Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,526,541 (GRCm39) |
I581N |
probably damaging |
Het |
Abcb10 |
A |
G |
8: 124,697,763 (GRCm39) |
F187S |
probably benign |
Het |
Actl11 |
T |
A |
9: 107,808,203 (GRCm39) |
V842E |
possibly damaging |
Het |
Akap12 |
A |
G |
10: 4,307,291 (GRCm39) |
D1367G |
probably benign |
Het |
Aoc1l1 |
T |
A |
6: 48,952,474 (GRCm39) |
L133Q |
probably damaging |
Het |
Aoc1l3 |
T |
A |
6: 48,964,509 (GRCm39) |
F172L |
probably benign |
Het |
AU040320 |
A |
T |
4: 126,717,509 (GRCm39) |
H362L |
possibly damaging |
Het |
Bmpr1a |
C |
T |
14: 34,146,999 (GRCm39) |
V258M |
probably damaging |
Het |
Bptf |
T |
A |
11: 106,972,193 (GRCm39) |
K892* |
probably null |
Het |
Cap2 |
A |
G |
13: 46,801,840 (GRCm39) |
*422W |
probably null |
Het |
Cars2 |
G |
T |
8: 11,567,854 (GRCm39) |
H414N |
probably benign |
Het |
Ccnt1 |
A |
C |
15: 98,442,124 (GRCm39) |
S381R |
probably benign |
Het |
Cdyl2 |
A |
T |
8: 117,321,794 (GRCm39) |
C244* |
probably null |
Het |
Cers2 |
A |
G |
3: 95,228,305 (GRCm39) |
E115G |
probably null |
Het |
Cpt1b |
G |
A |
15: 89,303,477 (GRCm39) |
P553S |
probably benign |
Het |
Cuedc1 |
A |
G |
11: 88,068,136 (GRCm39) |
E128G |
probably damaging |
Het |
Dll4 |
T |
A |
2: 119,156,968 (GRCm39) |
V80D |
probably damaging |
Het |
Dop1b |
T |
C |
16: 93,536,874 (GRCm39) |
L113P |
probably damaging |
Het |
Fam98a |
A |
G |
17: 75,845,810 (GRCm39) |
I312T |
probably damaging |
Het |
Gnrhr |
T |
G |
5: 86,345,473 (GRCm39) |
K71T |
possibly damaging |
Het |
Gtf3c3 |
A |
T |
1: 54,445,032 (GRCm39) |
L674Q |
probably damaging |
Het |
Hipk2 |
A |
T |
6: 38,795,212 (GRCm39) |
H352Q |
probably damaging |
Het |
Hivep1 |
T |
C |
13: 42,313,115 (GRCm39) |
V1785A |
probably damaging |
Het |
Hspa4 |
A |
T |
11: 53,153,810 (GRCm39) |
I687N |
probably damaging |
Het |
Krt18 |
A |
T |
15: 101,936,955 (GRCm39) |
D81V |
probably damaging |
Het |
Lama3 |
A |
C |
18: 12,685,912 (GRCm39) |
D1142A |
probably damaging |
Het |
Lnpep |
A |
G |
17: 17,766,727 (GRCm39) |
I713T |
possibly damaging |
Het |
Man2b2 |
T |
A |
5: 36,967,677 (GRCm39) |
Y897F |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,412,738 (GRCm39) |
I1895F |
unknown |
Het |
Myh8 |
G |
A |
11: 67,177,089 (GRCm39) |
V414I |
probably damaging |
Het |
Myo1d |
A |
T |
11: 80,575,149 (GRCm39) |
|
probably null |
Het |
Nav2 |
A |
T |
7: 49,141,121 (GRCm39) |
M889L |
probably benign |
Het |
Oc90 |
C |
T |
15: 65,754,457 (GRCm39) |
G236D |
probably benign |
Het |
Or13a27 |
A |
G |
7: 139,925,548 (GRCm39) |
V118A |
probably benign |
Het |
Pak4 |
A |
G |
7: 28,267,631 (GRCm39) |
I11T |
probably damaging |
Het |
Papss2 |
T |
C |
19: 32,615,787 (GRCm39) |
I173T |
probably damaging |
Het |
Pcsk9 |
A |
T |
4: 106,320,988 (GRCm39) |
D40E |
probably benign |
Het |
Pdzrn3 |
G |
C |
6: 101,128,064 (GRCm39) |
H867Q |
probably damaging |
Het |
Plcb1 |
A |
T |
2: 135,094,696 (GRCm39) |
I174F |
possibly damaging |
Het |
Pom121l2 |
G |
A |
13: 22,166,015 (GRCm39) |
W95* |
probably null |
Het |
Prcp |
A |
T |
7: 92,577,843 (GRCm39) |
T336S |
probably benign |
Het |
Prdm11 |
A |
C |
2: 92,843,226 (GRCm39) |
S78A |
probably benign |
Het |
Ralgds |
T |
C |
2: 28,435,224 (GRCm39) |
I405T |
probably damaging |
Het |
Rasgrf1 |
A |
G |
9: 89,902,478 (GRCm39) |
R1208G |
probably damaging |
Het |
Rasgrp2 |
T |
A |
19: 6,458,864 (GRCm39) |
|
probably null |
Het |
Rb1 |
A |
T |
14: 73,450,566 (GRCm39) |
Y599* |
probably null |
Het |
Rnf141 |
A |
T |
7: 110,433,010 (GRCm39) |
F62L |
probably damaging |
Het |
Rsl24d1 |
T |
A |
9: 73,023,698 (GRCm39) |
F292I |
possibly damaging |
Het |
Scn10a |
C |
T |
9: 119,477,175 (GRCm39) |
V736I |
probably damaging |
Het |
Sim2 |
A |
T |
16: 93,905,598 (GRCm39) |
T141S |
probably benign |
