Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
A |
T |
4: 53,092,860 (GRCm39) |
V308E |
probably benign |
Het |
Amy1 |
A |
G |
3: 113,356,418 (GRCm39) |
|
probably benign |
Het |
Astn2 |
C |
T |
4: 66,103,379 (GRCm39) |
V345M |
unknown |
Het |
Brwd1 |
T |
C |
16: 95,844,286 (GRCm39) |
E756G |
probably damaging |
Het |
Ccpg1 |
C |
T |
9: 72,909,103 (GRCm39) |
L135F |
probably benign |
Het |
Cecr2 |
C |
T |
6: 120,734,845 (GRCm39) |
H694Y |
probably damaging |
Het |
Cfh |
G |
A |
1: 140,110,920 (GRCm39) |
T14I |
probably damaging |
Het |
Cfhr2 |
G |
A |
1: 139,741,172 (GRCm39) |
R268* |
probably null |
Het |
Clca3a1 |
T |
A |
3: 144,738,350 (GRCm39) |
I53L |
probably benign |
Het |
Clcn6 |
A |
G |
4: 148,123,206 (GRCm39) |
|
probably benign |
Het |
Cnfn |
C |
T |
7: 25,067,256 (GRCm39) |
V98I |
probably benign |
Het |
Cntnap1 |
C |
T |
11: 101,077,840 (GRCm39) |
R1122W |
probably damaging |
Het |
Cpne9 |
A |
T |
6: 113,272,024 (GRCm39) |
E384V |
probably damaging |
Het |
Ctr9 |
T |
C |
7: 110,648,705 (GRCm39) |
|
probably benign |
Het |
Ctsj |
T |
A |
13: 61,151,515 (GRCm39) |
|
probably benign |
Het |
Cyp2c39 |
A |
C |
19: 39,501,934 (GRCm39) |
|
probably benign |
Het |
Dock5 |
A |
C |
14: 68,046,481 (GRCm39) |
I767S |
probably damaging |
Het |
Eftud2 |
T |
C |
11: 102,737,446 (GRCm39) |
T552A |
probably damaging |
Het |
Epdr1 |
A |
G |
13: 19,778,715 (GRCm39) |
I25T |
probably damaging |
Het |
Fcgbp |
A |
T |
7: 27,789,138 (GRCm39) |
D568V |
probably damaging |
Het |
Fcgbpl1 |
T |
A |
7: 27,836,516 (GRCm39) |
V145D |
probably damaging |
Het |
Fhip1b |
T |
C |
7: 105,038,654 (GRCm39) |
E195G |
probably damaging |
Het |
Frem2 |
T |
A |
3: 53,555,342 (GRCm39) |
T1732S |
probably damaging |
Het |
Fuz |
T |
C |
7: 44,547,982 (GRCm39) |
V183A |
possibly damaging |
Het |
Grb7 |
T |
C |
11: 98,344,046 (GRCm39) |
S284P |
probably damaging |
Het |
Hoxb4 |
G |
T |
11: 96,209,713 (GRCm39) |
G40C |
probably damaging |
Het |
Kmt2d |
C |
A |
15: 98,733,088 (GRCm39) |
|
probably benign |
Het |
L3mbtl3 |
A |
G |
10: 26,203,732 (GRCm39) |
V366A |
unknown |
Het |
Ldlr |
G |
A |
9: 21,651,040 (GRCm39) |
R486H |
probably benign |
Het |
Lnpep |
A |
T |
17: 17,795,658 (GRCm39) |
|
probably benign |
Het |
Mical3 |
A |
T |
6: 121,006,602 (GRCm39) |
|
probably benign |
Het |
Myh15 |
T |
C |
16: 48,992,250 (GRCm39) |
|
probably benign |
Het |
Nup155 |
T |
A |
15: 8,159,716 (GRCm39) |
H542Q |
probably benign |
Het |
Opn4 |
A |
G |
14: 34,320,930 (GRCm39) |
|
probably benign |
Het |
Or13a20 |
T |
C |
7: 140,231,976 (GRCm39) |
F28S |
probably benign |
Het |
Or4a68 |
T |
A |
2: 89,269,698 (GRCm39) |
R308S |
possibly damaging |
Het |
Or6c68 |
A |
G |
10: 129,157,916 (GRCm39) |
I141M |
probably benign |
Het |
Or8g4 |
A |
T |
9: 39,662,414 (GRCm39) |
H244L |
probably damaging |
Het |
Or8h10 |
T |
C |
2: 86,809,126 (GRCm39) |
N5D |
probably damaging |
Het |
Pak3 |
TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC |
X: 142,526,889 (GRCm39) |
|
probably benign |
Het |
Parp14 |
T |
C |
16: 35,661,382 (GRCm39) |
K1522R |
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,594,335 (GRCm39) |
D1259E |
probably benign |
Het |
Pogz |
C |
T |
3: 94,786,664 (GRCm39) |
A1084V |
probably damaging |
Het |
Popdc3 |
G |
A |
10: 45,191,359 (GRCm39) |
V157M |
probably benign |
Het |
Prrt4 |
T |
C |
6: 29,171,183 (GRCm39) |
Y423C |
probably damaging |
Het |
Qrich1 |
C |
T |
9: 108,411,719 (GRCm39) |
H415Y |
probably damaging |
Het |
Rabgap1 |
A |
G |
2: 37,433,235 (GRCm39) |
N801D |
probably benign |
Het |
Rb1 |
A |
G |
14: 73,525,124 (GRCm39) |
|
probably benign |
Het |
Rp1 |
A |
T |
1: 4,418,060 (GRCm39) |
N1017K |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,650,445 (GRCm39) |
D356G |
