Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
G |
17: 24,536,212 (GRCm39) |
K485T |
probably benign |
Het |
Abcc12 |
G |
T |
8: 87,280,023 (GRCm39) |
L337M |
probably damaging |
Het |
Adcy4 |
T |
C |
14: 56,010,221 (GRCm39) |
D687G |
probably benign |
Het |
Aldoc |
T |
A |
11: 78,215,610 (GRCm39) |
I98N |
probably damaging |
Het |
Aoah |
T |
A |
13: 21,184,121 (GRCm39) |
V395D |
probably damaging |
Het |
Arap1 |
C |
T |
7: 101,036,403 (GRCm39) |
R397W |
probably damaging |
Het |
Arl16 |
A |
T |
11: 120,357,526 (GRCm39) |
M63K |
probably damaging |
Het |
Atf7 |
T |
C |
15: 102,502,144 (GRCm39) |
D4G |
probably damaging |
Het |
Atp6v0d2 |
A |
T |
4: 19,922,397 (GRCm39) |
V34D |
probably benign |
Het |
Calhm4 |
T |
A |
10: 33,917,661 (GRCm39) |
K263N |
probably benign |
Het |
Camk1g |
C |
G |
1: 193,044,408 (GRCm39) |
G2A |
probably damaging |
Het |
Cenpe |
A |
G |
3: 134,929,001 (GRCm39) |
T302A |
probably damaging |
Het |
Cps1 |
T |
C |
1: 67,253,246 (GRCm39) |
V1246A |
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,560,139 (GRCm39) |
D1397G |
|
Het |
Ddx39b |
T |
A |
17: 35,463,435 (GRCm39) |
S115T |
probably benign |
Het |
Dnaja3 |
C |
A |
16: 4,514,383 (GRCm39) |
T305K |
probably benign |
Het |
Dusp7 |
C |
G |
9: 106,248,241 (GRCm39) |
H290D |
probably benign |
Het |
Emilin2 |
T |
A |
17: 71,582,282 (GRCm39) |
D148V |
possibly damaging |
Het |
Erbin |
C |
T |
13: 104,022,824 (GRCm39) |
R5Q |
probably damaging |
Het |
Foxn3 |
T |
C |
12: 99,162,951 (GRCm39) |
S317G |
probably benign |
Het |
Gipc1 |
T |
A |
8: 84,388,919 (GRCm39) |
M177K |
possibly damaging |
Het |
Grpel2 |
A |
C |
18: 61,851,823 (GRCm39) |
|
probably benign |
Het |
Htr1a |
G |
C |
13: 105,581,101 (GRCm39) |
A114P |
probably damaging |
Het |
Iqch |
A |
T |
9: 63,452,195 (GRCm39) |
M210K |
possibly damaging |
Het |
Kdelr3 |
T |
C |
15: 79,410,052 (GRCm39) |
I179T |
possibly damaging |
Het |
Lat2 |
C |
T |
5: 134,635,553 (GRCm39) |
|
probably benign |
Het |
Mcrip1 |
A |
G |
11: 120,435,605 (GRCm39) |
V10A |
probably damaging |
Het |
Mib1 |
C |
T |
18: 10,755,643 (GRCm39) |
L350F |
probably benign |
Het |
Nhlrc2 |
T |
A |
19: 56,583,344 (GRCm39) |
V605E |
probably benign |
Het |
Nup133 |
AAGAGA |
AAGA |
8: 124,638,627 (GRCm39) |
900 |
probably null |
Het |
Nutm2 |
A |
T |
13: 50,623,989 (GRCm39) |
I229F |
probably benign |
Het |
Or6f1 |
G |
A |
7: 85,970,989 (GRCm39) |
T57M |
probably damaging |
Het |
Phkb |
T |
C |
8: 86,745,156 (GRCm39) |
V611A |
possibly damaging |
Het |
Polg2 |
A |
T |
11: 106,670,208 (GRCm39) |
Y21N |
probably benign |
Het |
Prss28 |
T |
A |
17: 25,528,627 (GRCm39) |
I23N |
probably benign |
Het |
Ptprz1 |
G |
A |
6: 23,030,661 (GRCm39) |
V1856I |
probably benign |
Het |
Slc22a22 |
A |
T |
