Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018B08Rik |
T |
G |
8: 122,267,293 (GRCm39) |
K38T |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,248,661 (GRCm39) |
T2803A |
probably benign |
Het |
Adam23 |
A |
G |
1: 63,596,613 (GRCm39) |
D565G |
probably damaging |
Het |
Adcy3 |
A |
G |
12: 4,262,150 (GRCm39) |
T1067A |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,251,819 (GRCm39) |
Y1921* |
probably null |
Het |
Apc2 |
A |
G |
10: 80,149,757 (GRCm39) |
N1604D |
probably benign |
Het |
Atxn7 |
A |
T |
14: 14,089,446 (GRCm38) |
R321* |
probably null |
Het |
Axin1 |
T |
A |
17: 26,361,968 (GRCm39) |
I104N |
probably damaging |
Het |
Bahd1 |
T |
C |
2: 118,747,619 (GRCm39) |
S413P |
probably benign |
Het |
Baz2b |
C |
T |
2: 59,732,073 (GRCm39) |
C2024Y |
probably damaging |
Het |
Cacna1i |
T |
A |
15: 80,262,448 (GRCm39) |
V1388E |
probably damaging |
Het |
Cntn3 |
G |
A |
6: 102,255,301 (GRCm39) |
T199I |
probably damaging |
Het |
Col6a4 |
A |
T |
9: 105,952,191 (GRCm39) |
L569* |
probably null |
Het |
Ctnna2 |
A |
G |
6: 77,120,892 (GRCm39) |
I12T |
probably benign |
Het |
Dhx37 |
A |
G |
5: 125,496,196 (GRCm39) |
M754T |
probably benign |
Het |
Dmrt1 |
T |
A |
19: 25,523,395 (GRCm39) |
S249T |
possibly damaging |
Het |
Ell |
G |
T |
8: 71,025,553 (GRCm39) |
S59I |
probably damaging |
Het |
Fam89a |
G |
A |
8: 125,467,982 (GRCm39) |
S110F |
probably damaging |
Het |
Fer1l4 |
A |
C |
2: 155,889,834 (GRCm39) |
F278V |
possibly damaging |
Het |
Fyn |
T |
C |
10: 39,427,398 (GRCm39) |
I427T |
probably damaging |
Het |
Galnt14 |
T |
C |
17: 73,832,365 (GRCm39) |
D250G |
probably damaging |
Het |
Glp1r |
T |
C |
17: 31,143,546 (GRCm39) |
V194A |
probably damaging |
Het |
Glt1d1 |
T |
A |
5: 127,721,360 (GRCm39) |
|
probably null |
Het |
Gm7995 |
A |
G |
14: 42,133,327 (GRCm39) |
K69R |
probably benign |
Het |
Grip1 |
A |
G |
10: 119,822,329 (GRCm39) |
T379A |
possibly damaging |
Het |
Gtpbp2 |
G |
T |
17: 46,479,147 (GRCm39) |
A570S |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,459,029 (GRCm39) |
I5192V |
probably benign |
Het |
Igfl3 |
A |
T |
7: 17,913,844 (GRCm39) |
I65F |
possibly damaging |
Het |
Igsf10 |
G |
T |
3: 59,236,992 (GRCm39) |
T1063K |
probably benign |
Het |
Itfg1 |
A |
G |
8: 86,466,930 (GRCm39) |
V381A |
probably benign |
Het |
Itprid1 |
A |
G |
6: 55,953,405 (GRCm39) |
D907G |
probably damaging |
Het |
Jmjd8 |
T |
A |
17: 26,048,086 (GRCm39) |
V16E |
probably benign |
Het |
Kank1 |
A |
G |
19: 25,387,449 (GRCm39) |
Y374C |
probably damaging |
Het |
Kcnma1 |
C |
T |
14: 23,386,165 (GRCm39) |
V891I |
possibly damaging |
Het |
Kif20a |
C |
A |
18: 34,762,543 (GRCm39) |
T472K |
possibly damaging |
Het |
Klhl32 |
A |
T |
4: 24,711,578 (GRCm39) |
|
probably benign |
Het |
Lrrc37a |
A |
G |
11: 103,347,486 (GRCm39) |
S3070P |
unknown |
Het |
Mettl21e |
T |
G |
1: 44,249,425 (GRCm39) |
Y77S |
probably damaging |
Het |
Mlst8 |
G |
T |
17: 24,696,935 (GRCm39) |
D82E |
probably benign |
Het |
Mrgprx2 |
A |
T |
7: 48,132,617 (GRCm39) |
L67Q |
probably damaging |
Het |
Mylk |
T |
A |
16: 34,750,237 (GRCm39) |
L1192Q |
possibly damaging |
Het |
Myt1l |
A |
T |
12: 29,882,365 (GRCm39) |
Y520F |
unknown |
Het |
Naip2 |
A |
T |
13: 100,297,193 (GRCm39) |
W948R |
probably benign |
Het |
Nlrp9a |
A |
C |
7: 26,250,311 (GRCm39) |
K25N |
probably damaging |
Het |
Nsd3 |
T |
C |
8: 26,204,212 (GRCm39) |
C414R |
probably damaging |
Het |
Oit3 |
A |
T |
10: 59,274,374 (GRCm39) |
V142D |
possibly damaging |
Het |
Or2aj6 |
C |
T |
16: 19,443,194 (GRCm39) |
V219M |
probably benign |
Het |
P2ry6 |
T |
C |
7: 100,587,580 (GRCm39) |
T260A |
probably damaging |
Het |
Papola |
A |
G |
12: 105,771,196 (GRCm39) |
Q87R |
probably benign |
Het |
Pla2g4a |
T |
A |
1: 149,727,086 (GRCm39) |
R557* |
probably null |
Het |
Rgs13 |
G |
T |
1: 144,016,576 (GRCm39) |
H56N |
probably damaging |
Het |
Sbf1 |
T |
C |
15: 89,189,111 (GRCm39) |
S537G |
probably benign |
Het |
Sntg1 |
A |
C |
1: 8,653,508 (GRCm39) |
L243R |
possibly damaging |
Het |
Spata31h1 |
A |
T |
10: 82,125,138 (GRCm39) |
L2624Q |
possibly damaging |
Het |
Stam2 |
T |
C |
2: 52,610,954 (GRCm39) |
T23A |
probably benign |
Het |
Tbl1xr1 |
C |
A |
3: 22,258,141 (GRCm39) |
