Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578G10Rik |
T |
G |
4: 42,760,998 (GRCm39) |
W6G |
unknown |
Het |
Aatk |
A |
T |
11: 119,901,094 (GRCm39) |
C1101S |
probably benign |
Het |
Ankrd61 |
T |
C |
5: 143,828,322 (GRCm39) |
T218A |
possibly damaging |
Het |
Cacna1b |
T |
C |
2: 24,540,058 (GRCm39) |
E1467G |
probably damaging |
Het |
Ccdc186 |
T |
C |
19: 56,802,016 (GRCm39) |
T34A |
probably benign |
Het |
Cdc42bpb |
G |
A |
12: 111,261,372 (GRCm39) |
P1656S |
probably benign |
Het |
Cdk13 |
A |
C |
13: 17,902,747 (GRCm39) |
C934W |
probably damaging |
Het |
Cebpg |
T |
C |
7: 34,750,080 (GRCm39) |
N61S |
probably benign |
Het |
Cldn13 |
T |
A |
5: 134,943,843 (GRCm39) |
E114V |
probably benign |
Het |
Clec9a |
T |
A |
6: 129,398,023 (GRCm39) |
I187K |
possibly damaging |
Het |
Cr2 |
G |
T |
1: 194,840,416 (GRCm39) |
L509M |
probably damaging |
Het |
Creb3l2 |
C |
A |
6: 37,311,446 (GRCm39) |
G448W |
probably damaging |
Het |
Csf2rb |
T |
A |
15: 78,229,760 (GRCm39) |
|
probably null |
Het |
Cyth1 |
C |
T |
11: 118,076,206 (GRCm39) |
|
probably null |
Het |
Dapk1 |
A |
T |
13: 60,910,203 (GRCm39) |
D1441V |
unknown |
Het |
Dnhd1 |
A |
T |
7: 105,352,889 (GRCm39) |
N2681Y |
possibly damaging |
Het |
Dnm1 |
T |
C |
2: 32,213,739 (GRCm39) |
M476V |
probably benign |
Het |
Dock1 |
T |
G |
7: 134,592,279 (GRCm39) |
I938S |
probably benign |
Het |
Duox1 |
G |
A |
2: 122,160,023 (GRCm39) |
V713I |
possibly damaging |
Het |
Dusp16 |
T |
C |
6: 134,695,226 (GRCm39) |
H535R |
probably benign |
Het |
Eif3j2 |
TGCCGCCGCCGCCGCCGCCGCCGCCGCC |
TGCCGCCGCCGCCGCCGCCGCCGCC |
18: 43,610,782 (GRCm39) |
|
probably benign |
Het |
Fancd2os |
T |
A |
6: 113,574,994 (GRCm39) |
Y4F |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,037,886 (GRCm39) |
Q3846L |
probably benign |
Het |
Fbxw10 |
A |
C |
11: 62,743,814 (GRCm39) |
H240P |
probably benign |
Het |
Fer1l5 |
T |
C |
1: 36,442,662 (GRCm39) |
L727P |
probably damaging |
Het |
Fezf1 |
A |
C |
6: 23,247,845 (GRCm39) |
F77V |
probably benign |
Het |
Fli1 |
T |
C |
9: 32,335,493 (GRCm39) |
D313G |
probably damaging |
Het |
Frmd4a |
A |
G |
2: 4,608,324 (GRCm39) |
T731A |
probably benign |
Het |
Gfy |
T |
C |
7: 44,828,090 (GRCm39) |
Q2R |
possibly damaging |
Het |
Ggt5 |
T |
C |
10: 75,445,139 (GRCm39) |
V382A |
probably benign |
Het |
Hira |
A |
G |
16: 18,772,789 (GRCm39) |
D867G |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,462,127 (GRCm39) |
S5184P |
probably benign |
Het |
Ighv1-26 |
A |
C |
12: 114,752,407 (GRCm39) |
F7V |
probably benign |
Het |
Igkv4-81 |
C |
T |
6: 68,967,796 (GRCm39) |
E102K |
possibly damaging |
Het |
Inmt |
G |
T |
6: 55,147,990 (GRCm39) |
S213Y |
possibly damaging |
Het |
Ints2 |
T |
A |
11: 86,135,335 (GRCm39) |
