Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
A |
T |
10: 28,849,882 (GRCm39) |
Y230* |
probably null |
Het |
9230104M06Rik |
A |
T |
12: 112,963,692 (GRCm39) |
|
probably benign |
Het |
Arhgap20 |
A |
G |
9: 51,697,088 (GRCm39) |
D53G |
probably damaging |
Het |
Arl2 |
T |
C |
19: 6,187,776 (GRCm39) |
T54A |
probably damaging |
Het |
Baz2a |
G |
A |
10: 127,960,762 (GRCm39) |
G1521S |
probably damaging |
Het |
Begain |
A |
G |
12: 108,999,818 (GRCm39) |
S523P |
probably damaging |
Het |
Car10 |
T |
C |
11: 93,075,984 (GRCm39) |
|
probably null |
Het |
Cenpe |
A |
G |
3: 134,922,140 (GRCm39) |
I66V |
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,286,864 (GRCm39) |
V895E |
unknown |
Het |
Coro1b |
T |
C |
19: 4,199,418 (GRCm39) |
Y26H |
probably damaging |
Het |
Crebbp |
T |
C |
16: 3,932,727 (GRCm39) |
E1017G |
possibly damaging |
Het |
Cwf19l2 |
T |
C |
9: 3,428,709 (GRCm39) |
S232P |
probably damaging |
Het |
Cyp7b1 |
T |
A |
3: 18,126,728 (GRCm39) |
I473F |
probably damaging |
Het |
Efcab5 |
A |
T |
11: 77,004,507 (GRCm39) |
I937N |
probably damaging |
Het |
Fam53c |
A |
C |
18: 34,901,743 (GRCm39) |
E220A |
probably damaging |
Het |
Gsn |
A |
G |
2: 35,188,883 (GRCm39) |
Y434C |
probably damaging |
Het |
Igkv2-137 |
T |
C |
6: 67,532,971 (GRCm39) |
S45P |
possibly damaging |
Het |
Katnip |
T |
C |
7: 125,466,841 (GRCm39) |
|
probably null |
Het |
Kif13b |
C |
A |
14: 65,041,024 (GRCm39) |
T1704K |
probably benign |
Het |
Mapk7 |
A |
G |
11: 61,380,068 (GRCm39) |
S697P |
possibly damaging |
Het |
Mrgpra1 |
T |
A |
7: 46,985,446 (GRCm39) |
I78F |
probably damaging |
Het |
N6amt1 |
T |
C |
16: 87,153,854 (GRCm39) |
V97A |
possibly damaging |
Het |
Oas3 |
T |
C |
5: 120,907,420 (GRCm39) |
T406A |
probably benign |
Het |
Or4f61 |
A |
G |
2: 111,923,026 (GRCm39) |
S7P |
probably damaging |
Het |
Or8c17 |
C |
T |
9: 38,179,826 (GRCm39) |
Q6* |
probably null |
Het |
Paxip1 |
T |
C |
5: 27,977,095 (GRCm39) |
|
probably benign |
Het |
Pfn4 |
A |
T |
12: 4,824,486 (GRCm39) |
Y71F |
probably damaging |
Het |
Plin4 |
C |
A |
17: 56,410,762 (GRCm39) |
G1090C |
probably damaging |
Het |
Ptk2b |
C |
T |
14: 66,394,518 (GRCm39) |
G859S |
probably benign |
Het |
Rbl2 |
T |
A |
8: 91,849,047 (GRCm39) |
D1084E |
probably damaging |
Het |
Robo1 |
T |
G |
16: 72,757,090 (GRCm39) |
S350R |
probably damaging |
Het |
Sbno2 |
A |
G |
10: 79,922,161 (GRCm39) |
V4A |
possibly damaging |
Het |
Sh3rf1 |
T |
C |
8: 61,806,888 (GRCm39) |
|
probably null |
Het |
Smgc |
T |
C |
15: 91,738,764 (GRCm39) |
V474A |
possibly damaging |
Het |
Snx13 |
A |
G |
12: 35,136,917 (GRCm39) |
D126G |
possibly damaging |
Het |
Sox9 |
C |
A |
11: 112,673,803 (GRCm39) |
H131Q |
probably benign |
Het |
Spag6 |
T |
C |
2: 18,704,054 (GRCm39) |
I34T |
probably benign |
Het |
Speer2 |
T |
A |
16: 69,654,860 (GRCm39) |
T202S |
possibly damaging |
Het |
Sspo |
T |
A |
6: 48,459,621 (GRCm39) |
C3327S |
probably damaging |
Het |
Vcpip1 |
G |
T |
1: 9,818,299 (GRCm39) |
A28E |
unknown |
Het |
Zfp329 |
T |
C |
7: 12,544,559 (GRCm39) |
K322E |
probably damaging |
Het |
Zfp932 |
G |
A |
5: 110,157,052 (GRCm39) |
G250D |
probably damaging |
Het |
Zscan26 |
A |
G |
13: 21,629,427 (GRCm39) |
C359R |
probably damaging |
Het |
|
Other mutations in Vstm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01597:Vstm5
|
APN |
9 |
15,168,675 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01781:Vstm5
|
APN |
9 |
15,168,968 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02940:Vstm5
|
APN |
9 |
15,168,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R1155:Vstm5
|
UTSW |
9 |
15,168,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Vstm5
|
UTSW |
9 |
15,168,663 (GRCm39) |
missense |
probably benign |
0.13 |
R2368:Vstm5
|
UTSW |
9 |
15,169,027 (GRCm39) |
missense |
probably benign |
0.00 |
R3160:Vstm5
|
UTSW |
9 |
15,168,594 (GRCm39) |
missense |
probably benign |
0.02 |
R3161:Vstm5
|
UTSW |
9 |
15,168,594 (GRCm39) |
missense |
probably benign |
0.02 |
R3162:Vstm5
|
UTSW |
9 |
15,168,594 (GRCm39) |
missense |
probably benign |
0.02 |
R4612:Vstm5
|
UTSW |
9 |
15,168,789 (GRCm39) |
missense |
probably benign |
0.22 |
R4950:Vstm5
|
UTSW |
9 |
15,169,090 (GRCm39) |
splice site |
probably null |
|
R5088:Vstm5
|
UTSW |
9 |
15,168,601 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6351:Vstm5
|
UTSW |
9 |
15,168,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7063:Vstm5
|
UTSW |
9 |
15,150,549 (GRCm39) |
start gained |
probably benign |
|
R7720:Vstm5
|
UTSW |
9 |
15,150,652 (GRCm39) |
missense |
probably benign |
0.08 |
R9300:Vstm5
|
UTSW |
9 |
15,168,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R9491:Vstm5
|
UTSW |
9 |
15,168,586 (GRCm39) |
missense |
probably damaging |
0.99 |
|