Other mutations in this stock |
Total: 120 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402J07Rik |
C |
A |
8: 88,295,121 (GRCm39) |
Y86* |
probably null |
Het |
Aadac |
A |
G |
3: 59,947,118 (GRCm39) |
E272G |
probably damaging |
Het |
Abcc8 |
A |
T |
7: 45,816,326 (GRCm39) |
D271E |
probably benign |
Het |
Acan |
T |
C |
7: 78,748,783 (GRCm39) |
F1185L |
probably benign |
Het |
Adam1a |
A |
T |
5: 121,657,683 (GRCm39) |
C537S |
probably damaging |
Het |
Ago2 |
A |
G |
15: 72,995,814 (GRCm39) |
V395A |
probably benign |
Het |
Alox15 |
A |
G |
11: 70,241,578 (GRCm39) |
V101A |
probably damaging |
Het |
Ankra2 |
T |
C |
13: 98,407,632 (GRCm39) |
I194T |
probably damaging |
Het |
Apobec4 |
C |
A |
1: 152,631,981 (GRCm39) |
P3H |
probably damaging |
Het |
Arid3b |
G |
T |
9: 57,703,960 (GRCm39) |
Y329* |
probably null |
Het |
Atm |
A |
T |
9: 53,379,312 (GRCm39) |
S1993T |
probably benign |
Het |
Bpgm |
T |
G |
6: 34,464,669 (GRCm39) |
S129A |
probably benign |
Het |
Brat1 |
A |
G |
5: 140,704,264 (GRCm39) |
D839G |
possibly damaging |
Het |
Ccdc15 |
A |
T |
9: 37,253,866 (GRCm39) |
S128T |
probably benign |
Het |
Cd300lg |
A |
T |
11: 101,937,032 (GRCm39) |
|
probably benign |
Het |
Cdc34b |
C |
A |
11: 94,633,303 (GRCm39) |
Q168K |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,308,626 (GRCm39) |
V1767E |
probably benign |
Het |
Cep350 |
T |
C |
1: 155,829,397 (GRCm39) |
D169G |
probably benign |
Het |
Col7a1 |
A |
T |
9: 108,798,633 (GRCm39) |
D1762V |
possibly damaging |
Het |
Coro7 |
A |
G |
16: 4,448,298 (GRCm39) |
L724P |
probably damaging |
Het |
Crb1 |
T |
A |
1: 139,164,750 (GRCm39) |
I1125F |
probably damaging |
Het |
Ctif |
T |
A |
18: 75,653,012 (GRCm39) |
D415V |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dhrs2 |
A |
G |
14: 55,478,298 (GRCm39) |
D237G |
probably benign |
Het |
Dhx9 |
T |
C |
1: 153,341,499 (GRCm39) |
Q582R |
probably damaging |
Het |
Dnajc1 |
C |
T |
2: 18,224,524 (GRCm39) |
R443Q |
probably damaging |
Het |
Dnm2 |
C |
T |
9: 21,416,977 (GRCm39) |
R837W |
possibly damaging |
Het |
Dpf2 |
C |
A |
19: 5,956,643 (GRCm39) |
Q70H |
probably damaging |
Het |
Dqx1 |
T |
A |
6: 83,043,088 (GRCm39) |
D608E |
probably damaging |
Het |
Dync2h1 |
T |
A |
9: 7,049,166 (GRCm39) |
T3245S |
probably benign |
Het |
Ect2l |
A |
G |
10: 18,075,781 (GRCm39) |
L35P |
probably damaging |
Het |
Efcab5 |
A |
T |
11: 76,994,132 (GRCm39) |
L1285Q |
probably damaging |
Het |
Eif4g1 |
G |
C |
16: 20,500,617 (GRCm39) |
R697P |
probably damaging |
Het |
Entpd3 |
A |
G |
9: 120,387,485 (GRCm39) |
I227M |
probably damaging |
Het |
Epn1 |
T |
A |
7: 5,092,997 (GRCm39) |
V103E |
probably damaging |
Het |
Esrra |
T |
C |
19: 6,889,378 (GRCm39) |
D337G |
probably benign |
Het |
Fam83e |
A |
T |
7: 45,378,193 (GRCm39) |
K406* |
probably null |
Het |
Fam83e |
A |
T |
