Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
T |
12: 71,219,903 (GRCm39) |
I817L |
probably benign |
Het |
Adcy8 |
A |
T |
15: 64,573,939 (GRCm39) |
W1055R |
probably damaging |
Het |
Anks4b |
A |
G |
7: 119,781,923 (GRCm39) |
E318G |
probably benign |
Het |
Arid3a |
A |
G |
10: 79,767,889 (GRCm39) |
T229A |
probably benign |
Het |
Cckar |
T |
C |
5: 53,858,580 (GRCm39) |
K247E |
possibly damaging |
Het |
Cfap52 |
A |
T |
11: 67,844,571 (GRCm39) |
|
probably null |
Het |
Cped1 |
T |
C |
6: 22,059,953 (GRCm39) |
|
probably null |
Het |
Ctsf |
T |
G |
19: 4,906,567 (GRCm39) |
F165V |
probably damaging |
Het |
Cyp4v3 |
G |
T |
8: 45,785,954 (GRCm39) |
A21E |
probably benign |
Het |
Cytip |
T |
C |
2: 58,037,944 (GRCm39) |
E140G |
probably damaging |
Het |
D130043K22Rik |
A |
C |
13: 25,077,406 (GRCm39) |
Q1013P |
probably damaging |
Het |
Dpp6 |
A |
G |
5: 27,928,370 (GRCm39) |
M763V |
probably benign |
Het |
Eps15 |
T |
A |
4: 109,178,340 (GRCm39) |
Y193N |
probably damaging |
Het |
Ghrhr |
T |
C |
6: 55,356,083 (GRCm39) |
W59R |
probably damaging |
Het |
Hdac4 |
A |
G |
1: 91,861,402 (GRCm39) |
V1056A |
possibly damaging |
Het |
Ipcef1 |
T |
C |
10: 6,850,668 (GRCm39) |
T312A |
probably damaging |
Het |
Itpr3 |
T |
C |
17: 27,331,002 (GRCm39) |
|
probably null |
Het |
Kif6 |
A |
G |
17: 49,993,453 (GRCm39) |
I182V |
probably damaging |
Het |
Lcn3 |
A |
G |
2: 25,656,389 (GRCm39) |
K90E |
probably damaging |
Het |
Lig3 |
T |
C |
11: 82,681,342 (GRCm39) |
S446P |
probably damaging |
Het |
Ncln |
G |
A |
10: 81,326,103 (GRCm39) |
Q283* |
probably null |
Het |
Nlrp4c |
A |
G |
7: 6,069,322 (GRCm39) |
T408A |
probably damaging |
Het |
Oas1h |
T |
C |
5: 121,009,962 (GRCm39) |
F346L |
probably damaging |
Het |
Olig2 |
AGCCGCCGCCGCCGCCGCAGCCGCCGCCGCCGC |
AGCCGCCGCCGCCGCAGCCGCCGCCGCCGC |
16: 91,023,962 (GRCm39) |
|
probably benign |
Het |
Or2ad1 |
A |
T |
13: 21,326,356 (GRCm39) |
Y290* |
probably null |
Het |
Or52b4 |
T |
C |
7: 102,184,623 (GRCm39) |
I223T |
probably damaging |
Het |
Or52s1b |
A |
T |
7: 102,822,062 (GRCm39) |
F261I |
probably damaging |
Het |
Or8b55 |
A |
G |
9: 38,727,536 (GRCm39) |
I246V |
probably benign |
Het |
Pdcd1 |
A |
T |
1: 93,969,186 (GRCm39) |
V44E |
probably damaging |
Het |
Prdm13 |
A |
T |
4: 21,679,932 (GRCm39) |
I186N |
unknown |
Het |
Prpf4b |
A |
G |
13: 35,085,428 (GRCm39) |
D958G |
probably damaging |
Het |
Prss59 |
A |
T |
6: 40,903,022 (GRCm39) |
Y117N |
probably benign |
Het |
Prune2 |
A |
G |
19: 17,156,223 (GRCm39) |
N2792S |
probably damaging |
Het |
Robo1 |
T |
A |
16: 72,780,760 (GRCm39) |
I830N |
possibly damaging |
Het |
Scaper |
A |
G |
9: 55,669,611 (GRCm39) |
V355A |
probably damaging |
Het |
Scn3b |
C |
T |
9: 40,193,846 (GRCm39) |
A191V |
probably benign |
Het |
Slc13a3 |
G |
C |
2: 165,272,155 (GRCm39) |
S296C |
probably benign |
Het |
Slc6a16 |
T |
A |
7: 44,917,477 (GRCm39) |
I445N |
possibly damaging |
Het |
Snrnp35 |
A |
G |
5: 124,628,565 (GRCm39) |
Y126C |
possibly damaging |
Het |
Spock2 |
A |
G |
10: 59,957,554 (GRCm39) |
H98R |
possibly damaging |
Het |
Sptssb |
A |
T |
3: 69,728,286 (GRCm39) |
Y50* |
probably null |
Het |
Syne1 |
A |
G |
10: 5,066,965 (GRCm39) |
|
probably null |
Het |
Tcf21 |
T |
C |
10: 22,695,706 (GRCm39) |
T33A |
probably benign |
Het |
Tecta |
A |
G |
