Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
G |
5: 77,049,957 (GRCm39) |
V13A |
probably benign |
Het |
Atp8b5 |
T |
A |
4: 43,305,774 (GRCm39) |
I106K |
possibly damaging |
Het |
Cdh15 |
T |
C |
8: 123,592,111 (GRCm39) |
S633P |
probably benign |
Het |
Celsr3 |
A |
G |
9: 108,723,134 (GRCm39) |
T228A |
probably benign |
Het |
Cfap90 |
T |
A |
13: 68,759,312 (GRCm39) |
F95L |
probably benign |
Het |
Chrng |
A |
G |
1: 87,137,606 (GRCm39) |
|
probably null |
Het |
Coprs |
T |
C |
8: 13,935,782 (GRCm39) |
E79G |
probably damaging |
Het |
Cpb2 |
A |
C |
14: 75,520,758 (GRCm39) |
Y391S |
probably damaging |
Het |
Cyp2j8 |
A |
T |
4: 96,358,815 (GRCm39) |
I368N |
probably damaging |
Het |
Ddah1 |
T |
C |
3: 145,464,842 (GRCm39) |
F76L |
probably benign |
Het |
Exoc6b |
T |
A |
6: 84,835,411 (GRCm39) |
M375L |
probably benign |
Het |
Fasn |
T |
C |
11: 120,706,502 (GRCm39) |
E994G |
probably damaging |
Het |
Fem1a |
T |
A |
17: 56,565,640 (GRCm39) |
C578S |
probably benign |
Het |
Garnl3 |
A |
G |
2: 32,936,606 (GRCm39) |
S188P |
probably damaging |
Het |
Gpn3 |
T |
C |
5: 122,516,551 (GRCm39) |
V60A |
possibly damaging |
Het |
Hnrnpr |
A |
G |
4: 136,043,690 (GRCm39) |
D59G |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,145,094 (GRCm39) |
E815V |
probably damaging |
Het |
Itga9 |
C |
T |
9: 118,487,601 (GRCm39) |
T228M |
probably damaging |
Het |
Kpna7 |
T |
C |
5: 144,930,884 (GRCm39) |
I320M |
probably damaging |
Het |
Lnpep |
T |
C |
17: 17,791,234 (GRCm39) |
T437A |
probably damaging |
Het |
Ltf |
C |
T |
9: 110,868,015 (GRCm39) |
T48I |
probably benign |
Het |
Masp1 |
T |
G |
16: 23,313,476 (GRCm39) |
D153A |
probably damaging |
Het |
Mcpt9 |
T |
A |
14: 56,264,373 (GRCm39) |
R241* |
probably null |
Het |
Msantd4 |
T |
A |
9: 4,384,787 (GRCm39) |
S171T |
probably damaging |
Het |
Nos1 |
G |
A |
5: 118,081,382 (GRCm39) |
V1229M |
probably damaging |
Het |
Npc1l1 |
A |
G |
11: 6,179,246 (GRCm39) |
S55P |
probably benign |
Het |
Oc90 |
T |
C |
15: 65,759,983 (GRCm39) |
K212R |
probably benign |
Het |
Or2a12 |
A |
G |
6: 42,904,830 (GRCm39) |
I222V |
probably benign |
Het |
Or5t15 |
C |
T |
2: 86,681,130 (GRCm39) |
R304K |
probably benign |
Het |
Or6c202 |
C |
A |
10: 128,996,439 (GRCm39) |
C138F |
probably damaging |
Het |
Prr12 |
T |
A |
7: 44,697,980 (GRCm39) |
Q645L |
unknown |
Het |
Psmd9 |
A |
G |
5: 123,384,278 (GRCm39) |
I145V |
probably benign |
Het |
Rbks |
T |
C |
5: 31,817,407 (GRCm39) |
I121V |
probably benign |
Het |
Rnase2b |
A |
T |
14: 51,400,264 (GRCm39) |
Y115F |
probably damaging |
Het |
Sarnp |
A |
G |
10: 128,675,723 (GRCm39) |
E78G |
probably benign |
Het |
Sltm |
A |
G |
9: 70,498,946 (GRCm39) |
S1007G |
probably benign |
Het |
Spata31d1c |
T |
A |
13: 65,182,759 (GRCm39) |
Y100* |
probably null |
Het |
Srrm2 |
T |
C |
17: 24,029,720 (GRCm39) |
S222P |
probably benign |
Het |
Sult3a1 |
G |
A |
10: 33,740,046 (GRCm39) |
R35Q |
possibly damaging |
Het |
Tfap4 |
T |
C |
16: 4,369,224 (GRCm39) |
D132G |
probably damaging |
Het |
Tmem53 |
C |
T |
4: 117,125,285 (GRCm39) |
Q111* |
probably null |
Het |
Togaram1 |
T |
A |
12: 65,068,274 (GRCm39) |
V1709D |
probably damaging |
Het |
Trpm3 |
A |
T |
19: 22,878,483 (GRCm39) |
D628V |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,544,838 (GRCm39) |
K31009* |
probably null |
Het |
Vldlr |
A |
G |
19: 27,217,120 (GRCm39) |
I58V |
probably benign |
Het |
Vmn1r4 |
T |
C |
6: 56,934,231 (GRCm39) |
F245S |
probably benign |
Het |
Vrtn |
T |
A |
12: 84,695,258 (GRCm39) |
S3T |
probably damaging |
Het |
Vwa7 |
A |
G |
17: 35,242,476 (GRCm39) |
|
probably null |
Het |
Wrnip1 |
T |
A |
13: 33,006,053 (GRCm39) |
Y632N |
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 |
|
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 |
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 |
|