Other mutations in this stock |
Total: 129 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I07Rik |
A |
T |
14: 67,175,823 (GRCm39) |
H6L |
unknown |
Het |
Abca13 |
G |
A |
11: 9,217,622 (GRCm39) |
|
probably null |
Het |
Acad12 |
C |
T |
5: 121,745,511 (GRCm39) |
R260Q |
possibly damaging |
Het |
Actn1 |
G |
A |
12: 80,306,874 (GRCm39) |
|
probably benign |
Het |
Acvrl1 |
A |
G |
15: 101,034,030 (GRCm39) |
T182A |
probably damaging |
Het |
Adam23 |
T |
C |
1: 63,607,003 (GRCm39) |
|
probably benign |
Het |
Adamtsl1 |
A |
T |
4: 86,261,358 (GRCm39) |
T1190S |
probably benign |
Het |
Adh6b |
A |
T |
3: 138,063,411 (GRCm39) |
Y330F |
probably benign |
Het |
Ak7 |
A |
G |
12: 105,732,876 (GRCm39) |
E540G |
probably damaging |
Het |
Akr1c19 |
T |
A |
13: 4,287,099 (GRCm39) |
L106Q |
probably damaging |
Het |
Ankrd12 |
A |
T |
17: 66,356,847 (GRCm39) |
S57T |
probably damaging |
Het |
Aoc3 |
G |
A |
11: 101,222,964 (GRCm39) |
R400Q |
possibly damaging |
Het |
Arel1 |
A |
T |
12: 84,988,611 (GRCm39) |
I46N |
probably damaging |
Het |
Armc5 |
A |
G |
7: 127,843,463 (GRCm39) |
D752G |
probably damaging |
Het |
Atp11b |
T |
C |
3: 35,891,163 (GRCm39) |
V812A |
probably damaging |
Het |
Axin1 |
A |
G |
17: 26,403,215 (GRCm39) |
H131R |
possibly damaging |
Het |
Bpifb3 |
A |
G |
2: 153,765,789 (GRCm39) |
E184G |
probably benign |
Het |
Cacna2d2 |
T |
C |
9: 107,401,582 (GRCm39) |
|
probably benign |
Het |
Catsperd |
T |
C |
17: 56,969,828 (GRCm39) |
F641L |
probably benign |
Het |
Ccdc83 |
A |
C |
7: 89,877,591 (GRCm39) |
L284V |
probably damaging |
Het |
Ccn2 |
T |
A |
10: 24,472,364 (GRCm39) |
C136S |
probably damaging |
Het |
Ccnt2 |
T |
A |
1: 127,730,902 (GRCm39) |
V593E |
probably damaging |
Het |
Cd53 |
T |
A |
3: 106,669,444 (GRCm39) |
I185F |
probably benign |
Het |
Cep350 |
A |
T |
1: 155,724,366 (GRCm39) |
D3077E |
possibly damaging |
Het |
Ces1h |
C |
A |
8: 94,083,628 (GRCm39) |
|
probably null |
Het |
Chrna3 |
T |
A |
9: 54,923,290 (GRCm39) |
T173S |
probably benign |
Het |
Clca4b |
T |
C |
3: 144,627,717 (GRCm39) |
D418G |
probably benign |
Het |
Col11a2 |
T |
C |
17: 34,270,302 (GRCm39) |
|
probably benign |
Het |
Coq2 |
T |
A |
5: 100,815,889 (GRCm39) |
I97F |
possibly damaging |
Het |
Cr2 |
A |
G |
1: 194,842,667 (GRCm39) |
|
probably benign |
Het |
D2hgdh |
A |
G |
1: 93,754,099 (GRCm39) |
Y24C |
probably damaging |
Het |
D630045J12Rik |
G |
A |
6: 38,168,628 (GRCm39) |
R974C |
probably damaging |
Het |
Dach1 |
A |
G |
14: 98,140,715 (GRCm39) |
V429A |
possibly damaging |
Het |
Ddr1 |
G |
A |
17: 35,995,899 (GRCm39) |
T660I |
probably damaging |
Het |
Dlg1 |
A |
C |
16: 31,615,682 (GRCm39) |
|
probably null |
Het |
Dmbt1 |
T |
C |
7: 130,651,631 (GRCm39) |
|
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,301,120 (GRCm39) |
D2330E |
probably benign |
Het |
Dnai4 |
T |
C |
4: 102,953,815 (GRCm39) |
N128S |
possibly damaging |
Het |
Doc2a |
A |
G |
7: 126,447,983 (GRCm39) |
T5A |
probably benign |
Het |
Dock2 |
G |
A |
11: 34,595,545 (GRCm39) |
|
probably benign |
Het |
Dok4 |
T |
A |
8: 95,591,866 (GRCm39) |
Y290F |
probably damaging |
Het |
Dop1a |
A |
G |
9: 86,367,550 (GRCm39) |
D11G |
probably damaging |
Het |
E230025N22Rik |
T |
C |
18: 36,821,987 (GRCm39) |
H235R |
probably benign |
