Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
C |
T |
1: 183,765,702 (GRCm39) |
S119N |
probably benign |
Het |
4930550C14Rik |
A |
G |
9: 53,332,917 (GRCm39) |
I93V |
probably benign |
Het |
Abcg5 |
A |
C |
17: 84,989,477 (GRCm39) |
I77S |
possibly damaging |
Het |
Adam3 |
T |
C |
8: 25,171,545 (GRCm39) |
Y762C |
probably benign |
Het |
Agap1 |
T |
C |
1: 89,716,962 (GRCm39) |
S26P |
probably damaging |
Het |
Ago1 |
T |
C |
4: 126,347,426 (GRCm39) |
Y441C |
probably damaging |
Het |
B3gnt3 |
A |
G |
8: 72,146,481 (GRCm39) |
L16S |
possibly damaging |
Het |
Btaf1 |
T |
A |
19: 36,982,002 (GRCm39) |
D1677E |
probably damaging |
Het |
Cd5l |
T |
A |
3: 87,268,206 (GRCm39) |
S18T |
probably benign |
Het |
Cdca2 |
T |
A |
14: 67,931,131 (GRCm39) |
R521W |
probably damaging |
Het |
Cfap61 |
C |
A |
2: 145,792,981 (GRCm39) |
S64* |
probably null |
Het |
Cryzl2 |
T |
A |
1: 157,298,174 (GRCm39) |
|
probably benign |
Het |
Cul7 |
T |
A |
17: 46,974,116 (GRCm39) |
L1467H |
probably damaging |
Het |
Dhrs1 |
T |
C |
14: 55,981,162 (GRCm39) |
K83E |
probably benign |
Het |
Dmrt2 |
T |
A |
19: 25,655,980 (GRCm39) |
F526L |
probably benign |
Het |
Dnajb14 |
T |
A |
3: 137,614,115 (GRCm39) |
M342K |
possibly damaging |
Het |
Dpf3 |
A |
G |
12: 83,378,761 (GRCm39) |
V101A |
probably benign |
Het |
Dthd1 |
A |
C |
5: 62,979,302 (GRCm39) |
T321P |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Fras1 |
G |
A |
5: 96,856,530 (GRCm39) |
R1971Q |
probably benign |
Het |
Fry |
A |
G |
5: 150,419,754 (GRCm39) |
N608S |
probably damaging |
Het |
Gabrr3 |
T |
A |
16: 59,281,998 (GRCm39) |
V451D |
probably damaging |
Het |
Glg1 |
A |
G |
8: 111,924,235 (GRCm39) |
L251P |
probably benign |
Het |
Gli2 |
T |
A |
1: 118,781,080 (GRCm39) |
S222C |
probably damaging |
Het |
Gsr |
A |
G |
8: 34,159,949 (GRCm39) |
E99G |
probably damaging |
Het |
H1f5 |
T |
C |
13: 21,964,451 (GRCm39) |
T92A |
possibly damaging |
Het |
Hlx |
G |
T |
1: 184,464,184 (GRCm39) |
A52D |
probably damaging |
Het |
Hus1b |
T |
C |
13: 31,131,679 (GRCm39) |
|
probably benign |
Het |
Igf1r |
T |
A |
7: 67,844,774 (GRCm39) |
I849N |
possibly damaging |
Het |
Itih5 |
A |
G |
2: 10,256,323 (GRCm39) |
T930A |
probably benign |
Het |
Ivns1abp |
T |
A |
1: 151,235,860 (GRCm39) |
M309K |
probably benign |
Het |
Kdm3b |
T |
A |
18: 34,952,864 (GRCm39) |
F1078Y |
probably damaging |
Het |
Krt40 |
T |
G |
11: 99,431,059 (GRCm39) |
E150A |
probably damaging |
Het |
Lcn11 |
G |
T |
2: 25,669,115 (GRCm39) |
|
probably benign |
Het |
Lcor |
G |
T |
19: 41,574,502 (GRCm39) |
G1086C |
probably damaging |
Het |
Liph |
A |
G |
16: 21,802,898 (GRCm39) |
I57T |
possibly damaging |
Het |
Lrrc46 |
C |
T |
11: 96,926,997 (GRCm39) |
V107M |
probably damaging |
Het |
Ltb4r1 |
T |
C |
14: 56,004,832 (GRCm39) |
I45T |
probably damaging |
Het |
Mapkbp1 |
A |
G |
2: 119,841,554 (GRCm39) |
|
probably benign |
Het |
Mark3 |
C |
T |
12: 111,584,831 (GRCm39) |
|
probably benign |
Het |
Mug2 |
C |
T |
6: 122,036,014 (GRCm39) |
A642V |
probably benign |
Het |
Myh11 |
A |
G |
16: 14,019,991 (GRCm39) |
S1814P |
possibly damaging |
Het |
Ndst1 |
T |
A |
18: 60,830,218 (GRCm39) |
S631C |
probably damaging |
Het |
Nrbf2 |
A |
T |
10: 67,103,691 (GRCm39) |
D137E |
possibly damaging |
Het |
Or2ag16 |
A |
T |
7: 106,351,989 (GRCm39) |
M202K |
probably benign |
Het |
Or51l4 |
A |
G |
7: 103,404,183 (GRCm39) |
V203A |
probably benign |
Het |
Or6c208 |
T |
A |
10: 129,224,090 (GRCm39) |
M196K |
probably benign |
Het |
Parn |
A |
G |
16: 13,485,449 (GRCm39) |
Y16H |
probably damaging |
Het |
Parp14 |
A |
G |
16: 35,664,785 (GRCm39) |
|
probably benign |
Het |
Prl3d1 |
C |
T |
13: 27,283,992 (GRCm39) |
T187I |
probably benign |
