Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
T |
C |
5: 125,590,273 (GRCm39) |
Y511H |
probably damaging |
Het |
Abca7 |
T |
G |
10: 79,849,743 (GRCm39) |
Y1948D |
probably damaging |
Het |
Adgrl2 |
C |
A |
3: 148,564,611 (GRCm39) |
G319V |
probably damaging |
Het |
Adgrv1 |
T |
A |
13: 81,715,461 (GRCm39) |
D909V |
probably benign |
Het |
Anapc16 |
T |
C |
10: 59,824,579 (GRCm39) |
E119G |
possibly damaging |
Het |
C1qtnf12 |
T |
C |
4: 156,050,886 (GRCm39) |
V285A |
possibly damaging |
Het |
Cbr1 |
A |
C |
16: 93,405,119 (GRCm39) |
N89T |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,146,916 (GRCm39) |
Q2778L |
probably benign |
Het |
Clca4c-ps |
A |
G |
3: 144,595,340 (GRCm39) |
|
noncoding transcript |
Het |
Cst9 |
T |
C |
2: 148,677,269 (GRCm39) |
F47L |
probably damaging |
Het |
Dqx1 |
T |
C |
6: 83,043,408 (GRCm39) |
|
probably benign |
Het |
E2f2 |
A |
T |
4: 135,907,728 (GRCm39) |
K142* |
probably null |
Het |
Eif2ak4 |
T |
A |
2: 118,276,785 (GRCm39) |
H169Q |
probably benign |
Het |
Fmo9 |
C |
T |
1: 166,490,904 (GRCm39) |
A525T |
probably benign |
Het |
Gm42878 |
T |
C |
5: 121,683,247 (GRCm39) |
D6G |
probably benign |
Het |
Igfals |
A |
G |
17: 25,099,056 (GRCm39) |
Y49C |
probably damaging |
Het |
Il22b |
T |
C |
10: 118,126,069 (GRCm39) |
N176S |
possibly damaging |
Het |
Ipo7 |
T |
C |
7: 109,629,055 (GRCm39) |
|
probably benign |
Het |
Itga1 |
T |
C |
13: 115,121,657 (GRCm39) |
E784G |
probably damaging |
Het |
Jcad |
G |
T |
18: 4,672,855 (GRCm39) |
E206* |
probably null |
Het |
Kif24 |
A |
T |
4: 41,392,978 (GRCm39) |
|
probably benign |
Het |
Lrrc2 |
T |
A |
9: 110,809,886 (GRCm39) |
|
probably null |
Het |
Ltbp1 |
A |
G |
17: 75,534,240 (GRCm39) |
|
probably benign |
Het |
Man2c1 |
C |
T |
9: 57,045,244 (GRCm39) |
T451I |
possibly damaging |
Het |
Manba |
T |
A |
3: 135,248,150 (GRCm39) |
N346K |
probably damaging |
Het |
Nell1 |
T |
C |
7: 49,825,964 (GRCm39) |
|
probably benign |
Het |
Nfat5 |
T |
C |
8: 108,094,273 (GRCm39) |
V744A |
probably damaging |
Het |
Nms |
T |
C |
1: 38,985,192 (GRCm39) |
M98T |
possibly damaging |
Het |
Nos1 |
A |
T |
5: 118,076,339 (GRCm39) |
K1120* |
probably null |
Het |
Or11g25 |
C |
A |
14: 50,722,998 (GRCm39) |
Q28K |
probably benign |
Het |
Plekho1 |
C |
T |
3: 95,898,147 (GRCm39) |
R172H |
probably damaging |
Het |
Pot1b |
A |
T |
17: 55,976,750 (GRCm39) |
C391S |
possibly damaging |
Het |
Scn1a |
G |
A |
2: 66,162,645 (GRCm39) |
|
probably benign |
Het |
Sgce |
T |
G |
6: 4,711,326 (GRCm39) |
N149H |
probably damaging |
Het |
Slc45a1 |
A |
G |
4: 150,728,426 (GRCm39) |
W126R |
probably damaging |
Het |
Slc9a1 |
G |
A |
4: 133,147,404 (GRCm39) |
|
probably benign |
Het |
Tmem131l |
T |
A |
3: 83,845,362 (GRCm39) |
K423* |
probably null |
Het |
Tnrc18 |
C |
T |
5: 142,750,642 (GRCm39) |
E1444K |
possibly damaging |
Het |
Tpp1 |
T |
C |
7: 105,396,857 (GRCm39) |
|
probably benign |
Het |
Trip12 |
A |
C |
1: 84,705,999 (GRCm39) |
S610R |
probably benign |
Het |
Ushbp1 |
G |
T |
8: 71,840,076 (GRCm39) |
A525E |
probably benign |
Het |
Vmn2r106 |
A |
T |
17: 20,488,314 (GRCm39) |
M695K |
possibly damaging |
Het |
Vmn2r118 |
A |
G |
17: 55,915,585 (GRCm39) |
I455T |
probably benign |
Het |
Zbtb41 |
T |
C |
1: 139,370,621 (GRCm39) |
F686S |
probably damaging |
Het |
|
Other mutations in Dus4l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Dus4l
|
APN |
12 |
31,691,668 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01299:Dus4l
|
APN |
12 |
31,690,823 (GRCm39) |
missense |
probably benign |
|
IGL01443:Dus4l
|
APN |
12 |
31,702,409 (GRCm39) |
unclassified |
probably benign |
|
IGL02234:Dus4l
|
APN |
12 |
31,691,495 (GRCm39) |
splice site |
probably benign |
|
IGL02385:Dus4l
|
APN |
12 |
31,690,674 (GRCm39) |
utr 3 prime |
probably benign |
|
R0483:Dus4l
|
UTSW |
12 |
31,691,656 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1432:Dus4l
|
UTSW |
12 |
31,698,770 (GRCm39) |
missense |
probably benign |
0.03 |
R1514:Dus4l
|
UTSW |
12 |
31,690,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R1880:Dus4l
|
UTSW |
12 |
31,690,869 (GRCm39) |
missense |
probably benign |
0.00 |
R4362:Dus4l
|
UTSW |
12 |
31,698,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R5425:Dus4l
|
UTSW |
12 |
31,690,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Dus4l
|
UTSW |
12 |
31,696,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7188:Dus4l
|
UTSW |
12 |
31,696,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8184:Dus4l
|
UTSW |
12 |
31,690,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R8900:Dus4l
|
UTSW |
12 |
31,690,692 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9696:Dus4l
|
UTSW |
12 |
31,696,647 (GRCm39) |
missense |
probably damaging |
0.97 |
R9801:Dus4l
|
UTSW |
12 |
31,698,827 (GRCm39) |
missense |
probably damaging |
0.99 |
|