Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,349,180 (GRCm39) |
W3585R |
probably null |
Het |
Ajm1 |
G |
T |
2: 25,467,043 (GRCm39) |
S956* |
probably null |
Het |
Babam1 |
G |
C |
8: 71,850,424 (GRCm39) |
E18Q |
probably damaging |
Het |
Bcan |
G |
T |
3: 87,901,519 (GRCm39) |
S394R |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,999,232 (GRCm39) |
F4653L |
probably damaging |
Het |
Camsap2 |
A |
T |
1: 136,209,832 (GRCm39) |
H559Q |
probably benign |
Het |
Cars2 |
G |
T |
8: 11,580,430 (GRCm39) |
|
probably null |
Het |
Ccdc93 |
T |
A |
1: 121,389,712 (GRCm39) |
|
probably benign |
Het |
Ccna2 |
C |
A |
3: 36,624,879 (GRCm39) |
|
probably benign |
Het |
Cdc6 |
T |
A |
11: 98,803,037 (GRCm39) |
L326I |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,255,478 (GRCm39) |
|
probably benign |
Het |
Cenpe |
T |
A |
3: 134,976,661 (GRCm39) |
S2423T |
probably benign |
Het |
Cftr |
A |
G |
6: 18,225,936 (GRCm39) |
M295V |
probably benign |
Het |
Cxcl2 |
A |
G |
5: 91,051,871 (GRCm39) |
H23R |
probably benign |
Het |
Cyp4a12b |
A |
G |
4: 115,291,181 (GRCm39) |
T370A |
probably damaging |
Het |
Daam2 |
A |
G |
17: 49,803,148 (GRCm39) |
|
probably benign |
Het |
Dclk3 |
T |
C |
9: 111,298,276 (GRCm39) |
F607L |
probably damaging |
Het |
Des |
T |
G |
1: 75,337,230 (GRCm39) |
S57A |
probably benign |
Het |
Drd1 |
A |
T |
13: 54,206,964 (GRCm39) |
S410T |
probably damaging |
Het |
Ecm1 |
G |
A |
3: 95,643,275 (GRCm39) |
R342C |
probably damaging |
Het |
Fanci |
T |
C |
7: 79,082,941 (GRCm39) |
L639P |
probably damaging |
Het |
Fancm |
A |
G |
12: 65,140,463 (GRCm39) |
E395G |
probably benign |
Het |
Grik3 |
A |
G |
4: 125,601,790 (GRCm39) |
D889G |
probably benign |
Het |
Heyl |
A |
G |
4: 123,135,192 (GRCm39) |
S62G |
probably damaging |
Het |
Hmox1 |
C |
T |
8: 75,826,577 (GRCm39) |
P267L |
probably damaging |
Het |
Il12rb2 |
G |
T |
6: 67,333,576 (GRCm39) |
F234L |
probably benign |
Het |
Il4i1 |
T |
A |
7: 44,488,811 (GRCm39) |
S233T |
probably damaging |
Het |
Itga4 |
A |
G |
2: 79,146,032 (GRCm39) |
S745G |
probably benign |
Het |
Kalrn |
T |
A |
16: 33,830,918 (GRCm39) |
I734F |
possibly damaging |
Het |
Klk1b16 |
T |
C |
7: 43,790,425 (GRCm39) |
I200T |
probably benign |
Het |
Lrrc4c |
T |
A |
2: 97,461,117 (GRCm39) |
M581K |
probably benign |
Het |
M6pr |
A |
T |
6: 122,292,033 (GRCm39) |
I122L |
probably benign |
Het |
Magi3 |
T |
C |
3: 103,954,169 (GRCm39) |
|
probably benign |
Het |
Mybpc2 |
T |
G |
7: 44,163,111 (GRCm39) |
T480P |
probably benign |
Het |
Or14c44 |
T |
C |
7: 86,061,575 (GRCm39) |
S43P |
probably benign |
Het |
Or1j17 |
A |
G |
2: 36,578,770 (GRCm39) |
Y252C |
probably damaging |
Het |
Or51ab3 |
A |
T |
7: 103,201,372 (GRCm39) |
I127F |
possibly damaging |
Het |
Or8g23 |
T |
C |
9: 38,971,437 (GRCm39) |
N175S |
probably benign |
Het |
Pcx |
T |
A |
19: 4,669,114 (GRCm39) |
I704N |
probably damaging |
Het |
Pde3a |
G |
T |
6: 141,404,824 (GRCm39) |
A350S |
probably damaging |
Het |
Ppox |
A |
T |
1: 171,107,580 (GRCm39) |
|
probably benign |
Het |
Prb1a |
T |
A |
6: 132,185,507 (GRCm39) |
Y42F |
unknown |
Het |
Rsph4a |
T |
A |
10: 33,785,727 (GRCm39) |
V546E |
probably damaging |
Het |
Saxo4 |
T |
C |
19: 10,458,770 (GRCm39) |
T87A |
probably benign |
Het |
Sf3b1 |
C |
G |
1: 55,058,554 (GRCm39) |
E12Q |
possibly damaging |
Het |
Sh3tc1 |
A |
G |
5: 35,860,693 (GRCm39) |
|
probably null |
Het |
Slc22a2 |
T |
C |
17: 12,803,298 (GRCm39) |
F44S |
probably damaging |
Het |
Slco6c1 |
T |
A |
1: 97,026,223 (GRCm39) |
D334V |
probably damaging |
Het |
Smim19 |
T |
C |
8: 22,953,352 (GRCm39) |
D105G |
probably damaging |
Het |
Smpdl3a |
A |
G |
10: 57,683,588 (GRCm39) |
T233A |
probably damaging |
Het |
St8sia5 |
G |
A |
18: 77,299,460 (GRCm39) |
|
probably null |
Het |
Stk32a |
