Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp7 |
A |
G |
7: 28,310,409 (GRCm39) |
|
probably null |
Het |
Adap2 |
G |
T |
11: 80,047,859 (GRCm39) |
C105F |
probably damaging |
Het |
Bace2 |
T |
C |
16: 97,223,201 (GRCm39) |
|
probably null |
Het |
Bpifc |
A |
G |
10: 85,829,286 (GRCm39) |
S94P |
probably damaging |
Het |
C2cd3 |
A |
G |
7: 100,044,459 (GRCm39) |
D347G |
possibly damaging |
Het |
Cad |
T |
C |
5: 31,219,018 (GRCm39) |
V613A |
possibly damaging |
Het |
Ccdc47 |
T |
C |
11: 106,093,667 (GRCm39) |
H6R |
probably benign |
Het |
Celsr3 |
A |
G |
9: 108,714,338 (GRCm39) |
T1956A |
probably benign |
Het |
Cep128 |
T |
A |
12: 90,986,118 (GRCm39) |
D1006V |
probably damaging |
Het |
Cog3 |
T |
C |
14: 75,984,641 (GRCm39) |
|
probably null |
Het |
Csmd1 |
C |
T |
8: 15,967,405 (GRCm39) |
V3153M |
probably damaging |
Het |
Ctnna2 |
T |
C |
6: 77,630,127 (GRCm39) |
E122G |
possibly damaging |
Het |
Cts8 |
T |
A |
13: 61,398,772 (GRCm39) |
I245F |
probably damaging |
Het |
Ddx27 |
T |
A |
2: 166,868,166 (GRCm39) |
V333E |
probably damaging |
Het |
Dmpk |
A |
G |
7: 18,821,579 (GRCm39) |
Y279C |
probably damaging |
Het |
Dpagt1 |
A |
G |
9: 44,239,292 (GRCm39) |
I111V |
probably benign |
Het |
Dvl2 |
C |
A |
11: 69,899,695 (GRCm39) |
P546T |
possibly damaging |
Het |
Fat4 |
G |
T |
3: 38,946,089 (GRCm39) |
A1661S |
probably benign |
Het |
Gcm1 |
A |
G |
9: 77,971,734 (GRCm39) |
N225S |
probably damaging |
Het |
Gcnt2 |
A |
T |
13: 41,072,082 (GRCm39) |
M242L |
probably benign |
Het |
Golgb1 |
A |
G |
16: 36,715,211 (GRCm39) |
R226G |
probably damaging |
Het |
Grik2 |
A |
G |
10: 49,116,868 (GRCm39) |
L631P |
probably damaging |
Het |
Hapln3 |
T |
C |
7: 78,771,484 (GRCm39) |
D135G |
probably benign |
Het |
Il31ra |
C |
A |
13: 112,666,885 (GRCm39) |
V398F |
probably damaging |
Het |
Ipp |
G |
T |
4: 116,381,446 (GRCm39) |
R315L |
possibly damaging |
Het |
Kcmf1 |
A |
G |
6: 72,838,830 (GRCm39) |
L32P |
probably damaging |
Het |
Klf17 |
T |
A |
4: 117,617,805 (GRCm39) |
Q184L |
possibly damaging |
Het |
Lrp2 |
C |
T |
2: 69,262,328 (GRCm39) |
V4442I |
probably benign |
Het |
Lrrfip2 |
A |
T |
9: 111,051,278 (GRCm39) |
E293D |
probably damaging |
Het |
Oit3 |
A |
G |
10: 59,274,713 (GRCm39) |
I29T |
probably damaging |
Het |
Or1a1 |
G |
A |
11: 74,086,901 (GRCm39) |
D191N |
probably benign |
Het |
Or1j21 |
T |
C |
2: 36,683,574 (GRCm39) |
C109R |
possibly damaging |
Het |
Or51h1 |
T |
C |
7: 102,308,688 (GRCm39) |
V220A |
probably benign |
Het |
Plb1 |
T |
A |
5: 32,485,373 (GRCm39) |
M842K |
possibly damaging |
Het |
Ppt1 |
T |
C |
4: 122,730,100 (GRCm39) |
C18R |
probably benign |
Het |
Pstpip2 |
T |
C |
18: 77,959,477 (GRCm39) |
Y191H |
probably damaging |
Het |
Ryr1 |
C |
T |
7: 28,774,373 (GRCm39) |
V2361I |
probably damaging |
Het |
Serpinb11 |
A |
G |
1: 107,305,338 (GRCm39) |
N238S |
probably benign |
Het |
Skor2 |
A |
T |
18: 76,946,973 (GRCm39) |
K232* |
probably null |
Het |
Slc13a5 |
A |
T |
11: 72,148,214 (GRCm39) |
W231R |
probably damaging |
Het |
Svs5 |
A |
T |
2: 164,175,313 (GRCm39) |
E55V |
probably benign |
Het |
Tfcp2 |
A |
T |
15: 100,423,481 (GRCm39) |
W142R |
probably damaging |
Het |
Trpc2 |
A |
T |
7: 101,744,441 (GRCm39) |
I738F |
possibly damaging |
Het |
Vmn2r61 |
T |
A |
7: 41,916,067 (GRCm39) |
S227T |
possibly damaging |
Het |
Zfhx4 |
A |
G |
3: 5,464,386 (GRCm39) |
T1540A |
probably damaging |
Het |
Zfp616 |
A |
G |
11: 73,962,561 (GRCm39) |
T74A |
probably benign |
Het |
|
Other mutations in Gpr63 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01576:Gpr63
|
APN |
4 |
25,008,445 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01673:Gpr63
|
APN |
4 |
25,008,014 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01861:Gpr63
|
APN |
4 |
25,008,545 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02082:Gpr63
|
APN |
4 |
25,008,564 (GRCm39) |
utr 3 prime |
probably benign |
|
R0003:Gpr63
|
UTSW |
4 |
25,007,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R0554:Gpr63
|
UTSW |
4 |
25,007,447 (GRCm39) |
missense |
probably benign |
|
R0729:Gpr63
|
UTSW |
4 |
25,007,480 (GRCm39) |
missense |
probably benign |
0.02 |
R1506:Gpr63
|
UTSW |
4 |
25,008,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R3694:Gpr63
|
UTSW |
4 |
25,007,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R4021:Gpr63
|
UTSW |
4 |
25,008,470 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4807:Gpr63
|
UTSW |
4 |
25,007,446 (GRCm39) |
missense |
probably benign |
|
R4967:Gpr63
|
UTSW |
4 |
25,008,368 (GRCm39) |
nonsense |
probably null |
|
R5047:Gpr63
|
UTSW |
4 |
25,008,202 (GRCm39) |
missense |
probably benign |
0.44 |
R5325:Gpr63
|
UTSW |
4 |
25,007,294 (GRCm39) |
missense |
probably benign |
0.00 |
R5382:Gpr63
|
UTSW |
4 |
25,007,952 (GRCm39) |
missense |
probably benign |
|
R7047:Gpr63
|
UTSW |
4 |
25,007,320 (GRCm39) |
missense |
probably benign |
0.00 |
R7216:Gpr63
|
UTSW |
4 |
25,008,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8317:Gpr63
|
UTSW |
4 |
25,008,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R8387:Gpr63
|
UTSW |
4 |
25,008,301 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8989:Gpr63
|
UTSW |
4 |
25,007,357 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9324:Gpr63
|
UTSW |
4 |
25,008,432 (GRCm39) |
missense |
possibly damaging |
0.64 |
|