7: 45,378,194 (GRCm39) |
K406M |
possibly damaging |
Het |
Fat2 |
A |
G |
11: 55,202,384 (GRCm39) |
I230T |
probably damaging |
Het |
Fbxl16 |
A |
G |
17: 26,035,420 (GRCm39) |
I6V |
probably benign |
Het |
Fgf23 |
T |
C |
6: 127,050,156 (GRCm39) |
I55T |
probably damaging |
Het |
Fibcd1 |
T |
A |
2: 31,711,561 (GRCm39) |
D288V |
probably damaging |
Het |
Flnb |
T |
C |
14: 7,892,113 (GRCm38) |
I594T |
probably damaging |
Het |
Gabbr2 |
T |
C |
4: 46,739,823 (GRCm39) |
E449G |
probably benign |
Het |
Gbf1 |
T |
G |
19: 46,260,476 (GRCm39) |
S1130A |
possibly damaging |
Het |
Gipc3 |
T |
C |
10: 81,177,099 (GRCm39) |
E157G |
probably damaging |
Het |
Glra3 |
G |
T |
8: 56,393,942 (GRCm39) |
A18S |
probably benign |
Het |
Gm6625 |
A |
C |
8: 89,873,462 (GRCm39) |
|
noncoding transcript |
Het |
Gpx4 |
A |
G |
10: 79,891,870 (GRCm39) |
|
probably benign |
Het |
Grb10 |
A |
G |
11: 11,896,029 (GRCm39) |
F264L |
possibly damaging |
Het |
Grik3 |
T |
C |
4: 125,587,931 (GRCm39) |
Y684H |
probably damaging |
Het |
Gstp1 |
C |
T |
19: 4,086,795 (GRCm39) |
|
probably benign |
Het |
H2bc27 |
A |
T |
11: 58,839,928 (GRCm39) |
I55F |
possibly damaging |
Het |
Haus8 |
G |
A |
8: 71,708,767 (GRCm39) |
|
probably benign |
Het |
Hip1 |
G |
A |
5: 135,463,995 (GRCm39) |
|
probably null |
Het |
Hspbap1 |
T |
A |
16: 35,639,134 (GRCm39) |
|
probably null |
Het |
Htr2b |
T |
A |
1: 86,027,151 (GRCm39) |
I452F |
possibly damaging |
Het |
Hydin |
T |
A |
8: 111,296,440 (GRCm39) |
H3656Q |
probably benign |
Het |
Klb |
T |
A |
5: 65,506,180 (GRCm39) |
D142E |
probably benign |
Het |
Lamb3 |
A |
T |
1: 193,016,924 (GRCm39) |
T777S |
possibly damaging |
Het |
Lins1 |
C |
A |
7: 66,364,070 (GRCm39) |
T650K |
probably damaging |
Het |
Loxhd1 |
A |
G |
18: 77,369,667 (GRCm39) |
K5R |
possibly damaging |
Het |
Lpp |
G |
A |
16: 24,580,405 (GRCm39) |
M40I |
probably damaging |
Het |
Mia2 |
A |
T |
12: 59,217,037 (GRCm39) |
|
probably benign |
Het |
Miip |
A |
C |
4: 147,947,549 (GRCm39) |
F204V |
probably damaging |
Het |
Mmp21 |
T |
C |
7: 133,278,882 (GRCm39) |
R323G |
probably benign |
Het |
Mta3 |
T |
A |
17: 84,062,980 (GRCm39) |
|
probably benign |
Het |
Myh1 |
A |
G |
11: 67,104,456 (GRCm39) |
K1004R |
probably benign |
Het |
Myh14 |
T |
A |
7: 44,281,853 (GRCm39) |
I810F |
probably damaging |
Het |
Nbas |
A |
C |
12: 13,463,598 (GRCm39) |
D1295A |
probably damaging |
Het |
Niban3 |
T |
C |
8: 72,056,413 (GRCm39) |
M371T |
possibly damaging |
Het |
Npr2 |
T |
G |
4: 43,632,384 (GRCm39) |
V67G |
probably benign |
Het |
Oas1f |
C |
A |
5: 120,993,492 (GRCm39) |
Q235K |
probably damaging |
Het |
Or12d17 |
T |
A |
17: 37,777,938 (GRCm39) |
S280R |
probably damaging |
Het |
Or13a27 |
T |
A |
7: 139,925,900 (GRCm39) |
M1L |
probably benign |
Het |
Or1p1 |
G |
T |
11: 74,180,039 (GRCm39) |
C189F |
probably damaging |
