Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
T |
3: 59,654,744 (GRCm39) |
T193S |
probably benign |
Het |
Abca7 |
T |
A |
10: 79,844,805 (GRCm39) |
V1509E |
probably damaging |
Het |
Abraxas2 |
A |
G |
7: 132,485,085 (GRCm39) |
D376G |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 75,985,059 (GRCm39) |
T159A |
|
Het |
Ahnak2 |
G |
A |
12: 112,750,656 (GRCm39) |
R89W |
|
Het |
Ajm1 |
T |
G |
2: 25,467,262 (GRCm39) |
D883A |
|
Het |
Arhgef40 |
A |
C |
14: 52,241,165 (GRCm39) |
D1396A |
probably damaging |
Het |
Atp13a5 |
A |
T |
16: 29,066,928 (GRCm39) |
F1060I |
probably damaging |
Het |
Atp6v1c1 |
T |
A |
15: 38,677,789 (GRCm39) |
F105I |
probably damaging |
Het |
Atp9b |
C |
T |
18: 80,809,015 (GRCm39) |
E635K |
|
Het |
Brix1 |
T |
A |
15: 10,479,682 (GRCm39) |
Q124L |
possibly damaging |
Het |
Cep68 |
A |
G |
11: 20,180,418 (GRCm39) |
|
probably benign |
Het |
Cfap46 |
A |
G |
7: 139,195,565 (GRCm39) |
S2208P |
unknown |
Het |
Crisp1 |
T |
A |
17: 40,605,310 (GRCm39) |
K234* |
probably null |
Het |
Cryzl1 |
C |
T |
16: 91,509,092 (GRCm39) |
V70I |
probably benign |
Het |
Cybc1 |
C |
T |
11: 121,119,549 (GRCm39) |
|
probably benign |
Het |
Dnah7b |
T |
C |
1: 46,230,953 (GRCm39) |
Y1404H |
probably damaging |
Het |
Dot1l |
A |
G |
10: 80,607,033 (GRCm39) |
H109R |
possibly damaging |
Het |
E330034G19Rik |
A |
C |
14: 24,359,576 (GRCm39) |
H329P |
unknown |
Het |
Erbb4 |
A |
T |
1: 68,114,627 (GRCm39) |
L939Q |
probably damaging |
Het |
Fst |
A |
T |
13: 114,592,364 (GRCm39) |
C118S |
probably damaging |
Het |
Gfra3 |
A |
G |
18: 34,844,189 (GRCm39) |
V117A |
possibly damaging |
Het |
Gldc |
C |
G |
19: 30,078,212 (GRCm39) |
M928I |
probably benign |
Het |
Greb1 |
A |
G |
12: 16,738,520 (GRCm39) |
M1481T |
probably benign |
Het |
Hecw2 |
G |
A |
1: 53,930,305 (GRCm39) |
R1045C |
probably damaging |
Het |
Hexb |
C |
T |
13: 97,330,762 (GRCm39) |
V84I |
probably benign |
Het |
Hpse |
T |
C |
5: 100,843,452 (GRCm39) |
E240G |
probably benign |
Het |
Hspa12a |
T |
C |
19: 58,793,895 (GRCm39) |
D322G |
possibly damaging |
Het |
Hspa9 |
A |
T |
18: 35,081,157 (GRCm39) |
|
probably null |
Het |
Kif9 |
A |
G |
9: 110,353,998 (GRCm39) |
K790R |
probably damaging |
Het |
Klc2 |
C |
T |
19: 5,160,394 (GRCm39) |
|
probably null |
Het |
Ldha |
C |
G |
7: 46,499,702 (GRCm39) |
N144K |
probably benign |
Het |
Mical2 |
A |
G |
7: 111,980,403 (GRCm39) |
T126A |
probably benign |
Het |
Mrpl15 |
A |
T |
1: 4,852,807 (GRCm39) |
V137D |
probably damaging |
Het |
Muc16 |
G |
A |
9: 18,557,365 (GRCm39) |
T2976I |
unknown |
Het |
Mybpc2 |
A |
T |
7: 44,161,965 (GRCm39) |
V495D |
probably damaging |
Het |
Or10a5 |
A |
G |
7: 106,635,889 (GRCm39) |
N176D |
probably benign |
Het |
Or52ab2 |
A |
G |
7: 102,970,212 (GRCm39) |
K198R |
|
Het |
Or6c203 |
A |
T |
10: 129,010,715 (GRCm39) |
Y58* |
probably null |
Het |
Pcnt |
G |
A |
10: 76,218,008 (GRCm39) |
T2089I |
probably benign |
Het |
Pdzd7 |
T |
C |
19: 45,021,512 (GRCm39) |
D563G |
probably damaging |
Het |
Phlpp1 |
T |
G |
1: 106,278,333 (GRCm39) |
L915R |
probably damaging |
Het |
Plekhh2 |
T |
A |
17: 84,829,231 (GRCm39) |
I34N |
probably damaging |
Het |
Pou6f2 |
T |
A |
13: 18,553,083 (GRCm39) |
T84S |
|
Het |
Prxl2c |
G |
A |
13: 64,445,114 (GRCm39) |
Q170* |
probably null |
Het |
Ptprq |
A |
G |
10: 107,422,556 (GRCm39) |
V1612A |
possibly damaging |
Het |
Pvrig-ps |
T |
G |
5: 138,340,410 (GRCm39) |
|
probably benign |
Het |
Rasl10b |
A |
T |
11: 83,303,502 (GRCm39) |
I20F |
probably damaging |
Het |
Rimbp3 |
T |
A |
16: 17,026,870 (GRCm39) |
V98E |
probably damaging |
Het |
Rims2 |
T |
C |
15: 39,300,758 (GRCm39) |
I355T |
possibly damaging |
Het |
Slc1a2 |
A |
G |
2: 102,566,360 (GRCm39) |
