Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts1 |
A |
T |
16: 85,594,896 (GRCm39) |
N617K |
probably benign |
Het |
Adnp2 |
A |
T |
18: 80,174,185 (GRCm39) |
C75S |
probably damaging |
Het |
Agmo |
T |
C |
12: 37,407,673 (GRCm39) |
F186L |
possibly damaging |
Het |
Ahnak2 |
T |
C |
12: 112,749,872 (GRCm39) |
Y122C |
|
Het |
Ahnak2 |
T |
C |
12: 112,750,709 (GRCm39) |
E71G |
|
Het |
Aldh5a1 |
A |
G |
13: 25,102,524 (GRCm39) |
V313A |
probably damaging |
Het |
Ankib1 |
C |
A |
5: 3,822,643 (GRCm39) |
C21F |
probably benign |
Het |
Aqr |
A |
G |
2: 113,949,358 (GRCm39) |
Y947H |
probably damaging |
Het |
Atp1a2 |
T |
A |
1: 172,103,547 (GRCm39) |
Y991F |
probably benign |
Het |
Atp8b3 |
G |
A |
10: 80,365,923 (GRCm39) |
T309M |
possibly damaging |
Het |
Blzf1 |
T |
A |
1: 164,125,859 (GRCm39) |
D259V |
possibly damaging |
Het |
Cacng5 |
T |
C |
11: 107,772,510 (GRCm39) |
I113V |
probably benign |
Het |
Catsper3 |
T |
C |
13: 55,953,657 (GRCm39) |
M269T |
probably benign |
Het |
Ccdc142 |
A |
C |
6: 83,079,233 (GRCm39) |
Y190S |
probably damaging |
Het |
Ccdc159 |
C |
A |
9: 21,845,051 (GRCm39) |
Q306K |
probably benign |
Het |
Ccdc180 |
A |
T |
4: 45,920,842 (GRCm39) |
|
probably null |
Het |
Cebpz |
A |
G |
17: 79,229,081 (GRCm39) |
F955S |
possibly damaging |
Het |
Cftr |
C |
T |
6: 18,274,696 (GRCm39) |
T938I |
probably damaging |
Het |
Col28a1 |
T |
C |
6: 8,013,133 (GRCm39) |
K973R |
probably benign |
Het |
Cyp2c29 |
T |
C |
19: 39,310,138 (GRCm39) |
|
probably benign |
Het |
Ddx1 |
A |
G |
12: 13,293,859 (GRCm39) |
|
probably benign |
Het |
Duox2 |
A |
C |
2: 122,119,826 (GRCm39) |
Y867* |
probably null |
Het |
Esrrb |
T |
A |
12: 86,565,724 (GRCm39) |
L417Q |
probably damaging |
Het |
Fbxw7 |
G |
A |
3: 84,859,684 (GRCm39) |
R2H |
unknown |
Het |
Galnt6 |
C |
T |
15: 100,592,501 (GRCm39) |
V569I |
probably benign |
Het |
Gm14226 |
G |
A |
2: 154,866,094 (GRCm39) |
C17Y |
unknown |
Het |
Gpr150 |
T |
G |
13: 76,204,642 (GRCm39) |
D101A |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,565,296 (GRCm39) |
L1004Q |
probably benign |
Het |
Gtf2a1l |
T |
A |
17: 89,022,351 (GRCm39) |
D447E |
probably damaging |
Het |
Gtf2ird1 |
C |
T |
5: 134,444,064 (GRCm39) |
V64M |
probably damaging |
Het |
Ifi206 |
A |
T |
1: 173,308,074 (GRCm39) |
W641R |
|
Het |
Ifi214 |
T |
A |
1: 173,355,486 (GRCm39) |
E107D |
possibly damaging |
Het |
Kif19a |
T |
C |
11: 114,675,599 (GRCm39) |
V357A |
probably damaging |
Het |
Klhdc7b |
T |
A |
15: 89,271,025 (GRCm39) |
S636T |
probably benign |
Het |
Klhl25 |
C |
T |
7: 75,515,420 (GRCm39) |
R109C |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,853,124 (GRCm39) |
E835G |
probably benign |
Het |
Marchf1 |
A |
G |
8: 66,921,000 (GRCm39) |
K226E |
probably damaging |
Het |
Mcpt1 |
T |
C |
14: 56,256,170 (GRCm39) |
|
probably benign |
Het |
Myrf |
C |
A |
19: 10,192,434 (GRCm39) |
R639L |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,359,604 (GRCm39) |
H544R |
possibly damaging |
Het |
Nccrp1 |
T |
C |
7: 28,245,769 (GRCm39) |
I132V |
probably benign |
Het |
Nprl3 |
C |
T |
11: 32,187,334 (GRCm39) |
V333I |
possibly damaging |
Het |
Or13a25 |
C |
T |
7: 140,248,052 (GRCm39) |
S277L |
possibly damaging |
Het |
Or14n1-ps1 |
T |
C |
7: 86,092,923 (GRCm39) |
S245P |
probably damaging |
Het |
Or2o1 |
T |
C |
11: 49,051,297 (GRCm39) |
M152T |
probably benign |
Het |
Or2y1 |
T |
A |
11: 49,385,671 (GRCm39) |
S104T |
probably benign |
Het |
Or4b1d |
A |
T |
2: 89,969,114 (GRCm39) |
I123N |
probably damaging |
