Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf2 |
A |
G |
17: 43,024,063 (GRCm39) |
I136T |
probably damaging |
Het |
Bbs7 |
T |
C |
3: 36,646,572 (GRCm39) |
D416G |
probably damaging |
Het |
Commd4 |
G |
T |
9: 57,062,718 (GRCm39) |
D179E |
probably benign |
Het |
Cyp3a57 |
T |
C |
5: 145,327,213 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,314,007 (GRCm39) |
N1941S |
probably null |
Het |
Dynap |
T |
C |
18: 70,374,055 (GRCm39) |
D157G |
unknown |
Het |
Entrep2 |
A |
G |
7: 64,469,658 (GRCm39) |
|
probably benign |
Het |
Fbxo25 |
A |
G |
8: 13,985,222 (GRCm39) |
Y305C |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Fxr2 |
A |
G |
11: 69,530,241 (GRCm39) |
D36G |
probably benign |
Het |
Gas2l3 |
T |
C |
10: 89,249,805 (GRCm39) |
T438A |
probably benign |
Het |
Gcm1 |
A |
T |
9: 77,971,923 (GRCm39) |
Y288F |
possibly damaging |
Het |
Gm3164 |
C |
A |
14: 4,442,719 (GRCm38) |
S218R |
probably benign |
Het |
Hipk2 |
C |
T |
6: 38,675,491 (GRCm39) |
R1029H |
probably damaging |
Het |
Htra3 |
T |
C |
5: 35,811,453 (GRCm39) |
I392M |
probably damaging |
Het |
Kansl1l |
T |
C |
1: 66,840,515 (GRCm39) |
M262V |
possibly damaging |
Het |
Lrrc47 |
T |
C |
4: 154,104,344 (GRCm39) |
|
probably null |
Het |
Macf1 |
A |
T |
4: 123,326,718 (GRCm39) |
N4926K |
probably damaging |
Het |
Mllt10 |
T |
C |
2: 18,201,406 (GRCm39) |
S631P |
probably benign |
Het |
Nlrp14 |
A |
G |
7: 106,781,220 (GRCm39) |
H139R |
probably benign |
Het |
Or1e34 |
T |
A |
11: 73,778,688 (GRCm39) |
N170I |
probably benign |
Het |
Or5w20 |
A |
T |
2: 87,727,013 (GRCm39) |
T157S |
probably benign |
Het |
Ptger2 |
T |
C |
14: 45,226,590 (GRCm39) |
C57R |
probably benign |
Het |
Rhot1 |
T |
C |
11: 80,114,769 (GRCm39) |
V59A |
probably damaging |
Het |
Rmdn2 |
G |
A |
17: 79,975,458 (GRCm39) |
|
probably null |
Het |
Rxfp2 |
G |
T |
5: 149,967,584 (GRCm39) |
K148N |
probably benign |
Het |
Sec23a |
G |
A |
12: 59,018,057 (GRCm39) |
T623M |
probably damaging |
Het |
Smcr8 |
T |
C |
11: 60,669,269 (GRCm39) |
L139P |
probably damaging |
Het |
Spag6l |
A |
T |
16: 16,584,960 (GRCm39) |
|
probably benign |
Het |
Taar1 |
T |
C |
10: 23,796,971 (GRCm39) |
I223T |
probably damaging |
Het |
Tdo2 |
G |
T |
3: 81,870,065 (GRCm39) |
A269E |
probably damaging |
Het |
Tnfsf18 |
A |
G |
1: 161,331,156 (GRCm39) |
Y102C |
possibly damaging |
Het |
Tns1 |
A |
G |
1: 73,964,740 (GRCm39) |
L1297P |
probably benign |
Het |
Txndc8 |
C |
T |
4: 57,984,245 (GRCm39) |
|
probably benign |
Het |
Ubr5 |
T |
C |
15: 37,973,235 (GRCm39) |
N2622S |
probably damaging |
Het |
Vmn2r99 |
T |
A |
17: 19,599,305 (GRCm39) |
F330I |
probably benign |
Het |
Zdhhc2 |
T |
A |
8: 40,925,948 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Eri3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00678:Eri3
|
APN |
4 |
117,422,088 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01392:Eri3
|
APN |
4 |
117,446,356 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01781:Eri3
|
APN |
4 |
117,421,874 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02737:Eri3
|
APN |
4 |
117,422,057 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02969:Eri3
|
APN |
4 |
117,506,508 (GRCm39) |
missense |
probably damaging |
1.00 |
chewed_out
|
UTSW |
4 |
117,506,604 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4280001:Eri3
|
UTSW |
4 |
117,439,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0993:Eri3
|
UTSW |
4 |
117,421,860 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1331:Eri3
|
UTSW |
4 |
117,422,104 (GRCm39) |
splice site |
probably benign |
|
R1538:Eri3
|
UTSW |
4 |
117,439,836 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1854:Eri3
|
UTSW |
4 |
117,506,562 (GRCm39) |
missense |
probably benign |
0.01 |
R1971:Eri3
|
UTSW |
4 |
117,421,964 (GRCm39) |
missense |
probably benign |
0.10 |
R5340:Eri3
|
UTSW |
4 |
117,530,991 (GRCm39) |
missense |
probably damaging |
0.99 |
R5511:Eri3
|
UTSW |
4 |
117,472,386 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5569:Eri3
|
UTSW |
4 |
117,506,553 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6052:Eri3
|
UTSW |
4 |
117,421,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R7140:Eri3
|
UTSW |
4 |
117,506,604 (GRCm39) |
critical splice donor site |
probably null |
|
R7187:Eri3
|
UTSW |
4 |
117,446,343 (GRCm39) |
missense |
probably benign |
0.03 |
R7268:Eri3
|
UTSW |
4 |
117,506,580 (GRCm39) |
missense |
probably benign |
|
R8083:Eri3
|
UTSW |
4 |
117,450,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R8557:Eri3
|
UTSW |
4 |
117,472,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9430:Eri3
|
UTSW |
4 |
117,439,868 (GRCm39) |
nonsense |
probably null |
|
R9563:Eri3
|
UTSW |
4 |
117,422,013 (GRCm39) |
missense |
probably benign |
0.15 |
R9565:Eri3
|
UTSW |
4 |
117,422,013 (GRCm39) |
missense |
probably benign |
0.15 |
|