Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam22 |
A |
C |
5: 8,208,830 (GRCm39) |
S200A |
probably benign |
Het |
Adgrg3 |
G |
A |
8: 95,766,556 (GRCm39) |
R409H |
probably benign |
Het |
Aldh1l2 |
C |
T |
10: 83,342,506 (GRCm39) |
V548M |
possibly damaging |
Het |
Ampd1 |
T |
A |
3: 102,992,676 (GRCm39) |
C143* |
probably null |
Het |
Angpt4 |
A |
G |
2: 151,771,467 (GRCm39) |
Q261R |
probably damaging |
Het |
Ccar1 |
T |
C |
10: 62,601,191 (GRCm39) |
K491E |
probably damaging |
Het |
Cd177 |
A |
T |
7: 24,457,501 (GRCm39) |
M180K |
possibly damaging |
Het |
Dcst2 |
C |
T |
3: 89,280,553 (GRCm39) |
R620C |
probably damaging |
Het |
Dcun1d4 |
T |
A |
5: 73,688,832 (GRCm39) |
|
probably benign |
Het |
Dhrs1 |
T |
A |
14: 55,980,978 (GRCm39) |
T103S |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,384,087 (GRCm39) |
L1043P |
possibly damaging |
Het |
Eci3 |
A |
T |
13: 35,144,405 (GRCm39) |
N19K |
probably benign |
Het |
Ets1 |
A |
T |
9: 32,649,614 (GRCm39) |
D317V |
probably damaging |
Het |
Fem1c |
T |
C |
18: 46,638,668 (GRCm39) |
I445V |
possibly damaging |
Het |
Gabpb1 |
T |
C |
2: 126,492,484 (GRCm39) |
I176M |
possibly damaging |
Het |
Gm6563 |
A |
T |
19: 23,653,429 (GRCm39) |
K73I |
probably damaging |
Het |
Grap2 |
A |
G |
15: 80,532,140 (GRCm39) |
R252G |
possibly damaging |
Het |
Gsx1 |
T |
C |
5: 147,126,651 (GRCm39) |
L158P |
probably damaging |
Het |
Hand2 |
T |
A |
8: 57,775,468 (GRCm39) |
V176E |
probably benign |
Het |
Hey2 |
G |
T |
10: 30,718,622 (GRCm39) |
T8K |
possibly damaging |
Het |
Igsf3 |
T |
C |
3: 101,334,532 (GRCm39) |
I203T |
probably benign |
Het |
Itgax |
G |
A |
7: 127,739,066 (GRCm39) |
|
probably null |
Het |
Kcnn2 |
A |
G |
18: 45,725,139 (GRCm39) |
I212V |
possibly damaging |
Het |
Kcnu1 |
G |
T |
8: 26,403,708 (GRCm39) |
V740L |
probably damaging |
Het |
Kcnv1 |
A |
G |
15: 44,972,797 (GRCm39) |
I362T |
probably damaging |
Het |
Klhdc9 |
C |
T |
1: 171,186,488 (GRCm39) |
G316D |
probably damaging |
Het |
Mcmbp |
T |
C |
7: 128,317,738 (GRCm39) |
E169G |
probably damaging |
Het |
Muc20 |
G |
T |
16: 32,599,490 (GRCm39) |
H645N |
probably benign |
Het |
Nrm |
A |
G |
17: 36,175,423 (GRCm39) |
T52A |
probably benign |
Het |
Or13a23-ps1 |
T |
C |
7: 140,119,197 (GRCm39) |
S256P |
unknown |
Het |
Or14c41 |
A |
G |
7: 86,235,259 (GRCm39) |
K259E |
probably benign |
Het |
Or2y3 |
A |
T |
17: 38,392,925 (GRCm39) |
*315K |
probably null |
Het |
Or4c105 |
T |
A |
2: 88,648,043 (GRCm39) |
M176K |
possibly damaging |
Het |
Or4g7 |
T |
A |
2: 111,309,934 (GRCm39) |
D268E |
probably damaging |
Het |
Or51f23 |
T |
C |
7: 102,453,348 (GRCm39) |
V221A |
probably benign |
Het |
Pde11a |
A |
T |
2: 75,889,334 (GRCm39) |
N713K |
probably damaging |
Het |
Pfpl |
T |
C |
19: 12,405,944 (GRCm39) |
L65S |
probably damaging |
Het |
Prox1 |
A |
G |
1: 189,894,238 (GRCm39) |
V69A |
possibly damaging |
Het |
Prss39 |
A |
G |
1: 34,539,198 (GRCm39) |
H146R |
probably damaging |
Het |
Pxt1 |
A |
T |
17: 29,153,702 (GRCm39) |
F44I |
possibly damaging |
Het |
Rbp3 |
A |
G |
14: 33,677,795 (GRCm39) |
D581G |
probably benign |
