Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933405L10Rik |
A |
T |
8: 106,436,554 (GRCm39) |
H241L |
possibly damaging |
Het |
Acap1 |
T |
C |
11: 69,777,893 (GRCm39) |
D115G |
probably damaging |
Het |
Acvr2b |
T |
C |
9: 119,262,469 (GRCm39) |
V510A |
possibly damaging |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Agr2 |
A |
T |
12: 36,045,591 (GRCm39) |
K26* |
probably null |
Het |
Aox4 |
T |
A |
1: 58,256,685 (GRCm39) |
I69N |
probably damaging |
Het |
Asb4 |
G |
A |
6: 5,390,699 (GRCm39) |
G31R |
probably benign |
Het |
Atp6v1c2 |
C |
A |
12: 17,351,187 (GRCm39) |
E105* |
probably null |
Het |
Bend6 |
A |
G |
1: 33,917,509 (GRCm39) |
Y44H |
probably damaging |
Het |
Bltp3b |
T |
G |
10: 89,641,195 (GRCm39) |
S789A |
probably benign |
Het |
Btn2a2 |
C |
T |
13: 23,672,015 (GRCm39) |
V25M |
possibly damaging |
Het |
Cab39l |
T |
A |
14: 59,737,039 (GRCm39) |
L53Q |
probably damaging |
Het |
Cc2d1b |
C |
T |
4: 108,490,422 (GRCm39) |
R825W |
probably damaging |
Het |
Cdc14b |
C |
T |
13: 64,353,338 (GRCm39) |
|
probably benign |
Het |
Cenpu |
A |
G |
8: 47,015,615 (GRCm39) |
R177G |
probably benign |
Het |
Chit1 |
C |
A |
1: 134,074,381 (GRCm39) |
Y229* |
probably null |
Het |
Crybg2 |
C |
A |
4: 133,808,450 (GRCm39) |
S1350R |
probably damaging |
Het |
Ctdspl2 |
A |
G |
2: 121,809,373 (GRCm39) |
|
probably null |
Het |
Ctsr |
A |
T |
13: 61,308,345 (GRCm39) |
H266Q |
probably benign |
Het |
Dynlt5 |
A |
G |
4: 102,849,766 (GRCm39) |
E63G |
possibly damaging |
Het |
Efcab3 |
T |
G |
11: 104,746,386 (GRCm39) |
I2279S |
probably benign |
Het |
Extl3 |
T |
A |
14: 65,313,584 (GRCm39) |
M533L |
probably benign |
Het |
Fbxo28 |
T |
C |
1: 182,157,454 (GRCm39) |
K121R |
probably damaging |
Het |
Fsip2 |
A |
C |
2: 82,820,227 (GRCm39) |
E5320A |
possibly damaging |
Het |
Galc |
A |
T |
12: 98,225,421 (GRCm39) |
D56E |
probably damaging |
Het |
Gm5468 |
A |
G |
15: 25,414,481 (GRCm39) |
|
probably benign |
Het |
Hk1 |
T |
A |
10: 62,135,038 (GRCm39) |
H24L |
probably damaging |
Het |
Igkv5-43 |
A |
G |
6: 69,752,965 (GRCm39) |
V39A |
possibly damaging |
Het |
Lemd2 |
G |
A |
17: 27,411,976 (GRCm39) |
Q439* |
probably null |
Het |
Lgi1 |
A |
G |
19: 38,294,257 (GRCm39) |
N295S |
probably benign |
Het |
Macc1 |
T |
G |
12: 119,409,785 (GRCm39) |
S184R |
probably damaging |
Het |
Msmo1 |
A |
G |
8: 65,180,918 (GRCm39) |
|
probably benign |
Het |
Muc5b |
C |
A |
7: 141,405,333 (GRCm39) |
R914S |
unknown |
Het |
Or10d1 |
G |
A |
9: 39,483,776 (GRCm39) |
P260S |
possibly damaging |
Het |
Or1e16 |
G |
A |
11: 73,286,299 (GRCm39) |
A183V |
probably benign |
Het |
Or1e17 |
G |
A |
11: 73,831,635 (GRCm39) |
A188T |
possibly damaging |
Het |
Or4k2 |
C |
A |
14: 50,424,135 (GRCm39) |
D180Y |
probably damaging |
Het |
Or5b110-ps1 |
A |
G |
19: 13,260,290 (GRCm39) |
I44T |
