Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss1 |
A |
T |
2: 150,466,792 (GRCm39) |
|
probably benign |
Het |
Akr1c21 |
A |
T |
13: 4,630,300 (GRCm39) |
N198Y |
probably damaging |
Het |
Anapc11 |
A |
T |
11: 120,490,102 (GRCm39) |
K6I |
probably benign |
Het |
Angel1 |
G |
A |
12: 86,752,060 (GRCm39) |
L554F |
probably benign |
Het |
Arhgap11a |
A |
T |
2: 113,663,320 (GRCm39) |
*988K |
probably null |
Het |
Arnt |
T |
A |
3: 95,402,631 (GRCm39) |
|
probably null |
Het |
Atp1a3 |
T |
A |
7: 24,689,901 (GRCm39) |
D519V |
possibly damaging |
Het |
Bdp1 |
C |
A |
13: 100,187,861 (GRCm39) |
A1575S |
probably benign |
Het |
Bglap |
G |
A |
3: 88,291,715 (GRCm39) |
T3I |
unknown |
Het |
Brca2 |
C |
T |
5: 150,490,500 (GRCm39) |
P3054L |
probably damaging |
Het |
Btn2a2 |
C |
A |
13: 23,662,976 (GRCm39) |
E316* |
probably null |
Het |
C1qtnf9 |
C |
T |
14: 61,017,388 (GRCm39) |
T306I |
probably benign |
Het |
Caprin2 |
T |
C |
6: 148,744,360 (GRCm39) |
T1022A |
probably damaging |
Het |
Cd109 |
T |
C |
9: 78,598,581 (GRCm39) |
Y940H |
probably damaging |
Het |
Cd300ld |
A |
G |
11: 114,875,076 (GRCm39) |
L186S |
probably benign |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Chd6 |
A |
T |
2: 160,807,618 (GRCm39) |
S1865R |
probably benign |
Het |
Chrna2 |
T |
C |
14: 66,386,889 (GRCm39) |
V345A |
probably benign |
Het |
Dnah1 |
T |
G |
14: 31,014,597 (GRCm39) |
E1756A |
probably benign |
Het |
Dnah3 |
C |
T |
7: 119,564,720 (GRCm39) |
A2637T |
probably benign |
Het |
Ern2 |
A |
G |
7: 121,782,122 (GRCm39) |
F80S |
probably damaging |
Het |
Ero1b |
A |
G |
13: 12,619,322 (GRCm39) |
I439V |
possibly damaging |
Het |
Eva1a |
T |
G |
6: 82,048,211 (GRCm39) |
S30A |
probably benign |
Het |
Fer1l4 |
A |
G |
2: 155,887,648 (GRCm39) |
L516P |
probably benign |
Het |
Garin2 |
T |
A |
12: 78,780,989 (GRCm39) |
|
probably benign |
Het |
Hexim2 |
T |
C |
11: 103,029,103 (GRCm39) |
S52P |
probably damaging |
Het |
Hoxb9 |
A |
T |
11: 96,165,554 (GRCm39) |
M208L |
possibly damaging |
Het |
Lbr |
A |
G |
1: 181,659,778 (GRCm39) |
V139A |
probably benign |
Het |
Lcn10 |
G |
A |
2: 25,574,032 (GRCm39) |
|
probably benign |
Het |
Letm2 |
A |
G |
8: 26,076,789 (GRCm39) |
I271T |
probably damaging |
Het |
Lrrc34 |
T |
C |
3: 30,685,441 (GRCm39) |
S303G |
possibly damaging |
Het |
Matn2 |
C |
A |
15: 34,388,885 (GRCm39) |
A325D |
probably benign |
Het |
Mboat4 |
T |
C |
8: 34,582,258 (GRCm39) |
L4P |
probably damaging |
Het |
Mmp1a |
T |
A |
9: 7,464,301 (GRCm39) |
|
probably benign |
Het |
Naip2 |
T |
A |
13: 100,325,685 (GRCm39) |
R74S |
probably benign |
Het |
Neb |
G |
T |
2: 52,133,862 (GRCm39) |
Q3374K |
probably damaging |
Het |
Nup210l |
A |
G |
3: 90,044,157 (GRCm39) |
E486G |
possibly damaging |
Het |
Or4b13 |
A |
G |
2: 90,082,699 (GRCm39) |
I211T |
possibly damaging |
Het |
Or4k51 |
A |
C |
2: 111,584,699 (GRCm39) |
Y35S |
probably damaging |
Het |
Or5m12 |
A |
G |
2: 85,735,293 (GRCm39) |
V35A |
probably benign |
Het |
Or6c69 |
A |
T |
10: 129,747,200 (GRCm39) |
|
probably benign |
Het |
Pde8a |
A |
C |
7: 80,976,090 (GRCm39) |
N677H |
probably damaging |
Het |
Plag1 |
G |
A |
4: 3,903,812 (GRCm39) |
Q460* |
probably null |
Het |
Podnl1 |
A |
G |
8: 84,858,824 (GRCm39) |
T550A |
probably benign |
Het |
Ptpn22 |
A |
G |
3: 103,781,382 (GRCm39) |
|
probably benign |
Het |
Pycr3 |
A |
T |
15: 75,790,565 (GRCm39) |
I98N |
probably damaging |
Het |
Rtn4r |
A |
G |
16: 17,969,052 (GRCm39) |
Y160C |
probably damaging |
Het |
Slc27a4 |
A |
G |
2: 29,701,238 (GRCm39) |