M360L |
probably benign |
Het |
Itih3 |
A |
G |
14: 30,631,416 (GRCm39) |
S827P |
probably benign |
Het |
Klhl2 |
T |
C |
8: 65,202,113 (GRCm39) |
N521S |
probably benign |
Het |
Kmt2a |
A |
T |
9: 44,734,531 (GRCm39) |
F2104I |
unknown |
Het |
Kndc1 |
G |
A |
7: 139,510,031 (GRCm39) |
S1291N |
probably benign |
Het |
Mettl21a |
T |
C |
1: 64,647,285 (GRCm39) |
T91A |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,120,407 (GRCm39) |
I426V |
possibly damaging |
Het |
Mrpl2 |
T |
C |
17: 46,958,440 (GRCm39) |
V74A |
probably benign |
Het |
Msantd4 |
A |
G |
9: 4,385,007 (GRCm39) |
D244G |
probably benign |
Het |
Mtfmt |
C |
T |
9: 65,343,147 (GRCm39) |
R18C |
probably benign |
Het |
Ncam2 |
A |
G |
16: 81,420,341 (GRCm39) |
*838W |
probably null |
Het |
Ncor1 |
CTG |
CTGATG |
11: 62,324,442 (GRCm39) |
|
probably benign |
Het |
Nsf |
T |
C |
11: 103,763,988 (GRCm39) |
N365S |
probably damaging |
Het |
Osbpl3 |
C |
T |
6: 50,313,194 (GRCm39) |
|
probably null |
Het |
Pam |
C |
T |
1: 97,826,065 (GRCm39) |
|
probably null |
Het |
Parn |
A |
T |
16: 13,358,942 (GRCm39) |
M600K |
probably benign |
Het |
Pcdha11 |
C |
A |
18: 37,139,532 (GRCm39) |
T387N |
probably benign |
Het |
Ptprt |
A |
C |
2: 161,397,381 (GRCm39) |
C1129G |
probably damaging |
Het |
Ralgapb |
T |
A |
2: 158,285,856 (GRCm39) |
S645T |
probably damaging |
Het |
Rara |
C |
T |
11: 98,860,983 (GRCm39) |
S157L |
probably benign |
Het |
Rnf40 |
T |
A |
7: 127,201,808 (GRCm39) |
I1000N |
probably damaging |
Het |
Sap25 |
C |
T |
5: 137,640,494 (GRCm39) |
T141I |
probably null |
Het |
Scube2 |
C |
T |
7: 109,430,969 (GRCm39) |
G410E |
probably damaging |
Het |
Sh3gl2 |
A |
G |
4: 85,304,089 (GRCm39) |
E264G |
probably benign |
Het |
Smc4 |
T |
G |
3: 68,914,662 (GRCm39) |
S92A |
probably damaging |
Het |
Sorcs1 |
C |
T |
19: 50,666,521 (GRCm39) |
R129Q |
probably benign |
Het |
Spata31e4 |
A |
G |
13: 50,856,149 (GRCm39) |
T596A |
possibly damaging |
Het |
Spef2 |
T |
C |
15: 9,713,203 (GRCm39) |
R390G |
probably damaging |
Het |
Speg |
T |
C |
1: 75,377,768 (GRCm39) |
F842S |
probably damaging |
Het |
Stk17b |
G |
T |
1: 53,796,898 (GRCm39) |
H290N |
probably damaging |
Het |
Stpg3 |
A |
T |
2: 25,103,516 (GRCm39) |
V191D |
probably benign |
Het |
Supt6 |
C |
T |
11: 78,120,290 (GRCm39) |
R350H |
probably damaging |
Het |
Taf1b |
G |
A |
12: 24,566,947 (GRCm39) |
A214T |
possibly damaging |
Het |
Tet3 |
T |
C |
6: 83,380,935 (GRCm39) |
E411G |
possibly damaging |
Het |
Tet3 |
T |
A |
6: 83,381,808 (GRCm39) |
|
probably null |
Het |
Tg |
T |
C |
15: 66,545,913 (GRCm39) |
Y212H |
probably damaging |
Het |
Tns3 |
A |
G |
11: 8,395,702 (GRCm39) |
I1234T |
probably damaging |
Het |
Traf6 |
C |
T |
2: 101,521,825 (GRCm39) |
