably damaging |
Het |
Pitrm1 |
A |
G |
13: 6,623,141 (GRCm39) |
R801G |
probably benign |
Het |
Pthlh |
G |
A |
6: 147,154,073 (GRCm39) |
T174M |
probably benign |
Het |
Sco2 |
T |
C |
15: 89,255,924 (GRCm39) |
I243M |
probably benign |
Het |
Sema5a |
G |
A |
15: 32,681,641 (GRCm39) |
V907M |
probably benign |
Het |
Semp2l1 |
A |
G |
1: 32,584,735 (GRCm39) |
S392P |
possibly damaging |
Het |
Spata31e2 |
T |
C |
1: 26,724,253 (GRCm39) |
E309G |
probably benign |
Het |
Stac2 |
T |
A |
11: 97,934,387 (GRCm39) |
K106* |
probably null |
Het |
Tas2r105 |
T |
A |
6: 131,663,815 (GRCm39) |
R204S |
probably damaging |
Het |
Tgm5 |
A |
G |
2: 120,877,156 (GRCm39) |
|
probably null |
Het |
Trpm1 |
A |
G |
7: 63,893,312 (GRCm39) |
I939V |
probably damaging |
Het |
Ttll11 |
T |
A |
2: 35,674,205 (GRCm39) |
N574I |
probably damaging |
Het |
Zfyve26 |
G |
A |
12: 79,307,644 (GRCm39) |
H312Y |
probably benign |
Het |
|
Other mutations in Zfand3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01676:Zfand3
|
APN |
17 |
30,354,337 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02931:Zfand3
|
APN |
17 |
30,411,611 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03052:Zfand3
|
UTSW |
17 |
30,279,798 (GRCm39) |
missense |
probably benign |
0.03 |
R0083:Zfand3
|
UTSW |
17 |
30,354,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Zfand3
|
UTSW |
17 |
30,354,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R0661:Zfand3
|
UTSW |
17 |
30,354,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Zfand3
|
UTSW |
17 |
30,411,630 (GRCm39) |
missense |
probably benign |
0.06 |
R3732:Zfand3
|
UTSW |
17 |
30,411,630 (GRCm39) |
missense |
probably benign |
0.06 |
R3733:Zfand3
|
UTSW |
17 |
30,411,630 (GRCm39) |
missense |
probably benign |
0.06 |
R4694:Zfand3
|
UTSW |
17 |
30,354,362 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8029:Zfand3
|
UTSW |
17 |
30,354,407 (GRCm39) |
missense |
probably benign |
0.01 |
R9383:Zfand3
|
UTSW |
17 |
30,354,479 (GRCm39) |
missense |
probably benign |
0.01 |
R9546:Zfand3
|
UTSW |
17 |
30,372,302 (GRCm39) |
missense |
probably benign |
0.00 |
|