Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
C |
17: 24,595,717 (GRCm39) |
S357P |
possibly damaging |
Het |
Adam39 |
A |
G |
8: 41,279,018 (GRCm39) |
I470V |
probably benign |
Het |
Agrn |
A |
T |
4: 156,253,447 (GRCm39) |
C1708S |
probably benign |
Het |
Agtpbp1 |
A |
G |
13: 59,621,557 (GRCm39) |
I42T |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,186,626 (GRCm39) |
C1347R |
probably damaging |
Het |
Antxr1 |
A |
G |
6: 87,157,165 (GRCm39) |
L452P |
probably damaging |
Het |
Arhgef33 |
T |
A |
17: 80,677,704 (GRCm39) |
V417D |
probably damaging |
Het |
Brca2 |
A |
G |
5: 150,462,688 (GRCm39) |
I817M |
possibly damaging |
Het |
Casp4 |
A |
T |
9: 5,321,521 (GRCm39) |
|
probably benign |
Het |
Cdh20 |
T |
C |
1: 104,861,882 (GRCm39) |
Y21H |
possibly damaging |
Het |
Cdr2 |
C |
T |
7: 120,557,557 (GRCm39) |
V323M |
possibly damaging |
Het |
Cebpa |
G |
A |
7: 34,819,283 (GRCm39) |
R147H |
probably benign |
Het |
Cetn4 |
C |
A |
3: 37,364,118 (GRCm39) |
E31* |
probably null |
Het |
Cobll1 |
G |
A |
2: 64,964,115 (GRCm39) |
Q189* |
probably null |
Het |
Colec12 |
A |
G |
18: 9,846,825 (GRCm39) |
T74A |
possibly damaging |
Het |
Crisp4 |
A |
G |
1: 18,198,934 (GRCm39) |
S124P |
probably damaging |
Het |
Eddm3b |
T |
A |
14: 51,354,178 (GRCm39) |
D55E |
probably damaging |
Het |
Elmo1 |
C |
A |
13: 20,633,656 (GRCm39) |
N439K |
probably benign |
Het |
Fabp12 |
T |
C |
3: 10,315,167 (GRCm39) |
N60S |
probably benign |
Het |
Fat2 |
T |
A |
11: 55,178,704 (GRCm39) |
H1452L |
probably benign |
Het |
Flacc1 |
A |
G |
1: 58,730,919 (GRCm39) |
S46P |
possibly damaging |
Het |
Flrt2 |
T |
C |
12: 95,746,712 (GRCm39) |
V350A |
possibly damaging |
Het |
Ganab |
T |
C |
19: 8,889,301 (GRCm39) |
F626S |
probably damaging |
Het |
Ghr |
T |
C |
15: 3,349,561 (GRCm39) |
Y539C |
probably benign |
Het |
Gm6871 |
T |
C |
7: 41,197,525 (GRCm39) |
T112A |
probably damaging |
Het |
Gm7133 |
T |
A |
1: 97,110,848 (GRCm39) |
|
noncoding transcript |
Het |
Gon4l |
A |
C |
3: 88,802,835 (GRCm39) |
I1149L |
probably benign |
Het |
Greb1l |
G |
A |
18: 10,511,409 (GRCm39) |
D45N |
probably benign |
Het |
H2-K2 |
A |
G |
17: 34,215,989 (GRCm39) |
|
probably benign |
Het |
Herc2 |
C |
T |
7: 55,818,618 (GRCm39) |
R2770* |
probably null |
Het |
Insyn2b |
G |
A |
11: 34,352,788 (GRCm39) |
E277K |
probably damaging |
Het |
Itsn2 |
A |
G |
12: 4,683,553 (GRCm39) |
|
probably benign |
Het |
Klb |
A |
G |
5: 65,506,140 (GRCm39) |
D129G |
probably damaging |
Het |
Klf1 |
A |
G |
8: 85,629,969 (GRCm39) |
I265V |
probably benign |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Map3k10 |
T |
C |
7: 27,357,957 (GRCm39) |
E607G |
probably benign |
Het |
Melk |
C |
T |
4: 44,363,730 (GRCm39) |
T592M |
probably damaging |
Het |
Mroh6 |
A |
G |
15: 75,757,639 (GRCm39) |
L457P |
probably damaging |
Het |
Mrpl21 |
T |
A |
19: 3,337,012 (GRCm39) |
C128S |
probably damaging |
Het |
Or51f23 |
T |
C |
7: 102,453,327 (GRCm39) |
V214A |
probably benign |
Het |
Paqr4 |
G |
T |
17: 23,957,187 (GRCm39) |
H105Q |
probably damaging |
Het |
Pcdhga10 |
A |
G |
18: 37,881,747 (GRCm39) |
I503V |
probably benign |
Het |
Pds5a |
T |
C |
5: 65,821,271 (GRCm39) |
N151S |
probably damaging |
Het |
Pif1 |
A |
G |
9: 65,499,111 (GRCm39) |
T444A |
possibly damaging |
Het |
Ppp2r3d |
T |
C |
9: 101,031,064 (GRCm39) |
R851G |
probably damaging |
Het |
