Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,197,179 (GRCm39) |
F251I |
possibly damaging |
Het |
Abcb11 |
C |
T |
2: 69,108,146 (GRCm39) |
G717D |
probably benign |
Het |
Abcc1 |
G |
A |
16: 14,207,763 (GRCm39) |
W47* |
probably null |
Het |
Ahnak2 |
A |
G |
12: 112,748,641 (GRCm39) |
I402T |
|
Het |
Ankfy1 |
G |
A |
11: 72,650,769 (GRCm39) |
R984Q |
probably benign |
Het |
Apaf1 |
A |
G |
10: 90,890,242 (GRCm39) |
I598T |
probably benign |
Het |
Apobec1 |
G |
T |
6: 122,558,521 (GRCm39) |
P78Q |
possibly damaging |
Het |
Asap1 |
A |
T |
15: 63,991,974 (GRCm39) |
I737N |
probably benign |
Het |
Aste1 |
T |
A |
9: 105,279,904 (GRCm39) |
|
probably null |
Het |
Bcr |
A |
C |
10: 74,996,162 (GRCm39) |
D902A |
possibly damaging |
Het |
Bicra |
T |
C |
7: 15,723,367 (GRCm39) |
|
probably null |
Het |
Ccdc27 |
T |
C |
4: 154,117,424 (GRCm39) |
T508A |
probably benign |
Het |
Ccz1 |
T |
A |
5: 143,928,401 (GRCm39) |
N383I |
probably damaging |
Het |
Cdh24 |
T |
C |
14: 54,869,637 (GRCm39) |
D760G |
possibly damaging |
Het |
Cdhr2 |
T |
C |
13: 54,865,728 (GRCm39) |
I242T |
probably benign |
Het |
Cdk4 |
T |
A |
10: 126,900,106 (GRCm39) |
M1K |
probably null |
Het |
Cfap96 |
A |
G |
8: 46,415,331 (GRCm39) |
V225A |
probably benign |
Het |
Cntn5 |
A |
T |
9: 9,970,570 (GRCm39) |
S302T |
probably damaging |
Het |
Col25a1 |
G |
T |
3: 130,378,350 (GRCm39) |
G601V |
probably damaging |
Het |
Cpb1 |
A |
G |
3: 20,324,488 (GRCm39) |
L62P |
possibly damaging |
Het |
Cpne1 |
T |
C |
2: 155,919,857 (GRCm39) |
T264A |
probably benign |
Het |
Cpvl |
T |
A |
6: 53,924,727 (GRCm39) |
N198Y |
probably damaging |
Het |
Cyp2u1 |
A |
C |
3: 131,091,596 (GRCm39) |
L308R |
probably damaging |
Het |
Ddx54 |
G |
T |
5: 120,762,789 (GRCm39) |
V637L |
probably benign |
Het |
Dglucy |
C |
A |
12: 100,823,310 (GRCm39) |
P472T |
possibly damaging |
Het |
Dync2h1 |
A |
G |
9: 7,124,855 (GRCm39) |
Y2006H |
probably benign |
Het |
Emsy |
A |
G |
7: 98,264,762 (GRCm39) |
V545A |
possibly damaging |
Het |
Ezh1 |
G |
A |
11: 101,091,726 (GRCm39) |
L480F |
possibly damaging |
Het |
Fbln2 |
T |
A |
6: 91,242,845 (GRCm39) |
|
probably null |
Het |
Gja10 |
T |
A |
4: 32,602,058 (GRCm39) |
K109* |
probably null |
Het |
Gm28042 |
A |
G |
2: 119,870,438 (GRCm39) |
N762S |
probably benign |
Het |
Gnb1l |
C |
A |
16: 18,359,220 (GRCm39) |
P7Q |
possibly damaging |
Het |
Grem2 |
A |
T |
1: 174,664,685 (GRCm39) |
S55T |
probably damaging |
Het |
Gsn |
A |
T |
2: 35,186,433 (GRCm39) |
N393I |
possibly damaging |
Het |
H6pd |
T |
A |
4: 150,067,093 (GRCm39) |
Q439L |
probably benign |
Het |
Hmcn2 |
G |
A |
2: 31,310,842 (GRCm39) |
G3362E |
probably damaging |
Het |
Ighv11-2 |
T |
C |
12: 114,011,978 (GRCm39) |
Y79C |
probably damaging |
Het |
Ikzf2 |
T |
A |
1: 69,578,544 (GRCm39) |
N322Y |
probably benign |
Het |
Il25 |
A |
G |
14: 55,170,459 (GRCm39) |
I11V |
probably benign |
Het |
Jak2 |
C |
T |
19: 29,275,783 (GRCm39) |
T741I |
probably damaging |
Het |
Kdm3b |
T |
C |
18: 34,957,934 (GRCm39) |
S1300P |
probably damaging |
Het |
Ldb3 |
T |
A |
14: 34,289,402 (GRCm39) |
Q268L |
probably damaging |
Het |
Lrrc23 |
T |
A |
6: 124,756,075 (GRCm39) |
D6V |