Het |
Slc6a15 |
G |
T |
10: 103,244,067 (GRCm39) |
V436L |
probably damaging |
Het |
Smarca2 |
T |
C |
19: 26,668,772 (GRCm39) |
S924P |
probably damaging |
Het |
Tacc1 |
T |
C |
8: 25,671,881 (GRCm39) |
E449G |
probably benign |
Het |
Tlr3 |
A |
T |
8: 45,852,137 (GRCm39) |
N253K |
possibly damaging |
Het |
Tmem198 |
G |
A |
1: 75,456,500 (GRCm39) |
A82T |
probably benign |
Het |
Tom1l2 |
A |
T |
11: 60,133,648 (GRCm39) |
L54* |
probably null |
Het |
Trav12-2 |
A |
G |
14: 53,854,356 (GRCm39) |
Y110C |
probably benign |
Het |
Trdn |
T |
A |
10: 33,209,247 (GRCm39) |
|
probably null |
Het |
Trim36 |
G |
T |
18: 46,300,565 (GRCm39) |
P690Q |
probably damaging |
Het |
Trpc4 |
A |
T |
3: 54,206,599 (GRCm39) |
M600L |
probably damaging |
Het |
Trpm2 |
T |
A |
10: 77,759,355 (GRCm39) |
Q1143L |
probably benign |
Het |
Usp34 |
T |
A |
11: 23,283,739 (GRCm39) |
D144E |
probably benign |
Het |
Vwa1 |
A |
G |
4: 155,855,369 (GRCm39) |
V248A |
probably benign |
Het |
Wdr75 |
T |
C |
1: 45,838,211 (GRCm39) |
V40A |
probably damaging |
Het |
|
Other mutations in Vps18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01627:Vps18
|
APN |
2 |
119,127,672 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02311:Vps18
|
APN |
2 |
119,120,732 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02332:Vps18
|
APN |
2 |
119,124,291 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03089:Vps18
|
APN |
2 |
119,123,658 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03114:Vps18
|
APN |
2 |
119,124,132 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03334:Vps18
|
APN |
2 |
119,127,963 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Vps18
|
UTSW |
2 |
119,127,709 (GRCm39) |
missense |
probably benign |
0.22 |
R0311:Vps18
|
UTSW |
2 |
119,127,846 (GRCm39) |
missense |
probably benign |
0.05 |
R0346:Vps18
|
UTSW |
2 |
119,127,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Vps18
|
UTSW |
2 |
119,124,386 (GRCm39) |
missense |
probably damaging |
0.99 |
R0637:Vps18
|
UTSW |
2 |
119,124,386 (GRCm39) |
missense |
probably damaging |
0.99 |
R1493:Vps18
|
UTSW |
2 |
119,127,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Vps18
|
UTSW |
2 |
119,119,538 (GRCm39) |
missense |
probably benign |
0.03 |
R1734:Vps18
|
UTSW |
2 |
119,124,423 (GRCm39) |
missense |
probably benign |
0.01 |
R4297:Vps18
|
UTSW |
2 |
119,127,812 (GRCm39) |
nonsense |
probably null |
|
R4633:Vps18
|
UTSW |
2 |
119,123,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Vps18
|
UTSW |
2 |
119,124,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R5034:Vps18
|
UTSW |
2 |
119,123,787 (GRCm39) |
missense |
probably benign |
0.00 |
R5162:Vps18
|
UTSW |
2 |
119,123,423 (GRCm39) |
missense |
probably benign |
0.19 |
R5857:Vps18
|
UTSW |
2 |
119,128,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R6105:Vps18
|
UTSW |
2 |
119,119,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R6150:Vps18
|
UTSW |
2 |
119,128,073 (GRCm39) |
nonsense |
probably null |
|
R7934:Vps18
|
UTSW |
2 |
119,124,122 (GRCm39) |
missense |
probably benign |
0.11 |
R8018:Vps18
|
UTSW |
2 |
119,124,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R8147:Vps18
|
UTSW |
2 |
119,123,237 (GRCm39) |
missense |
probably benign |
0.19 |
R8401:Vps18
|
UTSW |
2 |
119,127,973 (GRCm39) |
missense |
probably damaging |
0.96 |
R8525:Vps18
|
UTSW |
2 |
119,120,711 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9044:Vps18
|
UTSW |
2 |
119,128,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R9719:Vps18
|
UTSW |
2 |
119,127,553 (GRCm39) |
missense |
probably damaging |
1.00 |
RF002:Vps18
|
UTSW |
2 |
119,127,871 (GRCm39) |
missense |
probably damaging |
1.00 |
V7583:Vps18
|
UTSW |
2 |
119,127,709 (GRCm39) |
missense |
probably benign |
0.22 |
|