Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ash1l |
T |
A |
3: 88,961,693 (GRCm39) |
V2355E |
probably damaging |
Het |
Baz2a |
AGCGGCGGTACTTGCGGG |
AG |
10: 127,960,946 (GRCm39) |
|
probably null |
Het |
Bmp4 |
G |
A |
14: 46,623,438 (GRCm39) |
A36V |
probably benign |
Het |
Ccdc191 |
T |
C |
16: 43,751,573 (GRCm39) |
F301S |
probably damaging |
Het |
Cdh9 |
T |
C |
15: 16,855,900 (GRCm39) |
S647P |
probably damaging |
Het |
Cntln |
C |
T |
4: 84,875,406 (GRCm39) |
T280M |
possibly damaging |
Het |
Coch |
A |
G |
12: 51,650,204 (GRCm39) |
T398A |
probably benign |
Het |
Col6a3 |
T |
C |
1: 90,744,024 (GRCm39) |
R515G |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 17,077,247 (GRCm39) |
Y137H |
probably damaging |
Het |
Ctnnal1 |
G |
A |
4: 56,813,246 (GRCm39) |
L662F |
probably benign |
Het |
Cyp19a1 |
T |
C |
9: 54,094,083 (GRCm39) |
I60V |
probably benign |
Het |
Cyp2c68 |
C |
T |
19: 39,722,757 (GRCm39) |
V264I |
probably benign |
Het |
Dbx1 |
A |
T |
7: 49,286,417 (GRCm39) |
L16H |
probably damaging |
Het |
Dgkg |
T |
A |
16: 22,394,091 (GRCm39) |
T321S |
probably damaging |
Het |
Dnah7c |
T |
A |
1: 46,837,439 (GRCm39) |
Y3951N |
probably damaging |
Het |
Emc10 |
G |
A |
7: 44,142,616 (GRCm39) |
R109W |
probably damaging |
Het |
Fam124b |
T |
A |
1: 80,190,748 (GRCm39) |
I212F |
probably damaging |
Het |
Fam187b |
A |
G |
7: 30,676,665 (GRCm39) |
D58G |
probably benign |
Het |
Galnt4 |
T |
C |
10: 98,945,243 (GRCm39) |
Y323H |
probably benign |
Het |
Gfpt1 |
A |
G |
6: 87,034,628 (GRCm39) |
D142G |
probably benign |
Het |
Gm5174 |
A |
G |
10: 86,492,519 (GRCm39) |
|
noncoding transcript |
Het |
Gtf2ird2 |
G |
A |
5: 134,237,756 (GRCm39) |
D278N |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,785,103 (GRCm39) |
D1480E |
probably benign |
Het |
Hnf4g |
T |
G |
3: 3,717,916 (GRCm39) |
S388R |
probably benign |
Het |
Il1rap |
A |
G |
16: 26,541,502 (GRCm39) |
E581G |
probably benign |
Het |
Itpr2 |
A |
T |
6: 146,214,335 (GRCm39) |
|
probably null |
Het |
Lgr6 |
A |
G |
1: 134,928,210 (GRCm39) |
|
probably null |
Het |
Lmod2 |
A |
C |
6: 24,604,471 (GRCm39) |
K482T |
probably damaging |
Het |
Magi3 |
A |
G |
3: 103,958,636 (GRCm39) |
V483A |
probably damaging |
Het |
Ncam2 |
A |
G |
16: 81,262,598 (GRCm39) |
|
probably benign |
Het |
Nphs1 |
C |
A |
7: 30,166,965 (GRCm39) |
S724* |
probably null |
Het |
Or5t9 |
T |
C |
2: 86,660,035 (GRCm39) |
M313T |
probably benign |
Het |
Osgep |
T |
C |
14: 51,154,286 (GRCm39) |
T225A |
probably benign |
Het |
Pcdhgc5 |
A |
G |
18: 37,954,727 (GRCm39) |
E667G |
possibly damaging |
Het |
Plce1 |
C |
T |
19: 38,608,963 (GRCm39) |
P424L |
probably benign |
Het |
Plekhg5 |
C |
T |
4: 152,196,635 (GRCm39) |
T694M |
probably damaging |
Het |
Prkag2 |
T |
A |
5: 25,076,067 (GRCm39) |
K233* |
probably null |
Het |
Prune2 |
T |
A |
19: 17,096,520 (GRCm39) |
S675T |
probably damaging |
Het |
Sars1 |
C |
T |
3: 108,336,621 (GRCm39) |
R302H |
probably damaging |
Het |
Sfmbt1 |
G |
A |
14: 30,539,753 (GRCm39) |
C847Y |
probably damaging |
Het |
Sparcl1 |
T |
C |