Het |
Or52ae9 |
T |
C |
7: 103,390,381 (GRCm39) |
N22S |
probably benign |
Het |
Or7e166 |
C |
T |
9: 19,624,386 (GRCm39) |
H88Y |
probably benign |
Het |
Pafah2 |
GCCCC |
GCCCCC |
4: 134,152,852 (GRCm39) |
|
probably null |
Het |
Pde1b |
A |
G |
15: 103,433,767 (GRCm39) |
|
probably null |
Het |
Pdilt |
T |
C |
7: 119,088,607 (GRCm39) |
T465A |
probably benign |
Het |
Plxnd1 |
T |
C |
6: 115,943,507 (GRCm39) |
H1233R |
probably damaging |
Het |
Ppm1b |
T |
A |
17: 85,301,552 (GRCm39) |
M144K |
probably benign |
Het |
Prkdc |
T |
C |
16: 15,625,922 (GRCm39) |
L3316S |
probably benign |
Het |
Prm2 |
T |
A |
16: 10,609,455 (GRCm39) |
|
probably benign |
Het |
Prmt7 |
T |
C |
8: 106,963,640 (GRCm39) |
V240A |
probably benign |
Het |
Prx |
C |
A |
7: 27,218,313 (GRCm39) |
A938E |
possibly damaging |
Het |
Rbm7 |
A |
G |
9: 48,402,194 (GRCm39) |
V131A |
probably benign |
Het |
Ric1 |
T |
A |
19: 29,578,213 (GRCm39) |
|
probably null |
Het |
Rnf150 |
A |
T |
8: 83,590,639 (GRCm39) |
M1L |
possibly damaging |
Het |
Rnf20 |
C |
T |
4: 49,644,628 (GRCm39) |
R298W |
probably damaging |
Het |
Rp1 |
T |
A |
1: 4,417,455 (GRCm39) |
Y1219F |
possibly damaging |
Het |
Scn7a |
A |
G |
2: 66,514,357 (GRCm39) |
|
probably null |
Het |
Sdad1 |
A |
G |
5: 92,440,510 (GRCm39) |
|
probably null |
Het |
Septin9 |
T |
C |
11: 117,243,909 (GRCm39) |
|
probably benign |
Het |
Serinc3 |
T |
C |
2: 163,487,409 (GRCm39) |
|
probably benign |
Het |
Shc3 |
C |
T |
13: 51,615,424 (GRCm39) |
G178R |
probably damaging |
Het |
Slc4a10 |
A |
T |
2: 62,146,950 (GRCm39) |
K1090M |
probably damaging |
Het |
Slco1a1 |
T |
C |
6: 141,868,837 (GRCm39) |
I376V |
probably benign |
Het |
Slmap |
A |
T |
14: 26,143,729 (GRCm39) |
F719L |
probably benign |
Het |
Smgc |
A |
G |
15: 91,743,956 (GRCm39) |
N573D |
possibly damaging |
Het |
Spx |
G |
A |
6: 142,359,805 (GRCm39) |
|
probably null |
Het |
Srrt |
C |
G |
5: 137,295,207 (GRCm39) |
E308Q |
probably damaging |
Het |
Tas2r130 |
T |
A |
6: 131,607,560 (GRCm39) |
R78S |
probably benign |
Het |
Tchhl1 |
A |
G |
3: 93,378,408 (GRCm39) |
R371G |
probably damaging |
Het |
Teddm2 |
C |
T |
1: 153,726,194 (GRCm39) |
A174T |
probably benign |
Het |
Tktl2 |
G |
A |
8: 66,964,999 (GRCm39) |
V186M |
probably damaging |
Het |
Trim33 |
T |
C |
3: 103,231,956 (GRCm39) |
|
probably benign |
Het |
Tspan31 |
A |
G |
10: 126,905,327 (GRCm39) |
V40A |
probably damaging |
Het |
Uevld |
A |
G |
7: 46,594,975 (GRCm39) |
|
probably benign |
Het |
Vcl |
G |
T |
14: 21,059,063 (GRCm39) |
A560S |
probably benign |
Het |
Vmn2r24 |
T |
A |
6: 123,793,183 (GRCm39) |
C837S |
probably damaging |
Het |
Vmn2r57 |
C |
T |
7: 41,077,531 (GRCm39) |
V212M |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,843,622 (GRCm39) |
T1968A |
probably benign |
Het |
Vtn |
A |
G |
11: 78,391,393 (GRCm39) |
R269G |
