Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl9 |
A |
T |
17: 33,652,098 (GRCm39) |
I53F |
probably damaging |
Het |
Apol7b |
T |
A |
15: 77,308,873 (GRCm39) |
D75V |
probably damaging |
Het |
Brd8 |
C |
T |
18: 34,741,528 (GRCm39) |
A387T |
probably damaging |
Het |
Cacybp |
T |
C |
1: 160,036,169 (GRCm39) |
|
probably null |
Het |
Calcoco1 |
T |
C |
15: 102,618,875 (GRCm39) |
K444E |
probably damaging |
Het |
Cers2 |
G |
A |
3: 95,228,320 (GRCm39) |
R120H |
probably benign |
Het |
Chd4 |
T |
A |
6: 125,099,086 (GRCm39) |
C1587S |
possibly damaging |
Het |
Col11a1 |
A |
T |
3: 113,888,593 (GRCm39) |
K286N |
possibly damaging |
Het |
Creld2 |
A |
G |
15: 88,709,413 (GRCm39) |
N308S |
probably damaging |
Het |
Cyp2d12 |
T |
C |
15: 82,440,934 (GRCm39) |
S151P |
probably damaging |
Het |
Dlec1 |
A |
G |
9: 118,955,242 (GRCm39) |
H642R |
probably benign |
Het |
Eif6 |
T |
C |
2: 155,665,206 (GRCm39) |
Y151C |
probably damaging |
Het |
Erbb4 |
A |
T |
1: 68,079,462 (GRCm39) |
M1206K |
probably benign |
Het |
Fbxo10 |
A |
G |
4: 45,059,035 (GRCm39) |
F234S |
probably benign |
Het |
Gcc2 |
A |
T |
10: 58,094,064 (GRCm39) |
E13D |
probably damaging |
Het |
Gm19410 |
C |
A |
8: 36,239,733 (GRCm39) |
A143E |
probably damaging |
Het |
Gtf3c5 |
T |
C |
2: 28,460,499 (GRCm39) |
K367E |
probably damaging |
Het |
Ifi204 |
T |
C |
1: 173,589,269 (GRCm39) |
E54G |
probably benign |
Het |
Kalrn |
A |
T |
16: 33,848,346 (GRCm39) |
I492N |
probably damaging |
Het |
Kifbp |
T |
C |
10: 62,410,923 (GRCm39) |
N140S |
possibly damaging |
Het |
Map2k5 |
A |
G |
9: 63,229,528 (GRCm39) |
Y168H |
probably benign |
Het |
Mbip |
A |
C |
12: 56,384,383 (GRCm39) |
|
probably null |
Het |
Mcmdc2 |
C |
T |
1: 10,004,242 (GRCm39) |
T574I |
probably damaging |
Het |
Or10a3b |
T |
C |
7: 108,444,747 (GRCm39) |
T157A |
probably benign |
Het |
Or52j3 |
T |
G |
7: 102,836,511 (GRCm39) |
D234E |
probably benign |
Het |
Or5w22 |
A |
T |
2: 87,363,285 (GRCm39) |
M303L |
probably benign |
Het |
Or8d2 |
T |
A |
9: 38,760,085 (GRCm39) |
I225N |
probably damaging |
Het |
Or8g33 |
T |
C |
9: 39,337,836 (GRCm39) |
Y177C |
probably damaging |
Het |
Or9s27 |
A |
T |
1: 92,516,768 (GRCm39) |
R239W |
probably damaging |
Het |
Pdzd8 |
A |
G |
19: 59,287,957 (GRCm39) |
*1148Q |
probably null |
Het |
Phactr1 |
T |
A |
13: 43,286,445 (GRCm39) |
I582N |
probably damaging |
Het |
Phf20l1 |
T |
G |
15: 66,502,762 (GRCm39) |
L714R |
probably damaging |
Het |
Pramel32 |
T |
C |
4: 88,548,291 (GRCm39) |
E38G |
probably damaging |
Het |
Rcor3 |
T |
C |
1: 191,822,179 (GRCm39) |
E6G |
possibly damaging |
Het |
Skic3 |
T |
C |
13: 76,333,298 (GRCm39) |
S1516P |
probably damaging |
Het |
Sptlc2 |
G |
A |
12: 87,397,069 (GRCm39) |
T239I |
possibly damaging |
Het |
Tmc1 |
A |
T |
19: 20,772,880 (GRCm39) |
V707D |
probably damaging |
Het |
Tmem63b |
T |
A |
17: 45,971,734 (GRCm39) |
E827V |
probably benign |
Het |
Triml1 |
A |
G |
8: 43,594,258 (GRCm39) |
S58P |
probably damaging |
Het |
Zdbf2 |
A |
G |
1: 63,347,687 (GRCm39) |
H2022R |
possibly damaging |
Het |
|
Other mutations in Fam178b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01070:Fam178b
|
APN |
1 |
36,603,484 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01128:Fam178b
|
APN |
1 |
36,683,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01859:Fam178b
|
APN |
1 |
36,698,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R0398:Fam178b
|
UTSW |
1 |
36,671,487 (GRCm39) |
splice site |
probably benign |
|
R1116:Fam178b
|
UTSW |
1 |
36,617,669 (GRCm39) |
nonsense |
probably null |
|
R1613:Fam178b
|
UTSW |
1 |
36,639,273 (GRCm39) |
missense |
probably benign |
0.01 |
R1623:Fam178b
|
UTSW |
1 |
36,683,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R2276:Fam178b
|
UTSW |
1 |
36,671,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R3706:Fam178b
|
UTSW |
1 |
36,647,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R4535:Fam178b
|
UTSW |
1 |
36,639,606 (GRCm39) |
missense |
probably benign |
0.43 |
R4784:Fam178b
|
UTSW |
1 |
36,671,496 (GRCm39) |
splice site |
probably null |
|
R5372:Fam178b
|
UTSW |
1 |
36,603,929 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5431:Fam178b
|
UTSW |
1 |
36,671,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Fam178b
|
UTSW |
1 |
36,639,548 (GRCm39) |
missense |
probably benign |
0.04 |
R7308:Fam178b
|
UTSW |
1 |
36,698,488 (GRCm39) |
missense |
probably benign |
|
R7573:Fam178b
|
UTSW |
1 |
36,671,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Fam178b
|
UTSW |
1 |
36,603,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R9786:Fam178b
|
UTSW |
1 |
36,603,517 (GRCm39) |
missense |
probably damaging |
0.97 |
|