Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acoxl |
G |
A |
2: 127,722,423 (GRCm39) |
|
probably null |
Het |
AI606181 |
A |
C |
19: 41,582,170 (GRCm39) |
K113N |
unknown |
Het |
Ankrd11 |
T |
C |
8: 123,618,914 (GRCm39) |
D1646G |
possibly damaging |
Het |
Ap2m1 |
T |
A |
16: 20,360,990 (GRCm39) |
I334N |
possibly damaging |
Het |
Arih2 |
T |
A |
9: 108,482,291 (GRCm39) |
H490L |
possibly damaging |
Het |
Ccdc168 |
T |
A |
1: 44,100,257 (GRCm39) |
K280N |
possibly damaging |
Het |
Cdhr1 |
T |
C |
14: 36,802,633 (GRCm39) |
Y610C |
probably damaging |
Het |
Cdkal1 |
C |
A |
13: 29,875,579 (GRCm39) |
|
probably null |
Het |
Cep76 |
A |
T |
18: 67,767,850 (GRCm39) |
N227K |
probably benign |
Het |
Clca4b |
A |
T |
3: 144,619,112 (GRCm39) |
Y676N |
probably damaging |
Het |
Cog2 |
T |
C |
8: 125,255,797 (GRCm39) |
|
probably null |
Het |
Col6a4 |
A |
T |
9: 105,957,746 (GRCm39) |
V26D |
probably damaging |
Het |
Dcaf11 |
T |
C |
14: 55,806,537 (GRCm39) |
V446A |
probably damaging |
Het |
Dync1h1 |
C |
A |
12: 110,606,378 (GRCm39) |
Q2483K |
probably benign |
Het |
Enpp3 |
A |
T |
10: 24,652,679 (GRCm39) |
D759E |
probably damaging |
Het |
Etfbkmt |
C |
T |
6: 149,052,082 (GRCm39) |
R96W |
probably benign |
Het |
Glipr1l2 |
A |
G |
10: 111,928,477 (GRCm39) |
D124G |
probably benign |
Het |
Gucy2e |
T |
C |
11: 69,126,402 (GRCm39) |
D326G |
probably benign |
Het |
Hnrnph3 |
T |
A |
10: 62,853,994 (GRCm39) |
R41S |
probably benign |
Het |
Hnrnph3 |
T |
A |
10: 62,855,279 (GRCm39) |
D2V |
probably damaging |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Itpr2 |
T |
C |
6: 146,319,477 (GRCm39) |
T188A |
possibly damaging |
Het |
Krt23 |
T |
A |
11: 99,377,608 (GRCm39) |
I133L |
probably damaging |
Het |
Krt74 |
T |
C |
15: 101,671,751 (GRCm39) |
|
noncoding transcript |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Map1a |
A |
T |
2: 121,136,255 (GRCm39) |
H2357L |
probably benign |
Het |
Mbl1 |
A |
G |
14: 40,880,706 (GRCm39) |
N198S |
probably damaging |
Het |
Mcf2l |
A |
G |
8: 13,047,337 (GRCm39) |
D233G |
probably damaging |
Het |
Mdga2 |
T |
C |
12: 66,517,700 (GRCm39) |
K45E |
possibly damaging |
Het |
Mdn1 |
A |
G |
4: 32,738,619 (GRCm39) |
N3524S |
probably benign |
Het |
Mospd3 |
A |
G |
5: 137,595,294 (GRCm39) |
L233P |
probably damaging |
Het |
Msto1 |
A |
G |
3: 88,818,848 (GRCm39) |
L269P |
probably benign |
Het |
Or4a39 |
A |
T |
2: 89,237,135 (GRCm39) |
M96K |
probably damaging |
Het |
Or5p5 |
T |
C |
7: 107,413,895 (GRCm39) |
Y35H |
probably damaging |
Het |
Or5w15 |
A |
G |
2: 87,567,825 (GRCm39) |
V281A |
probably damaging |
Het |
Or8b12i |
T |
C |
9: 20,082,561 (GRCm39) |
Y102C |
probably benign |
Het |
Or8g27 |
G |
A |
9: 39,129,024 (GRCm39) |
V124I |
possibly damaging |
Het |
Parp2 |
T |
A |
14: 51,057,130 (GRCm39) |
Y361N |
probably damaging |
Het |
Pcf11 |
G |
A |
7: 92,307,039 (GRCm39) |
P1043L |
probably damaging |
Het |
Phf24 |
G |
T |
4: 42,933,761 (GRCm39) |
V48L |
possibly damaging |
Het |
Pkn1 |
C |
A |
8: 84,398,953 (GRCm39) |
C678F |
probably damaging |
Het |
Plcl2 |
T |
C |
17: 50,915,010 (GRCm39) |
L673P |
probably damaging |
Het |
Ppp1r3c |
A |
T |
19: 36,711,617 (GRCm39) |
F51Y |
possibly damaging |
Het |
Rem2 |
T |
C |
14: 54,713,754 (GRCm39) |
|
probably benign |
Het |
Smpdl3b |
A |
G |
4: 132,472,449 (GRCm39) |
V108A |
probably damaging |
Het |
Sncaip |
A |
G |
18: 53,001,781 (GRCm39) |
T101A |
probably benign |
Het |
Stk11 |
T |
C |
10: 79,961,920 (GRCm39) |
