Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
C |
11: 9,242,438 (GRCm39) |
M1434L |
probably benign |
Het |
Acta2 |
T |
A |
19: 34,220,836 (GRCm39) |
I291F |
possibly damaging |
Het |
Arhgap10 |
A |
G |
8: 78,146,714 (GRCm39) |
I230T |
probably damaging |
Het |
Ark2c |
A |
T |
18: 77,550,610 (GRCm39) |
L106Q |
probably damaging |
Het |
Copb1 |
A |
C |
7: 113,826,011 (GRCm39) |
S658A |
probably benign |
Het |
Crtc3 |
A |
T |
7: 80,254,116 (GRCm39) |
C244* |
probably null |
Het |
Cyp4a14 |
G |
A |
4: 115,352,134 (GRCm39) |
R93* |
probably null |
Het |
Dclk2 |
A |
G |
3: 86,706,334 (GRCm39) |
F586L |
probably damaging |
Het |
Dmtn |
G |
T |
14: 70,842,259 (GRCm39) |
F358L |
probably damaging |
Het |
Ercc6 |
A |
G |
14: 32,284,531 (GRCm39) |
T765A |
probably damaging |
Het |
Gtf3c4 |
T |
C |
2: 28,724,092 (GRCm39) |
K547E |
probably damaging |
Het |
Hdc |
G |
T |
2: 126,445,814 (GRCm39) |
A230D |
probably benign |
Het |
Hipk3 |
A |
T |
2: 104,302,198 (GRCm39) |
|
probably benign |
Het |
Kidins220 |
A |
G |
12: 25,044,999 (GRCm39) |
I264M |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 41,401,494 (GRCm39) |
V387I |
probably benign |
Het |
Mmp8 |
T |
G |
9: 7,567,441 (GRCm39) |
F434V |
probably benign |
Het |
Nr3c2 |
C |
A |
8: 77,635,224 (GRCm39) |
Y108* |
probably null |
Het |
Or4k5 |
T |
G |
14: 50,386,173 (GRCm39) |
S53R |
probably benign |
Het |
Or5b119 |
T |
C |
19: 13,456,729 (GRCm39) |
M278V |
probably benign |
Het |
Pnpt1 |
A |
T |
11: 29,104,306 (GRCm39) |
D560V |
probably damaging |
Het |
Rbbp8nl |
T |
C |
2: 179,921,488 (GRCm39) |
S299G |
probably benign |
Het |
Slc9a4 |
A |
T |
1: 40,646,958 (GRCm39) |
N484I |
probably damaging |
Het |
Sncaip |
C |
T |
18: 53,002,109 (GRCm39) |
S210F |
probably damaging |
Het |
Tiam1 |
G |
T |
16: 89,695,260 (GRCm39) |
Q66K |
possibly damaging |
Het |
Ttc39a |
C |
A |
4: 109,290,281 (GRCm39) |
Y330* |
probably null |
Het |
Ush2a |
T |
G |
1: 188,169,154 (GRCm39) |
D1098E |
probably damaging |
Het |
Vmn2r103 |
A |
G |
17: 20,019,470 (GRCm39) |
E518G |
probably benign |
Het |
|
Other mutations in Enam |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00769:Enam
|
APN |
5 |
88,649,343 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01611:Enam
|
APN |
5 |
88,651,608 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02220:Enam
|
APN |
5 |
88,652,418 (GRCm39) |
nonsense |
probably null |
|
IGL02371:Enam
|
APN |
5 |
88,650,668 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02596:Enam
|
APN |
5 |
88,650,885 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03026:Enam
|
APN |
5 |
88,651,158 (GRCm39) |
missense |
probably benign |
0.38 |
IGL03303:Enam
|
APN |
5 |
88,652,450 (GRCm39) |
missense |
probably benign |
0.12 |
opinionated
|
UTSW |
5 |
88,650,885 (GRCm39) |
missense |
probably benign |
0.04 |
recalcitrant
|
UTSW |
5 |
88,651,650 (GRCm39) |
nonsense |
probably null |
|
R0200:Enam
|
UTSW |
5 |
88,640,886 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0230:Enam
|
UTSW |
5 |
88,637,514 (GRCm39) |
splice site |
probably benign |
|
R0395:Enam
|
UTSW |
5 |
88,649,367 (GRCm39) |
missense |
probably damaging |
0.99 |
R0548:Enam
|
UTSW |
5 |
88,650,964 (GRCm39) |
missense |
probably damaging |
0.96 |
R0608:Enam
|
UTSW |
5 |
88,640,886 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0724:Enam
|
UTSW |
5 |
88,649,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R0927:Enam
|
UTSW |
5 |
88,641,919 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1023:Enam
|
UTSW |
5 |
88,649,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R1053:Enam
|
UTSW |
5 |
88,651,878 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1169:Enam
|
UTSW |
5 |
88,651,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R1230:Enam
|
UTSW |
5 |
88,641,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R1324:Enam
|
UTSW |
5 |
88,641,927 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1663:Enam
|
UTSW |
5 |
88,651,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Enam
|
UTSW |
5 |
88,651,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R1750:Enam
