Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck1 |
T |
C |
12: 88,427,831 (GRCm39) |
S483P |
possibly damaging |
Het |
Agr3 |
T |
A |
12: 35,997,593 (GRCm39) |
|
probably null |
Het |
Anxa4 |
T |
C |
6: 86,718,873 (GRCm39) |
D282G |
probably damaging |
Het |
Aplp2 |
A |
C |
9: 31,074,640 (GRCm39) |
|
probably null |
Het |
Arfgef2 |
G |
A |
2: 166,701,754 (GRCm39) |
V714M |
probably damaging |
Het |
Cep295 |
A |
T |
9: 15,244,278 (GRCm39) |
F1393I |
probably benign |
Het |
Cfap206 |
G |
A |
4: 34,728,897 (GRCm39) |
P3S |
possibly damaging |
Het |
Chd5 |
T |
A |
4: 152,463,261 (GRCm39) |
D1410E |
probably damaging |
Het |
Chd8 |
T |
C |
14: 52,455,184 (GRCm39) |
Y1101C |
probably damaging |
Het |
Chtf8 |
A |
G |
8: 107,612,938 (GRCm39) |
V121A |
possibly damaging |
Het |
Dnajc3 |
A |
T |
14: 119,207,994 (GRCm39) |
|
probably null |
Het |
Dpys |
C |
T |
15: 39,710,010 (GRCm39) |
D140N |
probably benign |
Het |
Dsg1c |
A |
G |
18: 20,415,029 (GRCm39) |
Y642C |
probably damaging |
Het |
Gm45861 |
T |
C |
8: 28,057,823 (GRCm39) |
M1127T |
unknown |
Het |
Gnpnat1 |
A |
G |
14: 45,618,388 (GRCm39) |
|
probably null |
Het |
Hsd3b6 |
T |
A |
3: 98,713,456 (GRCm39) |
D281V |
possibly damaging |
Het |
Kng2 |
T |
A |
16: 22,806,672 (GRCm39) |
Q509L |
probably benign |
Het |
Lipo2 |
A |
T |
19: 33,726,880 (GRCm39) |
D52E |
probably benign |
Het |
Ly6g6c |
A |
G |
17: 35,287,867 (GRCm39) |
Y27C |
probably damaging |
Het |
Mcc |
G |
A |
18: 44,892,299 (GRCm39) |
T105I |
probably benign |
Het |
Neurl4 |
A |
G |
11: 69,801,891 (GRCm39) |
K1279E |
probably benign |
Het |
Ntmt2 |
A |
G |
1: 163,544,819 (GRCm39) |
Y55H |
probably damaging |
Het |
Ntn4 |
A |
C |
10: 93,576,918 (GRCm39) |
K529Q |
probably damaging |
Het |
Or4f57 |
C |
A |
2: 111,790,652 (GRCm39) |
M255I |
probably benign |
Het |
P2ry14 |
C |
T |
3: 59,022,867 (GRCm39) |
V198M |
probably damaging |
Het |
Pclo |
T |
A |
5: 14,727,560 (GRCm39) |
D2139E |
unknown |
Het |
Plxnb1 |
T |
A |
9: 108,929,573 (GRCm39) |
V143E |
probably damaging |
Het |
Prune2 |
G |
T |
19: 17,097,357 (GRCm39) |
D954Y |
probably damaging |
Het |
Qrsl1 |
G |
A |
10: 43,760,749 (GRCm39) |
P278L |
probably damaging |
Het |
Rnf17 |
C |
T |
14: 56,724,479 (GRCm39) |
R1108C |
probably benign |
Het |
Sipa1l2 |
T |
C |
8: 126,145,907 (GRCm39) |
S1716G |
probably benign |
Het |
Slfn4 |
A |
T |
11: 83,079,831 (GRCm39) |
H507L |
probably benign |
Het |
Snx18 |
T |
C |
13: 113,753,685 (GRCm39) |
E416G |
probably damaging |
Het |
Srp9 |
T |
C |
1: 181,959,001 (GRCm39) |
V81A |
probably benign |
Het |
Tex101 |
G |
A |
7: 24,369,778 (GRCm39) |
T62M |
probably damaging |
Het |
Utp25 |
G |
A |
1: 192,802,671 (GRCm39) |
L349F |
probably benign |
Het |
Wdfy4 |
G |
A |
14: 32,826,072 (GRCm39) |
P1193L |
|
Het |
Zbtb42 |
G |
T |
12: 112,646,275 (GRCm39) |
C150F |
probably damaging |
Het |
|
Other mutations in Eif2ak4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Eif2ak4
|
APN |
2 |
118,294,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00806:Eif2ak4
|
APN |
2 |
118,271,647 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01343:Eif2ak4
|
APN |
2 |
118,252,570 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01796:Eif2ak4
|
APN |
2 |
118,276,785 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02263:Eif2ak4
|
APN |
2 |
118,292,259 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02391:Eif2ak4
|
APN |
2 |
118,251,272 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02516:Eif2ak4
|
APN |
2 |
118,266,735 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02603:Eif2ak4
|
APN |
2 |
118,280,807 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02731:Eif2ak4
|
APN |
2 |
118,219,295 (GRCm39) |
missense |
probably benign |
