Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf1 |
G |
A |
17: 36,271,069 (GRCm39) |
T463M |
probably damaging |
Het |
Arhgap35 |
C |
T |
7: 16,297,511 (GRCm39) |
G518D |
probably damaging |
Het |
Arhgdia |
A |
G |
11: 120,470,517 (GRCm39) |
Y110H |
probably damaging |
Het |
Atp8b3 |
T |
C |
10: 80,372,604 (GRCm39) |
|
probably null |
Het |
Bpifb6 |
T |
A |
2: 153,750,436 (GRCm39) |
I309N |
possibly damaging |
Het |
Cbr4 |
T |
C |
8: 61,943,061 (GRCm39) |
V77A |
possibly damaging |
Het |
Cers2 |
A |
G |
3: 95,227,534 (GRCm39) |
Y54C |
possibly damaging |
Het |
Cnbp |
A |
T |
6: 87,821,120 (GRCm39) |
H145Q |
probably damaging |
Het |
Csmd1 |
A |
T |
8: 16,073,905 (GRCm39) |
I2030N |
possibly damaging |
Het |
Csmd1 |
A |
G |
8: 16,760,522 (GRCm39) |
|
probably null |
Het |
Dhodh |
T |
C |
8: 110,328,170 (GRCm39) |
|
probably null |
Het |
Dnah11 |
T |
A |
12: 117,982,495 (GRCm39) |
Y2558F |
probably benign |
Het |
Dysf |
C |
A |
6: 84,074,697 (GRCm39) |
D499E |
probably damaging |
Het |
En1 |
A |
T |
1: 120,534,872 (GRCm39) |
Y387F |
unknown |
Het |
Ephb2 |
C |
A |
4: 136,423,363 (GRCm39) |
C305F |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,238,315 (GRCm39) |
V1477A |
probably benign |
Het |
Gimap3 |
A |
T |
6: 48,742,327 (GRCm39) |
L201Q |
probably benign |
Het |
Gm10801 |
T |
G |
2: 98,494,246 (GRCm39) |
|
probably null |
Het |
Grhl1 |
A |
G |
12: 24,636,132 (GRCm39) |
I283V |
possibly damaging |
Het |
Grid2ip |
T |
A |
5: 143,374,658 (GRCm39) |
L926H |
probably damaging |
Het |
Gtf2h2 |
G |
T |
13: 100,605,523 (GRCm39) |
C82* |
probably null |
Het |
Gtf2ird1 |
T |
C |
5: 134,433,588 (GRCm39) |
T280A |
probably benign |
Het |
Gzmd |
T |
C |
14: 56,367,698 (GRCm39) |
I192V |
probably null |
Het |
Hectd1 |
A |
G |
12: 51,834,695 (GRCm39) |
V855A |
possibly damaging |
Het |
Hey1 |
A |
G |
3: 8,730,963 (GRCm39) |
|
probably benign |
Het |
Hpx |
A |
G |
7: 105,249,243 (GRCm39) |
S19P |
probably benign |
Het |
Incenp |
G |
A |
19: 9,853,964 (GRCm39) |
R696W |
unknown |
Het |
Itgam |
T |
C |
7: 127,700,709 (GRCm39) |
V493A |
probably damaging |
Het |
Ldlrad3 |
A |
G |
2: 101,900,343 (GRCm39) |
I53T |
probably damaging |
Het |
Map3k7 |
G |
T |
4: 31,985,700 (GRCm39) |
E208* |
probably null |
Het |
Myh9 |
A |
T |
15: 77,671,717 (GRCm39) |
I458N |
probably damaging |
Het |
Myo1c |
C |
T |
11: 75,560,856 (GRCm39) |
R770* |
probably null |
Het |
Nectin3 |
T |
A |
16: 46,284,306 (GRCm39) |
Y126F |
possibly damaging |
Het |
Nek5 |
A |
T |
8: 22,573,443 (GRCm39) |
N504K |
probably damaging |
Het |
Nlrp4c |
T |
A |
7: 6,068,424 (GRCm39) |
H108Q |
probably benign |
Het |
Or10d5 |
A |
T |
9: 39,861,165 (GRCm39) |
L301M |
probably damaging |
Het |
Or2ak4 |
T |
C |
11: 58,649,013 (GRCm39) |
V174A |
possibly damaging |
Het |
Or2at1 |
A |
T |
7: 99,416,989 (GRCm39) |
I207F |
probably damaging |
Het |
Or5h17 |
A |
T |
16: 58,820,458 (GRCm39) |
T137S |
