Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
CGG |
CG |
5: 124,215,368 (GRCm39) |
|
probably null |
Het |
Aif1l |
T |
A |
2: 31,859,763 (GRCm39) |
F94L |
probably damaging |
Het |
Ankzf1 |
C |
T |
1: 75,171,895 (GRCm39) |
H209Y |
probably damaging |
Het |
Ate1 |
A |
T |
7: 130,117,895 (GRCm39) |
M30K |
probably damaging |
Het |
Cd27 |
A |
G |
6: 125,210,281 (GRCm39) |
Y189H |
probably damaging |
Het |
Cela1 |
A |
G |
15: 100,579,109 (GRCm39) |
I183T |
probably benign |
Het |
Copg2 |
A |
T |
6: 30,803,168 (GRCm39) |
L259* |
probably null |
Het |
Dennd2b |
A |
T |
7: 109,155,653 (GRCm39) |
S366T |
probably benign |
Het |
Efcab7 |
T |
A |
4: 99,719,823 (GRCm39) |
|
probably benign |
Het |
Fcrl5 |
A |
G |
3: 87,353,726 (GRCm39) |
E357G |
probably damaging |
Het |
Fzr1 |
C |
T |
10: 81,203,474 (GRCm39) |
|
probably null |
Het |
Il12rb2 |
C |
T |
6: 67,275,179 (GRCm39) |
A649T |
probably damaging |
Het |
Itfg1 |
C |
A |
8: 86,464,758 (GRCm39) |
V438F |
probably damaging |
Het |
Jaml |
A |
C |
9: 45,012,361 (GRCm39) |
I283L |
possibly damaging |
Het |
Kif28 |
A |
T |
1: 179,537,024 (GRCm39) |
H486Q |
probably damaging |
Het |
Lrch4 |
A |
G |
5: 137,636,810 (GRCm39) |
|
probably benign |
Het |
Lrfn2 |
A |
G |
17: 49,378,188 (GRCm39) |
E423G |
possibly damaging |
Het |
Lrp4 |
T |
A |
2: 91,332,299 (GRCm39) |
N1665K |
probably benign |
Het |
Mrpl32 |
A |
T |
13: 14,785,165 (GRCm39) |
V157E |
probably damaging |
Het |
Mta3 |
A |
G |
17: 84,070,417 (GRCm39) |
I193V |
probably damaging |
Het |
Myom2 |
G |
A |
8: 15,162,018 (GRCm39) |
V984I |
possibly damaging |
Het |
Nedd4l |
G |
A |
18: 65,342,790 (GRCm39) |
V909I |
possibly damaging |
Het |
Nlrp4a |
A |
G |
7: 26,163,623 (GRCm39) |
D930G |
probably benign |
Het |
Or10al5 |
T |
A |
17: 38,063,271 (GRCm39) |
C175* |
probably null |
Het |
Or5d47 |
A |
T |
2: 87,804,066 (GRCm39) |
N314K |
probably benign |
Het |
Or7a35 |
T |
C |
10: 78,854,022 (GRCm39) |
F289L |
probably damaging |
Het |
Ovch2 |
A |
T |
7: 107,394,122 (GRCm39) |
H110Q |
probably damaging |
Het |
Pcnx3 |
G |
A |
19: 5,733,367 (GRCm39) |
Q155* |
probably null |
Het |
Pcnx3 |
C |
G |
19: 5,733,368 (GRCm39) |
L1F |
probably null |
Het |
Pi4k2a |
G |
A |
19: 42,079,131 (GRCm39) |
R64Q |
probably damaging |
Het |
Ptpn12 |
G |
A |
5: 21,203,690 (GRCm39) |
P363S |
probably damaging |
Het |
Rbm27 |
T |
C |
18: 42,425,177 (GRCm39) |
|
probably benign |
Het |
Ripor3 |
A |
G |
2: 167,825,785 (GRCm39) |
|
probably benign |
Het |
Rpl13-ps3 |
A |
G |
14: 59,131,265 (GRCm39) |
|
noncoding transcript |
Het |
Sap18b |
G |
A |
8: 96,552,191 (GRCm39) |
R67H |
probably benign |
Het |
Sdhb |
T |
C |
4: 140,700,311 (GRCm39) |
V137A |
probably damaging |
Het |
Shmt2 |
T |
C |
10: 127,353,897 (GRCm39) |
T459A |
probably benign |
Het |
Siglecg |
A |
G |
7: 43,058,846 (GRCm39) |
S200G |
possibly damaging |
Het |
Slc6a15 |
T |
G |
10: 103,252,646 (GRCm39) |
I603S |
probably benign |
Het |
Smtn |
A |
T |
11: 3,482,865 (GRCm39) |
|
probably null |
Het |
Spata31d1a |
G |
A |
13: 59,851,702 (GRCm39) |
S142L |
probably benign |
Het |
Spopfm2 |
G |
A |
3: 94,082,854 (GRCm39) |
A319V |
possibly damaging |
Het |
Spopfm2 |
C |
A |
3: 94,082,855 (GRCm39) |
A319S |
possibly damaging |
Het |
Spopl |
C |
T |
2: 23,427,392 (GRCm39) |
R221Q |
probably damaging |
Het |
Strip1 |
A |
G |
3: 107,523,135 (GRCm39) |
V633A |
probably benign |
Het |
Sun2 |
A |
G |
