Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl1 |
A |
G |
2: 31,668,957 (GRCm39) |
Y88C |
probably damaging |
Het |
Acbd3 |
A |
G |
1: 180,579,783 (GRCm39) |
I476V |
possibly damaging |
Het |
Apba2 |
T |
C |
7: 64,399,912 (GRCm39) |
I689T |
probably damaging |
Het |
AU018091 |
A |
G |
7: 3,209,001 (GRCm39) |
Y362H |
probably damaging |
Het |
Cdh26 |
T |
C |
2: 178,128,724 (GRCm39) |
S759P |
probably damaging |
Het |
Clcc1 |
A |
G |
3: 108,582,056 (GRCm39) |
Q387R |
probably benign |
Het |
Cobl |
C |
T |
11: 12,315,167 (GRCm39) |
G259R |
probably benign |
Het |
Col4a1 |
C |
T |
8: 11,268,934 (GRCm39) |
R968Q |
possibly damaging |
Het |
Ddr2 |
A |
G |
1: 169,832,381 (GRCm39) |
|
probably benign |
Het |
Dera |
C |
A |
6: 137,773,846 (GRCm39) |
N201K |
probably damaging |
Het |
Dsg1a |
A |
C |
18: 20,471,725 (GRCm39) |
E659A |
probably damaging |
Het |
Dus2 |
G |
T |
8: 106,772,702 (GRCm39) |
|
probably null |
Het |
Ears2 |
T |
A |
7: 121,647,352 (GRCm39) |
I311F |
possibly damaging |
Het |
Eml4 |
T |
A |
17: 83,761,893 (GRCm39) |
M417K |
possibly damaging |
Het |
Exosc4 |
A |
T |
15: 76,213,616 (GRCm39) |
M147L |
probably benign |
Het |
Fam171a2 |
T |
A |
11: 102,330,548 (GRCm39) |
Y278F |
possibly damaging |
Het |
Fastk |
A |
C |
5: 24,648,921 (GRCm39) |
H155Q |
probably null |
Het |
Fem1b |
G |
T |
9: 62,704,125 (GRCm39) |
N378K |
possibly damaging |
Het |
Fut11 |
C |
A |
14: 20,745,427 (GRCm39) |
Y119* |
probably null |
Het |
Gm6797 |
T |
C |
X: 8,511,388 (GRCm39) |
|
noncoding transcript |
Het |
Gstt4 |
T |
C |
10: 75,653,148 (GRCm39) |
D138G |
probably benign |
Het |
Hprt1 |
G |
A |
X: 52,091,027 (GRCm39) |
C66Y |
probably damaging |
Het |
Inpp5d |
T |
A |
1: 87,595,799 (GRCm39) |
|
probably benign |
Het |
Ints6l |
T |
A |
X: 55,547,108 (GRCm39) |
S621T |
probably benign |
Het |
Ints6l |
C |
G |
X: 55,550,172 (GRCm39) |
A699G |
probably benign |
Het |
Kctd3 |
A |
G |
1: 188,729,247 (GRCm39) |
|
probably benign |
Het |
Kntc1 |
G |
T |
5: 123,928,979 (GRCm39) |
V1252L |
probably null |
Het |
Lama5 |
A |
T |
2: 179,822,511 (GRCm39) |
M2854K |
possibly damaging |
Het |
Lcn5 |
G |
T |
2: 25,551,113 (GRCm39) |
L187F |
probably damaging |
Het |
Lrp3 |
A |
T |
7: 34,901,545 (GRCm39) |
L758M |
possibly damaging |
Het |
Ltn1 |
T |
A |
16: 87,209,395 (GRCm39) |
I740F |
probably benign |
Het |
Mcm5 |
A |
G |
8: 75,853,876 (GRCm39) |
K710R |
probably benign |
Het |
Mllt10 |
A |
G |
2: 18,208,577 (GRCm39) |
|
probably benign |
Het |
Nbr1 |
T |
A |
11: 101,467,197 (GRCm39) |
M864K |
probably benign |
Het |
Nkiras2 |
T |
C |
11: 100,515,758 (GRCm39) |
|
probably null |
Het |
Nlrp4d |
T |
A |
7: 10,116,449 (GRCm39) |
E144V |
probably benign |
Het |
Nppc |
T |
C |
1: 86,597,356 (GRCm39) |
|
probably benign |
Het |
Ormdl2 |
T |
A |
10: 128,655,868 (GRCm39) |
Q94L |
probably damaging |
Het |
Paox |
G |
C |
7: 139,707,440 (GRCm39) |
D88H |
probably damaging |
Het |
Prl7a2 |
T |
C |
13: 27,846,671 (GRCm39) |
E114G |
probably damaging |
Het |
Prpsap2 |
A |
G |
11: 61,631,826 (GRCm39) |
I177T |
possibly damaging |
Het |
Prss54 |
T |
C |
8: 96,286,368 (GRCm39) |
D235G |
possibly damaging |
Het |
Rwdd3 |
T |
C |
3: 120,965,256 (GRCm39) |
M24V |
probably benign |
Het |
Serpinb6e |
T |
A |
13: 34,025,201 (GRCm39) |
N30I |
probably benign |
Het |
Sh3rf1 |
G |
A |
8: 61,825,594 (GRCm39) |
A530T |
probably benign |
Het |
Slc28a1 |
T |
C |
7: 80,774,648 (GRCm39) |
I165T |
probably benign |
Het |
Slco6d1 |
T |
A |
1: 98,355,994 (GRCm39) |
L143* |
probably null |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Snx27 |
A |
G |
3: 94,469,320 (GRCm39) |
L7P |
probably benign |
Het |
Spata31e2 |
T |
A |
1: 26,722,013 (GRCm39) |
T1056S |
possibly damaging |
Het |
Spsb1 |
C |
T |
4: 149,991,374 (GRCm39) |
V65I |
probably benign |
Het |
St8sia2 |
C |
T |
7: 73,610,588 (GRCm39) |
G232S |
probably benign |
Het |
Sun1 |
A |
G |
5: 139,216,918 (GRCm39) |
H255R |
possibly damaging |
Het |
Tent2 |
T |
A |
13: 93,291,547 (GRCm39) |
Q365L |
probably benign |
Het |
Ube2k |
A |
G |
5: 65,738,795 (GRCm39) |
I95V |
probably damaging |
Het |
Ube2m |
C |
A |
7: 12,769,679 (GRCm39) |
E126D |
probably damaging |
Het |
Vmn2r27 |
A |
T |
6: 124,169,147 (GRCm39) |
M661K |
probably benign |
Het |
Wdr47 |
A |
T |
3: 108,525,939 (GRCm39) |
D154V |
probably damaging |
Het |
Zfp113 |
A |
G |
5: 138,143,845 (GRCm39) |
V135A |
probably benign |
Het |
|
Other mutations in Castor2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01370:Castor2
|
APN |
5 |
134,167,111 (GRCm39) |
missense |
probably benign |
0.12 |
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 |
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 |
|