Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd6 |
A |
T |
14: 8,049,867 (GRCm38) |
I219F |
probably damaging |
Het |
Acvr1b |
A |
G |
15: 101,096,703 (GRCm39) |
I207V |
possibly damaging |
Het |
Adamtsl4 |
T |
C |
3: 95,585,252 (GRCm39) |
T839A |
probably benign |
Het |
Akap1 |
C |
T |
11: 88,736,578 (GRCm39) |
R61H |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,051,667 (GRCm39) |
D1478G |
probably benign |
Het |
Aloxe3 |
T |
A |
11: 69,026,775 (GRCm39) |
V547E |
possibly damaging |
Het |
Ano6 |
G |
A |
15: 95,860,148 (GRCm39) |
A757T |
probably damaging |
Het |
Armc10 |
A |
G |
5: 21,858,455 (GRCm39) |
T167A |
probably damaging |
Het |
BB019430 |
A |
C |
10: 58,539,869 (GRCm39) |
|
noncoding transcript |
Het |
Brms1 |
C |
T |
19: 5,096,435 (GRCm39) |
R82W |
probably damaging |
Het |
Btnl6 |
G |
A |
17: 34,733,062 (GRCm39) |
T267I |
probably benign |
Het |
Catsper4 |
A |
T |
4: 133,945,212 (GRCm39) |
F215L |
probably benign |
Het |
Ccdc188 |
T |
C |
16: 18,036,552 (GRCm39) |
F197S |
probably damaging |
Het |
Cers5 |
A |
C |
15: 99,634,212 (GRCm39) |
C379G |
probably benign |
Het |
Chchd6 |
A |
G |
6: 89,361,626 (GRCm39) |
L259P |
probably damaging |
Het |
Cntnap2 |
T |
A |
6: 46,736,763 (GRCm39) |
C730S |
probably damaging |
Het |
Coch |
T |
G |
12: 51,649,631 (GRCm39) |
V314G |
probably damaging |
Het |
Cog1 |
T |
A |
11: 113,543,130 (GRCm39) |
S213T |
possibly damaging |
Het |
Crot |
A |
T |
5: 9,037,828 (GRCm39) |
F163I |
probably damaging |
Het |
Cyp4f13 |
A |
T |
17: 33,148,932 (GRCm39) |
I162N |
probably damaging |
Het |
Dab2 |
A |
T |
15: 6,359,933 (GRCm39) |
|
probably benign |
Het |
Depdc1b |
C |
T |
13: 108,460,482 (GRCm39) |
R31W |
probably damaging |
Het |
Dlk1 |
T |
C |
12: 109,425,613 (GRCm39) |
F161S |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,137,965 (GRCm39) |
E913G |
probably damaging |
Het |
Dnajc6 |
A |
G |
4: 101,455,028 (GRCm39) |
Y5C |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,511,586 (GRCm39) |
T1508A |
probably damaging |
Het |
Dstyk |
A |
G |
1: 132,361,832 (GRCm39) |
|
probably benign |
Het |
Efcc1 |
T |
C |
6: 87,726,265 (GRCm39) |
|
probably benign |
Het |
Entpd1 |
T |
C |
19: 40,727,450 (GRCm39) |
Y533H |
probably benign |
Het |
Erich3 |
C |
T |
3: 154,401,402 (GRCm39) |
T17M |
probably damaging |
Het |
Ethe1 |
T |
C |
7: 24,307,899 (GRCm39) |
|
probably benign |
Het |
Fbxw15 |
A |
T |
9: 109,386,347 (GRCm39) |
M211K |
probably damaging |
Het |
Fhod3 |
G |
A |
18: 25,199,335 (GRCm39) |
V669M |
possibly damaging |
Het |
Fktn |
C |
T |
4: 53,747,003 (GRCm39) |
|
probably benign |
Het |
Foxred1 |
G |
A |
9: 35,122,130 (GRCm39) |
R20C |
probably benign |
Het |
Gbp9 |
A |
G |
5: 105,242,319 (GRCm39) |
L140P |
probably damaging |
Het |
Gga1 |
T |
C |
15: 78,773,230 (GRCm39) |
L286P |
probably damaging |
Het |
Gml |
T |
C |
15: 74,685,462 (GRCm39) |
|
probably benign |
Het |
Gsap |
A |
T |
5: 21,486,035 (GRCm39) |
K628N |
probably damaging |
Het |
Gtf3c4 |
G |
A |
2: 28,720,648 (GRCm39) |
|
probably benign |
Het |
H2-M10.6 |
A |
C |
17: 37,124,043 (GRCm39) |
Y169S |
probably benign |
Het |
Hal |
G |
A |
10: 93,330,490 (GRCm39) |
V245I |
probably benign |
Het |
Hebp2 |
T |
C |
10: 18,420,849 (GRCm39) |
Y72C |
probably damaging |
Het |
Helz2 |
T |
C |
2: 180,878,056 (GRCm39) |
E914G |
probably damaging |
Het |
Herc3 |
T |
C |
6: 58,893,455 (GRCm39) |
Y906H |
probably damaging |
Het |
Hfm1 |
A |
T |
5: 107,028,226 (GRCm39) |
|
probably null |