|
IGL02928:Eif2ak4
|
APN |
2 |
118,303,168 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02947:Eif2ak4
|
APN |
2 |
118,261,514 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03191:Eif2ak4
|
APN |
2 |
118,252,693 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03202:Eif2ak4
|
APN |
2 |
118,231,101 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03235:Eif2ak4
|
APN |
2 |
118,273,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03375:Eif2ak4
|
APN |
2 |
118,252,799 (GRCm39) |
missense |
probably benign |
0.08 |
absurdum
|
UTSW |
2 |
118,251,291 (GRCm39) |
nonsense |
probably null |
|
Ad
|
UTSW |
2 |
118,266,722 (GRCm39) |
missense |
probably damaging |
1.00 |
atchoum
|
UTSW |
2 |
118,231,134 (GRCm39) |
splice site |
probably benign |
|
reductio
|
UTSW |
2 |
118,266,639 (GRCm39) |
splice site |
probably null |
|
PIT4520001:Eif2ak4
|
UTSW |
2 |
118,292,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Eif2ak4
|
UTSW |
2 |
118,293,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R0358:Eif2ak4
|
UTSW |
2 |
118,294,410 (GRCm39) |
splice site |
probably null |
|
R0482:Eif2ak4
|
UTSW |
2 |
118,292,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Eif2ak4
|
UTSW |
2 |
118,261,517 (GRCm39) |
missense |
probably benign |
0.01 |
R0523:Eif2ak4
|
UTSW |
2 |
118,272,577 (GRCm39) |
critical splice donor site |
probably null |
|
R0578:Eif2ak4
|
UTSW |
2 |
118,305,472 (GRCm39) |
splice site |
probably benign |
|
R0615:Eif2ak4
|
UTSW |
2 |
118,266,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1300:Eif2ak4
|
UTSW |
2 |
118,294,464 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1531:Eif2ak4
|
UTSW |
2 |
118,273,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Eif2ak4
|
UTSW |
2 |
118,261,320 (GRCm39) |
missense |
probably damaging |
0.98 |
R1866:Eif2ak4
|
UTSW |
2 |
118,303,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Eif2ak4
|
UTSW |
2 |
118,278,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R1977:Eif2ak4
|
UTSW |
2 |
118,292,238 (GRCm39) |
nonsense |
probably null |
|
R2011:Eif2ak4
|
UTSW |
2 |
118,261,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R2046:Eif2ak4
|
UTSW |
2 |
118,281,889 (GRCm39) |
splice site |
probably benign |
|
R2122:Eif2ak4
|
UTSW |
2 |
118,286,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Eif2ak4
|
UTSW |
2 |
118,252,604 (GRCm39) |
missense |
probably benign |
0.02 |
R2126:Eif2ak4
|
UTSW |
2 |
118,252,604 (GRCm39) |
missense |
probably benign |
0.02 |
R2193:Eif2ak4
|
UTSW |
2 |
118,252,747 (GRCm39) |
missense |
probably benign |
0.12 |
R2259:Eif2ak4
|
UTSW |
2 |
118,286,264 (GRCm39) |
missense |
probably damaging |
0.97 |
R2513:Eif2ak4
|
UTSW |
2 |
118,257,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R3798:Eif2ak4
|
UTSW |
2 |
118,304,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R3898:Eif2ak4
|
UTSW |
2 |
118,261,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R3900:Eif2ak4
|
UTSW |
2 |
118,305,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R4375:Eif2ak4
|
UTSW |
2 |
118,258,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4423:Eif2ak4
|
UTSW |
2 |
118,269,547 (GRCm39) |
missense |
probably benign |
0.01 |
R4589:Eif2ak4
|
UTSW |
2 |
118,247,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R4734:Eif2ak4
|
UTSW |
2 |
118,252,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R5173:Eif2ak4
|
UTSW |
2 |
118,238,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R5367:Eif2ak4
|
UTSW |
2 |
118,266,639 (GRCm39) |
splice site |
probably null |
|
R5471:Eif2ak4
|
UTSW |
2 |
118,304,613 (GRCm39) |
missense |
probably benign |
0.02 |
R5528:Eif2ak4
|
UTSW |
2 |
118,258,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R5634:Eif2ak4
