Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg3 |
C |
T |
8: 95,763,536 (GRCm39) |
A279V |
probably benign |
Het |
Aggf1 |
G |
A |
13: 95,508,102 (GRCm39) |
P88L |
probably benign |
Het |
Asb18 |
T |
C |
1: 89,896,411 (GRCm39) |
T210A |
probably benign |
Het |
Cd8b1 |
C |
T |
6: 71,303,006 (GRCm39) |
S27L |
possibly damaging |
Het |
Cfap43 |
C |
T |
19: 47,728,236 (GRCm39) |
S1507N |
possibly damaging |
Het |
Col12a1 |
A |
T |
9: 79,547,247 (GRCm39) |
|
probably null |
Het |
Col19a1 |
G |
A |
1: 24,573,190 (GRCm39) |
T194M |
unknown |
Het |
Cpb1 |
T |
A |
3: 20,317,733 (GRCm39) |
T237S |
probably benign |
Het |
Cubn |
G |
A |
2: 13,470,841 (GRCm39) |
T517M |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,106,274 (GRCm39) |
N1769S |
probably benign |
Het |
Dnm1 |
A |
G |
2: 32,225,984 (GRCm39) |
I365T |
probably damaging |
Het |
E2f5 |
T |
A |
3: 14,668,823 (GRCm39) |
D238E |
probably benign |
Het |
Etv6 |
A |
G |
6: 134,210,497 (GRCm39) |
E115G |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Gapvd1 |
C |
T |
2: 34,618,747 (GRCm39) |
V209I |
probably damaging |
Het |
Gbp8 |
G |
A |
5: 105,198,928 (GRCm39) |
|
probably benign |
Het |
Gprc6a |
T |
C |
10: 51,504,639 (GRCm39) |
I68M |
probably benign |
Het |
Grb14 |
T |
C |
2: 64,783,966 (GRCm39) |
N54D |
probably damaging |
Het |
Gucy2g |
A |
T |
19: 55,226,269 (GRCm39) |
F216I |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,820,225 (GRCm39) |
L2849Q |
probably damaging |
Het |
Hsd17b4 |
G |
T |
18: 50,261,381 (GRCm39) |
|
probably benign |
Het |
Igkv9-129 |
T |
A |
6: 67,816,784 (GRCm39) |
M3K |
probably damaging |
Het |
Iqcd |
A |
T |
5: 120,740,485 (GRCm39) |
E272V |
probably damaging |
Het |
Itih2 |
A |
T |
2: 10,111,548 (GRCm39) |
Y463* |
probably null |
Het |
Kcna10 |
G |
A |
3: 107,102,781 (GRCm39) |
E471K |
possibly damaging |
Het |
Klf3 |
A |
T |
5: 64,986,347 (GRCm39) |
E294V |
possibly damaging |
Het |
Lancl1 |
A |
T |
1: 67,060,015 (GRCm39) |
|
probably null |
Het |
Ldaf1 |
T |
G |
7: 119,714,714 (GRCm39) |
F68V |
probably damaging |
Het |
Lrig3 |
T |
C |
10: 125,846,877 (GRCm39) |
F882L |
probably benign |
Het |
Man2c1 |
A |
G |
9: 57,046,367 (GRCm39) |
N474S |
probably damaging |
Het |
Map4k3 |
A |
G |
17: 80,922,444 (GRCm39) |
|
probably null |
Het |
Mast1 |
C |
A |
8: 85,647,520 (GRCm39) |
W572C |
probably damaging |
Het |
Mbd4 |
T |
A |
6: 115,826,076 (GRCm39) |
Q305L |
possibly damaging |
Het |
Mbl2 |
T |
A |
19: 30,216,916 (GRCm39) |
S243T |
probably benign |
Het |
Mcph1 |
C |
T |
8: 18,682,557 (GRCm39) |
P565S |
probably benign |
Het |
Mfsd1 |
G |
C |
3: 67,507,943 (GRCm39) |
V435L |
probably benign |
Het |
Mycbp2 |
C |
T |
14: 103,360,881 (GRCm39) |
G1183D |
probably damaging |
Het |
Myof |
A |
G |
19: 37,911,426 (GRCm39) |
S1502P |
probably damaging |
Het |
Noa1 |
A |
T |
5: 77,454,219 (GRCm39) |
S474T |
probably benign |
Het |
Nrde2 |
A |
G |
12: 100,096,843 (GRCm39) |
Y986H |
probably benign |
Het |