probably benign |
Het |
Or9a2 |
G |
T |
6: 41,748,442 (GRCm39) |
Q264K |
probably benign |
Het |
Or9i14 |
T |
A |
19: 13,792,814 (GRCm39) |
I47F |
possibly damaging |
Het |
Parp6 |
T |
C |
9: 59,549,052 (GRCm39) |
I507T |
probably damaging |
Het |
Pcdhb12 |
A |
G |
18: 37,570,548 (GRCm39) |
T565A |
probably benign |
Het |
Pclo |
A |
G |
5: 14,828,572 (GRCm39) |
N4676D |
unknown |
Het |
Pdlim1 |
T |
A |
19: 40,211,180 (GRCm39) |
H278L |
probably benign |
Het |
Pfkfb3 |
G |
A |
2: 11,498,719 (GRCm39) |
T46M |
probably damaging |
Het |
Plscr2 |
A |
G |
9: 92,173,067 (GRCm39) |
Y203C |
probably damaging |
Het |
Plxna1 |
T |
C |
6: 89,311,733 (GRCm39) |
D924G |
possibly damaging |
Het |
Postn |
T |
A |
3: 54,292,031 (GRCm39) |
|
probably benign |
Het |
Ptpn23 |
A |
G |
9: 110,217,924 (GRCm39) |
S674P |
possibly damaging |
Het |
Ranbp6 |
C |
T |
19: 29,788,984 (GRCm39) |
R456Q |
probably benign |
Het |
Rbm43 |
A |
T |
2: 51,819,728 (GRCm39) |
V46E |
probably damaging |
Het |
Rlig1 |
T |
C |
10: 100,414,243 (GRCm39) |
I139V |
probably benign |
Het |
Rtn4r |
A |
G |
16: 17,969,046 (GRCm39) |
Y158C |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,731,884 (GRCm39) |
I2352T |
probably damaging |
Het |
Sbk2 |
G |
T |
7: 4,960,577 (GRCm39) |
R198S |
possibly damaging |
Het |
Slc45a1 |
G |
A |
4: 150,722,697 (GRCm39) |
P396S |
probably benign |
Het |
Slc4a10 |
A |
G |
2: 62,087,861 (GRCm39) |
D418G |
probably null |
Het |
Smarcad1 |
A |
G |
6: 65,052,099 (GRCm39) |
T411A |
probably benign |
Het |
Smtn |
G |
A |
11: 3,474,663 (GRCm39) |
S716F |
probably damaging |
Het |
Stag1 |
G |
T |
9: 100,620,092 (GRCm39) |
R65L |
probably damaging |
Het |
Stat1 |
A |
T |
1: 52,165,680 (GRCm39) |
D92V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,582,428 (GRCm39) |
Y22822H |
probably damaging |
Het |
Vmn1r172 |
A |
G |
7: 23,359,606 (GRCm39) |
T164A |
probably benign |
Het |
Vmn2r118 |
A |
T |
17: 55,917,860 (GRCm39) |
D217E |
probably damaging |
Het |
Vmn2r26 |
A |
G |
6: 124,030,924 (GRCm39) |
E553G |
probably damaging |
Het |
Vmn2r96 |
T |
C |
17: 18,803,088 (GRCm39) |
F333L |
probably benign |
Het |
Ypel5 |
G |
A |
17: 73,155,726 (GRCm39) |
R98H |
probably benign |
Het |
Zfp719 |
C |
T |
7: 43,239,656 (GRCm39) |
H415Y |
probably damaging |
Het |
Zyg11a |
T |
C |
4: 108,062,268 (GRCm39) |
S176G |
probably benign |
Het |
|
Other mutations in Scube3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02019:Scube3
|
APN |
17 |
28,386,658 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02189:Scube3
|
APN |
17 |
28,381,970 (GRCm39) |
missense |
probably benign |
|
IGL02416:Scube3
|
APN |
17 |
28,383,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02904:Scube3
|
APN |
17 |
28,386,574 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03153:Scube3
|
APN |
17 |
28,386,032 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL03309:Scube3
|
APN |
17 |