probably benign |
Het |
Plekha5 |
T |
C |
6: 140,525,179 (GRCm39) |
S14P |
probably benign |
Het |
Pus10 |
A |
G |
11: 23,622,638 (GRCm39) |
K86R |
probably benign |
Het |
Rab37 |
T |
C |
11: 115,051,132 (GRCm39) |
V147A |
probably benign |
Het |
Sin3a |
T |
A |
9: 57,011,213 (GRCm39) |
I490N |
probably damaging |
Het |
Slc27a4 |
A |
G |
2: 29,695,762 (GRCm39) |
D99G |
probably benign |
Het |
Slc43a2 |
C |
T |
11: 75,459,206 (GRCm39) |
R413* |
probably null |
Het |
Syna |
G |
T |
5: 134,588,466 (GRCm39) |
T161N |
probably benign |
Het |
T |
A |
G |
17: 8,655,996 (GRCm39) |
D86G |
possibly damaging |
Het |
Tanc1 |
G |
A |
2: 59,674,366 (GRCm39) |
E1817K |
possibly damaging |
Het |
Tap2 |
C |
A |
17: 34,433,384 (GRCm39) |
Q516K |
possibly damaging |
Het |
Tcaf1 |
A |
T |
6: 42,653,741 (GRCm39) |
D717E |
probably damaging |
Het |
Tcf20 |
G |
T |
15: 82,736,187 (GRCm39) |
Q1755K |
possibly damaging |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Trpm7 |
G |
A |
2: 126,667,559 (GRCm39) |
P811S |
possibly damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,661,679 (GRCm39) |
V712A |
probably benign |
Het |
Vwc2l |
T |
A |
1: 70,768,180 (GRCm39) |
D34E |
probably damaging |
Het |
Wdr35 |
A |
G |
12: 9,077,632 (GRCm39) |
K1091E |
probably benign |
Het |
|
Other mutations in Fam162b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00567:Fam162b
|
APN |
10 |
51,466,390 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02948:Fam162b
|
APN |
10 |
51,463,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R0709:Fam162b
|
UTSW |
10 |
51,463,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Fam162b
|
UTSW |
10 |
51,466,439 (GRCm39) |
missense |
probably benign |
|
R1185:Fam162b
|
UTSW |
10 |
51,466,439 (GRCm39) |
missense |
probably benign |
|
R1185:Fam162b
|
UTSW |
10 |
51,466,439 (GRCm39) |
missense |
probably benign |
|
R1505:Fam162b
|
UTSW |
10 |
51,463,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R1735:Fam162b
|
UTSW |
10 |
51,463,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1961:Fam162b
|
UTSW |
10 |
51,466,430 (GRCm39) |
missense |
probably benign |
0.00 |
R2401:Fam162b
|
UTSW |
10 |
51,463,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R6059:Fam162b
|
UTSW |
10 |
51,466,403 (GRCm39) |
missense |
probably benign |
0.28 |
R6284:Fam162b
|
UTSW |
10 |
51,461,598 (GRCm39) |
missense |
probably damaging |
0.99 |
R6625:Fam162b
|
UTSW |
10 |
51,466,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R7324:Fam162b
|
UTSW |
10 |
51,466,282 (GRCm39) |
splice site |
probably null |
|
R7380:Fam162b
|
UTSW |
10 |
51,466,572 (GRCm39) |
start gained |
probably benign |
|
R8945:Fam162b
|
UTSW |
10 |
51,466,469 (GRCm39) |
missense |
probably benign |
0.02 |
R9415:Fam162b
|
UTSW |
10 |
51,466,155 (GRCm39) |
critical splice donor site |
probably null |
|
|