V47A |
probably damaging |
Het |
Tmpo |
A |
C |
10: 90,998,958 (GRCm39) |
I276M |
probably benign |
Het |
Trim55 |
G |
T |
3: 19,725,256 (GRCm39) |
V258L |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,560,756 (GRCm39) |
V29215A |
probably damaging |
Het |
Ubr4 |
T |
G |
4: 139,157,534 (GRCm39) |
S2364A |
probably benign |
Het |
Unc79 |
T |
A |
12: 103,045,329 (GRCm39) |
|
probably null |
Het |
Upb1 |
T |
C |
10: 75,250,917 (GRCm39) |
|
probably null |
Het |
Usp47 |
T |
C |
7: 111,655,787 (GRCm39) |
S155P |
possibly damaging |
Het |
Zfp628 |
A |
T |
7: 4,922,732 (GRCm39) |
Q318L |
probably benign |
Het |
Zfp729b |
A |
T |
13: 67,739,253 (GRCm39) |
V1004E |
probably benign |
Het |
|
Other mutations in Fam83a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01061:Fam83a
|
APN |
15 |
57,849,771 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01328:Fam83a
|
APN |
15 |
57,849,901 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01590:Fam83a
|
APN |
15 |
57,873,173 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02306:Fam83a
|
APN |
15 |
57,858,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03062:Fam83a
|
APN |
15 |
57,856,473 (GRCm39) |
splice site |
probably null |
|
R0110:Fam83a
|
UTSW |
15 |
57,873,322 (GRCm39) |
missense |
probably benign |
0.09 |
R0469:Fam83a
|
UTSW |
15 |
57,873,322 (GRCm39) |
missense |
probably benign |
0.09 |
R0533:Fam83a
|
UTSW |
15 |
57,873,207 (GRCm39) |
missense |
probably benign |
0.43 |
R1210:Fam83a
|
UTSW |
15 |
57,858,644 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1386:Fam83a
|
UTSW |
15 |
57,849,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Fam83a
|
UTSW |
15 |
57,873,272 (GRCm39) |
missense |
probably benign |
0.02 |
R1476:Fam83a
|
UTSW |
15 |
57,873,341 (GRCm39) |
missense |
probably benign |
0.00 |
R1969:Fam83a
|
UTSW |
15 |
57,849,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R4463:Fam83a
|
UTSW |
15 |
57,858,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Fam83a
|
UTSW |
15 |
57,873,196 (GRCm39) |
missense |
probably benign |
0.00 |
R5961:Fam83a
|
UTSW |
15 |
57,872,992 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6307:Fam83a
|
UTSW |
15 |
57,849,507 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6524:Fam83a
|
UTSW |
15 |
57,858,736 (GRCm39) |
critical splice donor site |
probably null |
|
R6676:Fam83a
|
UTSW |
15 |
57,856,439 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7412:Fam83a
|
UTSW |
15 |
57,849,821 (GRCm39) |
missense |
probably benign |
|
R7447:Fam83a
|
UTSW |
15 |
57,873,086 (GRCm39) |
missense |
probably benign |
0.00 |
R7493:Fam83a
|
UTSW |
15 |
57,849,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R8379:Fam83a
|
UTSW |
15 |
57,873,196 (GRCm39) |
missense |
probably benign |
0.00 |
R8424:Fam83a
|
UTSW |
15 |
57,873,046 (GRCm39) |
missense |
possibly damaging |
0.45 |
R8728:Fam83a
|
UTSW |
15 |
57,873,062 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8856:Fam83a
|
UTSW |
15 |
57,872,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R8925:Fam83a
|
UTSW |
15 |
57,873,313 (GRCm39) |
missense |
probably benign |
0.01 |
R8927:Fam83a
|
UTSW |
15 |
57,873,313 (GRCm39) |
missense |
probably benign |
0.01 |
R9514:Fam83a
|
UTSW |
15 |
57,849,765 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9721:Fam83a
|
UTSW |
15 |
57,849,513 (GRCm39) |
missense |
probably benign |
0.00 |
X0023:Fam83a
|
UTSW |
15 |
57,873,001 (GRCm39) |
missense |
possibly damaging |
0.72 |
|