Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
A |
T |
13: 61,001,414 (GRCm39) |
H104Q |
probably benign |
Het |
4933405L10Rik |
A |
G |
8: 106,436,201 (GRCm39) |
T158A |
possibly damaging |
Het |
A1cf |
T |
C |
19: 31,895,385 (GRCm39) |
M156T |
probably benign |
Het |
Abca15 |
A |
G |
7: 120,006,198 (GRCm39) |
Y1620C |
probably damaging |
Het |
Abca3 |
C |
T |
17: 24,593,274 (GRCm39) |
R224C |
probably damaging |
Het |
Ablim1 |
A |
G |
19: 57,062,285 (GRCm39) |
|
probably null |
Het |
Acox2 |
A |
T |
14: 8,241,374 (GRCm38) |
Y579* |
probably null |
Het |
Adnp |
A |
T |
2: 168,024,921 (GRCm39) |
S791R |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,071,665 (GRCm39) |
E329G |
probably damaging |
Het |
Alx3 |
G |
T |
3: 107,512,109 (GRCm39) |
S249I |
possibly damaging |
Het |
Apob |
A |
G |
12: 8,058,714 (GRCm39) |
T2366A |
probably benign |
Het |
Apool |
C |
T |
X: 111,259,540 (GRCm39) |
Q60* |
probably null |
Het |
Arid4a |
T |
C |
12: 71,091,853 (GRCm39) |
V213A |
probably benign |
Het |
Atp7a |
A |
G |
X: 105,153,374 (GRCm39) |
D1092G |
probably benign |
Het |
Bpifa5 |
A |
T |
2: 154,007,892 (GRCm39) |
E178V |
probably damaging |
Het |
Car4 |
G |
A |
11: 84,854,193 (GRCm39) |
E47K |
probably benign |
Het |
Catsper1 |
T |
C |
19: 5,390,074 (GRCm39) |
|
probably null |
Het |
Ccdc63 |
T |
A |
5: 122,259,118 (GRCm39) |
Q260L |
probably benign |
Het |
Ccdc83 |
A |
T |
7: 89,899,737 (GRCm39) |
F45Y |
probably damaging |
Het |
Cct8l1 |
G |
A |
5: 25,721,881 (GRCm39) |
V199I |
probably benign |
Het |
Cdc23 |
C |
A |
18: 34,784,742 (GRCm39) |
V7L |
unknown |
Het |
Ces5a |
C |
T |
8: 94,261,296 (GRCm39) |
V44M |
probably damaging |
Het |
Cltc |
A |
G |
11: 86,608,794 (GRCm39) |
I741T |
possibly damaging |
Het |
Cnst |
C |
A |
1: 179,450,451 (GRCm39) |
D638E |
possibly damaging |
Het |
Col13a1 |
A |
G |
10: 61,709,797 (GRCm39) |
|
silent |
Het |
Cyp2a22 |
A |
T |
7: 26,631,906 (GRCm39) |
F450Y |
probably benign |
Het |
Cyp2d10 |
C |
T |
15: 82,287,954 (GRCm39) |
R383H |
probably benign |
Het |
Cyp4a29 |
A |
G |
4: 115,104,860 (GRCm39) |
T123A |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,590,191 (GRCm39) |
|
probably null |
Het |
Dnaja3 |
A |
T |
16: 4,514,289 (GRCm39) |
T274S |
probably damaging |
Het |
Dot1l |
A |
G |
10: 80,620,480 (GRCm39) |
D514G |
possibly damaging |
Het |
Dysf |
A |
T |
6: 84,114,254 (GRCm39) |
K1226M |
probably damaging |
Het |
Fbxo42 |
T |
C |
4: 140,926,256 (GRCm39) |
W313R |
probably damaging |
Het |
Fign |
A |
T |
2: 63,810,037 (GRCm39) |
L411* |
probably null |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Fryl |
G |
A |
5: 73,232,110 (GRCm39) |
P1550L |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gprasp2 |
C |
T |
X: 134,743,346 (GRCm39) |
T235I |
possibly damaging |
Het |
Gtf2ird1 |
G |
T |
5: 134,419,787 (GRCm39) |
|
probably null |
Het |
H2ab3 |
T |
C |
X: 119,222,543 (GRCm39) |
T84A |
probably damaging |
Het |
H2ac20 |
C |
T |
3: 96,128,099 (GRCm39) |
|
probably benign |
Het |
Hal |
A |
T |
10: 93,349,904 (GRCm39) |
I555F |
probably damaging |
Het |
Hdac6 |
A |
G |
X: 7,811,036 (GRCm39) |
F104L |
probably damaging |
Homo |
