Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck1 |
A |
T |
12: 88,423,503 (GRCm39) |
|
probably benign |
Het |
Add1 |
C |
T |
5: 34,787,859 (GRCm39) |
T210I |
probably damaging |
Het |
Ajm1 |
T |
C |
2: 25,468,969 (GRCm39) |
E314G |
possibly damaging |
Het |
Alpk2 |
A |
T |
18: 65,483,662 (GRCm39) |
D115E |
possibly damaging |
Het |
Ankrd36 |
C |
T |
11: 5,534,019 (GRCm39) |
T290I |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,001,904 (GRCm39) |
I1283N |
probably benign |
Het |
Ccnt2 |
T |
C |
1: 127,731,250 (GRCm39) |
F709S |
possibly damaging |
Het |
Erc1 |
T |
C |
6: 119,801,426 (GRCm39) |
E197G |
probably damaging |
Het |
Ftsj3 |
G |
T |
11: 106,143,145 (GRCm39) |
R390S |
possibly damaging |
Het |
Gabrb3 |
G |
A |
7: 57,466,226 (GRCm39) |
A347T |
probably benign |
Het |
Gde1 |
A |
G |
7: 118,288,383 (GRCm39) |
|
probably benign |
Het |
Jhy |
A |
T |
9: 40,828,438 (GRCm39) |
N489K |
probably benign |
Het |
Kiss1r |
A |
G |
10: 79,754,658 (GRCm39) |
T51A |
probably benign |
Het |
Lama5 |
T |
C |
2: 179,839,193 (GRCm39) |
S772G |
possibly damaging |
Het |
Lamb2 |
G |
T |
9: 108,364,932 (GRCm39) |
|
probably null |
Het |
Loxl3 |
A |
G |
6: 83,026,468 (GRCm39) |
T475A |
probably damaging |
Het |
Lpl |
A |
T |
8: 69,340,220 (GRCm39) |
S72C |
possibly damaging |
Het |
Lrrc74a |
A |
T |
12: 86,801,204 (GRCm39) |
I352F |
probably damaging |
Het |
Mcoln2 |
T |
C |
3: 145,887,585 (GRCm39) |
I334T |
possibly damaging |
Het |
Mettl8 |
T |
G |
2: 70,812,383 (GRCm39) |
D49A |
probably damaging |
Het |
Ms4a3 |
T |
A |
19: 11,610,245 (GRCm39) |
T106S |
probably benign |
Het |
Obscn |
T |
A |
11: 58,886,389 (GRCm39) |
|
probably null |
Het |
Or14j2 |
T |
C |
17: 37,885,412 (GRCm39) |
I301V |
probably null |
Het |
Or1o11 |
C |
A |
17: 37,756,605 (GRCm39) |
H64Q |
probably benign |
Het |
Or1p1c |
G |
A |
11: 74,160,325 (GRCm39) |
V37I |
probably benign |
Het |
Or4n4 |
G |
T |
14: 50,519,689 (GRCm39) |
T7K |
probably damaging |
Het |
Or5b107 |
A |
T |
19: 13,142,663 (GRCm39) |
Y95F |
possibly damaging |
Het |
Pcnx2 |
T |
C |
8: 126,528,222 (GRCm39) |
K1333E |
probably damaging |
Het |
Pias3 |
T |
C |
3: 96,610,891 (GRCm39) |
F364L |
probably damaging |
Het |
Piezo2 |
T |
A |
18: 63,155,531 (GRCm39) |
I2438F |
probably damaging |
Het |
Plcb3 |
A |
C |
19: 6,940,192 (GRCm39) |
V465G |
probably damaging |
Het |
Plekho2 |
G |
T |
9: 65,465,912 (GRCm39) |
H159N |
probably damaging |
Het |
Polr2e |
A |
G |
10: 79,872,681 (GRCm39) |
|
probably benign |
Het |
Rab6b |
G |
T |
9: 103,041,094 (GRCm39) |
V163L |
probably benign |
Het |
Rabep1 |
A |
G |
11: 70,816,607 (GRCm39) |
M597V |
probably benign |
Het |
Rbm15 |
A |
G |
3: 107,238,326 (GRCm39) |
S691P |
probably damaging |
Het |
Sec24b |
G |
A |
3: 129,801,253 (GRCm39) |
|
probably benign |
Het |
Slc6a18 |
A |
G |
13: 73,815,150 (GRCm39) |
I386T |
probably damaging |
Het |
Stxbp3 |
A |
C |
3: 108,704,741 (GRCm39) |
Y497* |
probably null |
Het |
Styk1 |
T |
C |
6: 131,278,615 (GRCm39) |
K353R |
probably damaging |
Het |
Tbc1d10b |
A |
T |
7: 126,798,253 (GRCm39) |
H629Q |
probably damaging |
Het |
Tbc1d5 |
T |
A |
17: 51,273,755 (GRCm39) |
I119F |
probably benign |
Het |
Tcp11l1 |
G |
T |
2: 104,536,831 (GRCm39) |
D11E |
probably benign |
Het |
Tfap2d |
A |
G |
1: 19,175,009 (GRCm39) |
Y154C |
probably damaging |
Het |
Tgm5 |
T |
C |
2: 120,884,018 (GRCm39) |
N325S |
probably benign |
Het |
Thbs2 |
T |
C |
17: 14,910,327 (GRCm39) |
K91E |
possibly damaging |
Het |
Vmn2r26 |
T |
A |
6: 124,038,715 (GRCm39) |
F763L |
probably benign |
Het |
Washc4 |
A |
G |
10: 83,394,694 (GRCm39) |
E308G |
probably damaging |
Het |
Xpot |
C |
A |
10: 121,440,399 (GRCm39) |
A611S |
probably benign |
Het |
|
Other mutations in Castor2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01924:Castor2
|
APN |
5 |
134,164,441 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02302:Castor2
|
APN |
5 |
134,164,482 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0733:Castor2
|
UTSW |
5 |
134,165,054 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1485:Castor2
|
UTSW |
5 |
134,165,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Castor2
|
UTSW |
5 |
134,154,726 (GRCm39) |
missense |
probably damaging |
0.97 |
R2130:Castor2
|
UTSW |
5 |
134,164,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Castor2
|
UTSW |
5 |
134,164,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Castor2
|
UTSW |
5 |
134,164,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Castor2
|
UTSW |
5 |
134,164,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Castor2
|
UTSW |
5 |
134,154,783 (GRCm39) |
critical splice donor site |
probably null |
|
R6422:Castor2
|
UTSW |
5 |
134,164,549 (GRCm39) |
missense |
probably benign |
0.04 |
R6722:Castor2
|
UTSW |
5 |
134,164,458 (GRCm39) |
missense |
probably benign |
0.38 |
R6959:Castor2
|
UTSW |
5 |
134,164,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R7161:Castor2
|
UTSW |
5 |
134,164,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Castor2
|
UTSW |
5 |
134,165,936 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8348:Castor2
|
UTSW |
5 |
134,166,955 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8448:Castor2
|
UTSW |
5 |
134,166,955 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8821:Castor2
|
UTSW |
5 |
134,164,092 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9489:Castor2
|
UTSW |
5 |
134,164,536 (GRCm39) |
missense |
probably benign |
0.01 |
X0028:Castor2
|
UTSW |
5 |
134,166,902 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0064:Castor2
|
UTSW |
5 |
134,164,420 (GRCm39) |
missense |
probably benign |
0.40 |
|