Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
A |
G |
1: 120,096,814 (GRCm39) |
|
probably benign |
Het |
A530084C06Rik |
G |
A |
13: 31,743,178 (GRCm39) |
A25V |
unknown |
Het |
A730018C14Rik |
T |
C |
12: 112,381,472 (GRCm39) |
|
noncoding transcript |
Het |
Aasdh |
G |
T |
5: 77,024,058 (GRCm39) |
A198E |
probably damaging |
Het |
Abcb8 |
C |
T |
5: 24,607,101 (GRCm39) |
A328V |
probably damaging |
Het |
Ace3 |
C |
A |
11: 105,888,330 (GRCm39) |
H347N |
probably damaging |
Het |
Amy1 |
A |
T |
3: 113,355,569 (GRCm39) |
M302K |
possibly damaging |
Het |
Apol11b |
C |
T |
15: 77,524,747 (GRCm39) |
V13M |
probably null |
Het |
Arfgef2 |
T |
A |
2: 166,678,177 (GRCm39) |
V131E |
possibly damaging |
Het |
Arnt |
T |
A |
3: 95,398,037 (GRCm39) |
|
probably benign |
Het |
Atl1 |
T |
C |
12: 69,972,785 (GRCm39) |
V35A |
probably damaging |
Het |
BC061237 |
A |
T |
14: 44,738,730 (GRCm39) |
D43V |
possibly damaging |
Het |
Cracd |
A |
G |
5: 77,005,384 (GRCm39) |
T582A |
unknown |
Het |
Cyp4f17 |
T |
C |
17: 32,725,887 (GRCm39) |
S7P |
probably benign |
Het |
Ddx60 |
A |
G |
8: 62,393,774 (GRCm39) |
Y70C |
probably damaging |
Het |
Defb34 |
T |
C |
8: 19,176,468 (GRCm39) |
L53P |
probably damaging |
Het |
Dennd5a |
T |
C |
7: 109,518,567 (GRCm39) |
T525A |
probably benign |
Het |
Ephb3 |
T |
C |
16: 21,030,129 (GRCm39) |
|
probably benign |
Het |
Gramd2b |
A |
G |
18: 56,607,108 (GRCm39) |
D74G |
possibly damaging |
Het |
Hax1 |
A |
G |
3: 89,903,035 (GRCm39) |
|
probably benign |
Het |
Kcnh8 |
T |
C |
17: 53,263,804 (GRCm39) |
I767T |
probably benign |
Het |
Ldah |
G |
A |
12: 8,270,614 (GRCm39) |
V5I |
possibly damaging |
Het |
Nbeal2 |
A |
G |
9: 110,460,560 (GRCm39) |
V1758A |
probably damaging |
Het |
Nos1 |
A |
G |
5: 118,033,967 (GRCm39) |
D363G |
probably damaging |
Het |
Or14j6 |
C |
T |
17: 38,214,700 (GRCm39) |
R88* |
probably null |
Het |
Pdlim7 |
T |
A |
13: 55,646,501 (GRCm39) |
D445V |
probably damaging |
Het |
Phip |
T |
A |
9: 82,772,203 (GRCm39) |
M1115L |
probably benign |
Het |
Pigb |
C |
T |
9: 72,936,966 (GRCm39) |
A215T |
probably damaging |
Het |
Pkd1 |
A |
T |
17: 24,799,935 (GRCm39) |
S2952C |
probably damaging |
Het |
Plxnb2 |
T |
C |
15: 89,051,775 (GRCm39) |
D148G |
probably damaging |
Het |
Ppp1r36 |
T |
C |
12: 76,473,579 (GRCm39) |
F70S |
possibly damaging |
Het |
Rad52 |
G |
A |
6: 119,889,907 (GRCm39) |
|
probably benign |
Het |
Rasa2 |
T |
A |
9: 96,427,823 (GRCm39) |
T681S |
probably benign |
Het |
Rel |
A |
T |
11: 23,692,724 (GRCm39) |
Y436* |
probably null |
Het |
Sec16a |
G |
A |
2: 26,309,650 (GRCm39) |
P2119S |
probably benign |
Het |
Sema6d |
C |
A |
2: 124,506,262 (GRCm39) |
T733K |
probably benign |
Het |
Sf3b3 |
C |
T |
8: 111,541,266 (GRCm39) |
A950T |
probably benign |
Het |
Slc24a5 |
T |
A |
2: 124,927,591 (GRCm39) |
F297I |
probably damaging |
Het |
Spp2 |
A |
T |
1: 88,340,025 (GRCm39) |
D122V |