|
UTSW |
2 |
118,292,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Eif2ak4
|
UTSW |
2 |
118,273,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R5756:Eif2ak4
|
UTSW |
2 |
118,293,221 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5779:Eif2ak4
|
UTSW |
2 |
118,243,444 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5807:Eif2ak4
|
UTSW |
2 |
118,219,332 (GRCm39) |
missense |
probably benign |
|
R6045:Eif2ak4
|
UTSW |
2 |
118,219,296 (GRCm39) |
nonsense |
probably null |
|
R6187:Eif2ak4
|
UTSW |
2 |
118,287,638 (GRCm39) |
missense |
probably damaging |
0.98 |
R6193:Eif2ak4
|
UTSW |
2 |
118,231,081 (GRCm39) |
start gained |
probably benign |
|
R6468:Eif2ak4
|
UTSW |
2 |
118,266,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R6555:Eif2ak4
|
UTSW |
2 |
118,258,350 (GRCm39) |
missense |
probably damaging |
0.96 |
R6616:Eif2ak4
|
UTSW |
2 |
118,285,326 (GRCm39) |
nonsense |
probably null |
|
R6737:Eif2ak4
|
UTSW |
2 |
118,292,749 (GRCm39) |
frame shift |
probably null |
|
R6956:Eif2ak4
|
UTSW |
2 |
118,252,748 (GRCm39) |
missense |
probably damaging |
0.96 |
R7075:Eif2ak4
|
UTSW |
2 |
118,251,291 (GRCm39) |
nonsense |
probably null |
|
R7109:Eif2ak4
|
UTSW |
2 |
118,235,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7228:Eif2ak4
|
UTSW |
2 |
118,287,638 (GRCm39) |
missense |
probably damaging |
0.98 |
R7441:Eif2ak4
|
UTSW |
2 |
118,302,377 (GRCm39) |
missense |
probably benign |
0.01 |
R7555:Eif2ak4
|
UTSW |
2 |
118,247,764 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7567:Eif2ak4
|
UTSW |
2 |
118,280,795 (GRCm39) |
missense |
probably benign |
|
R8004:Eif2ak4
|
UTSW |
2 |
118,247,775 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8063:Eif2ak4
|
UTSW |
2 |
118,241,382 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8195:Eif2ak4
|
UTSW |
2 |
118,280,819 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8306:Eif2ak4
|
UTSW |
2 |
118,287,656 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8470:Eif2ak4
|
UTSW |
2 |
118,293,207 (GRCm39) |
missense |
probably damaging |
0.98 |
R8671:Eif2ak4
|
UTSW |
2 |
118,252,667 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8693:Eif2ak4
|
UTSW |
2 |
118,262,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R8714:Eif2ak4
|
UTSW |
2 |
118,292,765 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8744:Eif2ak4
|
UTSW |
2 |
118,261,474 (GRCm39) |
nonsense |
probably null |
|
R8813:Eif2ak4
|
UTSW |
2 |
118,278,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R8917:Eif2ak4
|
UTSW |
2 |
118,287,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Eif2ak4
|
UTSW |
2 |
118,258,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R9177:Eif2ak4
|
UTSW |
2 |
118,271,701 (GRCm39) |
critical splice donor site |
probably null |
|
R9189:Eif2ak4
|
UTSW |
2 |
118,258,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Eif2ak4
|
UTSW |
2 |
118,271,662 (GRCm39) |
missense |
probably benign |
0.00 |
R9268:Eif2ak4
|
UTSW |
2 |
118,271,701 (GRCm39) |
critical splice donor site |
probably null |
|
R9321:Eif2ak4
|
UTSW |
2 |
118,292,798 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9512:Eif2ak4
|
UTSW |
2 |
118,293,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R9569:Eif2ak4
|
UTSW |
2 |
118,251,316 (GRCm39) |
missense |
probably benign |
0.00 |
R9658:Eif2ak4
|
UTSW |
2 |
118,269,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Eif2ak4
|
UTSW |
2 |
118,247,730 (GRCm39) |
missense |
probably benign |
0.01 |
R9757:Eif2ak4
|
UTSW |
2 |
118,269,398 (GRCm39) |
missense |
probably benign |
0.02 |
R9766:Eif2ak4
|
UTSW |
2 |
118,261,313 (GRCm39) |
nonsense |
probably null |
|
X0061:Eif2ak4
|
UTSW |
2 |
118,298,657 (GRCm39) |
missense |
probably damaging |
1.00 |
|