15: 57,108,237 (GRCm39) |
I526N |
probably damaging |
Het |
Slc24a4 |
T |
C |
12: 102,180,133 (GRCm39) |
F68S |
probably damaging |
Het |
Slc37a3 |
A |
G |
6: 39,322,274 (GRCm39) |
S377P |
probably damaging |
Het |
Smoc2 |
T |
C |
17: 14,545,896 (GRCm39) |
S62P |
probably damaging |
Het |
Sox4 |
A |
G |
13: 29,136,911 (GRCm39) |
S32P |
probably damaging |
Het |
Stxbp2 |
A |
T |
8: 3,689,541 (GRCm39) |
Q426L |
|
Het |
Synrg |
T |
G |
11: 83,910,410 (GRCm39) |
S937A |
probably benign |
Het |
Tbr1 |
C |
A |
2: 61,642,196 (GRCm39) |
T487K |
possibly damaging |
Het |
Tll2 |
T |
C |
19: 41,195,012 (GRCm39) |
T25A |
probably benign |
Het |
Trim31 |
T |
C |
17: 37,210,875 (GRCm39) |
F169S |
probably benign |
Het |
Tro |
G |
A |
X: 149,438,555 (GRCm39) |
S34L |
unknown |
Het |
Tspear |
T |
C |
10: 77,665,463 (GRCm39) |
F83S |
probably benign |
Het |
Ubr5 |
C |
A |
15: 38,041,123 (GRCm39) |
A254S |
|
Het |
Ubtfl1 |
A |
G |
9: 18,321,459 (GRCm39) |
E329G |
probably benign |
Het |
Vmn2r45 |
A |
G |
7: 8,474,881 (GRCm39) |
W716R |
probably damaging |
Het |
Vmn2r67 |
T |
C |
7: 84,799,895 (GRCm39) |
M448V |
probably damaging |
Het |
Wwc2 |
T |
G |
8: 48,336,579 (GRCm39) |
I228L |
possibly damaging |
Het |
Zbtb20 |
T |
C |
16: 43,430,857 (GRCm39) |
V383A |
probably benign |
Het |
|
Other mutations in Fam3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00648:Fam3b
|
APN |
16 |
97,279,599 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01754:Fam3b
|
APN |
16 |
97,277,607 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02582:Fam3b
|
APN |
16 |
97,272,391 (GRCm39) |
nonsense |
probably null |
|
R4393:Fam3b
|
UTSW |
16 |
97,282,986 (GRCm39) |
critical splice donor site |
probably null |
|
R4394:Fam3b
|
UTSW |
16 |
97,282,986 (GRCm39) |
critical splice donor site |
probably null |
|
R4395:Fam3b
|
UTSW |
16 |
97,282,986 (GRCm39) |
critical splice donor site |
probably null |
|
R6115:Fam3b
|
UTSW |
16 |
97,276,568 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6388:Fam3b
|
UTSW |
16 |
97,279,591 (GRCm39) |
missense |
probably benign |
0.23 |
R6500:Fam3b
|
UTSW |
16 |
97,302,101 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8031:Fam3b
|
UTSW |
16 |
97,283,052 (GRCm39) |
nonsense |
probably null |
|
R8411:Fam3b
|
UTSW |
16 |
97,283,053 (GRCm39) |
missense |
probably benign |
0.29 |
R8992:Fam3b
|
UTSW |
16 |
97,277,594 (GRCm39) |
missense |
probably damaging |
0.97 |
R9128:Fam3b
|
UTSW |
16 |
97,302,200 (GRCm39) |
missense |
probably benign |
|
R9220:Fam3b
|
UTSW |
16 |
97,302,111 (GRCm39) |
missense |
probably benign |
0.02 |
Z1176:Fam3b
|
UTSW |
16 |
97,283,044 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fam3b
|
UTSW |
16 |
97,313,687 (GRCm39) |
missense |
probably benign |
0.03 |
|