Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933415A04Rik |
GTGTGTGTATGTGTGT |
GTGTGTGT |
11: 43,478,239 (GRCm39) |
|
probably null |
Het |
Adamts16 |
A |
G |
13: 70,984,265 (GRCm39) |
S133P |
probably damaging |
Het |
Adamts17 |
T |
C |
7: 66,774,802 (GRCm39) |
W1001R |
probably damaging |
Het |
Aox4 |
T |
A |
1: 58,270,251 (GRCm39) |
|
probably null |
Het |
B4galnt4 |
C |
T |
7: 140,644,988 (GRCm39) |
P221S |
probably damaging |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
BC034090 |
T |
C |
1: 155,108,410 (GRCm39) |
|
probably benign |
Het |
Best2 |
T |
A |
8: 85,736,143 (GRCm39) |
D312V |
probably damaging |
Het |
Bod1l |
A |
T |
5: 41,975,286 (GRCm39) |
D2009E |
probably benign |
Het |
Ccdc158 |
A |
C |
5: 92,793,373 (GRCm39) |
S672A |
probably benign |
Het |
Ccdc43 |
A |
T |
11: 102,588,443 (GRCm39) |
L31Q |
probably damaging |
Het |
Cdcp3 |
G |
A |
7: 130,904,466 (GRCm39) |
|
probably null |
Het |
Chaf1a |
T |
G |
17: 56,369,291 (GRCm39) |
H507Q |
probably benign |
Het |
Clptm1l |
A |
G |
13: 73,752,439 (GRCm39) |
Y28C |
probably damaging |
Het |
Cp |
G |
A |
3: 20,029,223 (GRCm39) |
|
probably null |
Het |
Crocc |
C |
T |
4: 140,752,597 (GRCm39) |
A1432T |
probably benign |
Het |
Crybg2 |
A |
G |
4: 133,801,137 (GRCm39) |
T457A |
probably benign |
Het |
Csnk2a1-ps3 |
C |
T |
1: 156,352,552 (GRCm39) |
T251I |
probably damaging |
Het |
Dennd4a |
A |
G |
9: 64,814,202 (GRCm39) |
D1473G |
probably damaging |
Het |
Diaph3 |
A |
G |
14: 87,274,940 (GRCm39) |
F172S |
probably benign |
Het |
Dnajc5b |
A |
G |
3: 19,629,006 (GRCm39) |
N100S |
probably benign |
Het |
Dusp13b |
G |
A |
14: 21,791,404 (GRCm39) |
T16I |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,403,948 (GRCm39) |
Y233C |
probably damaging |
Het |
Fcgbp |
T |
A |
7: 27,784,460 (GRCm39) |
Y173* |
probably null |
Het |
Fign |
T |
A |
2: 63,809,506 (GRCm39) |
D588V |
probably damaging |
Het |
Fignl2 |
C |
T |
15: 100,951,188 (GRCm39) |
V365M |
unknown |
Het |
Fnip2 |
A |
C |
3: 79,415,430 (GRCm39) |
Y203D |
probably benign |
Het |
Ftsj3 |
CCTTCTTCTTCTTCTTCT |
CCTTCTTCTTCTTCT |
11: 106,143,377 (GRCm39) |
|
probably benign |
Het |
Gfral |
C |
A |
9: 76,100,572 (GRCm39) |
V289L |
probably benign |
Het |
H2bc21 |
T |
A |
3: 96,128,487 (GRCm39) |
|
probably null |
Het |
Heatr5b |
G |
T |
17: 79,103,370 (GRCm39) |
T1161K |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,443,784 (GRCm39) |
I1335F |
possibly damaging |
Het |
Htt |
T |
A |
5: 35,040,336 (GRCm39) |
V2166D |
probably benign |
Het |
Ipo5 |
G |
C |
14: 121,170,537 (GRCm39) |
K436N |
possibly damaging |
Het |
Iqca1l |
A |
G |
5: 24,749,224 (GRCm39) |
L758P |
probably damaging |
Het |
Itga6 |
A |
G |
2: 71,671,879 (GRCm39) |
E794G |
probably damaging |
Het |
Itga9 |
G |
A |
9: 118,672,712 (GRCm39) |
C148Y |
|
Het |
Kcnip2 |
A |
C |
19: 45,785,524 (GRCm39) |
|
probably null |
Het |
Kcnk6 |
T |
C |
7: 28,925,269 (GRCm39) |
T116A |
possibly damaging |
Het |
Kctd21 |
A |
G |
7: 96,997,297 (GRCm39) |
I257V |
probably benign |
Het |
Kif19a |
G |
A |
11: 114,672,748 (GRCm39) |
R299Q |
probably damaging |
Het |
Kifc2 |
G |
A |
