Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts12 |
A |
G |
15: 11,152,134 (GRCm39) |
K208R |
probably benign |
Het |
Amh |
T |
C |
10: 80,642,443 (GRCm39) |
M242T |
possibly damaging |
Het |
Anpep |
T |
C |
7: 79,488,510 (GRCm39) |
Y440C |
probably damaging |
Het |
Atf7ip |
G |
T |
6: 136,538,263 (GRCm39) |
E499* |
probably null |
Het |
Clasp2 |
A |
G |
9: 113,735,065 (GRCm39) |
I967V |
probably benign |
Het |
Cyp26b1 |
T |
A |
6: 84,553,590 (GRCm39) |
Y263F |
probably benign |
Het |
Ecm2 |
C |
A |
13: 49,682,439 (GRCm39) |
Y489* |
probably null |
Het |
Gpr22 |
C |
A |
12: 31,759,853 (GRCm39) |
V90L |
probably benign |
Het |
Grip1 |
G |
A |
10: 119,836,438 (GRCm39) |
V516M |
probably benign |
Het |
Ipo5 |
C |
T |
14: 121,160,547 (GRCm39) |
S188L |
probably benign |
Het |
Kcnh6 |
T |
A |
11: 105,908,464 (GRCm39) |
I360N |
possibly damaging |
Het |
Lrp1b |
C |
A |
2: 41,392,029 (GRCm39) |
D512Y |
|
Het |
Lrpprc |
C |
T |
17: 85,059,736 (GRCm39) |
|
probably null |
Het |
Lta4h |
A |
G |
10: 93,318,850 (GRCm39) |
K547R |
probably benign |
Het |
Nacad |
G |
C |
11: 6,548,948 (GRCm39) |
P1340R |
possibly damaging |
Het |
Ncapd2 |
T |
C |
6: 125,156,301 (GRCm39) |
K495E |
probably benign |
Het |
Ndufaf7 |
A |
T |
17: 79,245,968 (GRCm39) |
|
probably null |
Het |
Nsrp1 |
A |
G |
11: 76,941,477 (GRCm39) |
V77A |
probably benign |
Het |
Or1f19 |
A |
T |
16: 3,411,132 (GRCm39) |
S291C |
probably damaging |
Het |
Or8k3b |
T |
C |
2: 86,521,139 (GRCm39) |
Y60C |
probably damaging |
Het |
P2ry12 |
A |
G |
3: 59,125,456 (GRCm39) |
V73A |
probably damaging |
Het |
Pafah1b1 |
G |
A |
11: 74,574,493 (GRCm39) |
T231I |
probably benign |
Het |
Parp11 |
C |
A |
6: 127,448,615 (GRCm39) |
Y77* |
probably null |
Het |
Phc3 |
T |
A |
3: 30,983,916 (GRCm39) |
T712S |
unknown |
Het |
Pkm |
T |
A |
9: 59,579,220 (GRCm39) |
I335N |
probably damaging |
Het |
Pmpca |
A |
G |
2: 26,283,581 (GRCm39) |
T417A |
probably benign |
Het |
Pot1b |
C |
T |
17: 56,006,991 (GRCm39) |
|
probably null |
Het |
Prrc1 |
T |
A |
18: 57,507,764 (GRCm39) |
|
probably null |
Het |
Psg18 |
A |
T |
7: 18,083,047 (GRCm39) |
N369K |
probably benign |
Het |
Pum3 |
T |
A |
19: 27,399,791 (GRCm39) |
Y214F |
probably damaging |
Het |
Reln |
G |
A |
5: 22,253,036 (GRCm39) |
T637M |
probably damaging |
Het |
Rpe65 |
A |
T |
3: 159,321,292 (GRCm39) |
Y368F |
probably damaging |
Het |
Serpina3a |
A |
G |
12: 104,082,362 (GRCm39) |
D45G |
probably benign |
Het |
Serpinb3c |
T |
A |
1: 107,199,731 (GRCm39) |
L263F |
probably damaging |
Het |
Slc25a23 |
C |
T |
17: 57,352,553 (GRCm39) |
V444I |
probably damaging |
Het |
Slc40a1 |
C |
T |
1: 45,948,621 (GRCm39) |
G553D |
probably benign |
Het |
Spata31e5 |
T |
C |
1: 28,816,037 (GRCm39) |
Q665R |
possibly damaging |
Het |
Spata31h1 |
A |
G |
10: 82,123,185 (GRCm39) |
I3275T |
