Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp8a1 |
A |
G |
5: 67,824,994 (GRCm39) |
V779A |
probably benign |
Het |
Atrn |
T |
C |
2: 130,844,715 (GRCm39) |
S1199P |
probably damaging |
Het |
BC051076 |
C |
A |
5: 88,112,549 (GRCm39) |
|
probably benign |
Het |
Cdh17 |
T |
C |
4: 11,784,621 (GRCm39) |
|
probably benign |
Het |
Ceacam20 |
T |
C |
7: 19,708,199 (GRCm39) |
V268A |
probably damaging |
Het |
Cntn2 |
T |
G |
1: 132,455,909 (GRCm39) |
D203A |
probably damaging |
Het |
Cped1 |
A |
G |
6: 22,051,300 (GRCm39) |
N148D |
probably benign |
Het |
Dnah10 |
T |
A |
5: 124,861,010 (GRCm39) |
V2131E |
probably damaging |
Het |
Dsn1 |
A |
G |
2: 156,841,054 (GRCm39) |
|
probably null |
Het |
Fam237b |
T |
A |
5: 5,625,475 (GRCm39) |
I57K |
probably damaging |
Het |
Gaa |
T |
C |
11: 119,175,003 (GRCm39) |
V868A |
probably benign |
Het |
Igf1r |
A |
G |
7: 67,843,189 (GRCm39) |
T767A |
probably benign |
Het |
Ints7 |
T |
A |
1: 191,347,905 (GRCm39) |
V759E |
possibly damaging |
Het |
Jarid2 |
A |
G |
13: 45,038,311 (GRCm39) |
T171A |
probably damaging |
Het |
Krt33b |
T |
C |
11: 99,917,378 (GRCm39) |
D158G |
probably damaging |
Het |
Krt87 |
T |
C |
15: 101,334,414 (GRCm39) |
R198G |
probably benign |
Het |
Mst1r |
C |
A |
9: 107,788,791 (GRCm39) |
R437S |
probably damaging |
Het |
Myh15 |
T |
A |
16: 48,920,585 (GRCm39) |
I458K |
possibly damaging |
Het |
Or8k37 |
T |
C |
2: 86,469,283 (GRCm39) |
I256M |
possibly damaging |
Het |
Scn9a |
A |
T |
2: 66,324,230 (GRCm39) |
N1418K |
probably benign |
Het |
Sppl2a |
A |
G |
2: 126,762,232 (GRCm39) |
|
probably null |
Het |
Styxl2 |
G |
T |
1: 165,927,941 (GRCm39) |
A557E |
probably benign |
Het |
Zfp595 |
A |
T |
13: 67,465,465 (GRCm39) |
I266K |
possibly damaging |
Het |
|
Other mutations in Eif5b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Eif5b
|
APN |
1 |
38,080,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01377:Eif5b
|
APN |
1 |
38,075,179 (GRCm39) |
missense |
probably benign |
|
IGL01395:Eif5b
|
APN |
1 |
38,076,339 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01615:Eif5b
|
APN |
1 |
38,084,787 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02141:Eif5b
|
APN |
1 |
38,071,403 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02260:Eif5b
|
APN |
1 |
38,084,537 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02308:Eif5b
|
APN |
1 |
38,080,828 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Eif5b
|
APN |
1 |
38,075,350 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03327:Eif5b
|
APN |
1 |
38,080,772 (GRCm39) |
splice site |
probably benign |
|
R0018:Eif5b
|
UTSW |
1 |
38,057,970 (GRCm39) |
missense |
unknown |
|
R0036:Eif5b
|
UTSW |
1 |
38,058,192 (GRCm39) |
missense |
probably benign |
0.23 |
R0137:Eif5b
|
UTSW |
1 |
38,058,324 (GRCm39) |
missense |
probably benign |
0.23 |
R0349:Eif5b
|
UTSW |
1 |
38,071,447 (GRCm39) |
missense |
probably benign |
0.18 |
R0606:Eif5b
|
UTSW |
1 |
38,087,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R1056:Eif5b
|
UTSW |
1 |
38,061,248 (GRCm39) |
missense |
unknown |
|
R1225:Eif5b
|
UTSW |
1 |
38,076,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R2043:Eif5b
|
UTSW |
1 |
38,080,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R2163:Eif5b
|
UTSW |
1 |
38,087,875 (GRCm39) |
missense |
probably benign |
0.32 |
R2225:Eif5b
|
UTSW |
1 |
38,058,304 (GRCm39) |
missense |