possibly damaging |
Het |
Stap1 |
A |
G |
5: 86,225,906 (GRCm39) |
K60R |
probably benign |
Het |
Stat1 |
A |
G |
1: 52,178,423 (GRCm39) |
K286E |
probably damaging |
Het |
Stn1 |
T |
C |
19: 47,505,568 (GRCm39) |
T129A |
probably benign |
Het |
Tagap |
C |
T |
17: 8,152,285 (GRCm39) |
T490I |
probably damaging |
Het |
Tbc1d2 |
T |
C |
4: 46,637,715 (GRCm39) |
E177G |
possibly damaging |
Het |
Tln2 |
A |
T |
9: 67,174,150 (GRCm39) |
L841Q |
probably damaging |
Het |
Tmem59 |
T |
A |
4: 107,047,754 (GRCm39) |
M71K |
probably damaging |
Het |
Ugt2a3 |
G |
A |
5: 87,484,406 (GRCm39) |
T206I |
probably damaging |
Het |
Utp20 |
G |
A |
10: 88,608,421 (GRCm39) |
H1539Y |
possibly damaging |
Het |
Vps13a |
T |
C |
19: 16,657,387 (GRCm39) |
N1794S |
probably benign |
Het |
Vsig10 |
A |
T |
5: 117,490,814 (GRCm39) |
|
probably null |
Het |
Zfp97 |
T |
A |
17: 17,365,087 (GRCm39) |
F195L |
possibly damaging |
Het |
|
Other mutations in Fam83d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02066:Fam83d
|
APN |
2 |
158,627,793 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02420:Fam83d
|
APN |
2 |
158,627,655 (GRCm39) |
missense |
probably benign |
0.00 |
R0277:Fam83d
|
UTSW |
2 |
158,627,467 (GRCm39) |
missense |
probably benign |
0.05 |
R0323:Fam83d
|
UTSW |
2 |
158,627,467 (GRCm39) |
missense |
probably benign |
0.05 |
R0349:Fam83d
|
UTSW |
2 |
158,621,768 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0571:Fam83d
|
UTSW |
2 |
158,627,611 (GRCm39) |
nonsense |
probably null |
|
R0799:Fam83d
|
UTSW |
2 |
158,621,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R1164:Fam83d
|
UTSW |
2 |
158,625,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1168:Fam83d
|
UTSW |
2 |
158,610,443 (GRCm39) |
missense |
probably benign |
0.01 |
R1186:Fam83d
|
UTSW |
2 |
158,627,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Fam83d
|
UTSW |
2 |
158,610,070 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2896:Fam83d
|
UTSW |
2 |
158,627,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4500:Fam83d
|
UTSW |
2 |
158,627,187 (GRCm39) |
missense |
probably benign |
0.10 |
R4597:Fam83d
|
UTSW |
2 |
158,627,142 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5416:Fam83d
|
UTSW |
2 |
158,627,552 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6328:Fam83d
|
UTSW |
2 |
158,627,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R6364:Fam83d
|
UTSW |
2 |
158,625,179 (GRCm39) |
critical splice donor site |
probably null |
|
R7031:Fam83d
|
UTSW |
2 |
158,627,227 (GRCm39) |
missense |
probably benign |
0.01 |
R8721:Fam83d
|
UTSW |
2 |
158,627,522 (GRCm39) |
missense |
probably benign |
0.33 |
R9208:Fam83d
|
UTSW |
2 |
158,610,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:Fam83d
|
UTSW |
2 |
158,610,310 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fam83d
|
UTSW |
2 |
158,627,108 (GRCm39) |
missense |
probably damaging |
1.00 |
|