28,383,331 (GRCm39) |
nonsense |
probably null |
|
dinklage
|
UTSW |
17 |
28,381,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Scube3
|
UTSW |
17 |
28,383,331 (GRCm39) |
nonsense |
probably null |
|
R0084:Scube3
|
UTSW |
17 |
28,381,935 (GRCm39) |
missense |
probably benign |
0.12 |
R0122:Scube3
|
UTSW |
17 |
28,385,502 (GRCm39) |
splice site |
probably benign |
|
R0544:Scube3
|
UTSW |
17 |
28,383,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Scube3
|
UTSW |
17 |
28,387,353 (GRCm39) |
splice site |
probably benign |
|
R1842:Scube3
|
UTSW |
17 |
28,384,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R1878:Scube3
|
UTSW |
17 |
28,371,387 (GRCm39) |
missense |
probably benign |
0.10 |
R1950:Scube3
|
UTSW |
17 |
28,383,274 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2011:Scube3
|
UTSW |
17 |
28,387,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R2164:Scube3
|
UTSW |
17 |
28,385,108 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4356:Scube3
|
UTSW |
17 |
28,383,283 (GRCm39) |
missense |
probably benign |
0.01 |
R4392:Scube3
|
UTSW |
17 |
28,383,762 (GRCm39) |
missense |
probably null |
|
R4528:Scube3
|
UTSW |
17 |
28,381,973 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4809:Scube3
|
UTSW |
17 |
28,384,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Scube3
|
UTSW |
17 |
28,384,989 (GRCm39) |
missense |
probably damaging |
0.98 |
R4841:Scube3
|
UTSW |
17 |
28,383,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Scube3
|
UTSW |
17 |
28,383,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Scube3
|
UTSW |
17 |
28,371,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R5889:Scube3
|
UTSW |
17 |
28,379,887 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5936:Scube3
|
UTSW |
17 |
28,384,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R6523:Scube3
|
UTSW |
17 |
28,381,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Scube3
|
UTSW |
17 |
28,386,573 (GRCm39) |
missense |
probably benign |
|
R7337:Scube3
|
UTSW |
17 |
28,387,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Scube3
|
UTSW |
17 |
28,386,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Scube3
|
UTSW |
17 |
28,386,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:Scube3
|
UTSW |
17 |
28,384,569 (GRCm39) |
missense |
probably benign |
|
R7950:Scube3
|
UTSW |
17 |
28,390,200 (GRCm39) |
missense |
probably benign |
0.11 |
R8991:Scube3
|
UTSW |
17 |
28,383,027 (GRCm39) |
missense |
probably damaging |
0.98 |
R9376:Scube3
|
UTSW |
17 |
28,383,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9469:Scube3
|
UTSW |
17 |
28,386,138 (GRCm39) |
nonsense |
probably null |
|
R9653:Scube3
|
UTSW |
17 |
28,375,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Scube3
|
UTSW |
17 |
28,371,414 (GRCm39) |
missense |
probably benign |
0.05 |
RF009:Scube3
|
UTSW |
17 |
28,387,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|