R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
Ros1 |
T |
G |
10: 51,927,104 (GRCm39) |
Q2172P |
probably damaging |
Het |
Rpe65 |
A |
G |
3: 159,309,984 (GRCm39) |
T86A |
probably benign |
Het |
Rpl18a |
G |
A |
8: 71,348,932 (GRCm39) |
R15C |
possibly damaging |
Het |
Sh3tc2 |
A |
G |
18: 62,108,684 (GRCm39) |
K258R |
probably benign |
Het |
Ska3 |
T |
A |
14: 58,059,573 (GRCm39) |
E84V |
possibly damaging |
Het |
Slc25a40 |
T |
A |
5: 8,497,409 (GRCm39) |
|
probably null |
Het |
Slf1 |
A |
T |
13: 77,252,700 (GRCm39) |
S274T |
probably benign |
Het |
Spata21 |
A |
T |
4: 140,830,332 (GRCm39) |
Q267H |
probably damaging |
Het |
Strbp |
A |
T |
2: 37,517,455 (GRCm39) |
W207R |
possibly damaging |
Het |
Taf6l |
T |
C |
19: 8,752,326 (GRCm39) |
E454G |
probably damaging |
Het |
Tcam1 |
C |
A |
11: 106,176,353 (GRCm39) |
L360I |
probably benign |
Het |
Tnxb |
G |
A |
17: 34,922,582 (GRCm39) |
R2465H |
possibly damaging |
Het |
Trim66 |
T |
A |
7: 109,056,797 (GRCm39) |
Y1120F |
probably benign |
Het |
Trp53 |
T |
A |
11: 69,480,031 (GRCm39) |
M243K |
probably damaging |
Het |
Ttl |
T |
A |
2: 128,910,831 (GRCm39) |
C72S |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,539,240 (GRCm39) |
V34582A |
probably benign |
Het |
Uqcrh |
T |
C |
4: 115,927,101 (GRCm39) |
T31A |
possibly damaging |
Het |
Usp40 |
A |
G |
1: 87,923,504 (GRCm39) |
C256R |
probably benign |
Het |
Wdr72 |
A |
T |
9: 74,064,653 (GRCm39) |
I562F |
probably damaging |
Het |
Wnt4 |
A |
G |
4: 137,005,061 (GRCm39) |
N24S |
probably benign |
Het |
|
Other mutations in Vmn1r168 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01761:Vmn1r168
|
APN |
7 |
23,241,070 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02621:Vmn1r168
|
APN |
7 |
23,240,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Vmn1r168
|
APN |
7 |
23,240,916 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4466001:Vmn1r168
|
UTSW |
7 |
23,240,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R0320:Vmn1r168
|
UTSW |
7 |
23,240,767 (GRCm39) |
missense |
probably benign |
0.12 |
R1595:Vmn1r168
|
UTSW |
7 |
23,240,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1618:Vmn1r168
|
UTSW |
7 |
23,240,725 (GRCm39) |
missense |
probably benign |
0.02 |
R1808:Vmn1r168
|
UTSW |
7 |
23,240,184 (GRCm39) |
missense |
probably benign |
0.05 |
R2418:Vmn1r168
|
UTSW |
7 |
23,240,824 (GRCm39) |
missense |
probably benign |
0.05 |
R2419:Vmn1r168
|
UTSW |
7 |
23,240,824 (GRCm39) |
missense |
probably benign |
0.05 |
R4846:Vmn1r168
|
UTSW |
7 |
23,240,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Vmn1r168
|
UTSW |
7 |
23,240,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R6265:Vmn1r168
|
UTSW |
7 |
23,240,961 (GRCm39) |
missense |
probably benign |
|
R6353:Vmn1r168
|
UTSW |
7 |
23,240,944 (GRCm39) |
missense |
probably benign |
0.02 |
R6768:Vmn1r168
|
UTSW |
7 |
23,240,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R6921:Vmn1r168
|
UTSW |
7 |
23,240,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Vmn1r168
|
UTSW |
7 |
23,240,487 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8749:Vmn1r168
|
UTSW |
7 |
23,240,428 (GRCm39) |
missense |
probably benign |
0.10 |
R9749:Vmn1r168
|
UTSW |
7 |
23,240,237 (GRCm39) |
missense |
probably damaging |
0.98 |
R9768:Vmn1r168
|
UTSW |
7 |
23,240,509 (GRCm39) |
missense |
probably benign |
0.02 |
|