Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano3 |
A |
G |
2: 110,488,564 (GRCm39) |
M956T |
probably damaging |
Het |
Ap2b1 |
T |
G |
11: 83,226,356 (GRCm39) |
V289G |
probably damaging |
Het |
Cacnb4 |
G |
T |
2: 52,355,682 (GRCm39) |
H208Q |
probably damaging |
Het |
Calhm6 |
A |
T |
10: 34,003,533 (GRCm39) |
C125S |
probably damaging |
Het |
Cd5l |
G |
A |
3: 87,275,118 (GRCm39) |
R219Q |
probably benign |
Het |
Dzip1l |
G |
T |
9: 99,545,739 (GRCm39) |
G663W |
probably damaging |
Het |
Ecel1 |
G |
A |
1: 87,077,577 (GRCm39) |
|
probably benign |
Het |
Eno1 |
A |
G |
4: 150,323,993 (GRCm39) |
T19A |
probably damaging |
Het |
Fndc3a |
G |
A |
14: 72,811,996 (GRCm39) |
T315I |
probably benign |
Het |
Galr1 |
T |
C |
18: 82,411,942 (GRCm39) |
N308S |
probably damaging |
Het |
Get3 |
G |
A |
8: 85,745,185 (GRCm39) |
A294V |
possibly damaging |
Het |
Maf |
A |
T |
8: 116,432,702 (GRCm39) |
S301T |
probably damaging |
Het |
Map3k5 |
C |
T |
10: 19,904,879 (GRCm39) |
R394* |
probably null |
Het |
Mroh8 |
C |
T |
2: 157,055,616 (GRCm39) |
G994D |
probably damaging |
Het |
Myo10 |
T |
C |
15: 25,799,634 (GRCm39) |
V653A |
possibly damaging |
Het |
Nucks1 |
A |
G |
1: 131,858,828 (GRCm39) |
K196E |
unknown |
Het |
Nup42 |
T |
C |
5: 24,386,101 (GRCm39) |
V211A |
probably benign |
Het |
Or4n4 |
C |
A |
14: 50,518,798 (GRCm39) |
R304L |
probably benign |
Het |
Or7e178 |
A |
T |
9: 20,226,015 (GRCm39) |
I59N |
probably damaging |
Het |
Or7g32 |
A |
T |
9: 19,408,070 (GRCm39) |
I9F |
probably benign |
Het |
Piwil1 |
C |
T |
5: 128,824,396 (GRCm39) |
T493I |
probably null |
Het |
Plcd1 |
T |
C |
9: 118,905,053 (GRCm39) |
H216R |
probably benign |
Het |
Pmp2 |
A |
T |
3: 10,247,541 (GRCm39) |
Y49* |
probably null |
Het |
Rnf38 |
A |
G |
4: 44,138,806 (GRCm39) |
V229A |
probably damaging |
Het |
Saxo2 |
T |
C |
7: 82,284,108 (GRCm39) |
D250G |
probably damaging |
Het |
Scn8a |
T |
G |
15: 100,866,938 (GRCm39) |
V98G |
probably damaging |
Het |
Scnn1a |
T |
A |
6: 125,315,900 (GRCm39) |
|
probably null |
Het |
Sepsecs |
C |
T |
5: 52,801,402 (GRCm39) |
R420Q |
probably benign |
Het |
Slit2 |
T |
C |
5: 48,395,759 (GRCm39) |
S725P |
probably benign |
Het |
Stk16 |
A |
G |
1: 75,189,835 (GRCm39) |
Q207R |
probably benign |
Het |
Tapt1 |
C |
T |
5: 44,336,332 (GRCm39) |
V446M |
probably damaging |
Het |
Tent5c |
A |
T |
3: 100,379,946 (GRCm39) |
M270K |
probably damaging |
Het |
Tnni3k |
A |
C |
3: 154,667,663 (GRCm39) |
V250G |
probably damaging |
Het |
Ttll8 |
C |
T |
15: 88,799,848 (GRCm39) |
G531E |
possibly damaging |
Het |
U2surp |
T |
A |
9: 95,346,472 (GRCm39) |
E862D |
possibly damaging |
Het |
U2surp |
A |
G |
9: 95,364,234 (GRCm39) |
F561L |
probably damaging |
Het |
Unc5d |
A |
G |
8: 29,142,819 (GRCm39) |
Y878H |
probably damaging |
Het |
Ust |
A |
G |
10: 8,173,842 (GRCm39) |
M221T |
probably benign |
Het |
Wasf3 |
T |
C |
5: 146,392,401 (GRCm39) |
F157S |
probably damaging |
Het |
Wdr64 |
G |
A |
1: 175,533,637 (GRCm39) |
C91Y |
probably damaging |
Het |
Zan |
T |
C |
5: 137,422,368 (GRCm39) |
Y2750C |
unknown |
Het |
|
Other mutations in Tex56 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02726:Tex56
|
APN |
13 |
35,136,943 (GRCm39) |
intron |
probably benign |
|
IGL03241:Tex56
|
APN |
13 |
35,128,313 (GRCm39) |
missense |
probably damaging |
0.98 |
R0324:Tex56
|
UTSW |
13 |
35,108,596 (GRCm39) |
missense |
probably benign |
|
R0394:Tex56
|
UTSW |
13 |
35,116,636 (GRCm39) |
splice site |
probably benign |
|
R0409:Tex56
|
UTSW |
13 |
35,108,532 (GRCm39) |
missense |
probably benign |
0.08 |
R1639:Tex56
|
UTSW |
13 |
35,128,233 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1861:Tex56
|
UTSW |
13 |
35,116,490 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2054:Tex56
|
UTSW |
13 |
35,108,574 (GRCm39) |
missense |
probably damaging |
0.99 |
R4625:Tex56
|
UTSW |
13 |
35,116,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R4932:Tex56
|
UTSW |
13 |
35,116,613 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5875:Tex56
|
UTSW |
13 |
35,116,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R7837:Tex56
|
UTSW |
13 |
35,128,359 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8836:Tex56
|
UTSW |
13 |
35,116,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R9266:Tex56
|
UTSW |
13 |
35,116,569 (GRCm39) |
missense |
possibly damaging |
0.95 |
|