Hspg2 |
T |
C |
4: 137,267,541 (GRCm39) |
S2050P |
probably damaging |
Het |
Irgc |
T |
C |
7: 24,132,196 (GRCm39) |
D207G |
probably benign |
Het |
Kif19a |
G |
A |
11: 114,658,053 (GRCm39) |
M37I |
probably benign |
Het |
Kiss1r |
C |
A |
10: 79,754,596 (GRCm39) |
S30* |
probably null |
Het |
Krtap1-4 |
C |
G |
11: 99,474,442 (GRCm39) |
|
probably benign |
Het |
Lrrfip2 |
A |
G |
9: 111,028,872 (GRCm39) |
E365G |
probably damaging |
Het |
Ly75 |
A |
G |
2: 60,206,307 (GRCm39) |
Y121H |
probably damaging |
Het |
Man2a1 |
G |
A |
17: 64,966,074 (GRCm39) |
|
probably null |
Het |
Mllt10 |
C |
A |
2: 18,114,685 (GRCm39) |
H52N |
possibly damaging |
Het |
Mrtfa |
A |
G |
15: 80,906,627 (GRCm39) |
V91A |
probably damaging |
Het |
Myo1a |
T |
C |
10: 127,543,288 (GRCm39) |
|
probably null |
Het |
Myo3b |
C |
A |
2: 69,925,593 (GRCm39) |
T20K |
possibly damaging |
Het |
Nipsnap2 |
A |
T |
5: 129,816,644 (GRCm39) |
K62N |
probably damaging |
Het |
Nr1i3 |
C |
T |
1: 171,044,382 (GRCm39) |
T169I |
probably benign |
Het |
Numbl |
G |
A |
7: 26,980,415 (GRCm39) |
D466N |
probably damaging |
Het |
Oprm1 |
A |
G |
10: 6,782,550 (GRCm39) |
S398G |
probably benign |
Het |
Or14c46 |
A |
G |
7: 85,918,799 (GRCm39) |
I66T |
probably damaging |
Het |
Or51k1 |
T |
A |
7: 103,661,325 (GRCm39) |
R195W |
probably damaging |
Het |
Or6k2 |
A |
T |
1: 173,986,527 (GRCm39) |
I63F |
probably damaging |
Het |
Or8h10 |
A |
T |
2: 86,808,666 (GRCm39) |
V158D |
possibly damaging |
Het |
Pebp1 |
G |
T |
5: 117,421,475 (GRCm39) |
D156E |
probably benign |
Het |
Pik3c2g |
T |
A |
6: 139,665,873 (GRCm39) |
C65S |
probably null |
Het |
Pilra |
A |
G |
5: 137,833,674 (GRCm39) |
F131L |
probably damaging |
Het |
Pitrm1 |
T |
C |
13: 6,603,226 (GRCm39) |
F91S |
probably damaging |
Het |
Ppl |
A |
T |
16: 4,906,742 (GRCm39) |
S1184R |
probably benign |
Het |
Prmt2 |
C |
T |
10: 76,058,390 (GRCm39) |
V140I |
probably damaging |
Het |
Psg29 |
T |
A |
7: 16,945,763 (GRCm39) |
D444E |
probably damaging |
Het |
Ptgs1 |
A |
T |
2: 36,141,272 (GRCm39) |
N573I |
probably damaging |
Het |
Pygb |
C |
T |
2: 150,643,498 (GRCm39) |
T95M |
probably damaging |
Het |
Rassf9 |
A |
G |
10: 102,381,766 (GRCm39) |
K383E |
probably damaging |
Het |
Rfk |
T |
A |
19: 17,375,963 (GRCm39) |
F86I |
possibly damaging |
Het |
Rims2 |
T |
C |
15: 39,325,986 (GRCm39) |
F773L |
probably benign |
Het |
Sdcbp |
A |
G |
4: 6,393,019 (GRCm39) |
I218V |
probably benign |
Het |
Slc4a2 |
G |
A |
5: 24,643,760 (GRCm39) |
S855N |
probably benign |
Het |
Slc8a2 |
T |
C |
7: 15,884,508 (GRCm39) |
L626P |
possibly damaging |
Het |
Snrpd3 |
G |
T |
10: 75,355,227 (GRCm39) |
C20F |
possibly damaging |
Het |
Spen |
A |
T |
4: 141,249,613 (GRCm39) |
S58R |
unknown |
Het |
St3gal2 |
T |
C |
8: 111,684,350 (GRCm39) |
C3R |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,699,422 (GRCm39) |
I481N |
probably benign |
Het |
Stat5b |
T |
C |
11: 100,699,361 (GRCm39) |
|
probably null |
Het |
Tmco3 |
G |
T |
8: 13,342,860 (GRCm39) |
E199* |
probably null |
Het |
Tmem26 |
A |
G |
10: 68,611,178 (GRCm39) |