probably null |
Het |
Skint8 |
C |
G |
4: 111,794,126 (GRCm39) |
P172R |
probably damaging |
Het |
Slc12a8 |
T |
G |
16: 33,478,600 (GRCm39) |
M643R |
possibly damaging |
Het |
Sult1c2 |
A |
T |
17: 54,271,113 (GRCm39) |
|
probably benign |
Het |
Tasor2 |
A |
G |
13: 3,640,321 (GRCm39) |
L272P |
probably damaging |
Het |
Tcaf1 |
T |
A |
6: 42,650,473 (GRCm39) |
M869L |
probably damaging |
Het |
Tecpr1 |
T |
C |
5: 144,154,219 (GRCm39) |
N78S |
probably damaging |
Het |
Tectb |
A |
T |
19: 55,170,356 (GRCm39) |
Y69F |
probably damaging |
Het |
Them4 |
A |
T |
3: 94,237,101 (GRCm39) |
N187I |
possibly damaging |
Het |
Tm9sf3 |
A |
G |
19: 41,244,582 (GRCm39) |
|
probably null |
Het |
Tnik |
G |
T |
3: 28,631,510 (GRCm39) |
|
probably benign |
Het |
Tns2 |
G |
T |
15: 102,018,020 (GRCm39) |
|
probably benign |
Het |
Tnxb |
A |
G |
17: 34,891,118 (GRCm39) |
D487G |
probably damaging |
Het |
Trim33 |
T |
A |
3: 103,217,660 (GRCm39) |
C202S |
probably damaging |
Het |
Trpm2 |
T |
A |
10: 77,759,350 (GRCm39) |
I1145F |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,483,596 (GRCm39) |
T478A |
probably benign |
Het |
Ube2e3 |
T |
C |
2: 78,750,334 (GRCm39) |
Y187H |
probably benign |
Het |
Ubxn11 |
A |
G |
4: 133,836,963 (GRCm39) |
R64G |
possibly damaging |
Het |
Wwtr1 |
T |
C |
3: 57,366,487 (GRCm39) |
T407A |
probably damaging |
Het |
Zfyve26 |
A |
T |
12: 79,315,502 (GRCm39) |
S1325T |
possibly damaging |
Het |
|
Other mutations in Kcnn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00492:Kcnn1
|
APN |
8 |
71,300,706 (GRCm39) |
missense |
probably benign |
|
IGL00498:Kcnn1
|
APN |
8 |
71,305,524 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00792:Kcnn1
|
APN |
8 |
71,307,360 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03122:Kcnn1
|
APN |
8 |
71,307,724 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03137:Kcnn1
|
APN |
8 |
71,303,381 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03222:Kcnn1
|
APN |
8 |
71,300,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03226:Kcnn1
|
APN |
8 |
71,299,135 (GRCm39) |
splice site |
probably benign |
|
R1218:Kcnn1
|
UTSW |
8 |
71,305,332 (GRCm39) |
missense |
probably benign |
0.07 |
R1437:Kcnn1
|
UTSW |
8 |
71,297,195 (GRCm39) |
missense |
probably benign |
0.03 |
R1510:Kcnn1
|
UTSW |
8 |
71,316,714 (GRCm39) |
unclassified |
probably benign |
|
R2434:Kcnn1
|
UTSW |
8 |
71,307,810 (GRCm39) |
small deletion |
probably benign |
|
R2860:Kcnn1
|
UTSW |
8 |
71,299,179 (GRCm39) |
missense |
probably benign |
0.36 |
R2861:Kcnn1
|
UTSW |
8 |
71,299,179 (GRCm39) |
missense |
probably benign |
0.36 |
R4327:Kcnn1
|
UTSW |
8 |
71,305,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R4807:Kcnn1
|
UTSW |
8 |
71,300,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R4947:Kcnn1
|
UTSW |
8 |
71,297,073 (GRCm39) |
missense |
probably benign |
0.02 |
R5265:Kcnn1
|
UTSW |
8 |
71,307,297 (GRCm39) |
missense |
probably benign |
0.07 |
R5685:Kcnn1
|
UTSW |
8 |
71,305,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R6108:Kcnn1
|
UTSW |
8 |
71,307,800 (GRCm39) |
missense |
probably benign |
0.27 |
R6523:Kcnn1
|
UTSW |
8 |
71,299,169 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7512:Kcnn1
|
UTSW |
8 |
71,307,293 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8219:Kcnn1
|
UTSW |
8 |
71,305,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8310:Kcnn1
|
UTSW |
8 |
71,305,449 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8809:Kcnn1
|
UTSW |
8 |
71,305,297 (GRCm39) |
critical splice donor site |
probably null |
|
R9084:Kcnn1
|
UTSW |
8 |
71,307,810 (GRCm39) |
small deletion |
probably benign |
|
R9308:Kcnn1
|
UTSW |
8 |
71,305,434 (GRCm39) |
missense |
probably damaging |
1.00 |
|