Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 137,772,048 (GRCm39) |
E412D |
probably benign |
Het |
Aak1 |
T |
A |
6: 86,933,274 (GRCm39) |
V415D |
probably damaging |
Het |
Ache |
A |
C |
5: 137,289,185 (GRCm39) |
D297A |
probably damaging |
Het |
Armc9 |
T |
C |
1: 86,084,687 (GRCm39) |
I4T |
possibly damaging |
Het |
Atp8b2 |
T |
A |
3: 89,851,492 (GRCm39) |
Y925F |
|
Het |
Avpr1b |
T |
C |
1: 131,528,029 (GRCm39) |
L184P |
probably damaging |
Het |
Cabin1 |
G |
A |
10: 75,581,069 (GRCm39) |
P419L |
probably damaging |
Het |
Ccdc88c |
T |
C |
12: 100,884,597 (GRCm39) |
S1578G |
probably benign |
Het |
Ccnd2 |
A |
T |
6: 127,127,617 (GRCm39) |
C40* |
probably null |
Het |
Col6a3 |
A |
T |
1: 90,744,155 (GRCm39) |
I471N |
probably damaging |
Het |
Cp |
A |
G |
3: 20,046,671 (GRCm39) |
|
probably null |
Het |
Cyfip2 |
C |
T |
11: 46,091,668 (GRCm39) |
R1084Q |
probably damaging |
Het |
Diaph1 |
A |
G |
18: 38,029,412 (GRCm39) |
|
probably null |
Het |
Dnah6 |
T |
C |
6: 73,012,330 (GRCm39) |
N3713S |
possibly damaging |
Het |
Dot1l |
G |
T |
10: 80,621,438 (GRCm39) |
R633L |
possibly damaging |
Het |
Ehmt1 |
A |
T |
2: 24,715,030 (GRCm39) |
M809K |
probably damaging |
Het |
Fcgbp |
C |
A |
7: 27,803,436 (GRCm39) |
A1680E |
possibly damaging |
Het |
Flt1 |
A |
G |
5: 147,515,207 (GRCm39) |
F1072L |
probably damaging |
Het |
Gm19410 |
G |
T |
8: 36,248,810 (GRCm39) |
A549S |
probably damaging |
Het |
Gm57859 |
C |
T |
11: 113,583,229 (GRCm39) |
Q519* |
probably null |
Het |
Gnat1 |
A |
T |
9: 107,553,511 (GRCm39) |
I249N |
|
Het |
Gp2 |
T |
C |
7: 119,053,433 (GRCm39) |
Y176C |
probably damaging |
Het |
Gpc2 |
G |
T |
5: 138,277,248 (GRCm39) |
Q60K |
probably benign |
Het |
Gpsm2 |
T |
A |
3: 108,610,397 (GRCm39) |
E21V |
probably damaging |
Het |
Igkv4-80 |
T |
A |
6: 68,993,793 (GRCm39) |
M33L |
probably benign |
Het |
Il20ra |
C |
A |
10: 19,618,751 (GRCm39) |
H66Q |
probably benign |
Het |
Kap |
C |
T |
6: 133,828,950 (GRCm39) |
D61N |
probably benign |
Het |
Magi3 |
C |
T |
3: 103,922,473 (GRCm39) |
A1415T |
probably benign |
Het |
Mpp7 |
A |
T |
18: 7,461,692 (GRCm39) |
Y60* |
probably null |
Het |
Neil1 |
T |
A |
9: 57,051,098 (GRCm39) |
R294* |
probably null |
Het |
Nkx6-3 |
A |
G |
8: 23,643,778 (GRCm39) |
S60G |
probably benign |
Het |
Noc2l |
T |
A |
4: 156,326,130 (GRCm39) |
S406T |
possibly damaging |
Het |
Or11m3 |
T |
C |
15: 98,396,247 (GRCm39) |
V298A |
possibly damaging |
Het |
Or14j2 |
A |
G |
17: 37,885,825 (GRCm39) |
I163T |
probably benign |
Het |
Or2h2c |
A |
G |
17: 37,422,205 (GRCm39) |
V223A |
probably damaging |
Het |
Or2t46 |
T |
C |
11: 58,472,104 (GRCm39) |
C145R |
probably benign |
Het |
Or51ac3 |
T |
G |
7: 103,214,049 (GRCm39) |
I146L |
probably benign |
Het |
Or5p81 |
T |
C |
7: 108,266,626 (GRCm39) |
M1T |
probably null |
Het |
Paqr4 |
A |
G |
17: 23,958,939 (GRCm39) |
F21L |
probably damaging |
Het |
Pcdha9 |
A |
G |
18: 37,131,527 (GRCm39) |
T199A |
probably benign |
Het |
Pcdhgb7 |
T |
C |
18: 37,884,917 (GRCm39) |
L29P |
probably benign |
Het |
Pfkl |
G |
A |
10: 77,831,172 (GRCm39) |
A323V |
probably damaging |
Het |
Pik3r4 |
C |
A |
9: 105,528,041 (GRCm39) |
P465T |