probably damaging |
Het |
Wdcp |
G |
A |
12: 4,900,245 (GRCm39) |
V34I |
possibly damaging |
Het |
Zc3h14 |
A |
G |
12: 98,719,091 (GRCm39) |
D152G |
possibly damaging |
Het |
Zfp189 |
C |
T |
4: 49,529,266 (GRCm39) |
P123L |
probably benign |
Het |
Zfp318 |
T |
C |
17: 46,716,981 (GRCm39) |
S1038P |
possibly damaging |
Het |
Zfp873 |
A |
G |
10: 81,896,406 (GRCm39) |
D416G |
probably benign |
Het |
|
Other mutations in Emsy |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01314:Emsy
|
APN |
7 |
98,242,662 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01357:Emsy
|
APN |
7 |
98,240,077 (GRCm39) |
nonsense |
probably null |
|
IGL01620:Emsy
|
APN |
7 |
98,275,831 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01750:Emsy
|
APN |
7 |
98,268,508 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02032:Emsy
|
APN |
7 |
98,239,987 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02388:Emsy
|
APN |
7 |
98,290,873 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03089:Emsy
|
APN |
7 |
98,286,473 (GRCm39) |
nonsense |
probably null |
|
IGL03272:Emsy
|
APN |
7 |
98,242,969 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03347:Emsy
|
APN |
7 |
98,259,892 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03400:Emsy
|
APN |
7 |
98,251,933 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02980:Emsy
|
UTSW |
7 |
98,268,587 (GRCm39) |
missense |
probably damaging |
0.97 |
R0576:Emsy
|
UTSW |
7 |
98,242,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R1102:Emsy
|
UTSW |
7 |
98,251,796 (GRCm39) |
missense |
probably damaging |
0.97 |
R1323:Emsy
|
UTSW |
7 |
98,259,864 (GRCm39) |
splice site |
probably benign |
|
R1438:Emsy
|
UTSW |
7 |
98,270,613 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1439:Emsy
|
UTSW |
7 |
98,250,048 (GRCm39) |
intron |
probably benign |
|
R1452:Emsy
|
UTSW |
7 |
98,249,881 (GRCm39) |
missense |
probably damaging |
0.96 |
R1515:Emsy
|
UTSW |
7 |
98,240,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Emsy
|
UTSW |
7 |
98,242,944 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1791:Emsy
|
UTSW |
7 |
98,297,087 (GRCm39) |
missense |
probably damaging |
0.99 |
R1829:Emsy
|
UTSW |
7 |
98,251,937 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1829:Emsy
|
UTSW |
7 |
98,251,936 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1861:Emsy
|
UTSW |
7 |
98,290,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Emsy
|
UTSW |
7 |
98,275,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R1957:Emsy
|
UTSW |
7 |
98,297,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R2221:Emsy
|
UTSW |
7 |
98,239,982 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2223:Emsy
|
UTSW |
7 |
98,239,982 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2271:Emsy
|
UTSW |
7 |
98,275,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R4078:Emsy
