Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acnat2 |
T |
G |
4: 49,380,647 (GRCm39) |
M244L |
possibly damaging |
Het |
Acnat2 |
A |
T |
4: 49,380,639 (GRCm39) |
C228* |
probably null |
Het |
Adam24 |
T |
C |
8: 41,133,218 (GRCm39) |
S229P |
probably damaging |
Het |
Alpk3 |
T |
C |
7: 80,727,643 (GRCm39) |
S258P |
probably benign |
Het |
Atad2b |
A |
G |
12: 5,068,037 (GRCm39) |
T1012A |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,013,017 (GRCm39) |
E1899G |
probably damaging |
Het |
C4b |
A |
T |
17: 34,953,382 (GRCm39) |
S1034T |
probably benign |
Het |
Cd300ld2 |
T |
A |
11: 114,901,249 (GRCm39) |
H277L |
possibly damaging |
Het |
Chrna4 |
C |
T |
2: 180,670,926 (GRCm39) |
V277I |
probably benign |
Het |
Col3a1 |
A |
G |
1: 45,364,963 (GRCm39) |
|
probably null |
Het |
Dpep2 |
C |
T |
8: 106,715,388 (GRCm39) |
V369M |
probably damaging |
Het |
Eml2 |
T |
A |
7: 18,940,055 (GRCm39) |
N815K |
probably damaging |
Het |
Enpp3 |
A |
G |
10: 24,685,746 (GRCm39) |
|
probably benign |
Het |
Git1 |
T |
C |
11: 77,390,413 (GRCm39) |
V86A |
probably benign |
Het |
Hivep2 |
C |
T |
10: 14,006,926 (GRCm39) |
P1175S |
probably benign |
Het |
Hydin |
T |
C |
8: 111,293,604 (GRCm39) |
I3517T |
probably benign |
Het |
Ift172 |
T |
A |
5: 31,410,992 (GRCm39) |
|
probably null |
Het |
Jmy |
A |
G |
13: 93,589,316 (GRCm39) |
I647T |
probably benign |
Het |
Kifap3 |
T |
A |
1: 163,653,440 (GRCm39) |
|
probably benign |
Het |
Lama3 |
G |
A |
18: 12,670,915 (GRCm39) |
|
probably null |
Het |
Lipa |
A |
C |
19: 34,471,522 (GRCm39) |
I351S |
possibly damaging |
Het |
Ltbp2 |
G |
T |
12: 84,832,091 (GRCm39) |
A1631D |
probably benign |
Het |
Masp2 |
A |
G |
4: 148,698,477 (GRCm39) |
I519M |
probably damaging |
Het |
Mfsd6 |
A |
G |
1: 52,702,436 (GRCm39) |
|
probably benign |
Het |
Numa1 |
T |
G |
7: 101,661,216 (GRCm39) |
D1846E |
probably benign |
Het |
Oog3 |
A |
T |
4: 143,885,920 (GRCm39) |
I226K |
probably damaging |
Het |
Or11h6 |
A |
G |
14: 50,880,658 (GRCm39) |
T301A |
probably benign |
Het |
Or5an6 |
A |
T |
19: 12,372,265 (GRCm39) |
I213F |
probably benign |
Het |
Or8b3b |
T |
C |
9: 38,584,209 (GRCm39) |
Y177C |
probably damaging |
Het |
Or8g53 |
T |
G |
9: 39,683,800 (GRCm39) |
T99P |
probably damaging |
Het |
Or9s13 |
A |
T |
1: 92,548,183 (GRCm39) |
Y185F |
probably benign |
Het |
Pkdcc |
T |
C |
17: 83,531,295 (GRCm39) |
S435P |
probably damaging |
Het |
Ppm1g |
A |
G |
5: 31,365,425 (GRCm39) |
Y70H |
probably damaging |
Het |
Prcc |
C |
T |
3: 87,776,984 (GRCm39) |
S330N |
probably damaging |
Het |
Ror2 |
A |
T |
13: 53,272,876 (GRCm39) |
L251Q |
probably damaging |
Het |
Scn11a |
A |
G |
9: 119,621,464 (GRCm39) |
L651P |
probably damaging |
Het |
Skint6 |
A |
T |
4: 112,805,737 (GRCm39) |
|
probably benign |
Het |
Slc23a4 |
A |
G |
6: 34,931,917 (GRCm39) |
F186L |
probably benign |
Het |
Slc30a8 |
A |
T |
15: 52,198,530 (GRCm39) |
D325V |
probably benign |
Het |
Son |
C |
T |
16: 91,452,099 (GRCm39) |
T282M |
possibly damaging |
Het |
Tas2r118 |
A |
T |