T216A |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,550,822 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,602,709 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
T |
2: 76,576,746 (GRCm39) |
V24716I |
probably damaging |
Het |
Uba5 |
T |
C |
9: 103,931,626 (GRCm39) |
E202G |
probably damaging |
Het |
Ufl1 |
A |
G |
4: 25,254,780 (GRCm39) |
Y559H |
probably benign |
Het |
Utrn |
A |
T |
10: 12,259,948 (GRCm39) |
|
probably null |
Het |
Vmn2r111 |
C |
A |
17: 22,767,022 (GRCm39) |
C825F |
probably damaging |
Het |
Vmn2r113 |
T |
A |
17: 23,177,329 (GRCm39) |
C704* |
probably null |
Het |
Vmn2r56 |
A |
G |
7: 12,427,983 (GRCm39) |
I761T |
probably benign |
Het |
Vmn2r98 |
C |
T |
17: 19,286,306 (GRCm39) |
T268I |
probably benign |
Het |
Zfp263 |
A |
G |
16: 3,564,704 (GRCm39) |
R240G |
possibly damaging |
Het |
Zfp473 |
T |
A |
7: 44,381,943 (GRCm39) |
I797F |
probably damaging |
Het |
Zfp68 |
A |
T |
5: 138,604,579 (GRCm39) |
D543E |
probably benign |
Het |
|
Other mutations in Epha4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01315:Epha4
|
APN |
1 |
77,375,194 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01350:Epha4
|
APN |
1 |
77,483,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01657:Epha4
|
APN |
1 |
77,403,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Epha4
|
APN |
1 |
77,359,676 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02366:Epha4
|
APN |
1 |
77,403,348 (GRCm39) |
nonsense |
probably null |
|
IGL02426:Epha4
|
APN |
1 |
77,421,514 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02428:Epha4
|
APN |
1 |
77,483,385 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02706:Epha4
|
APN |
1 |
77,403,482 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02716:Epha4
|
APN |
1 |
77,357,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03348:Epha4
|
APN |
1 |
77,483,809 (GRCm39) |
missense |
possibly damaging |
0.82 |
frog
|
UTSW |
1 |
77,481,076 (GRCm38) |
intron |
probably benign |
|
R0324:Epha4
|
UTSW |
1 |
77,360,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R0392:Epha4
|
UTSW |
1 |
77,483,610 (GRCm39) |
missense |
probably benign |
0.00 |
R0538:Epha4
|
UTSW |
1 |
77,365,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R0562:Epha4
|
UTSW |
1 |
77,365,124 (GRCm39) |
missense |
probably benign |
0.00 |
R0885:Epha4
|
UTSW |
1 |
77,359,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R1509:Epha4
|
UTSW |
1 |
77,357,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R1620:Epha4
|
UTSW |
1 |
77,351,563 (GRCm39) |
missense |
probably benign |
0.31 |
R1624:Epha4
|
UTSW |
1 |
77,376,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Epha4
|
UTSW |
1 |
77,351,405 (GRCm39) |
splice site |
probably null |
|
R1755:Epha4
|
UTSW |
1 |
77,364,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1807:Epha4
|
UTSW |
1 |
77,351,541 (GRCm39) |
missense |
probably benign |
0.05 |
R2046:Epha4
|
UTSW |
1 |
77,483,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Epha4
|
UTSW |
1 |
77,359,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Epha4
|
UTSW |
1 |
77,488,339 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2511:Epha4
|
UTSW |
1 |
