Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg7 |
T |
C |
16: 56,553,211 (GRCm39) |
T629A |
probably benign |
Het |
Afg3l2 |
A |
G |
18: 67,542,550 (GRCm39) |
V632A |
possibly damaging |
Het |
Ahnak |
G |
A |
19: 8,987,487 (GRCm39) |
E2924K |
probably damaging |
Het |
Ampd1 |
A |
G |
3: 102,995,786 (GRCm39) |
Y232C |
probably benign |
Het |
Ank1 |
G |
A |
8: 23,606,264 (GRCm39) |
G1219S |
probably null |
Het |
Atp8b4 |
A |
T |
2: 126,275,841 (GRCm39) |
N130K |
probably benign |
Het |
Cdh15 |
T |
C |
8: 123,584,256 (GRCm39) |
|
probably null |
Het |
Cep70 |
T |
C |
9: 99,181,829 (GRCm39) |
I613T |
possibly damaging |
Het |
Cfap54 |
C |
T |
10: 92,651,883 (GRCm39) |
V3056I |
probably benign |
Het |
Chrna2 |
T |
C |
14: 66,386,282 (GRCm39) |
F143L |
probably benign |
Het |
Cmya5 |
C |
T |
13: 93,228,572 (GRCm39) |
R2172H |
probably benign |
Het |
Col17a1 |
T |
C |
19: 47,657,898 (GRCm39) |
E424G |
probably benign |
Het |
Crybg1 |
T |
C |
10: 43,880,477 (GRCm39) |
E237G |
probably benign |
Het |
Ctnnd2 |
G |
A |
15: 30,881,316 (GRCm39) |
C732Y |
probably damaging |
Het |
Dcaf12 |
T |
C |
4: 41,299,411 (GRCm39) |
N264S |
probably benign |
Het |
Dennd4c |
A |
G |
4: 86,743,349 (GRCm39) |
S1064G |
probably benign |
Het |
Dsc2 |
A |
T |
18: 20,176,968 (GRCm39) |
Y360N |
probably damaging |
Het |
E2f3 |
T |
G |
13: 30,097,478 (GRCm39) |
D295A |
probably damaging |
Het |
Eef2 |
T |
C |
10: 81,015,487 (GRCm39) |
L336P |
possibly damaging |
Het |
Fanca |
A |
G |
8: 124,035,307 (GRCm39) |
S213P |
possibly damaging |
Het |
Fpgt |
A |
T |
3: 154,792,903 (GRCm39) |
S375T |
probably benign |
Het |
Gad1 |
G |
A |
2: 70,416,206 (GRCm39) |
V222I |
probably benign |
Het |
Gm5930 |
A |
T |
14: 44,568,858 (GRCm39) |
Y255N |
possibly damaging |
Het |
Grik2 |
T |
A |
10: 48,989,555 (GRCm39) |
I825F |
possibly damaging |
Het |
Hcn4 |
T |
C |
9: 58,731,482 (GRCm39) |
S230P |
unknown |
Het |
Kansl3 |
T |
C |
1: 36,393,861 (GRCm39) |
I222V |
probably benign |
Het |
Kif20b |
T |
C |
19: 34,927,203 (GRCm39) |
S822P |
probably benign |
Het |
Kremen2 |
T |
A |
17: 23,964,737 (GRCm39) |
|
probably benign |
Het |
Krt71 |
G |
T |
15: 101,651,100 (GRCm39) |
R128S |
possibly damaging |
Het |
Lrp4 |
A |
T |
2: 91,324,397 (GRCm39) |
N1244I |
possibly damaging |
Het |
Lrrc66 |
T |
C |
5: 73,765,244 (GRCm39) |
S600G |
possibly damaging |
Het |
Mrc2 |
T |
A |
11: 105,216,711 (GRCm39) |
C167S |
probably damaging |
Het |
Mrps17 |
T |
C |
5: 129,793,857 (GRCm39) |
V17A |
probably damaging |
Het |
Muc20 |
A |
T |
16: 32,614,840 (GRCm39) |
L179Q |
unknown |
Het |
Or13g1 |
A |
T |
7: 85,955,957 (GRCm39) |
Y121* |
probably null |
Het |
Or13p8 |
T |
A |
4: 118,583,565 (GRCm39) |
F40L |
probably benign |
Het |
Or4c29 |
G |
T |
2: 88,739,951 (GRCm39) |
T262K |
probably damaging |
Het |
Otop2 |
T |
C |
11: 115,214,431 (GRCm39) |
F63L |
probably benign |
Het |
Pde3b |
C |
T |
7: 114,015,695 (GRCm39) |
Q304* |
probably null |
Het |
Pex19 |
GTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTC |
GTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTC |
1: 171,956,150 (GRCm39) |
|
probably null |
Het |
Plekhg4 |
A |
G |
8: 106,105,332 (GRCm39) |
E599G |
possibly damaging |
Het |
Ppargc1a |
C |
A |
5: 51,630,251 (GRCm39) |
R622L |
unknown |
Het |
Ppip5k2 |
A |
G |
1: 97,655,139 (GRCm39) |
L879P |
probably damaging |
Het |
Prepl |
C |
T |
17: 85,376,366 (GRCm39) |
V563M |
possibly damaging |
Het |
Prom1 |
G |
T |
5: 44,204,870 (GRCm39) |
D201E |
probably damaging |
Het |
Psmd1 |
T |
A |
1: 86,054,231 (GRCm39) |
D723E |
probably damaging |
Het |
Sall2 |
A |
T |
14: 52,550,719 (GRCm39) |
N825K |
possibly damaging |
Het |
Sds |
A |
T |
5: 120,618,655 (GRCm39) |
M70L |
probably benign |
Het |
Sema4c |
C |
T |
1: 36,592,079 (GRCm39) |
R256H |
probably damaging |
Het |
Sik1 |
T |
C |
17: 32,070,545 (GRCm39) |
Y100C |
probably damaging |
Het |
Slc13a5 |
T |
A |
11: 72,138,588 (GRCm39) |
I452F |
probably damaging |
Het |
Slc25a24 |
A |
G |
3: 109,062,395 (GRCm39) |
I162V |
possibly damaging |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Tenm3 |
T |
A |
8: 48,707,668 (GRCm39) |
N1710I |
probably damaging |
Het |
Tmem115 |
T |
A |
9: 107,411,880 (GRCm39) |
M68K |
probably benign |
Het |
Tmem132d |
T |
C |
5: 127,866,936 (GRCm39) |
I655V |
probably benign |
Het |
Tmem132d |
T |
C |
5: 128,346,316 (GRCm39) |
I69V |
probably benign |
Het |
Tnfrsf11a |
G |
A |
1: 105,754,854 (GRCm39) |
A309T |
possibly damaging |
Het |
Trim9 |
A |
G |
12: 70,314,013 (GRCm39) |
M544T |
probably benign |
Het |
Ttll3 |
G |
A |
6: 113,389,850 (GRCm39) |
R745H |
probably benign |
Het |
Ttn |
G |
T |
2: 76,737,931 (GRCm39) |
L4249I |
unknown |
Het |
Unc79 |
G |
A |
12: 103,074,874 (GRCm39) |
|
probably null |
Het |
Vmn1r196 |
T |
C |
13: 22,478,254 (GRCm39) |
C298R |
probably benign |
Het |
Vmn1r216 |
A |
G |
13: 23,284,081 (GRCm39) |
I255V |
probably benign |
Het |
Zfp853 |
A |
G |
5: 143,274,243 (GRCm39) |
L474P |
unknown |
Het |
|
Other mutations in Gpr55 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01331:Gpr55
|
APN |
1 |
85,868,915 (GRCm39) |
unclassified |
probably benign |
|
IGL02087:Gpr55
|
APN |
1 |
85,868,969 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03296:Gpr55
|
APN |
1 |
85,868,753 (GRCm39) |
missense |
probably damaging |
0.98 |
R0119:Gpr55
|
UTSW |
1 |
85,869,146 (GRCm39) |
nonsense |
probably null |
|
R0166:Gpr55
|
UTSW |
1 |
85,868,858 (GRCm39) |
missense |
probably benign |
0.01 |
R0529:Gpr55
|
UTSW |
1 |
85,869,225 (GRCm39) |
missense |
probably benign |
0.00 |
R0664:Gpr55
|
UTSW |
1 |
85,868,739 (GRCm39) |
missense |
probably benign |
0.30 |
R1670:Gpr55
|
UTSW |
1 |
85,869,137 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4490:Gpr55
|
UTSW |
1 |
85,869,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R7719:Gpr55
|
UTSW |
1 |
85,869,059 (GRCm39) |
missense |
probably benign |
0.00 |
R8049:Gpr55
|
UTSW |
1 |
85,869,419 (GRCm39) |
missense |
probably benign |
0.00 |
R8371:Gpr55
|
UTSW |
1 |
85,868,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R9480:Gpr55
|
UTSW |
1 |
85,868,977 (GRCm39) |
nonsense |
probably null |
|
|