9: 42,306,258 (GRCm39) |
F57L |
probably damaging |
Het |
Tgs1 |
C |
A |
4: 3,586,215 (GRCm39) |
P364H |
probably benign |
Het |
Tmem242 |
A |
G |
17: 5,461,711 (GRCm39) |
I119T |
probably benign |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Vmn2r3 |
T |
A |
3: 64,186,235 (GRCm39) |
N150I |
probably damaging |
Het |
Vmn2r69 |
A |
G |
7: 85,060,762 (GRCm39) |
I274T |
possibly damaging |
Het |
Vwf |
T |
A |
6: 125,616,304 (GRCm39) |
L1206* |
probably null |
Het |
Zfp157 |
T |
A |
5: 138,445,833 (GRCm39) |
W63R |
probably benign |
Het |
Zfp455 |
T |
C |
13: 67,347,302 (GRCm39) |
Y10H |
probably benign |
Het |
Zfp654 |
T |
C |
16: 64,605,239 (GRCm39) |
T447A |
probably damaging |
Het |
Zhx2 |
T |
C |
15: 57,685,063 (GRCm39) |
I144T |
probably damaging |
Het |
|
Other mutations in Ckap4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02591:Ckap4
|
APN |
10 |
84,364,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03251:Ckap4
|
APN |
10 |
84,364,469 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Ckap4
|
UTSW |
10 |
84,363,630 (GRCm39) |
missense |
probably damaging |
0.99 |
R0866:Ckap4
|
UTSW |
10 |
84,363,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Ckap4
|
UTSW |
10 |
84,363,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Ckap4
|
UTSW |
10 |
84,363,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Ckap4
|
UTSW |
10 |
84,363,738 (GRCm39) |
missense |
probably benign |
|
R2113:Ckap4
|
UTSW |
10 |
84,369,387 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3723:Ckap4
|
UTSW |
10 |
84,364,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R3958:Ckap4
|
UTSW |
10 |
84,364,028 (GRCm39) |
missense |
probably benign |
0.01 |
R4735:Ckap4
|
UTSW |
10 |
84,369,384 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4746:Ckap4
|
UTSW |
10 |
84,369,384 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4857:Ckap4
|
UTSW |
10 |
84,369,352 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5308:Ckap4
|
UTSW |
10 |
84,364,238 (GRCm39) |
missense |
probably benign |
0.01 |
R5333:Ckap4
|
UTSW |
10 |
84,363,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R5848:Ckap4
|
UTSW |
10 |
84,369,354 (GRCm39) |
missense |
probably benign |
0.02 |
R7383:Ckap4
|
UTSW |
10 |
84,364,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Ckap4
|
UTSW |
10 |
84,363,863 (GRCm39) |
missense |
probably damaging |
0.99 |
R7453:Ckap4
|
UTSW |
10 |
84,364,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Ckap4
|
UTSW |
10 |
84,364,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Ckap4
|
UTSW |
10 |
84,369,499 (GRCm39) |
missense |
probably damaging |
0.96 |
R8337:Ckap4
|
UTSW |
10 |
84,364,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R8932:Ckap4
|
UTSW |
10 |
84,364,290 (GRCm39) |
missense |
probably benign |
0.29 |
R9099:Ckap4
|
UTSW |
10 |
84,369,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R9115:Ckap4
|
UTSW |
10 |
84,363,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R9193:Ckap4
|
UTSW |
10 |
84,363,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Ckap4
|
UTSW |
10 |
84,363,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R9462:Ckap4
|
UTSW |
10 |
84,363,924 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9592:Ckap4
|
UTSW |
10 |
84,364,175 (GRCm39) |
missense |
probably damaging |
1.00 |
|