77,488,339 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3441:Epha4
|
UTSW |
1 |
77,403,333 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3724:Epha4
|
UTSW |
1 |
77,403,180 (GRCm39) |
splice site |
probably benign |
|
R3901:Epha4
|
UTSW |
1 |
77,357,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R3950:Epha4
|
UTSW |
1 |
77,376,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R3951:Epha4
|
UTSW |
1 |
77,376,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R3952:Epha4
|
UTSW |
1 |
77,376,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4012:Epha4
|
UTSW |
1 |
77,366,731 (GRCm39) |
splice site |
probably benign |
|
R4321:Epha4
|
UTSW |
1 |
77,483,850 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4422:Epha4
|
UTSW |
1 |
77,488,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R4898:Epha4
|
UTSW |
1 |
77,366,712 (GRCm39) |
nonsense |
probably null |
|
R5270:Epha4
|
UTSW |
1 |
77,483,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R5281:Epha4
|
UTSW |
1 |
77,351,504 (GRCm39) |
missense |
probably benign |
|
R5315:Epha4
|
UTSW |
1 |
77,365,109 (GRCm39) |
critical splice donor site |
probably null |
|
R5531:Epha4
|
UTSW |
1 |
77,351,513 (GRCm39) |
missense |
probably benign |
|
R5621:Epha4
|
UTSW |
1 |
77,491,686 (GRCm39) |
utr 5 prime |
probably benign |
|
R5648:Epha4
|
UTSW |
1 |
77,375,162 (GRCm39) |
missense |
probably benign |
0.25 |
R5747:Epha4
|
UTSW |
1 |
77,483,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R5829:Epha4
|
UTSW |
1 |
77,421,631 (GRCm39) |
missense |
probably benign |
0.01 |
R6185:Epha4
|
UTSW |
1 |
77,483,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R6486:Epha4
|
UTSW |
1 |
77,360,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R6821:Epha4
|
UTSW |
1 |
77,359,582 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6978:Epha4
|
UTSW |
1 |
77,354,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Epha4
|
UTSW |
1 |
77,483,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7216:Epha4
|
UTSW |
1 |
77,421,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R7270:Epha4
|
UTSW |
1 |
77,376,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7444:Epha4
|
UTSW |
1 |
77,364,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R7737:Epha4
|
UTSW |
1 |
77,357,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Epha4
|
UTSW |
1 |
77,366,668 (GRCm39) |
critical splice donor site |
probably null |
|
R7950:Epha4
|
UTSW |
1 |
77,483,833 (GRCm39) |
missense |
probably damaging |
0.99 |
R8297:Epha4
|
UTSW |
1 |
77,483,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R8373:Epha4
|
UTSW |
1 |
77,483,716 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8429:Epha4
|
UTSW |
1 |
77,366,673 (GRCm39) |
missense |
probably benign |
0.08 |
R8907:Epha4
|
UTSW |
1 |
77,483,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R9024:Epha4
|
UTSW |
1 |
77,365,169 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1088:Epha4
|
UTSW |
1 |
77,483,299 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1176:Epha4
|
UTSW |
1 |
77,359,648 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Epha4
|
UTSW |
1 |
77,350,370 (GRCm39) |
makesense |
probably null |
|
|