Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh8a1 |
G |
A |
10: 21,271,470 (GRCm39) |
V399I |
probably benign |
Het |
Apold1 |
A |
G |
6: 134,960,869 (GRCm39) |
I108V |
probably benign |
Het |
Arpc5 |
G |
A |
1: 152,644,607 (GRCm39) |
|
probably benign |
Het |
Capn11 |
T |
A |
17: 45,964,682 (GRCm39) |
D45V |
probably damaging |
Het |
Dctpp1 |
G |
A |
7: 126,856,285 (GRCm39) |
R146C |
probably damaging |
Het |
Dlat |
C |
T |
9: 50,560,931 (GRCm39) |
|
probably null |
Het |
Dock10 |
T |
A |
1: 80,584,286 (GRCm39) |
D140V |
probably damaging |
Het |
Dtx3 |
A |
G |
10: 127,027,040 (GRCm39) |
V378A |
probably benign |
Het |
Ezh2 |
A |
G |
6: 47,521,516 (GRCm39) |
I414T |
probably benign |
Het |
Gm1979 |
C |
T |
5: 26,209,604 (GRCm39) |
W41* |
probably null |
Het |
Igf2bp2 |
T |
C |
16: 21,882,426 (GRCm39) |
N425S |
probably damaging |
Het |
Kdm5a |
T |
A |
6: 120,371,067 (GRCm39) |
Y504N |
probably damaging |
Het |
Map3k21 |
T |
A |
8: 126,637,924 (GRCm39) |
I170N |
probably damaging |
Het |
Nipal2 |
T |
G |
15: 34,600,207 (GRCm39) |
K203N |
possibly damaging |
Het |
Nlrp1b |
A |
G |
11: 71,063,911 (GRCm39) |
F621S |
probably damaging |
Het |
Nos3 |
G |
A |
5: 24,576,714 (GRCm39) |
V448M |
probably damaging |
Het |
Ntrk3 |
G |
T |
7: 78,112,695 (GRCm39) |
|
probably benign |
Het |
Or5b118 |
A |
T |
19: 13,448,561 (GRCm39) |
T76S |
possibly damaging |
Het |
P2rx1 |
T |
C |
11: 72,900,799 (GRCm39) |
C190R |
probably damaging |
Het |
Pdzrn4 |
T |
A |
15: 92,297,630 (GRCm39) |
D198E |
probably benign |
Het |
Ptar1 |
A |
G |
19: 23,664,824 (GRCm39) |
M1V |
probably null |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Purg |
T |
A |
8: 33,877,019 (GRCm39) |
L219* |
probably null |
Het |
Rbp3 |
G |
T |
14: 33,677,347 (GRCm39) |
V432L |
possibly damaging |
Het |
Scnn1b |
G |
T |
7: 121,513,555 (GRCm39) |
|
probably null |
Het |
Sgms1 |
A |
G |
19: 32,120,192 (GRCm39) |
V238A |
possibly damaging |
Het |
Slc16a14 |
G |
T |
1: 84,890,228 (GRCm39) |
S359* |
probably null |
Het |
Smarca2 |
G |
A |
19: 26,661,327 (GRCm39) |
|
probably null |
Het |
Spatc1l |
A |
G |
10: 76,398,323 (GRCm39) |
S42G |
probably benign |
Het |
Stra6 |
T |
A |
9: 58,042,473 (GRCm39) |
V34E |
probably damaging |
Het |
Tex14 |
A |
G |
11: 87,429,449 (GRCm39) |
|
probably null |
Het |
Tox4 |
T |
C |
14: 52,523,361 (GRCm39) |
|
probably null |
Het |
Tyr |
A |
G |
7: 87,087,148 (GRCm39) |
S455P |
probably benign |
Het |
Uggt2 |
T |
C |
14: 119,263,845 (GRCm39) |
N1062D |
possibly damaging |
Het |
Umod |
A |
C |
7: 119,075,913 (GRCm39) |
N284K |
possibly damaging |
Het |
Unc93b1 |
T |
C |
19: 3,993,572 (GRCm39) |
I338T |
probably damaging |
Het |
Vmn2r99 |
C |
T |
17: 19,598,832 (GRCm39) |
T172I |
possibly damaging |
Het |
Whrn |
G |
A |
4: 63,333,876 (GRCm39) |
Q415* |
probably null |
Het |
|
Other mutations in Mrgpra6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01645:Mrgpra6
|
APN |
7 |
46,835,681 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01780:Mrgpra6
|
APN |
7 |
46,838,497 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01801:Mrgpra6
|
APN |
7 |
46,835,572 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02158:Mrgpra6
|
APN |
7 |
46,835,700 (GRCm39) |
nonsense |
probably null |
|
IGL02715:Mrgpra6
|
APN |
7 |
46,838,396 (GRCm39) |
splice site |
probably benign |
|
IGL02896:Mrgpra6
|
APN |
7 |
46,838,655 (GRCm39) |
missense |
probably benign |
0.02 |
D4216:Mrgpra6
|
UTSW |
7 |
46,838,504 (GRCm39) |
missense |
probably damaging |
0.96 |
R1566:Mrgpra6
|
UTSW |
7 |
46,838,652 (GRCm39) |
missense |
probably benign |
0.02 |
R5051:Mrgpra6
|
UTSW |
7 |
46,835,690 (GRCm39) |
missense |
probably benign |
0.00 |
R5384:Mrgpra6
|
UTSW |
7 |
46,838,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Mrgpra6
|
UTSW |
7 |
46,838,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Mrgpra6
|
UTSW |
7 |
46,835,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R5860:Mrgpra6
|
UTSW |
7 |
46,839,099 (GRCm39) |
missense |
probably benign |
0.41 |
R6633:Mrgpra6
|
UTSW |
7 |
46,838,493 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6952:Mrgpra6
|
UTSW |
7 |
46,835,693 (GRCm39) |
missense |
probably benign |
0.01 |
R6980:Mrgpra6
|
UTSW |
7 |
46,838,697 (GRCm39) |
missense |
probably damaging |
0.97 |
R9455:Mrgpra6
|
UTSW |
7 |
46,838,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R9615:Mrgpra6
|
UTSW |
7 |
46,835,675 (GRCm39) |
missense |
probably benign |
0.06 |
R9701:Mrgpra6
|
UTSW |
7 |
46,835,533 (GRCm39) |
missense |
probably benign |
0.00 |
R9802:Mrgpra6
|
UTSW |
7 |
46,835,533 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Mrgpra6
|
UTSW |
7 |
46,838,910 (GRCm39) |
missense |
possibly damaging |
0.80 |
|