Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013D24Rik |
A |
G |
6: 124,333,863 (GRCm39) |
L39P |
probably damaging |
Het |
Abcc1 |
A |
G |
16: 14,211,877 (GRCm39) |
M138V |
probably benign |
Het |
Abl1 |
T |
A |
2: 31,691,739 (GRCm39) |
I1067N |
probably damaging |
Het |
Adam6a |
C |
T |
12: 113,508,194 (GRCm39) |
T189I |
probably benign |
Het |
Ankfy1 |
G |
A |
11: 72,605,310 (GRCm39) |
|
probably null |
Het |
Aplnr |
T |
C |
2: 84,967,310 (GRCm39) |
Y112H |
possibly damaging |
Het |
Arhgap17 |
A |
G |
7: 122,906,217 (GRCm39) |
F313S |
probably damaging |
Het |
Arid1b |
T |
C |
17: 5,046,069 (GRCm39) |
|
probably benign |
Het |
Bcas1 |
G |
C |
2: 170,220,735 (GRCm39) |
P394A |
probably benign |
Het |
Ccdc116 |
A |
G |
16: 16,960,051 (GRCm39) |
S213P |
probably damaging |
Het |
Cdh15 |
T |
C |
8: 123,590,162 (GRCm39) |
V365A |
probably damaging |
Het |
Cenpf |
A |
G |
1: 189,385,242 (GRCm39) |
I2346T |
probably benign |
Het |
Chd7 |
A |
G |
4: 8,785,658 (GRCm39) |
|
probably benign |
Het |
Ezh2 |
A |
C |
6: 47,521,482 (GRCm39) |
N390K |
probably benign |
Het |
Fbxo7 |
C |
A |
10: 85,857,759 (GRCm39) |
|
probably benign |
Het |
Fibin |
A |
G |
2: 110,193,035 (GRCm39) |
Y36H |
probably damaging |
Het |
Gpr37 |
C |
T |
6: 25,688,425 (GRCm39) |
R224H |
possibly damaging |
Het |
Hars2 |
A |
T |
18: 36,923,541 (GRCm39) |
N363I |
probably damaging |
Het |
Ip6k2 |
G |
A |
9: 108,682,847 (GRCm39) |
R319Q |
probably benign |
Het |
Itpr1 |
G |
A |
6: 108,371,316 (GRCm39) |
D1140N |
probably benign |
Het |
Lrig2 |
A |
G |
3: 104,374,511 (GRCm39) |
V190A |
probably benign |
Het |
Ltk |
T |
A |
2: 119,588,429 (GRCm39) |
|
probably benign |
Het |
Morc2a |
C |
A |
11: 3,633,868 (GRCm39) |
T660N |
probably benign |
Het |
Msh3 |
A |
G |
13: 92,490,519 (GRCm39) |
|
probably benign |
Het |
Myo15b |
T |
C |
11: 115,764,318 (GRCm39) |
S1311P |
probably benign |
Het |
Nbeal1 |
A |
T |
1: 60,331,029 (GRCm39) |
I2213L |
probably damaging |
Het |
Or10ag57 |
T |
A |
2: 87,218,187 (GRCm39) |
M46K |
possibly damaging |
Het |
Or5d16 |
A |
G |
2: 87,773,787 (GRCm39) |
Y62H |
probably damaging |
Het |
P2ry12 |
T |
C |
3: 59,125,262 (GRCm39) |
T138A |
probably benign |
Het |
Pirb |
T |
C |
7: 3,720,574 (GRCm39) |
D308G |
probably damaging |
Het |
Pkn3 |
A |
G |
2: 29,973,049 (GRCm39) |
|
probably benign |
Het |
Ripor1 |
T |
A |
8: 106,345,489 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,794,153 (GRCm39) |
T942A |
probably benign |
Het |
Spata31e5 |
A |
T |
1: 28,817,054 (GRCm39) |
V326D |
probably damaging |
Het |
Sptbn5 |
T |
A |
2: 119,895,010 (GRCm39) |
D798V |
possibly damaging |
Het |
Synpo2 |
T |
A |
3: 122,910,799 (GRCm39) |
D282V |
probably damaging |
Het |
Tnik |
T |
C |
3: 28,720,324 (GRCm39) |
F1287L |
probably damaging |
Het |
Tshz1 |
T |
G |
18: 84,032,314 (GRCm39) |
K698T |
probably benign |
Het |
Ttc23l |
A |
C |
15: 10,540,006 (GRCm39) |
V159G |
probably damaging |
Het |
Urb2 |
T |
A |
8: 124,773,979 (GRCm39) |
D1503E |
probably benign |
Het |
Usp29 |
T |
A |
7: 6,965,805 (GRCm39) |
N549K |
probably benign |
Het |
Zfp24 |
A |
G |
18: 24,147,626 (GRCm39) |
Y229H |
possibly damaging |
Het |
Zfp472 |
T |
A |
17: 33,197,189 (GRCm39) |
Y421* |
probably null |
Het |
Zkscan3 |
T |
C |
13: 21,578,119 (GRCm39) |
E256G |
possibly damaging |
Het |
|
Other mutations in Vmn2r39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02059:Vmn2r39
|
APN |
7 |
9,026,643 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03017:Vmn2r39
|
APN |
7 |
9,017,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R1314:Vmn2r39
|
UTSW |
7 |
9,017,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R1358:Vmn2r39
|
UTSW |
7 |
9,026,687 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1480:Vmn2r39
|
UTSW |
7 |
9,017,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Vmn2r39
|
UTSW |
7 |
9,026,673 (GRCm39) |
missense |
probably benign |
0.01 |
R4720:Vmn2r39
|
UTSW |
7 |
9,026,469 (GRCm39) |
critical splice donor site |
probably null |
|
R4990:Vmn2r39
|
UTSW |
7 |
9,026,675 (GRCm39) |
missense |
probably benign |
|
R5079:Vmn2r39
|
UTSW |
7 |
9,026,489 (GRCm39) |
missense |
probably benign |
0.05 |
R5695:Vmn2r39
|
UTSW |
7 |
9,028,150 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6131:Vmn2r39
|
UTSW |
7 |
9,017,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R6561:Vmn2r39
|
UTSW |
7 |
9,018,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R7108:Vmn2r39
|
UTSW |
7 |
9,026,667 (GRCm39) |
missense |
probably damaging |
0.96 |
R7122:Vmn2r39
|
UTSW |
7 |
9,017,761 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8793:Vmn2r39
|
UTSW |
7 |
9,028,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9324:Vmn2r39
|
UTSW |
7 |
9,030,684 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Vmn2r39
|
UTSW |
7 |
9,018,032 (GRCm39) |
missense |
probably damaging |
1.00 |
|