probably damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,274,189 (GRCm39) |
S307P |
probably damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,278,659 (GRCm39) |
Y191H |
probably damaging |
Het |
Plod3 |
G |
A |
5: 137,023,036 (GRCm39) |
V613I |
probably benign |
Het |
Prr23a2 |
C |
T |
9: 98,738,921 (GRCm39) |
T93I |
probably damaging |
Het |
Ptk6 |
T |
A |
2: 180,840,206 (GRCm39) |
M267L |
possibly damaging |
Het |
Rabl6 |
C |
T |
2: 25,492,432 (GRCm39) |
|
probably null |
Het |
Ralgapa2 |
T |
C |
2: 146,254,058 (GRCm39) |
H787R |
probably benign |
Het |
Rfx8 |
T |
G |
1: 39,724,669 (GRCm39) |
M231L |
probably benign |
Het |
Rnf126 |
A |
T |
10: 79,597,465 (GRCm39) |
I149N |
probably damaging |
Het |
Smpd4 |
A |
G |
16: 17,459,451 (GRCm39) |
I625V |
probably benign |
Het |
Tcf7l1 |
A |
G |
6: 72,765,740 (GRCm39) |
S66P |
probably damaging |
Het |
Tsc22d1 |
G |
A |
14: 76,743,899 (GRCm39) |
V1007M |
probably damaging |
Het |
Tspoap1 |
C |
T |
11: 87,665,535 (GRCm39) |
R758C |
probably damaging |
Het |
Zfp532 |
G |
A |
18: 65,818,714 (GRCm39) |
V857I |
probably benign |
Het |
Zfyve9 |
T |
C |
4: 108,501,538 (GRCm39) |
T593A |
probably benign |
Het |
|
Other mutations in Vmn1r210 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00938:Vmn1r210
|
APN |
13 |
23,011,538 (GRCm39) |
nonsense |
probably null |
|
IGL01541:Vmn1r210
|
APN |
13 |
23,011,778 (GRCm39) |
missense |
probably benign |
|
IGL01610:Vmn1r210
|
APN |
13 |
23,011,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01632:Vmn1r210
|
APN |
13 |
23,011,366 (GRCm39) |
makesense |
probably null |
|
IGL03268:Vmn1r210
|
APN |
13 |
23,011,405 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03340:Vmn1r210
|
APN |
13 |
23,011,644 (GRCm39) |
missense |
probably benign |
0.23 |
R0227:Vmn1r210
|
UTSW |
13 |
23,011,561 (GRCm39) |
missense |
probably benign |
0.02 |
R0629:Vmn1r210
|
UTSW |
13 |
23,012,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Vmn1r210
|
UTSW |
13 |
23,011,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R4125:Vmn1r210
|
UTSW |
13 |
23,011,779 (GRCm39) |
missense |
probably benign |
0.00 |
R4132:Vmn1r210
|
UTSW |
13 |
23,011,819 (GRCm39) |
missense |
probably benign |
0.00 |
R4773:Vmn1r210
|
UTSW |
13 |
23,011,374 (GRCm39) |
missense |
probably benign |
0.00 |
R5653:Vmn1r210
|
UTSW |
13 |
23,011,378 (GRCm39) |
nonsense |
probably null |
|
R6128:Vmn1r210
|
UTSW |
13 |
23,012,277 (GRCm39) |
nonsense |
probably null |
|
R6452:Vmn1r210
|
UTSW |
13 |
23,011,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R6501:Vmn1r210
|
UTSW |
13 |
23,011,705 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6864:Vmn1r210
|
UTSW |
13 |
23,011,713 (GRCm39) |
missense |
probably benign |
0.06 |
R7623:Vmn1r210
|
UTSW |
13 |
23,011,405 (GRCm39) |
missense |
probably benign |
0.40 |
R7991:Vmn1r210
|
UTSW |
13 |
23,011,684 (GRCm39) |
missense |
probably benign |
0.01 |
R9244:Vmn1r210
|
UTSW |
13 |
23,012,089 (GRCm39) |
missense |
probably benign |
0.02 |
R9538:Vmn1r210
|
UTSW |
13 |
23,011,837 (GRCm39) |
nonsense |
probably null |
|
R9732:Vmn1r210
|
UTSW |
13 |
23,011,379 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9794:Vmn1r210
|
UTSW |
13 |
23,011,432 (GRCm39) |
missense |
probably damaging |
0.97 |
|