Het |
Hgs |
C |
T |
11: 120,370,889 (GRCm39) |
P582S |
probably damaging |
Het |
Hoxa10 |
G |
A |
6: 52,211,469 (GRCm39) |
P149L |
probably damaging |
Het |
Inpp5j |
T |
A |
11: 3,454,738 (GRCm39) |
Q4L |
possibly damaging |
Het |
Ints8 |
A |
C |
4: 11,254,109 (GRCm39) |
M1R |
probably null |
Het |
Isg15 |
T |
C |
4: 156,284,447 (GRCm39) |
E27G |
possibly damaging |
Het |
Klf13 |
A |
T |
7: 63,541,513 (GRCm39) |
C205S |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,070,831 (GRCm39) |
Y830F |
probably benign |
Het |
Lama1 |
G |
A |
17: 68,004,378 (GRCm39) |
V17M |
unknown |
Het |
Lama3 |
A |
G |
18: 12,598,556 (GRCm39) |
N988D |
probably benign |
Het |
Lcat |
CAT |
C |
8: 106,668,446 (GRCm39) |
|
probably null |
Het |
Lct |
G |
T |
1: 128,228,994 (GRCm39) |
P833H |
probably damaging |
Het |
Lmf1 |
A |
T |
17: 25,874,184 (GRCm39) |
R403W |
probably damaging |
Het |
Me3 |
T |
G |
7: 89,282,230 (GRCm39) |
S38A |
probably benign |
Het |
Myg1 |
A |
T |
15: 102,240,264 (GRCm39) |
D30V |
probably benign |
Het |
Nbea |
A |
G |
3: 55,537,610 (GRCm39) |
I2841T |
possibly damaging |
Het |
Nek1 |
T |
A |
8: 61,542,847 (GRCm39) |
|
probably null |
Het |
Obsl1 |
C |
T |
1: 75,470,527 (GRCm39) |
R1043H |
probably benign |
Het |
Or4p23 |
G |
T |
2: 88,576,361 (GRCm39) |
D290E |
probably benign |
Het |
Or5b119 |
A |
C |
19: 13,456,971 (GRCm39) |
V197G |
possibly damaging |
Het |
Or6n2 |
A |
T |
1: 173,897,224 (GRCm39) |
Y120F |
probably damaging |
Het |
Or9m2 |
T |
G |
2: 87,820,926 (GRCm39) |
I157R |
probably damaging |
Het |
Osbpl9 |
A |
G |
4: 108,921,780 (GRCm39) |
Y613H |
probably damaging |
Het |
Per3 |
C |
T |
4: 151,127,249 (GRCm39) |
|
probably null |
Het |
Pex6 |
G |
T |
17: 47,034,424 (GRCm39) |
V758L |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,291,707 (GRCm39) |
I1309V |
probably damaging |
Het |
Pimreg |
A |
G |
11: 71,933,985 (GRCm39) |
E37G |
possibly damaging |
Het |
Pjvk |
G |
A |
2: 76,486,232 (GRCm39) |
V211I |
probably benign |
Het |
Plekhg4 |
T |
A |
8: 106,108,293 (GRCm39) |
V1112E |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,044,319 (GRCm39) |
M2106K |
probably damaging |
Het |
Rdh16f2 |
G |
T |
10: 127,712,765 (GRCm39) |
L254F |
probably benign |
Het |
Rictor |
G |
A |
15: 6,803,343 (GRCm39) |
R485Q |
possibly damaging |
Het |
Rnf146 |
G |
A |
10: 29,223,475 (GRCm39) |
T137M |
probably damaging |
Het |
Rrp9 |
T |
A |
9: 106,360,203 (GRCm39) |
C204S |
probably damaging |
Het |
Rxylt1 |
T |
C |
10: 121,924,920 (GRCm39) |
T261A |
probably benign |
Het |
Serpinb9h |
T |
C |
13: 33,583,336 (GRCm39) |
S150P |
probably benign |
Het |
Shkbp1 |
T |
C |
7: 27,041,776 (GRCm39) |
T693A |
probably benign |
Het |
Skint9 |
A |
G |
4: 112,271,159 (GRCm39) |
Y84H |
probably benign |
Het |
Slc22a12 |
A |
T |
19: 6,586,761 (GRCm39) |
|
probably null |
Het |
Slfn4 |
T |
C |
11: 83,076,211 (GRCm39) |
C26R |
possibly damaging |
Het |
Snrnp200 |
T |
C |
2: 127,074,363 (GRCm39) |
L1401P |
probably damaging |
Het |
Specc1 |
T |
A |
11: 62,010,110 (GRCm39) |
|
probably null |
Het |
Spef2 |
A |
T |
15: 9,717,568 (GRCm39) |
M316K |
probably damaging |
Het |
Tbc1d22b |
A |
G |
17: 29,790,647 (GRCm39) |
R204G |
probably damaging |
Het |
Tektl1 |
T |
C |
10: 78,583,058 (GRCm39) |
N442S |
probably benign |
Het |
Tgfbr3l |
C |
A |
8: 4,299,548 (GRCm39) |
D110E |
probably benign |
Het |
Ticrr |
T |
G |
7: 79,325,071 (GRCm39) |
S532R |
probably damaging |
Het |
Ticrr |
C |
A |
7: 79,328,794 (GRCm39) |
