Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
A |
G |
12: 72,954,644 (GRCm39) |
L209S |
possibly damaging |
Het |
Abcc2 |
G |
T |
19: 43,815,068 (GRCm39) |
V1152F |
probably damaging |
Het |
Adam9 |
C |
T |
8: 25,457,212 (GRCm39) |
V639I |
probably benign |
Het |
Cdc6 |
A |
G |
11: 98,805,989 (GRCm39) |
I388V |
probably benign |
Het |
Chrm5 |
C |
T |
2: 112,310,651 (GRCm39) |
W155* |
probably null |
Het |
Chrna9 |
A |
G |
5: 66,128,287 (GRCm39) |
D161G |
probably damaging |
Het |
Det1 |
A |
G |
7: 78,477,702 (GRCm39) |
V541A |
possibly damaging |
Het |
Efhc1 |
G |
T |
1: 21,060,911 (GRCm39) |
*649L |
probably null |
Het |
Ehbp1 |
C |
T |
11: 22,122,883 (GRCm39) |
V146M |
probably damaging |
Het |
Fam20b |
A |
T |
1: 156,530,035 (GRCm39) |
V133E |
probably benign |
Het |
Frem2 |
T |
A |
3: 53,563,130 (GRCm39) |
Q459L |
probably benign |
Het |
Gapdhs |
C |
T |
7: 30,429,866 (GRCm39) |
|
probably benign |
Het |
Gm3404 |
T |
A |
5: 146,465,157 (GRCm39) |
V299D |
possibly damaging |
Het |
Gorasp2 |
C |
A |
2: 70,519,604 (GRCm39) |
H310N |
possibly damaging |
Het |
Gpr157 |
T |
C |
4: 150,186,094 (GRCm39) |
S219P |
possibly damaging |
Het |
Gpt2 |
T |
A |
8: 86,246,167 (GRCm39) |
C375* |
probably null |
Het |
Gtf2h3 |
T |
C |
5: 124,733,748 (GRCm39) |
S274P |
probably damaging |
Het |
Hmg20b |
C |
T |
10: 81,183,309 (GRCm39) |
V83M |
probably benign |
Het |
Igf2r |
G |
T |
17: 12,944,302 (GRCm39) |
Y400* |
probably null |
Het |
Ipo9 |
A |
T |
1: 135,314,431 (GRCm39) |
W942R |
possibly damaging |
Het |
Iqch |
T |
C |
9: 63,403,519 (GRCm39) |
|
probably null |
Het |
Kcnh3 |
T |
C |
15: 99,127,383 (GRCm39) |
L393P |
probably benign |
Het |
Kcnk12 |
T |
A |
17: 88,104,495 (GRCm39) |
I130L |
probably benign |
Het |
Lcorl |
T |
C |
5: 45,904,434 (GRCm39) |
T205A |
probably damaging |
Het |
Lpar6 |
G |
T |
14: 73,476,878 (GRCm39) |
A280S |
probably damaging |
Het |
Mgarp |
A |
T |
3: 51,296,570 (GRCm39) |
V152E |
probably damaging |
Het |
Pard3b |
A |
G |
1: 62,677,021 (GRCm39) |
D1184G |
probably damaging |
Het |
Pcnt |
A |
G |
10: 76,272,258 (GRCm39) |
|
probably null |
Het |
Pde6b |
A |
G |
5: 108,551,262 (GRCm39) |
N182S |
possibly damaging |
Het |
Pom121 |
T |
C |
5: 135,412,526 (GRCm39) |
K516E |
unknown |
Het |
Psmg2 |
G |
A |
18: 67,786,293 (GRCm39) |
V218I |
probably benign |
Het |
Ptpn18 |
T |
C |
1: 34,498,898 (GRCm39) |
|
probably benign |
Het |
Rapgef5 |
C |
T |
12: 117,717,154 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,606,202 (GRCm39) |
L4460S |
possibly damaging |
Het |
Sema6b |
T |
C |
17: 56,436,969 (GRCm39) |
|
probably null |
Het |
Serpinb6d |
T |
A |
13: 33,850,375 (GRCm39) |
C67* |
probably null |
Het |
Sorbs2 |
T |
G |
8: 46,248,381 (GRCm39) |
V510G |
probably null |
Het |
Spic |
T |
A |
10: 88,511,864 (GRCm39) |
I131F |
possibly damaging |
Het |
Spire2 |
T |
C |
8: 124,086,137 (GRCm39) |
S290P |
probably damaging |
Het |
Tas2r117 |
C |
T |
6: 132,780,447 (GRCm39) |
S195F |
probably benign |
Het |
Tas2r117 |
T |
C |
6: 132,780,450 (GRCm39) |
V196A |
probably damaging |
Het |
Tff1 |
C |
T |
17: 31,381,703 (GRCm39) |
G58D |
probably damaging |
Het |
Tmprss11g |
T |
C |
5: 86,638,640 (GRCm39) |
T283A |
probably benign |
Het |
Toporsl |
T |
A |
4: 52,610,794 (GRCm39) |
L229H |
probably damaging |
Het |
Vmn2r80 |
G |
A |
10: 79,007,488 (GRCm39) |
G488D |
probably damaging |
Het |
Vps54 |
T |
A |
11: 21,261,082 (GRCm39) |
V583D |
probably damaging |
Het |
Vwa1 |
T |
C |
4: 155,855,255 (GRCm39) |
E286G |
possibly damaging |
Het |
Vwde |
A |
T |
6: 13,219,977 (GRCm39) |
I58N |
probably damaging |
Het |
Zbtb11 |
T |
C |
16: 55,800,973 (GRCm39) |
V109A |
probably damaging |
Het |
Zfp319 |
C |
T |
8: 96,055,540 (GRCm39) |
R221Q |
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 |
IGL01802:Enam
|
APN |
5 |
88,651,533 (GRCm39) |
missense |
possibly damaging |
0.93 |
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 |
|