Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam11 |
A |
G |
11: 102,663,682 (GRCm39) |
T287A |
probably damaging |
Het |
Afm |
G |
T |
5: 90,696,742 (GRCm39) |
|
probably benign |
Het |
Ankrd24 |
A |
G |
10: 81,465,571 (GRCm39) |
|
probably benign |
Het |
Ankrd53 |
G |
T |
6: 83,740,031 (GRCm39) |
E62* |
probably null |
Het |
Atg4b |
A |
G |
1: 93,706,032 (GRCm39) |
S162G |
probably damaging |
Het |
B530045E10Rik |
A |
T |
10: 99,258,177 (GRCm39) |
|
noncoding transcript |
Het |
Ccng1 |
A |
G |
11: 40,643,183 (GRCm39) |
V88A |
probably benign |
Het |
Ces1e |
T |
A |
8: 93,950,524 (GRCm39) |
M86L |
probably benign |
Het |
Chrne |
A |
T |
11: 70,509,498 (GRCm39) |
|
probably null |
Het |
Ctsh |
T |
C |
9: 89,946,260 (GRCm39) |
S109P |
probably damaging |
Het |
Eif4g1 |
A |
C |
16: 20,499,790 (GRCm39) |
I420L |
probably damaging |
Het |
Ep300 |
T |
A |
15: 81,524,224 (GRCm39) |
S1351T |
unknown |
Het |
Fgfr1 |
A |
G |
8: 26,063,569 (GRCm39) |
M732V |
possibly damaging |
Het |
Gata5 |
T |
G |
2: 179,969,138 (GRCm39) |
|
probably benign |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm3633 |
A |
T |
14: 42,461,234 (GRCm39) |
M18K |
probably damaging |
Het |
Gucy1b2 |
A |
G |
14: 62,657,595 (GRCm39) |
L211P |
probably damaging |
Het |
Hemgn |
T |
C |
4: 46,396,994 (GRCm39) |
N81D |
possibly damaging |
Het |
Irs2 |
A |
T |
8: 11,056,221 (GRCm39) |
M737K |
probably damaging |
Het |
Itgb7 |
C |
A |
15: 102,126,430 (GRCm39) |
C502F |
probably damaging |
Het |
Jakmip1 |
G |
T |
5: 37,278,324 (GRCm39) |
A534S |
probably damaging |
Het |
Kidins220 |
A |
G |
12: 25,107,728 (GRCm39) |
H1636R |
probably benign |
Het |
Kirrel1 |
T |
A |
3: 87,003,037 (GRCm39) |
I119F |
probably damaging |
Het |
Lrba |
T |
C |
3: 86,217,354 (GRCm39) |
V527A |
probably damaging |
Het |
Mitf |
A |
G |
6: 97,994,856 (GRCm39) |
E409G |
probably benign |
Het |
Mtrr |
T |
G |
13: 68,720,728 (GRCm39) |
K289T |
probably damaging |
Het |
Muc2 |
A |
T |
7: 141,306,477 (GRCm39) |
I739F |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,142,934 (GRCm39) |
T612A |
unknown |
Het |
Or12e7 |
T |
A |
2: 87,287,654 (GRCm39) |
N48K |
probably damaging |
Het |
Or1x2 |
A |
T |
11: 50,918,202 (GRCm39) |
R124S |
probably damaging |
Het |
Or6c213 |
T |
A |
10: 129,574,791 (GRCm39) |
|
probably benign |
Het |
Or8b42 |
T |
A |
9: 38,341,594 (GRCm39) |
N5K |
probably damaging |
Het |
P4ha3 |
T |
A |
7: 99,949,859 (GRCm39) |
C109S |
probably damaging |
Het |
Prkd3 |
T |
C |
17: 79,264,635 (GRCm39) |
E660G |
possibly damaging |
Het |
Rbm4b |
G |
A |
19: 4,812,219 (GRCm39) |
M209I |
probably benign |
Het |
Reln |
T |
A |
5: 22,109,715 (GRCm39) |
T3132S |
probably benign |
Het |
Selenbp2 |
T |
A |
3: 94,605,451 (GRCm39) |
D92E |
possibly damaging |
Het |
Slfn8 |
G |
T |
11: 82,894,905 (GRCm39) |
Q634K |
probably benign |
Het |
Sumo3 |
A |
T |
10: 77,449,832 (GRCm39) |
I57F |
probably benign |
Het |
Tacr1 |
A |
G |
6: 82,533,997 (GRCm39) |
Y341C |
probably benign |
Het |
Tlr4 |
T |
A |
4: 66,757,726 (GRCm39) |
L173Q |
probably damaging |
Het |
Tshz3 |
C |
T |
7: 36,469,385 (GRCm39) |
T458M |
probably damaging |
Het |
Vmn2r16 |
T |
C |
5: 109,478,277 (GRCm39) |
F11L |
probably benign |
Het |
Vmn2r28 |
T |
A |
7: 5,484,302 (GRCm39) |
M633L |
probably benign |
Het |
Vmn2r35 |
T |
C |
7: 7,819,772 (GRCm39) |
|
probably benign |
Het |
Vwc2l |
G |
T |
1: 70,768,172 (GRCm39) |
A79S |
probably benign |
Het |
Zfhx2 |
G |
A |
14: 55,301,372 (GRCm39) |
S2204F |
unknown |
Het |
|
Other mutations in Vmn1r91 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02125:Vmn1r91
|
APN |
7 |
19,835,429 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02263:Vmn1r91
|
APN |
7 |
19,835,768 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02338:Vmn1r91
|
APN |
7 |
19,835,671 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02708:Vmn1r91
|
APN |
7 |
19,835,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1880:Vmn1r91
|
UTSW |
7 |
19,835,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Vmn1r91
|
UTSW |
7 |
19,835,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R4730:Vmn1r91
|
UTSW |
7 |
19,835,695 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5362:Vmn1r91
|
UTSW |
7 |
19,835,386 (GRCm39) |
missense |
probably benign |
0.05 |
R5633:Vmn1r91
|
UTSW |
7 |
19,835,870 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5979:Vmn1r91
|
UTSW |
7 |
19,835,990 (GRCm39) |
missense |
probably benign |
0.00 |
R6151:Vmn1r91
|
UTSW |
7 |
19,835,360 (GRCm39) |
missense |
probably benign |
|
R6177:Vmn1r91
|
UTSW |
7 |
19,835,404 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7397:Vmn1r91
|
UTSW |
7 |
19,835,695 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7589:Vmn1r91
|
UTSW |
7 |
19,835,802 (GRCm39) |
missense |
probably benign |
0.07 |
R7872:Vmn1r91
|
UTSW |
7 |
19,835,839 (GRCm39) |
missense |
probably benign |
0.26 |
R7886:Vmn1r91
|
UTSW |
7 |
19,835,490 (GRCm39) |
missense |
probably benign |
|
R7903:Vmn1r91
|
UTSW |
7 |
19,835,135 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7953:Vmn1r91
|
UTSW |
7 |
19,835,218 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8043:Vmn1r91
|
UTSW |
7 |
19,835,218 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8202:Vmn1r91
|
UTSW |
7 |
19,835,749 (GRCm39) |
missense |
probably damaging |
1.00 |
|