Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427I04Rik |
A |
T |
4: 123,754,512 (GRCm39) |
H142L |
possibly damaging |
Het |
Aadacl2fm3 |
A |
G |
3: 59,772,689 (GRCm39) |
I64M |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,240,678 (GRCm39) |
E847G |
probably benign |
Het |
Abca9 |
T |
A |
11: 110,006,278 (GRCm39) |
T1276S |
probably benign |
Het |
Abcb11 |
C |
T |
2: 69,117,938 (GRCm39) |
|
probably null |
Het |
Alpk1 |
G |
C |
3: 127,474,616 (GRCm39) |
H462Q |
probably damaging |
Het |
Armh1 |
C |
A |
4: 117,070,938 (GRCm39) |
A396S |
probably benign |
Het |
Atm |
C |
T |
9: 53,356,807 (GRCm39) |
V2815M |
probably benign |
Het |
Braf |
T |
C |
6: 39,600,575 (GRCm39) |
I681V |
possibly damaging |
Het |
Casc3 |
C |
G |
11: 98,700,699 (GRCm39) |
R4G |
unknown |
Het |
Cilk1 |
G |
C |
9: 78,074,902 (GRCm39) |
V586L |
probably benign |
Het |
Crybg1 |
T |
C |
10: 43,874,831 (GRCm39) |
D759G |
probably damaging |
Het |
Csrp2 |
A |
G |
10: 110,773,624 (GRCm39) |
N103S |
probably benign |
Het |
Faf1 |
A |
T |
4: 109,719,034 (GRCm39) |
H380L |
probably damaging |
Het |
Farp1 |
G |
A |
14: 121,514,334 (GRCm39) |
A888T |
probably benign |
Het |
Fat4 |
A |
T |
3: 39,035,309 (GRCm39) |
Q2987L |
probably benign |
Het |
Fkbp15 |
T |
A |
4: 62,232,578 (GRCm39) |
T665S |
probably benign |
Het |
Gigyf1 |
T |
C |
5: 137,519,231 (GRCm39) |
S343P |
probably benign |
Het |
Glrx3 |
A |
G |
7: 137,060,954 (GRCm39) |
Y196C |
probably damaging |
Het |
Gm3278 |
T |
G |
14: 16,080,387 (GRCm39) |
L66R |
probably damaging |
Het |
Ift140 |
T |
G |
17: 25,270,798 (GRCm39) |
L708R |
probably damaging |
Het |
Ints13 |
A |
T |
6: 146,458,836 (GRCm39) |
L328M |
probably benign |
Het |
Itfg2 |
A |
G |
6: 128,401,709 (GRCm39) |
I23T |
probably damaging |
Het |
Ldha |
C |
T |
7: 46,499,681 (GRCm39) |
P100S |
unknown |
Het |
Lmtk2 |
T |
A |
5: 144,085,158 (GRCm39) |
L210H |
probably damaging |
Het |
Lrrc4 |
T |
A |
6: 28,829,816 (GRCm39) |
I600L |
probably benign |
Het |
Map2 |
C |
A |
1: 66,453,536 (GRCm39) |
P809T |
probably damaging |
Het |
Matn2 |
T |
A |
15: 34,423,874 (GRCm39) |
C577* |
probably null |
Het |
Matn2 |
A |
G |
15: 34,403,092 (GRCm39) |
K439R |
probably benign |
Het |
Mep1a |
C |
T |
17: 43,789,868 (GRCm39) |
G494S |
probably benign |
Het |
Mtmr4 |
T |
C |
11: 87,495,406 (GRCm39) |
F488L |
probably damaging |
Het |
Mtus1 |
G |
T |
8: 41,469,248 (GRCm39) |
T8K |
probably benign |
Het |
Mug1 |
C |
A |
6: 121,838,179 (GRCm39) |
H470N |
possibly damaging |
Het |
Mybpc1 |
T |
C |
10: 88,384,716 (GRCm39) |
T523A |
possibly damaging |
Het |
Ncoa3 |
C |
T |
2: 165,911,241 (GRCm39) |
P1334S |
probably benign |
Het |
Neb |
T |
G |
2: 52,139,451 (GRCm39) |
M119L |
|
Het |
Nox4 |
T |
C |
7: 87,019,230 (GRCm39) |
Y408H |
probably damaging |
Het |
Nxpe3 |
C |
T |
16: 55,664,690 (GRCm39) |
R510Q |
probably damaging |
Het |
Or4c58 |
T |
C |
2: 89,674,787 (GRCm39) |
T177A |
probably benign |