|
UTSW |
7 |
98,239,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R4707:Emsy
|
UTSW |
7 |
98,246,311 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4783:Emsy
|
UTSW |
7 |
98,295,686 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5453:Emsy
|
UTSW |
7 |
98,250,013 (GRCm39) |
missense |
probably damaging |
0.97 |
R5518:Emsy
|
UTSW |
7 |
98,242,818 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5828:Emsy
|
UTSW |
7 |
98,242,699 (GRCm39) |
missense |
probably benign |
|
R5945:Emsy
|
UTSW |
7 |
98,268,590 (GRCm39) |
missense |
probably damaging |
0.97 |
R6153:Emsy
|
UTSW |
7 |
98,260,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R6824:Emsy
|
UTSW |
7 |
98,242,614 (GRCm39) |
missense |
probably benign |
0.27 |
R7068:Emsy
|
UTSW |
7 |
98,259,968 (GRCm39) |
missense |
probably benign |
0.17 |
R7381:Emsy
|
UTSW |
7 |
98,240,010 (GRCm39) |
missense |
probably damaging |
0.98 |
R7417:Emsy
|
UTSW |
7 |
98,264,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R7488:Emsy
|
UTSW |
7 |
98,264,762 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7499:Emsy
|
UTSW |
7 |
98,279,538 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7646:Emsy
|
UTSW |
7 |
98,268,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Emsy
|
UTSW |
7 |
98,239,905 (GRCm39) |
missense |
probably damaging |
0.99 |
R7716:Emsy
|
UTSW |
7 |
98,248,973 (GRCm39) |
missense |
unknown |
|
R7789:Emsy
|
UTSW |
7 |
98,270,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Emsy
|
UTSW |
7 |
98,249,931 (GRCm39) |
missense |
probably benign |
0.30 |
R7832:Emsy
|
UTSW |
7 |
98,289,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Emsy
|
UTSW |
7 |
98,279,425 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7996:Emsy
|
UTSW |
7 |
98,242,888 (GRCm39) |
missense |
probably benign |
0.00 |
R8070:Emsy
|
UTSW |
7 |
98,275,922 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8221:Emsy
|
UTSW |
7 |
98,297,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R8472:Emsy
|
UTSW |
7 |
98,304,037 (GRCm39) |
start gained |
probably benign |
|
R8841:Emsy
|
UTSW |
7 |
98,264,768 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8998:Emsy
|
UTSW |
7 |
98,268,512 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9063:Emsy
|
UTSW |
7 |
98,295,684 (GRCm39) |
missense |
probably damaging |
0.96 |
R9259:Emsy
|
UTSW |
7 |
98,242,757 (GRCm39) |
missense |
probably benign |
|
R9366:Emsy
|
UTSW |
7 |
98,290,860 (GRCm39) |
missense |
probably benign |
0.23 |
R9660:Emsy
|
UTSW |
7 |
98,262,285 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9729:Emsy
|
UTSW |
7 |
98,262,256 (GRCm39) |
missense |
probably benign |
0.01 |
X0067:Emsy
|
UTSW |
7 |
98,279,447 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1088:Emsy
|
UTSW |
7 |
98,249,929 (GRCm39) |
missense |
probably damaging |
0.96 |
|