Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd17b |
T |
A |
19: 21,656,024 (GRCm39) |
V102D |
probably damaging |
Het |
Adam6b |
T |
A |
12: 113,454,087 (GRCm39) |
D301E |
probably benign |
Het |
Adnp |
A |
C |
2: 168,025,092 (GRCm39) |
D734E |
probably benign |
Het |
Ank2 |
T |
A |
3: 126,723,532 (GRCm39) |
T932S |
probably damaging |
Het |
Arhgap20 |
C |
A |
9: 51,760,277 (GRCm39) |
D709E |
possibly damaging |
Het |
Atoh1 |
A |
G |
6: 64,707,226 (GRCm39) |
D307G |
probably benign |
Het |
Aven |
C |
T |
2: 112,390,120 (GRCm39) |
R8W |
probably benign |
Het |
B3galt1 |
A |
G |
2: 67,948,530 (GRCm39) |
I82V |
probably benign |
Het |
Chd2 |
T |
C |
7: 73,118,285 (GRCm39) |
D1111G |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,059,468 (GRCm39) |
D2089G |
probably benign |
Het |
Dach1 |
T |
A |
14: 98,256,370 (GRCm39) |
H296L |
probably damaging |
Het |
Dennd4b |
T |
G |
3: 90,178,904 (GRCm39) |
L556R |
probably damaging |
Het |
Dop1a |
T |
A |
9: 86,405,151 (GRCm39) |
S326T |
probably benign |
Het |
Eif2b5 |
T |
A |
16: 20,321,306 (GRCm39) |
H286Q |
probably damaging |
Het |
Fcnb |
C |
T |
2: 27,968,330 (GRCm39) |
S209N |
possibly damaging |
Het |
Fn3k |
T |
A |
11: 121,341,222 (GRCm39) |
F292L |
probably damaging |
Het |
Gm1123 |
G |
A |
9: 98,905,309 (GRCm39) |
A67V |
probably benign |
Het |
Hey2 |
C |
T |
10: 30,710,273 (GRCm39) |
C160Y |
probably benign |
Het |
Jph2 |
T |
A |
2: 163,180,621 (GRCm39) |
|
probably null |
Het |
Lars1 |
A |
G |
18: 42,343,166 (GRCm39) |
S1084P |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,276,497 (GRCm39) |
D6084G |
probably damaging |
Het |
Mdfic |
G |
T |
6: 15,740,989 (GRCm39) |
A115S |
probably benign |
Het |
Mki67 |
T |
C |
7: 135,297,237 (GRCm39) |
E2599G |
probably damaging |
Het |
Mtus1 |
A |
G |
8: 41,509,689 (GRCm39) |
S131P |
probably benign |
Het |
Muc16 |
G |
T |
9: 18,556,630 (GRCm39) |
T3221K |
unknown |
Het |
Or1q1 |
T |
A |
2: 36,886,873 (GRCm39) |
I17N |
possibly damaging |
Het |
Or8b3 |
A |
G |
9: 38,314,904 (GRCm39) |
S245G |
probably damaging |
Het |
Or8b54 |
G |
A |
9: 38,686,577 (GRCm39) |
V9M |
noncoding transcript |
Het |
Pdgfc |
A |
G |
3: 80,944,811 (GRCm39) |
E23G |
possibly damaging |
Het |
Pfkp |
T |
C |
13: 6,655,698 (GRCm39) |
T312A |
probably benign |
Het |
Pxn |
A |
G |
5: 115,683,768 (GRCm39) |
E200G |
probably damaging |
Het |
Rai1 |
C |
T |
11: 60,076,796 (GRCm39) |
H287Y |
probably damaging |
Het |
Rap1gap |
G |
A |
4: 137,445,275 (GRCm39) |
V319I |
probably benign |
Het |
Rbm46 |
C |
T |
3: 82,772,775 (GRCm39) |
R119Q |
probably benign |
Het |
Selp |
A |
T |
1: 163,961,490 (GRCm39) |
D401V |
possibly damaging |
Het |
Sh3bp5 |
A |
G |
14: 31,139,399 (GRCm39) |
V58A |
probably benign |
Het |
Shpk |
A |
T |
11: 73,094,775 (GRCm39) |
I64F |
probably benign |
Het |
Slmap |
A |
G |
14: 26,189,646 (GRCm39) |
Y171H |
probably damaging |
Het |
Tmem67 |
T |
C |
4: 12,075,661 (GRCm39) |
T183A |
probably benign |
Het |
Tyw1 |
G |
T |
5: 130,328,862 (GRCm39) |
L549F |
probably damaging |
Het |
Uhrf2 |
T |
A |
19: 30,051,329 (GRCm39) |
M301K |
probably benign |
Het |
Uvssa |
G |
A |
5: 33,568,311 (GRCm39) |
V532I |
probably benign |
Het |
Zfp52 |
A |
G |
17: 21,782,156 (GRCm39) |
N668S |
possibly damaging |
Het |
|
Other mutations in Vmn2r113 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01318:Vmn2r113
|
APN |
17 |
23,177,309 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01386:Vmn2r113
|
APN |
17 |
23,175,024 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01743:Vmn2r113
|
APN |
17 |
23,177,285 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02224:Vmn2r113
|
APN |
17 |
23,174,960 (GRCm39) |
nonsense |
probably null |
|
IGL02498:Vmn2r113
|
APN |
17 |
23,177,349 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02969:Vmn2r113
|
APN |
17 |
23,177,591 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03010:Vmn2r113
|
APN |
17 |
23,175,038 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03240:Vmn2r113
|
APN |
17 |
23,174,931 (GRCm39) |
missense |
probably benign |
0.19 |
R1853:Vmn2r113
|
UTSW |
17 |
23,164,501 (GRCm39) |
missense |
probably benign |
|
R2058:Vmn2r113
|
UTSW |
17 |
23,177,223 (GRCm39) |
nonsense |
probably null |
|
R3010:Vmn2r113
|
UTSW |
17 |
23,177,105 (GRCm39) |
missense |
probably damaging |
0.97 |
R4942:Vmn2r113
|
UTSW |
17 |
23,177,321 (GRCm39) |
missense |
probably damaging |
0.97 |
R5072:Vmn2r113
|
UTSW |
17 |
23,177,329 (GRCm39) |
nonsense |
probably null |
|
R5755:Vmn2r113
|
UTSW |
17 |
23,176,955 (GRCm39) |
missense |
probably benign |
0.00 |
R6513:Vmn2r113
|
UTSW |
17 |
23,177,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R7164:Vmn2r113
|
UTSW |
17 |
23,167,137 (GRCm39) |
missense |
probably benign |
|
R7936:Vmn2r113
|
UTSW |
17 |
23,176,917 (GRCm39) |
missense |
probably benign |
0.05 |
R8087:Vmn2r113
|
UTSW |
17 |
23,177,711 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8193:Vmn2r113
|
UTSW |
17 |
23,164,501 (GRCm39) |
missense |
probably benign |
0.06 |
R8414:Vmn2r113
|
UTSW |
17 |
23,177,753 (GRCm39) |
nonsense |
probably null |
|
R8490:Vmn2r113
|
UTSW |
17 |
23,177,372 (GRCm39) |
missense |
probably benign |
0.18 |
|