|
UTSW |
5 |
88,651,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Enam
|
UTSW |
5 |
88,652,324 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1907:Enam
|
UTSW |
5 |
88,652,481 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2104:Enam
|
UTSW |
5 |
88,649,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Enam
|
UTSW |
5 |
88,640,779 (GRCm39) |
missense |
probably benign |
0.02 |
R2196:Enam
|
UTSW |
5 |
88,650,603 (GRCm39) |
missense |
probably damaging |
0.99 |
R2363:Enam
|
UTSW |
5 |
88,651,008 (GRCm39) |
missense |
probably benign |
0.24 |
R2497:Enam
|
UTSW |
5 |
88,650,553 (GRCm39) |
missense |
probably benign |
0.13 |
R3615:Enam
|
UTSW |
5 |
88,652,306 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3616:Enam
|
UTSW |
5 |
88,652,306 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3782:Enam
|
UTSW |
5 |
88,650,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R4067:Enam
|
UTSW |
5 |
88,651,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R4349:Enam
|
UTSW |
5 |
88,651,407 (GRCm39) |
missense |
probably damaging |
0.99 |
R4604:Enam
|
UTSW |
5 |
88,652,142 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4649:Enam
|
UTSW |
5 |
88,640,827 (GRCm39) |
missense |
probably benign |
0.02 |
R4702:Enam
|
UTSW |
5 |
88,651,650 (GRCm39) |
nonsense |
probably null |
|
R4703:Enam
|
UTSW |
5 |
88,651,650 (GRCm39) |
nonsense |
probably null |
|
R4704:Enam
|
UTSW |
5 |
88,651,650 (GRCm39) |
nonsense |
probably null |
|
R4705:Enam
|
UTSW |
5 |
88,651,650 (GRCm39) |
nonsense |
probably null |
|
R4714:Enam
|
UTSW |
5 |
88,651,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:Enam
|
UTSW |
5 |
88,649,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Enam
|
UTSW |
5 |
88,640,967 (GRCm39) |
nonsense |
probably null |
|
R4840:Enam
|
UTSW |
5 |
88,650,885 (GRCm39) |
missense |
probably benign |
0.04 |
R4856:Enam
|
UTSW |
5 |
88,636,593 (GRCm39) |
nonsense |
probably null |
|
R4886:Enam
|
UTSW |
5 |
88,636,593 (GRCm39) |
nonsense |
probably null |
|
R4910:Enam
|
UTSW |
5 |
88,650,173 (GRCm39) |
missense |
probably benign |
|
R4911:Enam
|
UTSW |
5 |
88,650,173 (GRCm39) |
missense |
probably benign |
|
R6103:Enam
|
UTSW |
5 |
88,650,187 (GRCm39) |
missense |
probably damaging |
0.96 |
R6651:Enam
|
UTSW |
5 |
88,650,776 (GRCm39) |
missense |
probably damaging |
0.98 |
R6759:Enam
|
UTSW |
5 |
88,649,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Enam
|
UTSW |
5 |
88,650,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R7365:Enam
|
UTSW |
5 |
88,649,347 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7392:Enam
|
UTSW |
5 |
88,649,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R7483:Enam
|
UTSW |
5 |
88,649,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R7647:Enam
|
UTSW |
5 |
88,650,884 (GRCm39) |
missense |
probably benign |
0.00 |
R7648:Enam
|
UTSW |
5 |
88,652,016 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7672:Enam
|
UTSW |
5 |
88,651,830 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7943:Enam
|
UTSW |
5 |
88,636,410 (GRCm39) |
splice site |
probably null |
|
R7999:Enam
|
UTSW |
5 |
88,651,561 (GRCm39) |
missense |
probably benign |
|
R8117:Enam
|
UTSW |
5 |
88,651,385 (GRCm39) |
missense |
probably benign |
0.00 |
R8419:Enam
|
UTSW |
5 |
88,651,209 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8528:Enam
|
UTSW |
5 |
88,650,078 (GRCm39) |
missense |
probably damaging |
0.98 |
R8836:Enam
|
UTSW |
5 |
88,639,124 (GRCm39) |
critical splice donor site |
probably null |
|
R8973:Enam
|
UTSW |
5 |
88,641,947 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9001:Enam
|
UTSW |
5 |
88,637,388 (GRCm39) |
missense |
probably benign |
0.11 |
R9033:Enam
|
UTSW |
5 |
88,646,475 (GRCm39) |
missense |
probably benign |
0.01 |
R9268:Enam
|
UTSW |
5 |
88,640,778 (GRCm39) |
missense |
probably benign |
0.01 |
R9723:Enam
|
UTSW |
5 |
88,652,241 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Enam
|
UTSW |
5 |
88,650,550 (GRCm39) |
nonsense |
probably null |
|
Z1176:Enam
|
UTSW |
5 |
88,640,830 (GRCm39) |
missense |
probably damaging |
0.99 |
|