H30R |
probably benign |
Het |
Slc28a1 |
G |
A |
7: 80,810,794 (GRCm39) |
V389M |
possibly damaging |
Het |
Slc7a13 |
T |
C |
4: 19,819,189 (GRCm39) |
S130P |
probably benign |
Het |
Sp140 |
TTTTTTTT |
TTTTTTTTTTTTT |
1: 85,572,295 (GRCm39) |
|
probably benign |
Het |
Spag17 |
T |
A |
3: 100,032,751 (GRCm39) |
H2320Q |
possibly damaging |
Het |
Speer4a1 |
T |
C |
5: 26,241,793 (GRCm39) |
E111G |
possibly damaging |
Het |
Ss18l1 |
T |
C |
2: 179,709,131 (GRCm39) |
Y397H |
unknown |
Het |
Tbck |
T |
C |
3: 132,543,818 (GRCm39) |
S890P |
probably damaging |
Het |
Tcp11 |
T |
C |
17: 28,299,204 (GRCm39) |
E17G |
probably benign |
Het |
Tesk2 |
C |
T |
4: 116,659,484 (GRCm39) |
R315C |
probably benign |
Het |
Tln1 |
T |
C |
4: 43,556,383 (GRCm39) |
N45S |
probably benign |
Het |
Trim10 |
C |
T |
17: 37,180,846 (GRCm39) |
P26S |
probably damaging |
Het |
Vmac |
C |
A |
17: 57,022,573 (GRCm39) |
G146C |
probably damaging |
Het |
Vmn1r14 |
G |
A |
6: 57,211,017 (GRCm39) |
M198I |
probably damaging |
Het |
Vmn1r78 |
G |
A |
7: 11,887,118 (GRCm39) |
C243Y |
probably damaging |
Het |
Wasf3 |
C |
T |
5: 146,403,672 (GRCm39) |
Q261* |
probably null |
Het |
Ybx2 |
A |
G |
11: 69,827,063 (GRCm39) |
K88R |
probably benign |
Het |
Zfhx4 |
G |
A |
3: 5,463,949 (GRCm39) |
R1394H |
probably damaging |
Het |
Zfp871 |
T |
C |
17: 32,993,901 (GRCm39) |
T425A |
probably benign |
Het |
Zfy2 |
C |
T |
Y: 2,106,600 (GRCm39) |
S678N |
possibly damaging |
Het |
Zswim4 |
T |
C |
8: 84,949,945 (GRCm39) |
E650G |
possibly damaging |
Het |
|
Other mutations in Vmn1r194 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01890:Vmn1r194
|
APN |
13 |
22,428,776 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02140:Vmn1r194
|
APN |
13 |
22,428,706 (GRCm39) |
missense |
probably benign |
0.08 |
R0066:Vmn1r194
|
UTSW |
13 |
22,428,641 (GRCm39) |
missense |
probably benign |
0.33 |
R0066:Vmn1r194
|
UTSW |
13 |
22,428,641 (GRCm39) |
missense |
probably benign |
0.33 |
R0109:Vmn1r194
|
UTSW |
13 |
22,429,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Vmn1r194
|
UTSW |
13 |
22,429,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1276:Vmn1r194
|
UTSW |
13 |
22,429,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R1426:Vmn1r194
|
UTSW |
13 |
22,429,236 (GRCm39) |
missense |
probably damaging |
0.99 |
R1620:Vmn1r194
|
UTSW |
13 |
22,429,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R4593:Vmn1r194
|
UTSW |
13 |
22,428,461 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4844:Vmn1r194
|
UTSW |
13 |
22,429,223 (GRCm39) |
missense |
probably benign |
0.02 |
R5011:Vmn1r194
|
UTSW |
13 |
22,429,058 (GRCm39) |
missense |
probably benign |
0.00 |
R5110:Vmn1r194
|
UTSW |
13 |
22,429,170 (GRCm39) |
missense |
probably benign |
0.07 |
R5588:Vmn1r194
|
UTSW |
13 |
22,428,512 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5810:Vmn1r194
|
UTSW |
13 |
22,428,597 (GRCm39) |
nonsense |
probably null |
|
R6648:Vmn1r194
|
UTSW |
13 |
22,428,694 (GRCm39) |
missense |
probably benign |
0.11 |
R7660:Vmn1r194
|
UTSW |
13 |
22,428,767 (GRCm39) |
missense |
not run |
|
R7663:Vmn1r194
|
UTSW |
13 |
22,428,911 (GRCm39) |
missense |
not run |
|
R7879:Vmn1r194
|
UTSW |
13 |
22,428,772 (GRCm39) |
missense |
probably benign |
0.06 |
R8344:Vmn1r194
|
UTSW |
13 |
22,429,247 (GRCm39) |
missense |
probably benign |
0.01 |
R9245:Vmn1r194
|
UTSW |
13 |
22,428,731 (GRCm39) |
missense |
probably benign |
0.44 |
R9291:Vmn1r194
|
UTSW |
13 |
22,428,875 (GRCm39) |
missense |
probably benign |
0.20 |
R9624:Vmn1r194
|
UTSW |
13 |
22,428,671 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn1r194
|
UTSW |
13 |
22,428,596 (GRCm39) |
missense |
probably benign |
0.08 |
|