Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34l |
T |
G |
8: 44,079,477 (GRCm39) |
Q249P |
probably benign |
Het |
Adgrv1 |
C |
T |
13: 81,255,017 (GRCm39) |
|
probably null |
Het |
Ccdc110 |
A |
G |
8: 46,387,761 (GRCm39) |
|
probably benign |
Het |
Cd200r1 |
T |
A |
16: 44,609,106 (GRCm39) |
|
probably benign |
Het |
Cdkl1 |
A |
T |
12: 69,836,809 (GRCm39) |
D40E |
probably benign |
Het |
Cdx1 |
A |
G |
18: 61,153,436 (GRCm39) |
|
probably benign |
Het |
Cenpp |
T |
A |
13: 49,801,108 (GRCm39) |
K103N |
possibly damaging |
Het |
Cep162 |
A |
G |
9: 87,093,862 (GRCm39) |
Y839H |
possibly damaging |
Het |
Chac1 |
T |
A |
2: 119,183,941 (GRCm39) |
L181* |
probably null |
Het |
Ciapin1 |
G |
T |
8: 95,554,938 (GRCm39) |
Q173K |
probably damaging |
Het |
Cmklr2 |
T |
A |
1: 63,222,690 (GRCm39) |
N182Y |
probably benign |
Het |
Dgcr2 |
A |
G |
16: 17,667,650 (GRCm39) |
C270R |
probably damaging |
Het |
Dlc1 |
A |
G |
8: 37,317,383 (GRCm39) |
S431P |
probably benign |
Het |
Ehbp1 |
A |
T |
11: 22,181,992 (GRCm39) |
|
probably benign |
Het |
Enpp3 |
A |
T |
10: 24,652,767 (GRCm39) |
V730D |
possibly damaging |
Het |
Fam174b |
A |
G |
7: 73,390,512 (GRCm39) |
T88A |
probably benign |
Het |
Fancl |
A |
G |
11: 26,421,337 (GRCm39) |
K364E |
probably benign |
Het |
Fbp2 |
A |
T |
13: 63,001,862 (GRCm39) |
F118I |
probably damaging |
Het |
Galc |
A |
G |
12: 98,188,906 (GRCm39) |
Y402H |
probably damaging |
Het |
Gga2 |
T |
C |
7: 121,598,123 (GRCm39) |
N324D |
possibly damaging |
Het |
Hc |
G |
T |
2: 34,918,086 (GRCm39) |
F732L |
probably damaging |
Het |
Heca |
T |
C |
10: 17,791,463 (GRCm39) |
M198V |
probably benign |
Het |
Herc6 |
C |
A |
6: 57,596,586 (GRCm39) |
H509N |
probably benign |
Het |
Irf2bpl |
A |
T |
12: 86,929,398 (GRCm39) |
M425K |
probably benign |
Het |
Mael |
C |
T |
1: 166,066,159 (GRCm39) |
G26D |
probably damaging |
Het |
Map1a |
A |
G |
2: 121,135,906 (GRCm39) |
T2241A |
probably benign |
Het |
Mcc |
C |
G |
18: 44,652,583 (GRCm39) |
|
probably benign |
Het |
Mdga2 |
A |
G |
12: 66,701,894 (GRCm39) |
S505P |
probably damaging |
Het |
Mdm1 |
A |
G |
10: 117,992,783 (GRCm39) |
|
probably benign |
Het |
Mex3b |
A |
T |
7: 82,518,312 (GRCm39) |
E209V |
probably damaging |
Het |
Mrgprx3-ps |
T |
C |
7: 46,959,154 (GRCm39) |
E279G |
possibly damaging |
Het |
Ms4a20 |
A |
T |
19: 11,093,801 (GRCm39) |
Y10* |
probably null |
Het |
Nfe2l1 |
A |
T |
11: 96,718,439 (GRCm39) |
L32Q |
probably damaging |
Het |
Npas1 |
C |
T |
7: 16,195,818 (GRCm39) |
V285I |
probably benign |
Het |
Or5e1 |
T |
A |
7: 108,354,781 (GRCm39) |
C239* |
probably null |
Het |
Or5h19 |
C |
T |
16: 58,856,456 (GRCm39) |
V215I |
probably benign |
Het |
Or9i14 |
T |
C |
19: 13,792,342 (GRCm39) |
N204S |
probably benign |
Het |
Osr1 |
A |
G |
12: 9,629,639 (GRCm39) |
T171A |
probably benign |
Het |
Ppp3cb |
A |
T |
14: 20,574,044 (GRCm39) |
C265S |
probably damaging |
Het |
Pramel27 |
A |
G |
4: 143,578,401 (GRCm39) |
I220M |
probably damaging |
