Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap31 |
A |
G |
16: 38,423,190 (GRCm39) |
S959P |
probably damaging |
Het |
Arrb2 |
G |
A |
11: 70,327,005 (GRCm39) |
G24D |
probably damaging |
Het |
Catsper4 |
A |
G |
4: 133,945,519 (GRCm39) |
I180T |
probably damaging |
Het |
Chst15 |
G |
A |
7: 131,872,186 (GRCm39) |
Q32* |
probably null |
Het |
Cntnap5c |
A |
T |
17: 58,469,200 (GRCm39) |
Y594F |
possibly damaging |
Het |
Cse1l |
T |
A |
2: 166,784,977 (GRCm39) |
|
probably benign |
Het |
Dab1 |
A |
T |
4: 104,538,798 (GRCm39) |
I201F |
possibly damaging |
Het |
Fkbp1b |
T |
C |
12: 4,888,220 (GRCm39) |
|
probably benign |
Het |
Fryl |
C |
A |
5: 73,245,792 (GRCm39) |
V1122F |
possibly damaging |
Het |
Gas2l2 |
A |
G |
11: 83,317,036 (GRCm39) |
|
probably benign |
Het |
Gstt2 |
A |
T |
10: 75,668,655 (GRCm39) |
|
probably null |
Het |
H4c14 |
T |
C |
3: 96,170,458 (GRCm39) |
T55A |
possibly damaging |
Het |
Hcst |
T |
G |
7: 30,118,036 (GRCm39) |
|
probably benign |
Het |
Hectd4 |
A |
G |
5: 121,466,445 (GRCm39) |
E2420G |
possibly damaging |
Het |
Ifi206 |
A |
T |
1: 173,308,344 (GRCm39) |
S551T |
probably benign |
Het |
Itgb3bp |
A |
G |
4: 99,657,724 (GRCm39) |
|
probably benign |
Het |
Krtap6-2 |
A |
G |
16: 89,216,644 (GRCm39) |
Y108H |
unknown |
Het |
Krtap6-5 |
T |
G |
16: 88,844,740 (GRCm39) |
|
probably benign |
Het |
Muc5b |
A |
G |
7: 141,415,699 (GRCm39) |
T2882A |
possibly damaging |
Het |
Nup214 |
C |
T |
2: 31,900,233 (GRCm39) |
T854M |
probably damaging |
Het |
Olfml2b |
A |
G |
1: 170,477,401 (GRCm39) |
K179E |
probably benign |
Het |
Or10d1b |
A |
G |
9: 39,613,871 (GRCm39) |
S65P |
probably damaging |
Het |
Or4k37 |
A |
T |
2: 111,159,229 (GRCm39) |
H155L |
probably damaging |
Het |
Per2 |
A |
T |
1: 91,351,950 (GRCm39) |
I852K |
possibly damaging |
Het |
Pkhd1 |
A |
T |
1: 20,187,247 (GRCm39) |
I3687N |
probably damaging |
Het |
Slc7a2 |
A |
T |
8: 41,369,410 (GRCm39) |
S622C |
probably damaging |
Het |
Smarcc2 |
G |
A |
10: 128,318,781 (GRCm39) |
V719I |
probably damaging |
Het |
Syne2 |
T |
C |
12: 75,972,209 (GRCm39) |
I1033T |
possibly damaging |
Het |
Tmod1 |
T |
C |
4: 46,096,999 (GRCm39) |
I264T |
probably damaging |
Het |
Tmtc3 |
G |
A |
10: 100,283,581 (GRCm39) |
A658V |
possibly damaging |
Het |
Top6bl |
T |
C |
19: 4,748,206 (GRCm39) |
E164G |
probably benign |
Het |
Tpm3 |
A |
G |
3: 89,981,079 (GRCm39) |
E56G |
possibly damaging |
Het |
Tra2b |
T |
C |
16: 22,065,993 (GRCm39) |
|
probably benign |
Het |
Trmu |
T |
A |
15: 85,779,138 (GRCm39) |
Y262N |
possibly damaging |
Het |
Uox |
C |
T |
3: 146,331,590 (GRCm39) |
T213I |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,818,517 (GRCm39) |
W2R |
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 |
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 |
R8092:Eif2ak4
|
UTSW |
2 |
118,272,513 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|