15: 79,612,114 (GRCm39) |
S522P |
possibly damaging |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Terb2 |
T |
A |
2: 122,028,913 (GRCm39) |
C157S |
probably benign |
Het |
Themis |
T |
A |
10: 28,739,376 (GRCm39) |
N615K |
possibly damaging |
Het |
Tlnrd1 |
A |
T |
7: 83,531,488 (GRCm39) |
D314E |
probably benign |
Het |
Vmn1r205 |
T |
A |
13: 22,776,566 (GRCm39) |
T179S |
probably benign |
Het |
Vsig10l |
G |
A |
7: 43,118,185 (GRCm39) |
R689H |
probably benign |
Het |
Wt1 |
G |
A |
2: 104,993,773 (GRCm39) |
|
probably benign |
Het |
Zfp423 |
G |
T |
8: 88,507,179 (GRCm39) |
A1034D |
possibly damaging |
Het |
Zyg11a |
G |
T |
4: 108,053,343 (GRCm39) |
Q440K |
possibly damaging |
Het |
|
Other mutations in Zfy2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02850:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02850:Zfy2
|
APN |
Y |
2,106,894 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02851:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02851:Zfy2
|
APN |
Y |
2,106,894 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02852:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02852:Zfy2
|
APN |
Y |
2,106,894 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4515001:Zfy2
|
UTSW |
Y |
2,117,096 (GRCm39) |
missense |
probably benign |
0.09 |
R0426:Zfy2
|
UTSW |
Y |
2,107,348 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0490:Zfy2
|
UTSW |
Y |
2,106,620 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1080:Zfy2
|
UTSW |
Y |
2,121,645 (GRCm39) |
missense |
probably benign |
0.00 |
R1513:Zfy2
|
UTSW |
Y |
2,116,185 (GRCm39) |
missense |
probably benign |
0.00 |
R1935:Zfy2
|
UTSW |
Y |
2,121,496 (GRCm39) |
missense |
probably benign |
0.02 |
R1936:Zfy2
|
UTSW |
Y |
2,121,496 (GRCm39) |
missense |
probably benign |
0.02 |
R4484:Zfy2
|
UTSW |
Y |
2,107,351 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4754:Zfy2
|
UTSW |
Y |
2,121,477 (GRCm39) |
missense |
probably benign |
0.02 |
R4777:Zfy2
|
UTSW |
Y |
2,116,194 (GRCm39) |
missense |
probably benign |
0.00 |
R4812:Zfy2
|
UTSW |
Y |
2,106,334 (GRCm39) |
missense |
probably benign |
0.08 |
R5045:Zfy2
|
UTSW |
Y |
2,107,159 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5363:Zfy2
|
UTSW |
Y |
2,106,555 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6256:Zfy2
|
UTSW |
Y |
2,116,267 (GRCm39) |
missense |
probably benign |
0.02 |
R6618:Zfy2
|
UTSW |
Y |
2,121,477 (GRCm39) |
missense |
probably benign |
0.10 |
R6941:Zfy2
|
UTSW |
Y |
2,121,491 (GRCm39) |
missense |
probably benign |
0.02 |
R7011:Zfy2
|
UTSW |
Y |
2,107,127 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7712:Zfy2
|
UTSW |
Y |
2,121,420 (GRCm39) |
missense |
probably benign |
0.05 |
R7759:Zfy2
|
UTSW |
Y |
2,117,083 (GRCm39) |
missense |
probably benign |
0.02 |
R7985:Zfy2
|
UTSW |
Y |
2,116,263 (GRCm39) |
missense |
probably benign |
0.00 |
R8051:Zfy2
|
UTSW |
Y |
2,117,380 (GRCm39) |
intron |
probably benign |
|
R8218:Zfy2
|
UTSW |
Y |
2,133,421 (GRCm39) |
missense |
unknown |
|
R8345:Zfy2
|
UTSW |
Y |
2,107,096 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8371:Zfy2
|
UTSW |
Y |
2,117,168 (GRCm39) |
missense |
probably benign |
0.00 |
R8830:Zfy2
|
UTSW |
Y |
2,106,600 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9448:Zfy2
|
UTSW |
Y |
2,109,904 (GRCm39) |
missense |
probably damaging |
0.98 |
R9537:Zfy2
|
UTSW |
Y |
2,108,596 (GRCm39) |
missense |
|
|
|