6: 23,969,891 (GRCm39) |
F57I |
probably damaging |
Het |
Tcf7l1 |
A |
G |
6: 72,606,966 (GRCm39) |
S447P |
probably benign |
Het |
Thsd1 |
T |
A |
8: 22,733,454 (GRCm39) |
V167E |
probably damaging |
Het |
Tle3 |
T |
C |
9: 61,322,063 (GRCm39) |
V696A |
probably damaging |
Het |
Tmem67 |
A |
T |
4: 12,069,463 (GRCm39) |
I405K |
possibly damaging |
Het |
Tmem71 |
A |
C |
15: 66,413,466 (GRCm39) |
V202G |
probably benign |
Het |
Trim6 |
T |
C |
7: 103,881,564 (GRCm39) |
|
probably benign |
Het |
Trip12 |
A |
G |
1: 84,721,535 (GRCm39) |
|
probably benign |
Het |
Ubr1 |
A |
C |
2: 120,694,854 (GRCm39) |
C1693G |
possibly damaging |
Het |
Ush2a |
G |
A |
1: 188,648,195 (GRCm39) |
R4600H |
probably damaging |
Het |
Vil1 |
A |
G |
1: 74,465,851 (GRCm39) |
I547M |
probably benign |
Het |
Vmn1r219 |
A |
T |
13: 23,347,266 (GRCm39) |
I152L |
probably benign |
Het |
Vmn2r45 |
T |
A |
7: 8,486,185 (GRCm39) |
K368* |
probably null |
Het |
Vmn2r68 |
C |
T |
7: 84,871,153 (GRCm39) |
W710* |
probably null |
Het |
Zfp808 |
T |
A |
13: 62,321,032 (GRCm39) |
*754R |
probably null |
Het |
Zyg11b |
C |
T |
4: 108,123,515 (GRCm39) |
E151K |
probably damaging |
Het |
|
Other mutations in Vmn1r26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02609:Vmn1r26
|
APN |
6 |
57,985,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R1121:Vmn1r26
|
UTSW |
6 |
57,985,647 (GRCm39) |
missense |
probably benign |
0.43 |
R1881:Vmn1r26
|
UTSW |
6 |
57,985,650 (GRCm39) |
missense |
probably benign |
0.20 |
R1958:Vmn1r26
|
UTSW |
6 |
57,985,286 (GRCm39) |
missense |
probably benign |
0.01 |
R1978:Vmn1r26
|
UTSW |
6 |
57,986,111 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2106:Vmn1r26
|
UTSW |
6 |
57,985,710 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2117:Vmn1r26
|
UTSW |
6 |
57,985,335 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2323:Vmn1r26
|
UTSW |
6 |
57,985,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Vmn1r26
|
UTSW |
6 |
57,985,808 (GRCm39) |
missense |
probably damaging |
0.99 |
R5695:Vmn1r26
|
UTSW |
6 |
57,985,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6355:Vmn1r26
|
UTSW |
6 |
57,985,536 (GRCm39) |
missense |
probably benign |
0.02 |
R6948:Vmn1r26
|
UTSW |
6 |
57,985,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R7114:Vmn1r26
|
UTSW |
6 |
57,985,755 (GRCm39) |
missense |
probably benign |
0.02 |
R7977:Vmn1r26
|
UTSW |
6 |
57,985,264 (GRCm39) |
nonsense |
probably null |
|
R7987:Vmn1r26
|
UTSW |
6 |
57,985,264 (GRCm39) |
nonsense |
probably null |
|
R8311:Vmn1r26
|
UTSW |
6 |
57,985,518 (GRCm39) |
missense |
probably benign |
0.39 |
R8442:Vmn1r26
|
UTSW |
6 |
57,985,728 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8784:Vmn1r26
|
UTSW |
6 |
57,985,440 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9129:Vmn1r26
|
UTSW |
6 |
57,985,373 (GRCm39) |
missense |
|
|
RF020:Vmn1r26
|
UTSW |
6 |
57,985,705 (GRCm39) |
missense |
probably benign |
0.35 |
Z1176:Vmn1r26
|
UTSW |
6 |
57,985,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|