Het |
Ptgir |
G |
A |
7: 16,641,055 (GRCm39) |
|
probably null |
Het |
Rabgap1l |
C |
T |
1: 160,059,445 (GRCm39) |
|
probably benign |
Het |
Rims4 |
C |
T |
2: 163,705,849 (GRCm39) |
V262M |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,368,055 (GRCm39) |
Y4697H |
probably benign |
Het |
Rps6ka4 |
T |
A |
19: 6,808,364 (GRCm39) |
I598F |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,684,855 (GRCm39) |
V3029M |
probably damaging |
Het |
Slc34a1 |
T |
C |
13: 24,003,920 (GRCm39) |
F335S |
probably damaging |
Het |
Spata6l |
T |
C |
19: 28,945,032 (GRCm39) |
M1V |
probably null |
Het |
Stau2 |
A |
T |
1: 16,510,585 (GRCm39) |
Y124* |
probably null |
Het |
Tbl3 |
A |
G |
17: 24,920,580 (GRCm39) |
I652T |
probably benign |
Het |
Trappc3 |
C |
T |
4: 126,166,759 (GRCm39) |
|
probably benign |
Het |
Trim60 |
A |
T |
8: 65,454,071 (GRCm39) |
F59L |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,648,453 (GRCm39) |
F4686S |
probably benign |
Het |
Vcan |
T |
C |
13: 89,840,529 (GRCm39) |
T1672A |
probably damaging |
Het |
Vmn1r215 |
T |
A |
13: 23,260,758 (GRCm39) |
I266N |
possibly damaging |
Het |
Vmn2r6 |
A |
T |
3: 64,445,487 (GRCm39) |
V657E |
possibly damaging |
Het |
Wdr95 |
G |
T |
5: 149,529,802 (GRCm39) |
A548S |
probably benign |
Het |
Zfp12 |
A |
G |
5: 143,231,500 (GRCm39) |
Y609C |
probably damaging |
Het |
Znfx1 |
C |
A |
2: 166,897,560 (GRCm39) |
E455* |
probably null |
Het |
|
Other mutations in Krt12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02968:Krt12
|
APN |
11 |
99,308,843 (GRCm39) |
missense |
probably damaging |
0.98 |
R0348:Krt12
|
UTSW |
11 |
99,308,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Krt12
|
UTSW |
11 |
99,311,650 (GRCm39) |
missense |
probably benign |
0.42 |
R1763:Krt12
|
UTSW |
11 |
99,306,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R1886:Krt12
|
UTSW |
11 |
99,309,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R2087:Krt12
|
UTSW |
11 |
99,309,459 (GRCm39) |
missense |
probably damaging |
0.98 |
R3859:Krt12
|
UTSW |
11 |
99,309,319 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3942:Krt12
|
UTSW |
11 |
99,312,922 (GRCm39) |
missense |
unknown |
|
R4030:Krt12
|
UTSW |
11 |
99,312,854 (GRCm39) |
missense |
unknown |
|
R4061:Krt12
|
UTSW |
11 |
99,306,841 (GRCm39) |
missense |
unknown |
|
R4672:Krt12
|
UTSW |
11 |
99,309,509 (GRCm39) |
intron |
probably benign |
|
R4867:Krt12
|
UTSW |
11 |
99,307,789 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4907:Krt12
|
UTSW |
11 |
99,309,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R5592:Krt12
|
UTSW |
11 |
99,311,650 (GRCm39) |
missense |
probably benign |
0.00 |
R6276:Krt12
|
UTSW |
11 |
99,312,728 (GRCm39) |
nonsense |
probably null |
|
R6326:Krt12
|
UTSW |
11 |
99,307,745 (GRCm39) |
missense |
probably benign |
|
R7108:Krt12
|
UTSW |
11 |
99,306,878 (GRCm39) |
missense |
unknown |
|
R7144:Krt12
|
UTSW |
11 |
99,306,839 (GRCm39) |
makesense |
probably null |
|
R7524:Krt12
|
UTSW |
11 |
99,310,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R7769:Krt12
|
UTSW |
11 |
99,308,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R7813:Krt12
|
UTSW |
11 |
99,309,309 (GRCm39) |
critical splice donor site |
probably null |
|
R9063:Krt12
|
UTSW |
11 |
99,307,757 (GRCm39) |
missense |
probably benign |
0.03 |
R9113:Krt12
|
UTSW |
11 |
99,309,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R9656:Krt12
|
UTSW |
11 |
99,309,471 (GRCm39) |
missense |
|
|
X0026:Krt12
|
UTSW |
11 |
99,310,410 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Krt12
|
UTSW |
11 |
99,311,587 (GRCm39) |
nonsense |
probably null |
|
Z1177:Krt12
|
UTSW |
11 |
99,312,930 (GRCm39) |
missense |
unknown |
|
|