Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
A |
7: 119,893,438 (GRCm39) |
L1296H |
probably damaging |
Het |
Abcb4 |
A |
T |
5: 9,008,988 (GRCm39) |
D1215V |
probably damaging |
Het |
Ache |
A |
C |
5: 137,289,025 (GRCm39) |
I244L |
probably benign |
Het |
Ankrd13d |
A |
T |
19: 4,332,250 (GRCm39) |
V58D |
probably damaging |
Het |
Ano3 |
A |
G |
2: 110,496,782 (GRCm39) |
L789S |
probably damaging |
Het |
Atp2a3 |
T |
C |
11: 72,863,290 (GRCm39) |
V129A |
probably damaging |
Het |
Cldn11 |
T |
C |
3: 31,217,410 (GRCm39) |
S193P |
possibly damaging |
Het |
Clpb |
A |
T |
7: 101,360,625 (GRCm39) |
R218S |
probably benign |
Het |
Cntln |
A |
G |
4: 84,875,258 (GRCm39) |
S231G |
probably benign |
Het |
Cntn4 |
T |
C |
6: 106,639,591 (GRCm39) |
Y574H |
probably damaging |
Het |
Col6a3 |
C |
T |
1: 90,709,523 (GRCm39) |
R2498H |
unknown |
Het |
Ctdnep1 |
T |
C |
11: 69,875,594 (GRCm39) |
V108A |
probably damaging |
Het |
Cyp2c67 |
A |
T |
19: 39,627,178 (GRCm39) |
N217K |
probably damaging |
Het |
Dao |
T |
A |
5: 114,147,901 (GRCm39) |
M1K |
probably null |
Het |
Dchs1 |
A |
G |
7: 105,414,981 (GRCm39) |
|
probably null |
Het |
Dennd4a |
A |
T |
9: 64,819,974 (GRCm39) |
I1809L |
probably benign |
Het |
Dnah7a |
T |
A |
1: 53,568,058 (GRCm39) |
|
probably null |
Het |
Epn1 |
A |
T |
7: 5,086,720 (GRCm39) |
|
probably benign |
Het |
Erich1 |
A |
G |
8: 14,080,719 (GRCm39) |
S267P |
probably damaging |
Het |
Gm17732 |
G |
T |
18: 62,795,936 (GRCm39) |
V41L |
probably damaging |
Het |
Gpaa1 |
C |
A |
15: 76,218,826 (GRCm39) |
T556K |
possibly damaging |
Het |
Gpr65 |
T |
A |
12: 98,241,523 (GRCm39) |
S59T |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,124,695 (GRCm39) |
V568A |
possibly damaging |
Het |
Itga1 |
T |
C |
13: 115,107,112 (GRCm39) |
H993R |
probably benign |
Het |
Itgax |
T |
C |
7: 127,747,935 (GRCm39) |
L1075P |
possibly damaging |
Het |
Itpr1 |
T |
A |
6: 108,326,638 (GRCm39) |
V120E |
probably damaging |
Het |
Kdm3b |
T |
C |
18: 34,970,718 (GRCm39) |
S1762P |
probably damaging |
Het |
Krt80 |
T |
A |
15: 101,247,978 (GRCm39) |
T221S |
unknown |
Het |
Lama2 |
T |
C |
10: 26,994,620 (GRCm39) |
D1763G |
probably benign |
Het |
Lrp5 |
T |
C |
19: 3,670,286 (GRCm39) |
D606G |
probably benign |
Het |
Map6d1 |
T |
C |
16: 20,059,933 (GRCm39) |
D44G |
probably benign |
Het |
Mtmr11 |
T |
A |
3: 96,072,372 (GRCm39) |
I282K |
probably benign |
Het |
Nalcn |
G |
A |
14: 123,515,713 (GRCm39) |
T1696M |
possibly damaging |
Het |
Nup214 |
T |
C |
2: 31,924,244 (GRCm39) |
V1591A |
probably benign |
Het |
Oas1f |
C |
A |
5: 120,986,243 (GRCm39) |
Y65* |
probably null |
Het |
Or1x6 |
T |
A |
11: 50,939,662 (GRCm39) |
C243S |
probably damaging |
Het |
Or2t43 |
T |
A |
11: 58,457,683 (GRCm39) |
T163S |
possibly damaging |
Het |
Or2t46 |
T |
C |
11: 58,472,636 (GRCm39) |
V322A |
probably benign |
Het |
Or51f1e |
A |
T |
7: 102,746,971 (GRCm39) |
T8S |
probably benign |
Het |
Or5p58 |
A |
T |
7: 107,694,471 (GRCm39) |
I102K |
possibly damaging |
Het |
Palld |
C |
T |
8: 61,969,691 (GRCm39) |
R1211H |
unknown |
Het |
Pigyl |
A |
G |
9: 22,069,324 (GRCm39) |
I12V |
probably benign |
Het |
Pno1 |
A |
T |
11: 17,158,791 (GRCm39) |
D202E |
probably benign |
Het |
Ppp5c |
A |
T |
7: 16,743,849 (GRCm39) |
M195K |
probably damaging |
Het |
Prrc2a |
A |
T |
17: 35,369,598 (GRCm39) |
F1905Y |
possibly damaging |
Het |
Ptpn11 |
C |
A |
5: 121,282,681 (GRCm39) |
D435Y |
probably damaging |
Het |
Rbm33 |
A |
G |
5: 28,544,164 (GRCm39) |