Y644* |
probably null |
Het |
Traf3ip1 |
A |
T |
1: 91,450,579 (GRCm39) |
T509S |
probably damaging |
Het |
Trmt10b |
T |
C |
4: 45,307,946 (GRCm39) |
Y209H |
probably damaging |
Het |
Trmt6 |
T |
C |
2: 132,652,157 (GRCm39) |
M172V |
probably damaging |
Het |
Tsc1 |
A |
G |
2: 28,576,125 (GRCm39) |
D978G |
probably benign |
Het |
Tshz2 |
C |
A |
2: 169,725,843 (GRCm39) |
F146L |
probably benign |
Het |
Tspyl4 |
G |
T |
10: 34,173,576 (GRCm39) |
E23* |
probably null |
Het |
Ulk2 |
A |
T |
11: 61,732,165 (GRCm39) |
|
probably benign |
Het |
Umodl1 |
A |
T |
17: 31,227,674 (GRCm39) |
I1336F |
probably damaging |
Het |
Vezt |
T |
C |
10: 93,806,425 (GRCm39) |
D662G |
probably benign |
Het |
Vnn1 |
G |
T |
10: 23,776,727 (GRCm39) |
Q359H |
probably benign |
Het |
Vnn1 |
A |
T |
10: 23,776,726 (GRCm39) |
Q359L |
possibly damaging |
Het |
Zdhhc16 |
A |
G |
19: 41,930,394 (GRCm39) |
N14S |
probably damaging |
Het |
Zfp455 |
T |
C |
13: 67,355,601 (GRCm39) |
S225P |
probably damaging |
Het |
Zfp74 |
T |
A |
7: 29,634,486 (GRCm39) |
E407D |
probably benign |
Het |
Zic2 |
T |
A |
14: 122,716,031 (GRCm39) |
H384Q |
possibly damaging |
Het |
|
Other mutations in Epha8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00946:Epha8
|
APN |
4 |
136,673,121 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00960:Epha8
|
APN |
4 |
136,679,150 (GRCm39) |
splice site |
probably null |
|
IGL01124:Epha8
|
APN |
4 |
136,663,394 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01550:Epha8
|
APN |
4 |
136,659,051 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01807:Epha8
|
APN |
4 |
136,658,993 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01844:Epha8
|
APN |
4 |
136,658,360 (GRCm39) |
makesense |
probably null |
|
IGL02167:Epha8
|
APN |
4 |
136,658,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R0255:Epha8
|
UTSW |
4 |
136,667,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R0445:Epha8
|
UTSW |
4 |
136,659,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Epha8
|
UTSW |
4 |
136,663,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R1936:Epha8
|
UTSW |
4 |
136,667,554 (GRCm39) |
missense |
probably benign |
0.08 |
R2291:Epha8
|
UTSW |
4 |
136,660,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R2359:Epha8
|
UTSW |
4 |
136,673,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R2372:Epha8
|
UTSW |
4 |
136,660,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R4581:Epha8
|
UTSW |
4 |
136,660,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Epha8
|
UTSW |
4 |
136,666,006 (GRCm39) |
frame shift |
probably null |
|
R4784:Epha8
|
UTSW |
4 |
136,660,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R5156:Epha8
|
UTSW |
4 |
136,666,037 (GRCm39) |
missense |
probably benign |
0.14 |
R5164:Epha8
|
UTSW |
4 |
136,672,983 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5335:Epha8
|
UTSW |
4 |
136,659,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Epha8
|
UTSW |
4 |
136,662,441 (GRCm39) |
missense |
probably benign |
|
R5552:Epha8
|
UTSW |
4 |
136,659,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R5830:Epha8
|
UTSW |
4 |
136,663,701 (GRCm39) |
nonsense |
probably null |
|
R6017:Epha8
|
UTSW |
4 |
136,659,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6450:Epha8
|
UTSW |
4 |
136,659,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Epha8
|
UTSW |
4 |
136,672,980 (GRCm39) |
missense |
probably benign |
0.00 |
R6799:Epha8
|
UTSW |
4 |
136,672,980 (GRCm39) |