Oca2 |
G |
T |
7: 56,064,182 (GRCm39) |
V726F |
possibly damaging |
Het |
Or2ag13 |
T |
A |
7: 106,472,580 (GRCm39) |
S291C |
probably damaging |
Het |
Or7a41 |
A |
T |
10: 78,871,244 (GRCm39) |
M205L |
probably benign |
Het |
Pip5k1a |
A |
G |
3: 94,975,370 (GRCm39) |
|
probably null |
Het |
Plekhn1 |
A |
T |
4: 156,309,730 (GRCm39) |
|
probably null |
Het |
Sec61a2 |
T |
C |
2: 5,887,670 (GRCm39) |
D104G |
probably benign |
Het |
Skic3 |
A |
T |
13: 76,303,784 (GRCm39) |
Y1234F |
probably damaging |
Het |
Slc25a36 |
T |
C |
9: 96,967,171 (GRCm39) |
T131A |
probably benign |
Het |
Slc5a11 |
A |
T |
7: 122,857,700 (GRCm39) |
D263V |
probably damaging |
Het |
Sorbs1 |
T |
C |
19: 40,384,189 (GRCm39) |
I35V |
probably benign |
Het |
Tbc1d1 |
T |
C |
5: 64,331,013 (GRCm39) |
V64A |
possibly damaging |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Vmn1r20 |
A |
G |
6: 57,409,042 (GRCm39) |
M123V |
probably benign |
Het |
Zwint |
T |
C |
10: 72,492,095 (GRCm39) |
L59P |
probably damaging |
Het |
|
Other mutations in Speer3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01663:Speer3
|
APN |
5 |
13,843,236 (GRCm39) |
nonsense |
probably null |
|
IGL02730:Speer3
|
APN |
5 |
13,843,285 (GRCm39) |
missense |
probably benign |
|
IGL03192:Speer3
|
APN |
5 |
13,841,702 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03301:Speer3
|
APN |
5 |
13,845,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Speer3
|
UTSW |
5 |
13,846,335 (GRCm39) |
missense |
probably benign |
|
R3028:Speer3
|
UTSW |
5 |
13,845,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R4091:Speer3
|
UTSW |
5 |
13,846,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4092:Speer3
|
UTSW |
5 |
13,846,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4368:Speer3
|
UTSW |
5 |
13,846,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4369:Speer3
|
UTSW |
5 |
13,846,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4450:Speer3
|
UTSW |
5 |
13,846,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4509:Speer3
|
UTSW |
5 |
13,846,368 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4594:Speer3
|
UTSW |
5 |
13,846,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4702:Speer3
|
UTSW |
5 |
13,846,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5096:Speer3
|
UTSW |
5 |
13,846,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5508:Speer3
|
UTSW |
5 |
13,844,678 (GRCm39) |
missense |
probably damaging |
0.97 |
R5583:Speer3
|
UTSW |
5 |
13,844,782 (GRCm39) |
critical splice donor site |
probably null |
|
R6061:Speer3
|
UTSW |
5 |
13,844,705 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6337:Speer3
|
UTSW |
5 |
13,843,369 (GRCm39) |
missense |
probably damaging |
0.96 |
R6518:Speer3
|
UTSW |
5 |
13,845,462 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7503:Speer3
|
UTSW |
5 |
13,843,348 (GRCm39) |
missense |
probably benign |
0.30 |
R9456:Speer3
|
UTSW |
5 |
13,846,368 (GRCm39) |
missense |
|
|
|