unknown |
|
R2432:Eif5b
|
UTSW |
1 |
38,058,423 (GRCm39) |
missense |
unknown |
|
R2922:Eif5b
|
UTSW |
1 |
38,057,100 (GRCm39) |
splice site |
probably benign |
|
R4357:Eif5b
|
UTSW |
1 |
38,089,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Eif5b
|
UTSW |
1 |
38,080,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Eif5b
|
UTSW |
1 |
38,084,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R4702:Eif5b
|
UTSW |
1 |
38,057,958 (GRCm39) |
missense |
unknown |
|
R4941:Eif5b
|
UTSW |
1 |
38,090,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Eif5b
|
UTSW |
1 |
38,090,792 (GRCm39) |
makesense |
probably null |
|
R5020:Eif5b
|
UTSW |
1 |
38,058,150 (GRCm39) |
nonsense |
probably null |
|
R5175:Eif5b
|
UTSW |
1 |
38,084,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R5375:Eif5b
|
UTSW |
1 |
38,084,835 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5566:Eif5b
|
UTSW |
1 |
38,084,765 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5566:Eif5b
|
UTSW |
1 |
38,090,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R5853:Eif5b
|
UTSW |
1 |
38,076,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R5978:Eif5b
|
UTSW |
1 |
38,037,361 (GRCm39) |
splice site |
probably null |
|
R6315:Eif5b
|
UTSW |
1 |
38,057,114 (GRCm39) |
missense |
unknown |
|
R6376:Eif5b
|
UTSW |
1 |
38,084,760 (GRCm39) |
missense |
probably damaging |
0.98 |
R6388:Eif5b
|
UTSW |
1 |
38,058,081 (GRCm39) |
missense |
unknown |
|
R6444:Eif5b
|
UTSW |
1 |
38,075,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Eif5b
|
UTSW |
1 |
38,058,108 (GRCm39) |
missense |
probably benign |
0.23 |
R6810:Eif5b
|
UTSW |
1 |
38,085,741 (GRCm39) |
missense |
probably benign |
0.45 |
R6877:Eif5b
|
UTSW |
1 |
38,089,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7130:Eif5b
|
UTSW |
1 |
38,080,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Eif5b
|
UTSW |
1 |
38,088,155 (GRCm39) |
missense |
probably damaging |
0.98 |
R7439:Eif5b
|
UTSW |
1 |
38,090,718 (GRCm39) |
missense |
probably benign |
0.28 |
R7488:Eif5b
|
UTSW |
1 |
38,089,387 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8140:Eif5b
|
UTSW |
1 |
38,090,357 (GRCm39) |
missense |
probably benign |
0.41 |
R8166:Eif5b
|
UTSW |
1 |
38,087,901 (GRCm39) |
missense |
probably benign |
0.11 |
R8191:Eif5b
|
UTSW |
1 |
38,075,283 (GRCm39) |
missense |
probably damaging |
0.98 |
R8304:Eif5b
|
UTSW |
1 |
38,084,774 (GRCm39) |
missense |
probably benign |
0.11 |
R8549:Eif5b
|
UTSW |
1 |
38,076,288 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8558:Eif5b
|
UTSW |
1 |
38,083,795 (GRCm39) |
missense |
probably damaging |
0.99 |
R8893:Eif5b
|
UTSW |
1 |
38,090,300 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9452:Eif5b
|
UTSW |
1 |
38,084,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R9487:Eif5b
|
UTSW |
1 |
38,084,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R9487:Eif5b
|
UTSW |
1 |
38,058,451 (GRCm39) |
nonsense |
probably null |
|
R9542:Eif5b
|
UTSW |
1 |
38,057,131 (GRCm39) |
nonsense |
probably null |
|
R9721:Eif5b
|
UTSW |
1 |
38,076,740 (GRCm39) |
critical splice donor site |
probably null |
|
R9745:Eif5b
|
UTSW |
1 |
38,084,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Eif5b
|
UTSW |
1 |
38,090,241 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF018:Eif5b
|
UTSW |
1 |
38,060,673 (GRCm39) |
critical splice acceptor site |
probably null |
|
|