Het |
Ear6 |
A |
G |
14: 52,091,909 (GRCm39) |
D152G |
probably damaging |
Het |
Ecscr |
T |
A |
18: 35,846,689 (GRCm39) |
|
probably benign |
Het |
Eml6 |
A |
T |
11: 29,710,010 (GRCm39) |
|
probably benign |
Het |
Exoc4 |
A |
G |
6: 33,948,998 (GRCm39) |
N947S |
probably benign |
Het |
Flg |
A |
G |
3: 93,186,767 (GRCm39) |
E73G |
probably damaging |
Het |
Fndc1 |
C |
T |
17: 8,003,173 (GRCm39) |
|
probably benign |
Het |
Gad1-ps |
T |
C |
10: 99,280,854 (GRCm39) |
|
noncoding transcript |
Het |
Gata6 |
A |
G |
18: 11,064,771 (GRCm39) |
T528A |
probably benign |
Het |
Gjd4 |
T |
C |
18: 9,280,244 (GRCm39) |
E278G |
probably benign |
Het |
Gm20091 |
T |
A |
10: 96,244,864 (GRCm39) |
|
noncoding transcript |
Het |
Gnb3 |
G |
A |
6: 124,812,659 (GRCm39) |
Q266* |
probably null |
Het |
Grm3 |
A |
G |
5: 9,562,446 (GRCm39) |
V468A |
possibly damaging |
Het |
Igf1r |
C |
T |
7: 67,857,574 (GRCm39) |
R1085C |
probably damaging |
Het |
Igsf10 |
T |
C |
3: 59,227,527 (GRCm39) |
T2049A |
probably damaging |
Het |
Jak3 |
A |
T |
8: 72,138,126 (GRCm39) |
D859V |
probably benign |
Het |
Kcnb2 |
G |
T |
1: 15,783,108 (GRCm39) |
|
probably benign |
Het |
Kcnh3 |
G |
A |
15: 99,138,839 (GRCm39) |
G858D |
probably benign |
Het |
Kif1a |
C |
A |
1: 92,971,360 (GRCm39) |
R1006L |
probably damaging |
Het |
Klhl23 |
C |
T |
2: 69,654,757 (GRCm39) |
A209V |
probably benign |
Het |
Mapk13 |
T |
C |
17: 28,994,229 (GRCm39) |
Y104H |
probably damaging |
Het |
Mbd4 |
A |
G |
6: 115,826,443 (GRCm39) |
S183P |
probably damaging |
Het |
Mga |
T |
C |
2: 119,750,187 (GRCm39) |
|
probably null |
Het |
Mipol1 |
G |
A |
12: 57,461,197 (GRCm39) |
|
probably null |
Het |
Mmp14 |
A |
G |
14: 54,676,166 (GRCm39) |
T299A |
possibly damaging |
Het |
Mmrn1 |
A |
G |
6: 60,953,453 (GRCm39) |
E578G |
probably benign |
Het |
Mov10l1 |
G |
A |
15: 88,879,063 (GRCm39) |
C193Y |
possibly damaging |
Het |
Mppe1 |
A |
G |
18: 67,370,548 (GRCm39) |
C50R |
probably damaging |
Het |
Msantd1 |
C |
A |
5: 35,075,069 (GRCm39) |
R44S |
probably damaging |
Het |
Myt1l |
T |
C |
12: 29,892,570 (GRCm39) |
V69A |
possibly damaging |
Het |
Nav1 |
A |
T |
1: 135,392,430 (GRCm39) |
|
probably benign |
Het |
Ncan |
A |
G |
8: 70,561,252 (GRCm39) |
S572P |
possibly damaging |
Het |
Nck2 |
T |
C |
1: 43,608,304 (GRCm39) |
|
probably benign |
Het |
Nemf |
A |
T |
12: 69,403,088 (GRCm39) |
D31E |
probably damaging |
Het |
Nlrp12 |
T |
C |
7: 3,297,892 (GRCm39) |
D93G |
possibly damaging |
Het |
Nsmaf |
A |
T |
4: 6,419,930 (GRCm39) |
|
probably null |
Het |
Nup98 |
T |
C |
7: 101,835,892 (GRCm39) |
T184A |
probably damaging |
Het |
Oog2 |
C |
A |
4: 143,922,654 (GRCm39) |
Y306* |
probably null |
Het |
Or13a18 |
A |
T |
7: 140,190,297 (GRCm39) |
N73Y |
probably damaging |
Het |
Or6ae1 |
A |
T |
7: 139,742,144 (GRCm39) |
S240T |
probably damaging |
Het |
Or6b2b |
A |
T |
1: 92,419,055 (GRCm39) |
C141S |
possibly damaging |
Het |
Osmr |
A |
G |
15: 6,871,419 (GRCm39) |
|
probably benign |
Het |
P2rx6 |
A |
G |
16: 17,386,162 (GRCm39) |
N275S |
probably benign |
Het |
Pbxip1 |
G |
T |
3: 89,354,926 (GRCm39) |
G482W |
possibly damaging |
Het |
Pcsk4 |
T |
G |
10: 80,161,168 (GRCm39) |
I249L |
probably damaging |
Het |
Pou4f2 |
C |
T |
8: 79,162,291 (GRCm39) |
G104E |
probably damaging |