H467Q |
probably damaging |
Het |
Tmem131l |
A |
G |
3: 83,820,587 (GRCm39) |
S1222P |
possibly damaging |
Het |
Tmem43 |
G |
T |
6: 91,455,759 (GRCm39) |
Q123H |
probably damaging |
Het |
Tmem43 |
T |
A |
6: 91,463,862 (GRCm39) |
I379N |
possibly damaging |
Het |
Trim43c |
A |
T |
9: 88,727,003 (GRCm39) |
I277F |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,703,211 (GRCm39) |
|
probably benign |
Het |
Vmn1r75 |
T |
A |
7: 11,615,003 (GRCm39) |
V245D |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vps53 |
A |
T |
11: 75,967,881 (GRCm39) |
M414K |
probably benign |
Het |
Wrn |
T |
G |
8: 33,809,248 (GRCm39) |
L249F |
probably benign |
Het |
Zc3h13 |
TGATGTCCGGGATGTCCGGGATGTCCGGGATGTCCGGGATGT |
TGATGTCCGGGATGTCCGGGATGTCCGGGATGT |
14: 75,560,998 (GRCm39) |
|
probably benign |
Het |
Zfp454 |
T |
C |
11: 50,764,950 (GRCm39) |
N161D |
probably benign |
Het |
Zfp619 |
G |
A |
7: 39,183,586 (GRCm39) |
G60R |
probably benign |
Het |
Zfp623 |
T |
A |
15: 75,820,308 (GRCm39) |
H421Q |
probably damaging |
Het |
Zfp827 |
A |
G |
8: 79,916,606 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ces4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00584:Ces4a
|
APN |
8 |
105,871,795 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01574:Ces4a
|
APN |
8 |
105,871,859 (GRCm39) |
splice site |
probably benign |
|
IGL01655:Ces4a
|
APN |
8 |
105,873,806 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03092:Ces4a
|
APN |
8 |
105,874,836 (GRCm39) |
splice site |
probably benign |
|
IGL03151:Ces4a
|
APN |
8 |
105,874,829 (GRCm39) |
critical splice donor site |
probably null |
|
F6893:Ces4a
|
UTSW |
8 |
105,873,859 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0266:Ces4a
|
UTSW |
8 |
105,868,598 (GRCm39) |
missense |
probably benign |
|
R0659:Ces4a
|
UTSW |
8 |
105,871,554 (GRCm39) |
splice site |
probably benign |
|
R1239:Ces4a
|
UTSW |
8 |
105,876,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Ces4a
|
UTSW |
8 |
105,864,667 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1467:Ces4a
|
UTSW |
8 |
105,864,667 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1505:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Ces4a
|
UTSW |
8 |
105,869,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1736:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1737:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1738:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1744:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2202:Ces4a
|
UTSW |
8 |
105,872,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R4512:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R4865:Ces4a
|
UTSW |
8 |
105,873,790 (GRCm39) |
missense |
probably benign |
0.05 |
R4934:Ces4a
|
UTSW |
8 |
105,864,613 (GRCm39) |
missense |
probably benign |
0.30 |
R4936:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R5255:Ces4a
|
UTSW |
8 |
105,869,121 (GRCm39) |
missense |
probably benign |
0.00 |
R5342:Ces4a
|
UTSW |
8 |
105,872,775 (GRCm39) |
missense |
probably benign |
0.07 |
R5647:Ces4a
|
UTSW |
8 |
105,872,712 (GRCm39) |
missense |
probably benign |
0.10 |
R6062:Ces4a
|
UTSW |
8 |
105,864,806 (GRCm39) |
critical splice donor site |
probably null |
|
R6606:Ces4a
|
UTSW |
8 |
105,876,010 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6876:Ces4a
|
UTSW |
8 |
105,871,624 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6901:Ces4a
|
UTSW |
8 |
105,873,330 (GRCm39) |
missense |
probably benign |
|
R7519:Ces4a
|
UTSW |
8 |
105,871,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Ces4a
|
UTSW |
8 |
105,873,297 (GRCm39) |
missense |
probably benign |
0.00 |
R8171:Ces4a
|
UTSW |
8 |
105,873,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R8329:Ces4a
|
UTSW |
8 |
105,874,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Ces4a
|
UTSW |
8 |
105,858,614 (GRCm39) |
missense |
probably benign |
0.00 |
R9168:Ces4a
|
UTSW |
8 |
105,876,050 (GRCm39) |
missense |
probably benign |
0.00 |
R9557:Ces4a
|
UTSW |
8 |
105,869,527 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9758:Ces4a
|
UTSW |
8 |
105,869,054 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Ces4a
|
UTSW |
8 |
105,858,609 (GRCm39) |
missense |
probably benign |
0.00 |
|