15: 76,548,328 (GRCm39) |
G391R |
probably benign |
Het |
Klrg2 |
A |
G |
6: 38,604,562 (GRCm39) |
V381A |
possibly damaging |
Het |
Mob1b |
A |
G |
5: 88,897,542 (GRCm39) |
|
probably null |
Het |
Or13p8 |
T |
C |
4: 118,584,106 (GRCm39) |
Y221H |
probably damaging |
Het |
Or6c69 |
T |
G |
10: 129,747,392 (GRCm39) |
S252R |
probably damaging |
Het |
Or6c75 |
T |
C |
10: 129,337,020 (GRCm39) |
V81A |
probably benign |
Het |
Or7c70 |
T |
C |
10: 78,683,447 (GRCm39) |
I101V |
probably benign |
Het |
Oxsm |
C |
A |
14: 16,240,925 (GRCm38) |
A375S |
possibly damaging |
Het |
Pcdha3 |
T |
C |
18: 37,081,193 (GRCm39) |
V645A |
probably damaging |
Het |
Pcdhb15 |
T |
A |
18: 37,607,788 (GRCm39) |
V340E |
possibly damaging |
Het |
Pced1a |
G |
A |
2: 130,264,435 (GRCm39) |
P132S |
probably damaging |
Het |
Pla2r1 |
C |
T |
2: 60,334,531 (GRCm39) |
V414M |
probably benign |
Het |
Plekhg4 |
A |
C |
8: 106,104,399 (GRCm39) |
I493L |
probably benign |
Het |
Plekhj1 |
T |
A |
10: 80,634,179 (GRCm39) |
|
probably benign |
Het |
Pmfbp1 |
G |
T |
8: 110,254,412 (GRCm39) |
K482N |
probably damaging |
Het |
Ppil3 |
T |
C |
1: 58,473,574 (GRCm39) |
N92S |
probably benign |
Het |
Ppt2 |
A |
G |
17: 34,844,686 (GRCm39) |
S156P |
probably benign |
Het |
Prss41 |
A |
T |
17: 24,056,087 (GRCm39) |
D255E |
probably benign |
Het |
Psg25 |
T |
A |
7: 18,255,227 (GRCm39) |
M430L |
probably benign |
Het |
Rffl |
A |
T |
11: 82,703,595 (GRCm39) |
C109* |
probably null |
Het |
Rock2 |
A |
G |
12: 17,021,111 (GRCm39) |
E991G |
probably benign |
Het |
Rpap2 |
A |
G |
5: 107,768,058 (GRCm39) |
I299V |
probably benign |
Het |
Rras |
T |
C |
7: 44,670,529 (GRCm39) |
S158P |
probably benign |
Het |
Serpinb10 |
G |
A |
1: 107,463,196 (GRCm39) |
|
probably benign |
Het |
Smyd3 |
A |
T |
1: 178,799,859 (GRCm39) |
I360N |
possibly damaging |
Het |
Synm |
A |
G |
7: 67,384,714 (GRCm39) |
S541P |
probably damaging |
Het |
Tasor |
A |
G |
14: 27,193,901 (GRCm39) |
T1034A |
probably benign |
Het |
Tbc1d31 |
C |
A |
15: 57,821,764 (GRCm39) |
T813K |
possibly damaging |
Het |
Trav7n-4 |
A |
G |
14: 53,329,103 (GRCm39) |
M38V |
probably benign |
Het |
Tulp3 |
A |
C |
6: 128,301,943 (GRCm39) |
N359K |
possibly damaging |
Het |
Twf1 |
T |
C |
15: 94,480,654 (GRCm39) |
K196E |
probably benign |
Het |
Usp24 |
A |
T |
4: 106,173,771 (GRCm39) |
N35Y |
probably damaging |
Het |
Usp46 |
T |
A |
5: 74,162,772 (GRCm39) |
E342D |
probably benign |
Het |
Vps50 |
T |
A |
6: 3,532,202 (GRCm39) |
|
probably null |
Het |
Vps8 |
T |
A |
16: 21,330,308 (GRCm39) |
I727N |
possibly damaging |
Het |
Wdr90 |
C |
T |
17: 26,065,300 (GRCm39) |
R1652Q |
probably damaging |
Het |
Zfp11 |
A |
T |
5: 129,734,027 (GRCm39) |
V478E |
possibly damaging |
Het |
Zfp493 |
A |
G |
13: 67,935,123 (GRCm39) |
K359E |
probably benign |
Het |
Zfp536 |
T |
C |
7: 37,268,126 (GRCm39) |
Y430C |
probably damaging |
Het |
Zfpm1 |
A |
G |
8: 123,063,689 (GRCm39) |
D916G |
unknown |
Het |
|
Other mutations in Epb42 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01535:Epb42
|
APN |
2 |
120,858,169 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01627:Epb42