T220I |
possibly damaging |
Het |
Tram2 |
C |
G |
1: 21,074,150 (GRCm39) |
A263P |
possibly damaging |
Het |
Treml1 |
T |
G |
17: 48,673,771 (GRCm39) |
S261A |
probably damaging |
Het |
Trim34b |
A |
G |
7: 103,980,503 (GRCm39) |
E197G |
probably damaging |
Het |
Tspan18 |
C |
T |
2: 93,050,462 (GRCm39) |
G54S |
probably damaging |
Het |
Wdtc1 |
A |
G |
4: 133,049,529 (GRCm39) |
V29A |
probably damaging |
Het |
Zdhhc16 |
T |
C |
19: 41,929,155 (GRCm39) |
Y253H |
probably damaging |
Het |
Zfp366 |
A |
G |
13: 99,365,874 (GRCm39) |
Y345C |
probably damaging |
Het |
Zfp423 |
T |
A |
8: 88,510,041 (GRCm39) |
D101V |
possibly damaging |
Het |
Zfp462 |
G |
A |
4: 55,080,735 (GRCm39) |
M2450I |
probably benign |
Het |
Zfp52 |
C |
T |
17: 21,782,218 (GRCm39) |
L689F |
possibly damaging |
Het |
Zim1 |
G |
A |
7: 6,690,739 (GRCm39) |
Q29* |
probably null |
Het |
|
Other mutations in Kcnk12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01103:Kcnk12
|
APN |
17 |
88,054,195 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01611:Kcnk12
|
APN |
17 |
88,104,495 (GRCm39) |
missense |
probably benign |
0.08 |
kiskadee
|
UTSW |
17 |
88,054,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Kcnk12
|
UTSW |
17 |
88,053,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R1672:Kcnk12
|
UTSW |
17 |
88,053,747 (GRCm39) |
missense |
probably benign |
0.16 |
R1806:Kcnk12
|
UTSW |
17 |
88,053,537 (GRCm39) |
missense |
probably benign |
0.34 |
R1807:Kcnk12
|
UTSW |
17 |
88,053,468 (GRCm39) |
missense |
probably benign |
0.04 |
R1873:Kcnk12
|
UTSW |
17 |
88,053,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Kcnk12
|
UTSW |
17 |
88,104,560 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4116:Kcnk12
|
UTSW |
17 |
88,053,584 (GRCm39) |
frame shift |
probably null |
|
R5202:Kcnk12
|
UTSW |
17 |
88,054,033 (GRCm39) |
nonsense |
probably null |
|
R5888:Kcnk12
|
UTSW |
17 |
88,054,077 (GRCm39) |
missense |
probably benign |
0.00 |
R6017:Kcnk12
|
UTSW |
17 |
88,054,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R7544:Kcnk12
|
UTSW |
17 |
88,053,493 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8298:Kcnk12
|
UTSW |
17 |
88,104,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:Kcnk12
|
UTSW |
17 |
88,054,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Kcnk12
|
UTSW |
17 |
88,053,538 (GRCm39) |
missense |
probably benign |
0.09 |
R9420:Kcnk12
|
UTSW |
17 |
88,104,507 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9436:Kcnk12
|
UTSW |
17 |
88,104,880 (GRCm39) |
start codon destroyed |
probably null |
|
R9476:Kcnk12
|
UTSW |
17 |
88,054,122 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:Kcnk12
|
UTSW |
17 |
88,053,471 (GRCm39) |
missense |
probably benign |
0.28 |
|