5: 104,241,203 (GRCm39) |
T74A |
probably benign |
Het |
Sppl2b |
A |
G |
10: 80,703,325 (GRCm39) |
E529G |
probably benign |
Het |
Stradb |
C |
A |
1: 59,031,450 (GRCm39) |
H212Q |
possibly damaging |
Het |
Tm4sf4 |
C |
T |
3: 57,345,043 (GRCm39) |
R150C |
possibly damaging |
Het |
Tmem212 |
T |
C |
3: 27,939,019 (GRCm39) |
S156G |
probably damaging |
Het |
Tmem51 |
T |
C |
4: 141,765,035 (GRCm39) |
N8D |
probably damaging |
Het |
Tmigd1 |
A |
G |
11: 76,801,124 (GRCm39) |
T204A |
possibly damaging |
Het |
Tsga10 |
G |
A |
1: 37,840,872 (GRCm39) |
L445F |
probably damaging |
Het |
Unc80 |
G |
A |
1: 66,662,450 (GRCm39) |
V1768I |
probably benign |
Het |
Urb1 |
C |
T |
16: 90,592,331 (GRCm39) |
V310I |
probably damaging |
Het |
Usp29 |
T |
A |
7: 6,965,052 (GRCm39) |
C298* |
probably null |
Het |
Usp8 |
T |
C |
2: 126,600,432 (GRCm39) |
V1050A |
probably damaging |
Het |
Vmn1r38 |
T |
C |
6: 66,753,430 (GRCm39) |
T229A |
probably benign |
Het |
Yes1 |
T |
C |
5: 32,810,515 (GRCm39) |
S195P |
probably damaging |
Het |
|
Other mutations in Tkfc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01066:Tkfc
|
APN |
19 |
10,571,892 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01149:Tkfc
|
APN |
19 |
10,578,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02726:Tkfc
|
APN |
19 |
10,573,576 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03069:Tkfc
|
APN |
19 |
10,576,518 (GRCm39) |
missense |
probably benign |
|
R1367:Tkfc
|
UTSW |
19 |
10,570,838 (GRCm39) |
missense |
probably benign |
0.19 |
R1476:Tkfc
|
UTSW |
19 |
10,572,690 (GRCm39) |
missense |
probably null |
0.55 |
R2081:Tkfc
|
UTSW |
19 |
10,574,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Tkfc
|
UTSW |
19 |
10,573,405 (GRCm39) |
missense |
probably damaging |
0.97 |
R2151:Tkfc
|
UTSW |
19 |
10,576,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R2443:Tkfc
|
UTSW |
19 |
10,571,902 (GRCm39) |
missense |
probably damaging |
0.97 |
R3105:Tkfc
|
UTSW |
19 |
10,574,357 (GRCm39) |
nonsense |
probably null |
|
R3106:Tkfc
|
UTSW |
19 |
10,574,357 (GRCm39) |
nonsense |
probably null |
|
R5027:Tkfc
|
UTSW |
19 |
10,570,023 (GRCm39) |
splice site |
probably null |
|
R5601:Tkfc
|
UTSW |
19 |
10,571,927 (GRCm39) |
missense |
probably benign |
|
R5637:Tkfc
|
UTSW |
19 |
10,571,897 (GRCm39) |
missense |
probably benign |
0.00 |
R5933:Tkfc
|
UTSW |
19 |
10,574,711 (GRCm39) |
missense |
probably benign |
0.17 |
R6792:Tkfc
|
UTSW |
19 |
10,571,888 (GRCm39) |
missense |
probably benign |
|
R6845:Tkfc
|
UTSW |
19 |
10,576,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R6909:Tkfc
|
UTSW |
19 |
10,573,630 (GRCm39) |
missense |
probably benign |
0.06 |
R7007:Tkfc
|
UTSW |
19 |
10,573,727 (GRCm39) |
missense |
probably benign |
|
R7883:Tkfc
|
UTSW |
19 |
10,572,394 (GRCm39) |
splice site |
probably null |
|
R8962:Tkfc
|
UTSW |
19 |
10,570,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R9039:Tkfc
|
UTSW |
19 |
10,573,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R9254:Tkfc
|
UTSW |
19 |
10,574,712 (GRCm39) |
missense |
probably damaging |
1.00 |
|