|
APN |
2 |
120,856,324 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02059:Epb42
|
APN |
2 |
120,855,188 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02869:Epb42
|
APN |
2 |
120,856,227 (GRCm39) |
missense |
probably benign |
|
R0279:Epb42
|
UTSW |
2 |
120,859,525 (GRCm39) |
splice site |
probably benign |
|
R0521:Epb42
|
UTSW |
2 |
120,859,631 (GRCm39) |
nonsense |
probably null |
|
R1457:Epb42
|
UTSW |
2 |
120,860,448 (GRCm39) |
critical splice donor site |
probably null |
|
R2157:Epb42
|
UTSW |
2 |
120,852,243 (GRCm39) |
missense |
probably benign |
|
R2392:Epb42
|
UTSW |
2 |
120,860,468 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2407:Epb42
|
UTSW |
2 |
120,855,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R2866:Epb42
|
UTSW |
2 |
120,856,402 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2993:Epb42
|
UTSW |
2 |
120,859,525 (GRCm39) |
splice site |
probably benign |
|
R3426:Epb42
|
UTSW |
2 |
120,860,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R3427:Epb42
|
UTSW |
2 |
120,860,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4192:Epb42
|
UTSW |
2 |
120,860,570 (GRCm39) |
splice site |
probably null |
|
R4940:Epb42
|
UTSW |
2 |
120,864,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Epb42
|
UTSW |
2 |
120,849,943 (GRCm39) |
missense |
probably benign |
0.22 |
R5771:Epb42
|
UTSW |
2 |
120,852,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R6048:Epb42
|
UTSW |
2 |
120,854,889 (GRCm39) |
missense |
probably benign |
0.00 |
R6362:Epb42
|
UTSW |
2 |
120,856,260 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6475:Epb42
|
UTSW |
2 |
120,857,614 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6711:Epb42
|
UTSW |
2 |
120,854,589 (GRCm39) |
intron |
probably benign |
|
R6843:Epb42
|
UTSW |
2 |
120,858,166 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6895:Epb42
|
UTSW |
2 |
120,867,104 (GRCm39) |
start gained |
probably benign |
|
R7154:Epb42
|
UTSW |
2 |
120,863,843 (GRCm39) |
missense |
probably benign |
0.01 |
R7192:Epb42
|
UTSW |
2 |
120,854,578 (GRCm39) |
missense |
unknown |
|
R7600:Epb42
|
UTSW |
2 |
120,852,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Epb42
|
UTSW |
2 |
120,858,200 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7779:Epb42
|
UTSW |
2 |
120,864,916 (GRCm39) |
missense |
probably benign |
0.14 |
R7781:Epb42
|
UTSW |
2 |
120,864,916 (GRCm39) |
missense |
probably benign |
0.14 |
R7783:Epb42
|
UTSW |
2 |
120,864,916 (GRCm39) |
missense |
probably benign |
0.14 |
R7784:Epb42
|
UTSW |
2 |
120,864,916 (GRCm39) |
missense |
probably benign |
0.14 |
R8737:Epb42
|
UTSW |
2 |
120,856,324 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8915:Epb42
|
UTSW |
2 |
120,849,987 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8930:Epb42
|
UTSW |
2 |
120,854,767 (GRCm39) |
missense |
probably benign |
0.00 |
R8932:Epb42
|
UTSW |
2 |
120,854,767 (GRCm39) |
missense |
probably benign |
0.00 |
R9746:Epb42
|
UTSW |
2 |
120,855,091 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Epb42
|
UTSW |
2 |
120,858,206 (GRCm39) |
missense |
probably damaging |
1.00 |
|