Y140C |
probably damaging |
Het |
Runx1t1 |
A |
G |
4: 13,865,225 (GRCm39) |
E339G |
possibly damaging |
Het |
Scube3 |
G |
T |
17: 28,383,670 (GRCm39) |
K480N |
possibly damaging |
Het |
Sephs1 |
T |
A |
2: 4,910,469 (GRCm39) |
M313K |
probably benign |
Het |
Tcaim |
T |
C |
9: 122,655,995 (GRCm39) |
W304R |
probably damaging |
Het |
Terf2ip |
C |
T |
8: 112,738,514 (GRCm39) |
T134I |
probably damaging |
Het |
Terf2ip |
A |
G |
8: 112,744,528 (GRCm39) |
T282A |
probably benign |
Het |
Tnfrsf18 |
G |
T |
4: 156,112,448 (GRCm39) |
A102S |
probably benign |
Het |
Trim10 |
A |
T |
17: 37,184,168 (GRCm39) |
I254F |
probably benign |
Het |
Triqk |
A |
G |
4: 12,962,987 (GRCm39) |
T9A |
probably benign |
Het |
Tshz2 |
G |
A |
2: 169,726,013 (GRCm39) |
S203N |
probably benign |
Het |
Zc3h13 |
G |
A |
14: 75,561,128 (GRCm39) |
V573I |
unknown |
Het |
Zfhx4 |
A |
G |
3: 5,306,833 (GRCm39) |
K20E |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,465,395 (GRCm39) |
D1876G |
probably benign |
Het |
|
Other mutations in Ifi205 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Ifi205
|
APN |
1 |
173,854,899 (GRCm39) |
splice site |
probably benign |
|
IGL02419:Ifi205
|
APN |
1 |
173,845,180 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02476:Ifi205
|
APN |
1 |
173,842,627 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03128:Ifi205
|
APN |
1 |
173,842,652 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03154:Ifi205
|
APN |
1 |
173,845,232 (GRCm39) |
splice site |
probably benign |
|
R0211:Ifi205
|
UTSW |
1 |
173,855,994 (GRCm39) |
missense |
probably benign |
|
R1932:Ifi205
|
UTSW |
1 |
173,855,980 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2397:Ifi205
|
UTSW |
1 |
173,845,141 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3115:Ifi205
|
UTSW |
1 |
173,855,901 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4534:Ifi205
|
UTSW |
1 |
173,845,207 (GRCm39) |
missense |
probably benign |
0.16 |
R4544:Ifi205
|
UTSW |
1 |
173,854,139 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4715:Ifi205
|
UTSW |
1 |
173,855,887 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4977:Ifi205
|
UTSW |
1 |
173,842,574 (GRCm39) |
missense |
probably benign |
0.07 |
R5844:Ifi205
|
UTSW |
1 |
173,854,258 (GRCm39) |
splice site |
probably null |
|
R6061:Ifi205
|
UTSW |
1 |
173,854,830 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6510:Ifi205
|
UTSW |
1 |
173,845,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R7032:Ifi205
|
UTSW |
1 |
173,855,916 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7196:Ifi205
|
UTSW |
1 |
173,854,109 (GRCm39) |
missense |
probably damaging |
0.96 |
R7244:Ifi205
|
UTSW |
1 |
173,845,210 (GRCm39) |
nonsense |
probably null |
|
R7419:Ifi205
|
UTSW |
1 |
173,855,874 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7431:Ifi205
|
UTSW |
1 |
173,855,943 (GRCm39) |
missense |
probably benign |
|
R7660:Ifi205
|
UTSW |
1 |
173,855,814 (GRCm39) |
missense |
probably benign |
0.27 |
R7787:Ifi205
|
UTSW |
1 |
173,842,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Ifi205
|
UTSW |
1 |
173,842,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Ifi205
|
UTSW |
1 |
173,855,841 (GRCm39) |
missense |
probably benign |
|
R9163:Ifi205
|
UTSW |
1 |
173,844,988 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9348:Ifi205
|
UTSW |
1 |
173,844,997 (GRCm39) |
missense |
probably benign |
0.24 |
R9477:Ifi205
|
UTSW |
1 |
173,854,155 (GRCm39) |
missense |
probably benign |
|
|