C |
A |
18: 43,376,149 (GRCm39) |
Q73K |
probably benign |
Het |
Tmem129 |
G |
T |
5: 33,815,100 (GRCm39) |
|
probably null |
Het |
Traf3ip3 |
A |
T |
1: 192,860,599 (GRCm39) |
L441Q |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,731,305 (GRCm39) |
|
probably benign |
Het |
Unc45b |
T |
C |
11: 82,808,672 (GRCm39) |
S253P |
possibly damaging |
Het |
Vars2 |
A |
G |
17: 35,977,150 (GRCm39) |
|
probably benign |
Het |
Vmn2r51 |
C |
T |
7: 9,836,372 (GRCm39) |
M136I |
possibly damaging |
Het |
Vmn2r51 |
A |
G |
7: 9,836,373 (GRCm39) |
M136T |
possibly damaging |
Het |
Zfp595 |
T |
C |
13: 67,465,127 (GRCm39) |
I379V |
possibly damaging |
Het |
|
Other mutations in Ifi213 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00678:Ifi213
|
APN |
1 |
173,421,619 (GRCm39) |
splice site |
probably benign |
|
IGL00908:Ifi213
|
APN |
1 |
173,422,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00964:Ifi213
|
APN |
1 |
173,421,518 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02217:Ifi213
|
APN |
1 |
173,422,598 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0709:Ifi213
|
UTSW |
1 |
173,417,366 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1518:Ifi213
|
UTSW |
1 |
173,417,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R1822:Ifi213
|
UTSW |
1 |
173,417,408 (GRCm39) |
missense |
probably damaging |
0.99 |
R1839:Ifi213
|
UTSW |
1 |
173,417,166 (GRCm39) |
missense |
probably damaging |
0.98 |
R1989:Ifi213
|
UTSW |
1 |
173,396,374 (GRCm39) |
critical splice donor site |
probably null |
|
R2108:Ifi213
|
UTSW |
1 |
173,396,668 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2696:Ifi213
|
UTSW |
1 |
173,417,590 (GRCm39) |
missense |
probably benign |
|
R3890:Ifi213
|
UTSW |
1 |
173,394,822 (GRCm39) |
missense |
probably benign |
0.33 |
R4544:Ifi213
|
UTSW |
1 |
173,409,693 (GRCm39) |
splice site |
probably null |
|
R4611:Ifi213
|
UTSW |
1 |
173,417,480 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4689:Ifi213
|
UTSW |
1 |
173,417,986 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4710:Ifi213
|
UTSW |
1 |
173,394,738 (GRCm39) |
utr 3 prime |
probably benign |
|
R5126:Ifi213
|
UTSW |
1 |
173,417,581 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5472:Ifi213
|
UTSW |
1 |
173,394,838 (GRCm39) |
splice site |
probably null |
|
R5625:Ifi213
|
UTSW |
1 |
173,396,629 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5789:Ifi213
|
UTSW |
1 |
173,396,360 (GRCm39) |
splice site |
probably benign |
|
R5898:Ifi213
|
UTSW |
1 |
173,396,545 (GRCm39) |
missense |
probably benign |
0.01 |
R6025:Ifi213
|
UTSW |
1 |
173,422,800 (GRCm39) |
missense |
probably damaging |
0.99 |
R6149:Ifi213
|
UTSW |
1 |
173,421,581 (GRCm39) |
missense |
probably benign |
0.18 |
R6348:Ifi213
|
UTSW |
1 |
173,417,848 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6564:Ifi213
|
UTSW |
1 |
173,422,862 (GRCm39) |
start codon destroyed |
probably null |
0.06 |
R7254:Ifi213
|
UTSW |
1 |
173,421,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R7292:Ifi213
|
UTSW |
1 |
173,422,691 (GRCm39) |
missense |
probably damaging |
0.99 |
R7752:Ifi213
|
UTSW |
1 |
173,394,784 (GRCm39) |
missense |
probably benign |
0.18 |
R7901:Ifi213
|
UTSW |
1 |
173,394,784 (GRCm39) |
missense |
probably benign |
0.18 |
R8100:Ifi213
|
UTSW |
1 |
173,422,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R8352:Ifi213
|
UTSW |
1 |
173,422,835 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8425:Ifi213
|
UTSW |
1 |
173,417,426 (GRCm39) |
missense |
probably benign |
|
R8452:Ifi213
|
UTSW |
1 |
173,422,835 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9357:Ifi213
|
UTSW |
1 |
173,396,392 (GRCm39) |
missense |
probably benign |
0.01 |
RF010:Ifi213
|
UTSW |
1 |
173,409,719 (GRCm39) |
missense |
probably damaging |
0.98 |
|