Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp2 |
A |
T |
2: 91,037,060 (GRCm39) |
|
probably null |
Het |
Aire |
G |
A |
10: 77,866,130 (GRCm39) |
A536V |
probably damaging |
Het |
Aox4 |
A |
G |
1: 58,294,645 (GRCm39) |
I951M |
probably benign |
Het |
Ash1l |
G |
T |
3: 88,950,848 (GRCm39) |
C2190F |
probably damaging |
Het |
C1s1 |
C |
T |
6: 124,510,359 (GRCm39) |
V363M |
probably damaging |
Het |
Diaph3 |
A |
T |
14: 87,352,456 (GRCm39) |
D48E |
possibly damaging |
Het |
Dnajc13 |
A |
G |
9: 104,095,763 (GRCm39) |
V559A |
probably benign |
Het |
Dzank1 |
T |
C |
2: 144,323,614 (GRCm39) |
I610V |
probably benign |
Het |
F7 |
A |
G |
8: 13,085,209 (GRCm39) |
I412V |
probably benign |
Het |
Flt1 |
A |
G |
5: 147,525,382 (GRCm39) |
S919P |
probably damaging |
Het |
Igkv4-70 |
C |
A |
6: 69,244,975 (GRCm39) |
R82L |
probably damaging |
Het |
Lnp1 |
T |
A |
16: 56,748,281 (GRCm39) |
R4* |
probably null |
Het |
Lrrc3b |
T |
C |
14: 15,358,018 (GRCm38) |
N196S |
probably benign |
Het |
Mlxip |
A |
G |
5: 123,588,558 (GRCm39) |
D816G |
probably damaging |
Het |
Myh7 |
C |
T |
14: 55,221,119 (GRCm39) |
E935K |
possibly damaging |
Het |
Myom3 |
A |
T |
4: 135,516,947 (GRCm39) |
H839L |
probably benign |
Het |
Nebl |
C |
T |
2: 17,381,433 (GRCm39) |
|
probably null |
Het |
Ninj1 |
T |
C |
13: 49,347,432 (GRCm39) |
I99T |
probably damaging |
Het |
Or11g1 |
A |
C |
14: 50,651,786 (GRCm39) |
M262L |
probably damaging |
Het |
Or2l5 |
A |
G |
16: 19,334,258 (GRCm39) |
S43P |
possibly damaging |
Het |
Or4a76 |
T |
A |
2: 89,460,448 (GRCm39) |
I265F |
possibly damaging |
Het |
Or8g55 |
A |
T |
9: 39,785,146 (GRCm39) |
T192S |
possibly damaging |
Het |
Otop1 |
A |
G |
5: 38,445,364 (GRCm39) |
H174R |
probably damaging |
Het |
Pcdhb16 |
A |
G |
18: 37,611,510 (GRCm39) |
N157D |
possibly damaging |
Het |
Prss44 |
A |
C |
9: 110,643,746 (GRCm39) |
Q130P |
probably damaging |
Het |
Ptpn4 |
T |
A |
1: 119,607,925 (GRCm39) |
M712L |
probably damaging |
Het |
Ptprh |
C |
A |
7: 4,574,987 (GRCm39) |
S344I |
probably benign |
Het |
Rps6kl1 |
T |
C |
12: 85,196,566 (GRCm39) |
I33V |
possibly damaging |
Het |
Scn1a |
T |
C |
2: 66,148,156 (GRCm39) |
S110G |
probably damaging |
Het |
Sdk2 |
C |
A |
11: 113,784,267 (GRCm39) |
K157N |
possibly damaging |
Het |
Serpina1d |
A |
T |
12: 103,733,815 (GRCm39) |
V163D |
probably damaging |
Het |
Serpina3g |
T |
C |
12: 104,205,428 (GRCm39) |
S56P |
probably benign |
Het |
Slc4a4 |
T |
C |
5: 89,318,640 (GRCm39) |
L636P |
probably benign |
Het |
Slc6a1 |
T |
C |
6: 114,288,863 (GRCm39) |
F474S |
probably benign |
Het |
Slco6d1 |
A |
G |
1: 98,356,141 (GRCm39) |
D235G |
probably damaging |
Het |
Srgn |
A |
T |
10: 62,330,763 (GRCm39) |
M114K |
possibly damaging |
Het |
Syne3 |
A |
T |
12: 104,929,491 (GRCm39) |
V243E |
probably damaging |
Het |
Tcf19 |
A |
G |
17: 35,825,804 (GRCm39) |
F118L |