Het |
Pramel28 |
T |
A |
4: 143,691,653 (GRCm39) |
T357S |
possibly damaging |
Het |
Prkdc |
G |
T |
16: 15,651,652 (GRCm39) |
R3763L |
probably damaging |
Het |
Ptpre |
A |
T |
7: 135,265,044 (GRCm39) |
I207F |
probably damaging |
Het |
Rapgef3 |
A |
T |
15: 97,655,698 (GRCm39) |
|
probably benign |
Het |
Rasgrp1 |
T |
G |
2: 117,115,428 (GRCm39) |
K685T |
probably benign |
Het |
Rnf148 |
C |
T |
6: 23,654,237 (GRCm39) |
R253Q |
probably damaging |
Het |
Rock1 |
T |
C |
18: 10,132,227 (GRCm39) |
I241V |
possibly damaging |
Het |
Rp1l1 |
T |
G |
14: 64,259,541 (GRCm39) |
V61G |
probably damaging |
Het |
Scin |
A |
C |
12: 40,131,770 (GRCm39) |
S255A |
probably damaging |
Het |
Scn8a |
A |
T |
15: 100,933,505 (GRCm39) |
K1570* |
probably null |
Het |
Sec14l4 |
A |
C |
11: 3,990,018 (GRCm39) |
M106L |
probably benign |
Het |
Sec63 |
G |
A |
10: 42,674,795 (GRCm39) |
R226H |
probably benign |
Het |
Septin2 |
T |
A |
1: 93,429,345 (GRCm39) |
N271K |
probably damaging |
Het |
Serac1 |
G |
T |
17: 6,099,101 (GRCm39) |
|
probably benign |
Het |
Shc2 |
T |
A |
10: 79,465,974 (GRCm39) |
|
probably benign |
Het |
Sipa1l1 |
T |
A |
12: 82,471,873 (GRCm39) |
D1284E |
probably benign |
Het |
Slc11a2 |
A |
G |
15: 100,306,097 (GRCm39) |
L105P |
probably damaging |
Het |
Slc1a3 |
T |
A |
15: 8,680,406 (GRCm39) |
T151S |
probably benign |
Het |
Smarca2 |
G |
T |
19: 26,668,762 (GRCm39) |
K920N |
probably damaging |
Het |
Sugp2 |
G |
A |
8: 70,711,598 (GRCm39) |
E964K |
probably damaging |
Het |
Tas2r122 |
A |
C |
6: 132,688,778 (GRCm39) |
N38K |
probably benign |
Het |
Tecpr1 |
G |
A |
5: 144,143,092 (GRCm39) |
R730C |
probably damaging |
Het |
Tent2 |
A |
T |
13: 93,312,123 (GRCm39) |
|
probably benign |
Het |
Themis3 |
G |
T |
17: 66,900,265 (GRCm39) |
N34K |
possibly damaging |
Het |
Traf3ip1 |
A |
G |
1: 91,427,341 (GRCm39) |
T104A |
unknown |
Het |
Trappc11 |
A |
G |
8: 47,956,447 (GRCm39) |
V843A |
probably benign |
Het |
Trmt61a |
T |
A |
12: 111,645,361 (GRCm39) |
L99Q |
probably damaging |
Het |
Trp53tg5 |
T |
A |
2: 164,313,401 (GRCm39) |
K91N |
probably damaging |
Het |
Ufsp2 |
T |
C |
8: 46,445,187 (GRCm39) |
S339P |
probably damaging |
Het |
Usp20 |
T |
A |
2: 30,894,462 (GRCm39) |
V126E |
probably damaging |
Het |
Vmn1r75 |
T |
A |
7: 11,614,797 (GRCm39) |
N176K |
probably damaging |
Het |
Vmn2r24 |
A |
G |
6: 123,793,012 (GRCm39) |
S780G |
probably benign |
Het |
Vmn2r89 |
A |
G |
14: 51,695,048 (GRCm39) |
|
probably null |
Het |
Vps13d |
A |
T |
4: 144,771,665 (GRCm39) |
S4038T |
probably damaging |
Het |
Vwa7 |
A |
G |
17: 35,241,627 (GRCm39) |
T421A |
probably damaging |
Het |
Wdr95 |
C |
A |
5: 149,504,271 (GRCm39) |
L332I |
probably damaging |
Het |
Wrn |
T |
A |
8: 33,826,119 (GRCm39) |
K181I |
probably damaging |
Het |
Zc3h6 |
T |
A |
2: 128,859,143 (GRCm39) |
I1058N |
possibly damaging |
Het |
Zfp423 |
T |
A |
8: 88,508,713 (GRCm39) |
I544F |
probably damaging |
Het |
Zfp446 |
T |
A |
7: 12,713,516 (GRCm39) |
S161T |
possibly damaging |
Het |
Zmym6 |
T |
A |
4: 127,017,162 (GRCm39) |
M889K |
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 |
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 |
|
R5072:Epha4
|
UTSW |
1 |
77,421,639 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|