Het |
Or4f52 |
C |
T |
2: 111,061,960 (GRCm39) |
M59I |
probably damaging |
Het |
Or5p60 |
A |
G |
7: 107,724,041 (GRCm39) |
V143A |
probably benign |
Het |
Or6c214 |
C |
A |
10: 129,590,432 (GRCm39) |
E296* |
probably null |
Het |
Or7g23 |
T |
C |
9: 19,086,804 (GRCm39) |
H56R |
probably benign |
Het |
Or8k31-ps1 |
A |
T |
2: 86,356,174 (GRCm39) |
S116T |
possibly damaging |
Het |
Paip1 |
C |
T |
13: 119,587,306 (GRCm39) |
T390I |
possibly damaging |
Het |
Pax8 |
T |
C |
2: 24,326,573 (GRCm39) |
Y263C |
probably benign |
Het |
Pcdha11 |
T |
A |
18: 37,138,904 (GRCm39) |
Y178N |
probably benign |
Het |
Pcdhga11 |
C |
T |
18: 37,890,183 (GRCm39) |
T397M |
possibly damaging |
Het |
Pdlim5 |
G |
T |
3: 141,964,946 (GRCm39) |
H428N |
probably damaging |
Het |
Pigg |
G |
A |
5: 108,486,485 (GRCm39) |
V713I |
probably benign |
Het |
Rgs3 |
A |
G |
4: 62,619,349 (GRCm39) |
D478G |
possibly damaging |
Het |
Scgb2b11 |
C |
T |
7: 31,909,883 (GRCm39) |
E68K |
probably damaging |
Het |
Sema4b |
C |
A |
7: 79,869,995 (GRCm39) |
Q428K |
probably benign |
Het |
Semp2l2a |
A |
T |
8: 13,887,995 (GRCm39) |
I32K |
probably benign |
Het |
Serpine2 |
T |
C |
1: 79,780,622 (GRCm39) |
T276A |
probably benign |
Het |
Sgo2b |
G |
A |
8: 64,393,108 (GRCm39) |
H110Y |
probably benign |
Het |
Slc12a7 |
T |
C |
13: 73,954,208 (GRCm39) |
L833S |
probably benign |
Het |
Slc6a15 |
T |
A |
10: 103,229,241 (GRCm39) |
|
probably null |
Het |
Srfbp1 |
G |
A |
18: 52,608,671 (GRCm39) |
V24I |
probably damaging |
Het |
Stpg2 |
A |
T |
3: 139,407,458 (GRCm39) |
N537Y |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,087,782 (GRCm39) |
S1766T |
probably benign |
Het |
Tiam2 |
T |
A |
17: 3,532,880 (GRCm39) |
M1K |
probably null |
Het |
Tmem245 |
A |
T |
4: 56,899,170 (GRCm39) |
I661K |
possibly damaging |
Het |
Trim5 |
T |
C |
7: 103,928,569 (GRCm39) |
H124R |
probably damaging |
Het |
Trim67 |
T |
A |
8: 125,547,024 (GRCm39) |
L478Q |
probably damaging |
Het |
Triml2 |
A |
G |
8: 43,646,357 (GRCm39) |
D282G |
probably damaging |
Het |
Txndc11 |
T |
C |
16: 10,905,793 (GRCm39) |
Y579C |
probably damaging |
Het |
Ube3c |
T |
A |
5: 29,824,629 (GRCm39) |
D551E |
probably damaging |
Het |
Vmn1r194 |
T |
C |
13: 22,428,767 (GRCm39) |
V128A |
not run |
Het |
Vmn2r130 |
T |
A |
17: 23,296,006 (GRCm39) |
D725E |
probably damaging |
Het |
Vmn2r70 |
T |
G |
7: 85,218,130 (GRCm39) |
N56T |
probably damaging |
Het |
Wdr95 |
T |
C |
5: 149,517,945 (GRCm39) |
V501A |
possibly damaging |
Het |
Zc3h8 |
T |
C |
2: 128,772,742 (GRCm39) |
T249A |
probably damaging |
Het |
Zfp54 |
T |
C |
17: 21,654,501 (GRCm39) |
C332R |
probably damaging |
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 |
|
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 |
R9376:Ifi205
|
UTSW |
1 |
173,854,221 (GRCm39) |
missense |
probably benign |
|
R9477:Ifi205
|
UTSW |
1 |
173,854,155 (GRCm39) |
missense |
probably benign |
|
|