unknown |
Het |
Megf10 |
A |
G |
18: 57,324,187 (GRCm39) |
Y76C |
probably damaging |
Het |
Neb |
A |
T |
2: 52,110,233 (GRCm39) |
M205K |
probably benign |
Het |
Or12e8 |
T |
C |
2: 87,188,597 (GRCm39) |
S270P |
probably damaging |
Het |
Or6c2b |
G |
T |
10: 128,947,605 (GRCm39) |
Q230K |
probably benign |
Het |
Or8a1 |
A |
G |
9: 37,641,983 (GRCm39) |
S99P |
probably damaging |
Het |
Pcnx3 |
G |
A |
19: 5,717,487 (GRCm39) |
R1541W |
possibly damaging |
Het |
Pdgfd |
A |
G |
9: 6,359,739 (GRCm39) |
Y270C |
probably damaging |
Het |
Pds5b |
A |
T |
5: 150,646,802 (GRCm39) |
D197V |
probably damaging |
Het |
Pknox2 |
A |
G |
9: 36,866,127 (GRCm39) |
M30T |
probably benign |
Het |
Plekhg1 |
A |
T |
10: 3,907,491 (GRCm39) |
S858C |
|
Het |
Por |
A |
T |
5: 135,762,498 (GRCm39) |
E400D |
probably benign |
Het |
Pou2af2 |
C |
A |
9: 51,201,360 (GRCm39) |
R232L |
probably damaging |
Het |
Psip1 |
A |
G |
4: 83,391,275 (GRCm39) |
|
probably null |
Het |
Retreg1 |
G |
T |
15: 25,889,628 (GRCm39) |
V111F |
|
Het |
Rock1 |
G |
A |
18: 10,122,762 (GRCm39) |
A353V |
probably damaging |
Het |
Rpl6 |
C |
G |
5: 121,346,591 (GRCm39) |
R231G |
probably benign |
Het |
Scn7a |
C |
T |
2: 66,587,574 (GRCm39) |
R43H |
probably benign |
Het |
Scnn1g |
T |
A |
7: 121,362,657 (GRCm39) |
N488K |
probably benign |
Het |
Slc24a1 |
A |
G |
9: 64,831,764 (GRCm39) |
V1111A |
probably benign |
Het |
Snapc1 |
C |
T |
12: 74,029,285 (GRCm39) |
S356L |
probably benign |
Het |
Spata31e2 |
T |
C |
1: 26,723,039 (GRCm39) |
T714A |
possibly damaging |
Het |
Ssbp2 |
T |
A |
13: 91,823,209 (GRCm39) |
N201K |
probably damaging |
Het |
Tfdp2 |
A |
G |
9: 96,179,695 (GRCm39) |
N43D |
probably damaging |
Het |
Tmprss11d |
A |
G |
5: 86,474,309 (GRCm39) |
I216T |
probably damaging |
Het |
Tmprss4 |
A |
G |
9: 45,086,853 (GRCm39) |
S303P |
probably benign |
Het |
Tnpo2 |
A |
G |
8: 85,781,663 (GRCm39) |
E815G |
probably benign |
Het |
Trav6-1 |
A |
C |
14: 52,875,972 (GRCm39) |
M1L |
possibly damaging |
Het |
Trpm3 |
T |
C |
19: 22,955,937 (GRCm39) |
V1133A |
probably damaging |
Het |
Trpv1 |
C |
T |
11: 73,129,355 (GRCm39) |
P91S |
probably benign |
Het |
Trpv2 |
T |
C |
11: 62,480,576 (GRCm39) |
Y338H |
probably damaging |
Het |
Txnip |
T |
C |
3: 96,467,539 (GRCm39) |
M336T |
probably benign |
Het |
Vmn1r61 |
A |
T |
7: 5,613,767 (GRCm39) |
H182Q |
possibly damaging |
Het |
Vmn2r105 |
A |
G |
17: 20,429,045 (GRCm39) |
V677A |
probably damaging |
Het |
Wwp1 |
G |
T |
4: 19,627,660 (GRCm39) |
T745K |
probably damaging |
Het |
Xkr5 |
C |
A |
8: 18,983,608 (GRCm39) |
E645* |
probably null |
Het |
Zfp451 |
C |
T |
1: 33,818,221 (GRCm39) |
R303H |
probably benign |
Het |
Zyg11b |
T |
C |
4: 108,123,655 (GRCm39) |
H104R |
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 |
IGL01572:Eif5b
|
APN |
1 |
38,061,335 (GRCm39) |
nonsense |
probably null |
|
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 |
38,090,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R5566:Eif5b
|
UTSW |
1 |
38,084,765 (GRCm39) |
missense |
possibly damaging |
0.90 |
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 |
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 |
|
|