Het |
Or4f62 |
A |
T |
2: 111,986,934 (GRCm39) |
I213F |
probably damaging |
Het |
Or52h1 |
T |
C |
7: 103,829,025 (GRCm39) |
N197D |
probably damaging |
Het |
Or56a41 |
C |
A |
7: 104,741,808 (GRCm39) |
V73F |
possibly damaging |
Het |
Or8c15 |
T |
C |
9: 38,121,099 (GRCm39) |
V248A |
probably benign |
Het |
Or8d6 |
T |
C |
9: 39,853,891 (GRCm39) |
S112P |
probably damaging |
Het |
Otx2 |
A |
G |
14: 48,896,521 (GRCm39) |
M179T |
probably damaging |
Het |
Pmfbp1 |
A |
G |
8: 110,265,309 (GRCm39) |
|
probably benign |
Het |
Ppfia3 |
T |
A |
7: 45,011,129 (GRCm39) |
T34S |
probably benign |
Het |
Prkcsh |
T |
C |
9: 21,924,375 (GRCm39) |
Y502H |
probably damaging |
Het |
Psd |
T |
C |
19: 46,301,775 (GRCm39) |
E937G |
probably damaging |
Het |
Rbbp6 |
T |
A |
7: 122,600,976 (GRCm39) |
I1661N |
unknown |
Het |
Rhobtb1 |
T |
A |
10: 69,106,587 (GRCm39) |
M446K |
probably damaging |
Het |
Sall3 |
T |
C |
18: 81,017,236 (GRCm39) |
I231V |
probably benign |
Het |
Slc12a9 |
C |
T |
5: 137,325,916 (GRCm39) |
V270I |
probably damaging |
Het |
Slc6a15 |
A |
G |
10: 103,225,112 (GRCm39) |
K67E |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,380,646 (GRCm39) |
D524G |
probably benign |
Het |
Smpdl3a |
A |
G |
10: 57,687,526 (GRCm39) |
D418G |
probably benign |
Het |
Sox6 |
T |
C |
7: 115,196,743 (GRCm39) |
T296A |
probably benign |
Het |
Ssu2 |
T |
C |
6: 112,361,399 (GRCm39) |
E19G |
probably damaging |
Het |
Tctn3 |
T |
C |
19: 40,600,170 (GRCm39) |
N90S |
probably damaging |
Het |
Tex24 |
A |
G |
8: 27,834,652 (GRCm39) |
Q60R |
possibly damaging |
Het |
Tlcd1 |
T |
A |
11: 78,070,470 (GRCm39) |
*128R |
probably null |
Het |
Tti1 |
A |
C |
2: 157,834,930 (GRCm39) |
L1010R |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,567,682 (GRCm39) |
L27737P |
probably damaging |
Het |
Ubqln5 |
T |
A |
7: 103,778,322 (GRCm39) |
K167N |
probably benign |
Het |
Unkl |
A |
G |
17: 25,450,689 (GRCm39) |
I492V |
possibly damaging |
Het |
Vmn1r8 |
G |
A |
6: 57,013,665 (GRCm39) |
V239I |
probably benign |
Het |
Vmn2r101 |
T |
A |
17: 19,811,397 (GRCm39) |
L494I |
probably benign |
Het |
Vmn2r54 |
G |
T |
7: 12,369,877 (GRCm39) |
T62K |
probably benign |
Het |
|
Other mutations in Ereg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Ereg
|
APN |
5 |
91,222,638 (GRCm39) |
missense |
probably benign |
|
IGL01643:Ereg
|
APN |
5 |
91,234,637 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01927:Ereg
|
APN |
5 |
91,234,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03355:Ereg
|
APN |
5 |
91,236,440 (GRCm39) |
splice site |
probably benign |
|
I0000:Ereg
|
UTSW |
5 |
91,237,068 (GRCm39) |
missense |
probably benign |
0.08 |
R0245:Ereg
|
UTSW |
5 |
91,222,659 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4366:Ereg
|
UTSW |
5 |
91,234,659 (GRCm39) |
missense |
probably benign |
0.21 |
R4958:Ereg
|
UTSW |
5 |
91,237,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R5422:Ereg
|
UTSW |
5 |
91,222,666 (GRCm39) |
critical splice donor site |
probably null |
|
R5911:Ereg
|
UTSW |
5 |
91,222,552 (GRCm39) |
utr 5 prime |
probably benign |
|
R6838:Ereg
|
UTSW |
5 |
91,236,323 (GRCm39) |
missense |
probably benign |
0.00 |
R8356:Ereg
|
UTSW |
5 |
91,237,993 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8456:Ereg
|
UTSW |
5 |
91,237,993 (GRCm39) |
missense |
possibly damaging |
0.58 |
X0009:Ereg
|
UTSW |
5 |
91,237,943 (GRCm39) |
missense |
probably benign |
0.29 |
Z1176:Ereg
|
UTSW |
5 |
91,237,979 (GRCm39) |
missense |
possibly damaging |
0.90 |
|