Het |
Sephs1 |
A |
G |
2: 4,904,371 (GRCm39) |
T250A |
probably benign |
Het |
Simc1 |
T |
C |
13: 54,674,417 (GRCm39) |
Y922H |
probably damaging |
Het |
Slc25a39 |
A |
G |
11: 102,297,056 (GRCm39) |
F56L |
probably benign |
Het |
Smg8 |
A |
G |
11: 86,976,948 (GRCm39) |
L211P |
probably damaging |
Het |
Sncaip |
A |
G |
18: 53,040,400 (GRCm39) |
S805G |
probably benign |
Het |
Sra1 |
T |
C |
18: 36,809,662 (GRCm39) |
|
probably benign |
Het |
Tas2r104 |
T |
G |
6: 131,662,055 (GRCm39) |
D218A |
probably damaging |
Het |
Unc45b |
A |
G |
11: 82,802,686 (GRCm39) |
|
probably benign |
Het |
Unc79 |
A |
G |
12: 103,075,040 (GRCm39) |
|
probably null |
Het |
Washc2 |
T |
A |
6: 116,225,007 (GRCm39) |
L785* |
probably null |
Het |
Zfp30 |
A |
G |
7: 29,493,063 (GRCm39) |
E439G |
probably damaging |
Het |
Zfp518a |
A |
G |
19: 40,901,072 (GRCm39) |
T334A |
probably benign |
Het |
|
Other mutations in Efcab12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00435:Efcab12
|
APN |
6 |
115,800,625 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02748:Efcab12
|
APN |
6 |
115,797,063 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03148:Efcab12
|
APN |
6 |
115,787,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:Efcab12
|
UTSW |
6 |
115,800,209 (GRCm39) |
splice site |
probably benign |
|
R2847:Efcab12
|
UTSW |
6 |
115,788,072 (GRCm39) |
missense |
probably damaging |
0.97 |
R4674:Efcab12
|
UTSW |
6 |
115,800,610 (GRCm39) |
missense |
probably damaging |
0.99 |
R4707:Efcab12
|
UTSW |
6 |
115,791,510 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5145:Efcab12
|
UTSW |
6 |
115,800,238 (GRCm39) |
missense |
probably damaging |
0.98 |
R5185:Efcab12
|
UTSW |
6 |
115,800,451 (GRCm39) |
missense |
probably benign |
0.00 |
R6168:Efcab12
|
UTSW |
6 |
115,791,577 (GRCm39) |
missense |
probably damaging |
0.97 |
R6960:Efcab12
|
UTSW |
6 |
115,815,273 (GRCm39) |
unclassified |
probably benign |
|
R7187:Efcab12
|
UTSW |
6 |
115,800,474 (GRCm39) |
missense |
not run |
|
R7297:Efcab12
|
UTSW |
6 |
115,787,997 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7324:Efcab12
|
UTSW |
6 |
115,800,555 (GRCm39) |
missense |
probably benign |
0.30 |
R7715:Efcab12
|
UTSW |
6 |
115,800,504 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7996:Efcab12
|
UTSW |
6 |
115,800,378 (GRCm39) |
missense |
probably benign |
0.30 |
R8418:Efcab12
|
UTSW |
6 |
115,799,076 (GRCm39) |
critical splice donor site |
probably null |
|
R8527:Efcab12
|
UTSW |
6 |
115,791,535 (GRCm39) |
missense |
probably benign |
0.02 |
R8923:Efcab12
|
UTSW |
6 |
115,787,982 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8924:Efcab12
|
UTSW |
6 |
115,800,664 (GRCm39) |
missense |
probably benign |
0.00 |
R9364:Efcab12
|
UTSW |
6 |
115,814,975 (GRCm39) |
missense |
probably benign |
0.00 |
R9433:Efcab12
|
UTSW |
6 |
115,792,995 (GRCm39) |
missense |
probably benign |
0.03 |
R9762:Efcab12
|
UTSW |
6 |
115,800,331 (GRCm39) |
missense |
possibly damaging |
0.72 |
|