Het |
Rims2 |
A |
G |
15: 39,381,239 (GRCm39) |
T1057A |
probably benign |
Het |
Robo1 |
G |
A |
16: 72,786,495 (GRCm39) |
G836R |
probably benign |
Het |
Slc34a3 |
A |
T |
2: 25,122,057 (GRCm39) |
S155T |
possibly damaging |
Het |
Slc35d1 |
T |
C |
4: 103,030,951 (GRCm39) |
Y308C |
|
Het |
Slfn9 |
T |
C |
11: 82,878,194 (GRCm39) |
I312V |
possibly damaging |
Het |
St3gal5 |
T |
A |
6: 72,130,461 (GRCm39) |
L351Q |
probably damaging |
Het |
Tanc1 |
A |
G |
2: 59,601,590 (GRCm39) |
D157G |
probably benign |
Het |
Tmprss11g |
C |
T |
5: 86,638,837 (GRCm39) |
|
probably null |
Het |
Tnpo1 |
A |
T |
13: 98,989,916 (GRCm39) |
I745N |
probably benign |
Het |
Uggt1 |
C |
A |
1: 36,236,624 (GRCm39) |
|
probably null |
Het |
Ugt8a |
G |
A |
3: 125,732,105 (GRCm39) |
|
probably benign |
Het |
Urod |
T |
C |
4: 116,850,729 (GRCm39) |
|
probably benign |
Het |
Vwa3a |
T |
A |
7: 120,381,910 (GRCm39) |
S582T |
probably damaging |
Het |
Zfp869 |
A |
T |
8: 70,159,177 (GRCm39) |
C465* |
probably null |
Het |
|
Other mutations in Vmn1r211 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Vmn1r211
|
APN |
13 |
23,036,272 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01583:Vmn1r211
|
APN |
13 |
23,036,571 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02735:Vmn1r211
|
APN |
13 |
23,036,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Vmn1r211
|
APN |
13 |
23,036,379 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02794:Vmn1r211
|
APN |
13 |
23,036,377 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Vmn1r211
|
APN |
13 |
23,036,376 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03292:Vmn1r211
|
APN |
13 |
23,036,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Vmn1r211
|
UTSW |
13 |
23,036,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Vmn1r211
|
UTSW |
13 |
23,035,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R1868:Vmn1r211
|
UTSW |
13 |
23,035,779 (GRCm39) |
missense |
probably benign |
0.07 |
R2002:Vmn1r211
|
UTSW |
13 |
23,035,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Vmn1r211
|
UTSW |
13 |
23,036,134 (GRCm39) |
missense |
probably damaging |
0.98 |
R2655:Vmn1r211
|
UTSW |
13 |
23,036,586 (GRCm39) |
missense |
probably benign |
0.42 |
R4837:Vmn1r211
|
UTSW |
13 |
23,036,296 (GRCm39) |
missense |
probably benign |
0.41 |
R6284:Vmn1r211
|
UTSW |
13 |
23,036,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R6701:Vmn1r211
|
UTSW |
13 |
23,035,779 (GRCm39) |
missense |
probably benign |
0.07 |
R6715:Vmn1r211
|
UTSW |
13 |
23,035,949 (GRCm39) |
missense |
probably benign |
0.00 |
R7058:Vmn1r211
|
UTSW |
13 |
23,036,063 (GRCm39) |
missense |
probably benign |
0.15 |
R7465:Vmn1r211
|
UTSW |
13 |
23,036,086 (GRCm39) |
missense |
probably benign |
0.13 |
R8085:Vmn1r211
|
UTSW |
13 |
23,035,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8720:Vmn1r211
|
UTSW |
13 |
23,036,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R9120:Vmn1r211
|
UTSW |
13 |
23,035,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R9725:Vmn1r211
|
UTSW |
13 |
23,036,506 (GRCm39) |
missense |
probably benign |
0.03 |
|