probably damaging |
Het |
Tln2 |
A |
T |
9: 67,165,742 (GRCm39) |
|
probably null |
Het |
Tnxb |
A |
G |
17: 34,907,672 (GRCm39) |
T1239A |
probably damaging |
Het |
Traip |
A |
G |
9: 107,848,241 (GRCm39) |
I453M |
probably benign |
Het |
Vmn1r157 |
C |
T |
7: 22,461,210 (GRCm39) |
A30V |
probably damaging |
Het |
Vps13d |
G |
A |
4: 144,822,854 (GRCm39) |
R2976* |
probably null |
Het |
Wdr75 |
T |
C |
1: 45,858,795 (GRCm39) |
F655L |
probably benign |
Het |
Wwp1 |
A |
G |
4: 19,650,114 (GRCm39) |
|
probably null |
Het |
Zc3h4 |
T |
C |
7: 16,166,909 (GRCm39) |
L747P |
unknown |
Het |
Zfp268 |
G |
A |
4: 145,349,126 (GRCm39) |
D188N |
possibly damaging |
Het |
|
Other mutations in Vmn1r233 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01843:Vmn1r233
|
APN |
17 |
21,214,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01912:Vmn1r233
|
APN |
17 |
21,214,467 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02642:Vmn1r233
|
APN |
17 |
21,214,291 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02730:Vmn1r233
|
APN |
17 |
21,214,057 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02754:Vmn1r233
|
APN |
17 |
21,214,886 (GRCm39) |
missense |
probably benign |
|
IGL02754:Vmn1r233
|
APN |
17 |
21,214,887 (GRCm39) |
missense |
probably benign |
0.37 |
BB018:Vmn1r233
|
UTSW |
17 |
21,214,125 (GRCm39) |
missense |
probably benign |
|
R0368:Vmn1r233
|
UTSW |
17 |
21,214,869 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1894:Vmn1r233
|
UTSW |
17 |
21,213,994 (GRCm39) |
missense |
probably benign |
0.02 |
R2507:Vmn1r233
|
UTSW |
17 |
21,214,110 (GRCm39) |
missense |
probably benign |
0.29 |
R4609:Vmn1r233
|
UTSW |
17 |
21,214,677 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4662:Vmn1r233
|
UTSW |
17 |
21,214,393 (GRCm39) |
missense |
probably benign |
0.16 |
R4686:Vmn1r233
|
UTSW |
17 |
21,214,368 (GRCm39) |
missense |
probably benign |
0.33 |
R4721:Vmn1r233
|
UTSW |
17 |
21,214,879 (GRCm39) |
missense |
probably benign |
|
R5559:Vmn1r233
|
UTSW |
17 |
21,214,839 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5651:Vmn1r233
|
UTSW |
17 |
21,214,279 (GRCm39) |
missense |
probably benign |
0.00 |
R6642:Vmn1r233
|
UTSW |
17 |
21,214,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R7285:Vmn1r233
|
UTSW |
17 |
21,214,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R7931:Vmn1r233
|
UTSW |
17 |
21,214,125 (GRCm39) |
missense |
probably benign |
|
R7936:Vmn1r233
|
UTSW |
17 |
21,214,237 (GRCm39) |
nonsense |
probably null |
|
R7984:Vmn1r233
|
UTSW |
17 |
21,214,417 (GRCm39) |
missense |
probably damaging |
0.99 |
R8059:Vmn1r233
|
UTSW |
17 |
21,214,698 (GRCm39) |
missense |
probably benign |
0.06 |
R9422:Vmn1r233
|
UTSW |
17 |
21,214,069 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1176:Vmn1r233
|
UTSW |
17 |
21,214,920 (GRCm39) |
missense |
probably damaging |
0.98 |
|