probably benign |
Het |
Taf7 |
C |
A |
18: 37,776,223 (GRCm39) |
D115Y |
probably damaging |
Het |
Tanc1 |
G |
C |
2: 59,673,766 (GRCm39) |
A1624P |
probably benign |
Het |
Tmed4 |
T |
C |
11: 6,224,405 (GRCm39) |
D85G |
probably benign |
Het |
Tmed6 |
A |
G |
8: 107,790,385 (GRCm39) |
V138A |
probably benign |
Het |
Tmem63b |
T |
C |
17: 45,977,517 (GRCm39) |
T370A |
probably benign |
Het |
Ttc38 |
A |
G |
15: 85,720,310 (GRCm39) |
T91A |
probably benign |
Het |
Ube4b |
C |
G |
4: 149,444,833 (GRCm39) |
A476P |
probably benign |
Het |
Vmn2r53 |
A |
G |
7: 12,315,435 (GRCm39) |
C795R |
probably benign |
Het |
|
Other mutations in Cpa6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00858:Cpa6
|
APN |
1 |
10,554,219 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00933:Cpa6
|
APN |
1 |
10,407,595 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01710:Cpa6
|
APN |
1 |
10,395,497 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02211:Cpa6
|
APN |
1 |
10,665,861 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02504:Cpa6
|
APN |
1 |
10,559,144 (GRCm39) |
missense |
probably benign |
0.19 |
R0487:Cpa6
|
UTSW |
1 |
10,479,487 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1260:Cpa6
|
UTSW |
1 |
10,395,544 (GRCm39) |
splice site |
probably null |
|
R2154:Cpa6
|
UTSW |
1 |
10,407,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R4705:Cpa6
|
UTSW |
1 |
10,551,283 (GRCm39) |
missense |
probably benign |
0.03 |
R4788:Cpa6
|
UTSW |
1 |
10,478,502 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4872:Cpa6
|
UTSW |
1 |
10,665,843 (GRCm39) |
critical splice donor site |
probably null |
|
R4941:Cpa6
|
UTSW |
1 |
10,479,562 (GRCm39) |
missense |
probably benign |
0.25 |
R5656:Cpa6
|
UTSW |
1 |
10,399,739 (GRCm39) |
missense |
probably benign |
0.19 |
R5969:Cpa6
|
UTSW |
1 |
10,559,108 (GRCm39) |
missense |
probably benign |
0.15 |
R6019:Cpa6
|
UTSW |
1 |
10,665,868 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6322:Cpa6
|
UTSW |
1 |
10,547,346 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6958:Cpa6
|
UTSW |
1 |
10,665,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R7154:Cpa6
|
UTSW |
1 |
10,407,694 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7274:Cpa6
|
UTSW |
1 |
10,479,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R8140:Cpa6
|
UTSW |
1 |
10,395,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8559:Cpa6
|
UTSW |
1 |
10,478,574 (GRCm39) |
nonsense |
probably null |
|
R9297:Cpa6
|
UTSW |
1 |
10,554,273 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9355:Cpa6
|
UTSW |
1 |
10,479,520 (GRCm39) |
missense |
probably benign |
0.09 |
R9498:Cpa6
|
UTSW |
1 |
10,479,546 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Cpa6
|
UTSW |
1 |
10,399,784 (GRCm39) |
critical splice acceptor site |
probably null |
|
|