N343S |
probably benign |
Het |
Slc2a4 |
A |
G |
11: 69,836,940 (GRCm39) |
Y43H |
probably damaging |
Het |
Sorbs1 |
A |
T |
19: 40,365,348 (GRCm39) |
L145Q |
probably damaging |
Het |
Sugp2 |
G |
T |
8: 70,696,449 (GRCm39) |
G474V |
probably damaging |
Het |
Syt3 |
C |
T |
7: 44,035,447 (GRCm39) |
S18L |
possibly damaging |
Het |
Tacc1 |
T |
C |
8: 25,691,159 (GRCm39) |
E48G |
probably damaging |
Het |
Tdrd6 |
A |
G |
17: 43,931,337 (GRCm39) |
V2083A |
probably benign |
Het |
Thra |
A |
T |
11: 98,655,185 (GRCm39) |
H355L |
probably benign |
Het |
Tmem35b |
C |
T |
4: 127,019,981 (GRCm39) |
Q34* |
probably null |
Het |
Unk |
G |
T |
11: 115,947,017 (GRCm39) |
G537V |
probably damaging |
Het |
Usp32 |
T |
A |
11: 84,974,632 (GRCm39) |
D92V |
probably damaging |
Het |
Vmn1r209 |
G |
T |
13: 22,990,290 (GRCm39) |
Y133* |
probably null |
Het |
Vmn1r42 |
A |
G |
6: 89,821,630 (GRCm39) |
V313A |
possibly damaging |
Het |
Vnn1 |
A |
G |
10: 23,780,520 (GRCm39) |
I503V |
probably benign |
Het |
Vwa2 |
G |
A |
19: 56,886,361 (GRCm39) |
G143R |
possibly damaging |
Het |
|
Other mutations in Speer2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00693:Speer2
|
APN |
16 |
69,657,406 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01115:Speer2
|
APN |
16 |
69,658,539 (GRCm39) |
nonsense |
probably null |
|
IGL01694:Speer2
|
APN |
16 |
69,655,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01694:Speer2
|
APN |
16 |
69,655,000 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03024:Speer2
|
APN |
16 |
69,655,003 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03062:Speer2
|
APN |
16 |
69,654,865 (GRCm39) |
missense |
probably damaging |
0.96 |
R0054:Speer2
|
UTSW |
16 |
69,655,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R1248:Speer2
|
UTSW |
16 |
69,653,955 (GRCm39) |
splice site |
probably null |
|
R1952:Speer2
|
UTSW |
16 |
69,654,052 (GRCm39) |
missense |
probably damaging |
0.96 |
R1993:Speer2
|
UTSW |
16 |
69,654,965 (GRCm39) |
missense |
probably benign |
0.01 |
R1995:Speer2
|
UTSW |
16 |
69,654,965 (GRCm39) |
missense |
probably benign |
0.01 |
R2063:Speer2
|
UTSW |
16 |
69,657,385 (GRCm39) |
missense |
probably benign |
0.02 |
R2155:Speer2
|
UTSW |
16 |
69,657,485 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2216:Speer2
|
UTSW |
16 |
69,655,730 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4547:Speer2
|
UTSW |
16 |
69,655,737 (GRCm39) |
missense |
probably damaging |
0.98 |
R4548:Speer2
|
UTSW |
16 |
69,655,737 (GRCm39) |
missense |
probably damaging |
0.98 |
R4625:Speer2
|
UTSW |
16 |
69,655,642 (GRCm39) |
nonsense |
probably null |
|
R4692:Speer2
|
UTSW |
16 |
69,654,860 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4841:Speer2
|
UTSW |
16 |
69,654,988 (GRCm39) |
missense |
probably benign |
0.26 |
R4842:Speer2
|
UTSW |
16 |
69,654,988 (GRCm39) |
missense |
probably benign |
0.26 |
R5035:Speer2
|
UTSW |
16 |
69,654,829 (GRCm39) |
critical splice donor site |
probably null |
|
R5133:Speer2
|
UTSW |
16 |
69,655,708 (GRCm39) |
missense |
probably null |
0.06 |
R5812:Speer2
|
UTSW |
16 |
69,655,783 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6348:Speer2
|
UTSW |
16 |
69,654,895 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6854:Speer2
|
UTSW |
16 |
69,655,775 (GRCm39) |
missense |
probably damaging |
0.96 |
R7446:Speer2
|
UTSW |
16 |
69,654,965 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8068:Speer2
|
UTSW |
16 |
69,657,412 (GRCm39) |
missense |
possibly damaging |
0.84 |
|