missense |
probably benign |
0.00 |
R7060:Epha8
|
UTSW |
4 |
136,658,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R7297:Epha8
|
UTSW |
4 |
136,673,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7344:Epha8
|
UTSW |
4 |
136,661,849 (GRCm39) |
missense |
probably benign |
0.14 |
R7467:Epha8
|
UTSW |
4 |
136,658,399 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7563:Epha8
|
UTSW |
4 |
136,666,100 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7826:Epha8
|
UTSW |
4 |
136,663,498 (GRCm39) |
missense |
probably benign |
0.09 |
R7845:Epha8
|
UTSW |
4 |
136,663,712 (GRCm39) |
missense |
probably benign |
0.04 |
R7863:Epha8
|
UTSW |
4 |
136,660,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Epha8
|
UTSW |
4 |
136,659,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7918:Epha8
|
UTSW |
4 |
136,661,877 (GRCm39) |
missense |
probably benign |
0.12 |
R8177:Epha8
|
UTSW |
4 |
136,672,974 (GRCm39) |
missense |
probably benign |
0.00 |
R8244:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8266:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8268:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8269:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8289:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8290:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8294:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8295:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8299:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8445:Epha8
|
UTSW |
4 |
136,659,600 (GRCm39) |
missense |
probably benign |
0.13 |
R8889:Epha8
|
UTSW |
4 |
136,661,850 (GRCm39) |
missense |
probably benign |
0.45 |
R8892:Epha8
|
UTSW |
4 |
136,661,850 (GRCm39) |
missense |
probably benign |
0.45 |
R8928:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8965:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8983:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8984:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R8988:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9081:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9231:Epha8
|
UTSW |
4 |
136,673,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Epha8
|
UTSW |
4 |
136,658,995 (GRCm39) |
missense |
probably benign |
|
R9370:Epha8
|
UTSW |
4 |
136,673,511 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9466:Epha8
|
UTSW |
4 |
136,662,414 (GRCm39) |
missense |
probably benign |
|
R9478:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9546:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9547:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9550:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9585:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9624:Epha8
|
UTSW |
4 |
136,659,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R9686:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9687:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9690:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9744:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9763:Epha8
|
UTSW |
4 |
136,665,897 (GRCm39) |
missense |
probably damaging |
0.98 |
R9794:Epha8
|
UTSW |
4 |
136,666,035 (GRCm39) |
missense |
probably benign |
0.16 |
RF025:Epha8
|
UTSW |
4 |
136,660,348 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF054:Epha8
|
UTSW |
4 |
136,660,348 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1176:Epha8
|
UTSW |
4 |
136,666,007 (GRCm39) |
missense |
probably benign |
0.01 |
|