Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930018P22Rik |
C |
T |
2: 103,953,564 (GRCm39) |
T130I |
probably benign |
Het |
Ahi1 |
T |
C |
10: 20,876,450 (GRCm39) |
L787P |
possibly damaging |
Het |
Atf3 |
A |
G |
1: 190,909,640 (GRCm39) |
S10P |
probably benign |
Het |
Cdr2l |
A |
G |
11: 115,281,726 (GRCm39) |
N77S |
probably damaging |
Het |
Cnp |
A |
G |
11: 100,467,525 (GRCm39) |
D156G |
probably benign |
Het |
Cntn3 |
A |
T |
6: 102,145,894 (GRCm39) |
D982E |
probably damaging |
Het |
Col22a1 |
A |
G |
15: 71,878,587 (GRCm39) |
L190S |
probably damaging |
Het |
Csmd3 |
C |
T |
15: 47,777,325 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,384,607 (GRCm39) |
D3117G |
probably damaging |
Het |
Dock5 |
T |
C |
14: 67,994,558 (GRCm39) |
E1834G |
probably null |
Het |
Eea1 |
A |
G |
10: 95,877,389 (GRCm39) |
T1368A |
probably benign |
Het |
Fam83f |
T |
C |
15: 80,556,350 (GRCm39) |
V78A |
probably benign |
Het |
Fcgbp |
G |
A |
7: 27,800,898 (GRCm39) |
V1315I |
probably damaging |
Het |
Fsd2 |
A |
T |
7: 81,198,671 (GRCm39) |
Y364* |
probably null |
Het |
Gm21976 |
G |
A |
13: 98,439,057 (GRCm39) |
G16R |
probably null |
Het |
Guca2b |
A |
G |
4: 119,514,885 (GRCm39) |
S59P |
probably damaging |
Het |
Hars2 |
A |
G |
18: 36,919,231 (GRCm39) |
E123G |
probably damaging |
Het |
Hdac2 |
A |
T |
10: 36,876,370 (GRCm39) |
K462* |
probably null |
Het |
Huwe1 |
T |
A |
X: 150,710,622 (GRCm39) |
|
probably benign |
Het |
Iqgap3 |
T |
A |
3: 87,997,611 (GRCm39) |
N262K |
probably benign |
Het |
Kat6b |
A |
G |
14: 21,719,826 (GRCm39) |
S1502G |
probably damaging |
Het |
Mapkapk3 |
A |
T |
9: 107,134,279 (GRCm39) |
D328E |
probably benign |
Het |
Naca |
C |
T |
10: 127,877,437 (GRCm39) |
|
probably benign |
Het |
Npffr1 |
T |
C |
10: 61,449,918 (GRCm39) |
V64A |
probably damaging |
Het |
Oga |
A |
G |
19: 45,750,682 (GRCm39) |
F671S |
probably damaging |
Het |
Or2t49 |
A |
G |
11: 58,393,211 (GRCm39) |
L57P |
probably damaging |
Het |
Or8b3b |
T |
A |
9: 38,584,564 (GRCm39) |
M72L |
probably damaging |
Het |
Pcca |
A |
G |
14: 123,126,945 (GRCm39) |
D718G |
probably damaging |
Het |
Pde6a |
A |
C |
18: 61,397,326 (GRCm39) |
D670A |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,320,417 (GRCm39) |
E292V |
probably benign |
Het |
Prmt9 |
A |
C |
8: 78,291,698 (GRCm39) |
M357L |
probably benign |
Het |
Ptgfr |
A |
T |
3: 151,540,963 (GRCm39) |
S182T |
probably benign |
Het |
Rtraf |
A |
T |
14: 19,866,260 (GRCm39) |
M152K |
possibly damaging |
Het |
Satb1 |
T |
C |
17: 52,049,717 (GRCm39) |
D579G |
possibly damaging |
Het |
Serpinb6a |
A |
G |
13: 34,115,453 (GRCm39) |
|
probably null |
Het |
Slc5a9 |
T |
C |
4: 111,747,497 (GRCm39) |
I297V |
possibly damaging |
Het |
Slf1 |
T |
A |
13: 77,195,223 (GRCm39) |
|
probably benign |
Het |
St8sia2 |
C |
T |
7: 73,616,559 (GRCm39) |
V139M |
probably damaging |
Het |
Tas2r114 |
T |
C |
6: 131,666,243 (GRCm39) |
M262V |
probably benign |
Het |
Tmem147 |
A |
G |
7: 30,428,847 (GRCm39) |
|
probably benign |
Het |
Tmem220 |
A |
G |
11: 66,924,933 (GRCm39) |
|
probably null |
Het |
Uspl1 |
A |
G |
5: 149,125,156 (GRCm39) |
N35S |
possibly damaging |
Het |
Vmn2r121 |
T |
G |
X: 123,037,591 (GRCm39) |
I810L |
probably damaging |
Het |
Wbp2nl |
A |
T |
15: 82,189,945 (GRCm39) |
T46S |
possibly damaging |
Het |
Zfp955b |
T |
A |
17: 33,519,940 (GRCm39) |
M57K |
probably benign |
Het |
|
Other mutations in Vmn1r170 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02005:Vmn1r170
|
APN |
7 |
23,306,338 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02150:Vmn1r170
|
APN |
7 |
23,306,465 (GRCm39) |
nonsense |
probably null |
|
IGL02216:Vmn1r170
|
APN |
7 |
23,305,915 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02749:Vmn1r170
|
APN |
7 |
23,305,716 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02807:Vmn1r170
|
APN |
7 |
23,305,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02828:Vmn1r170
|
APN |
7 |
23,305,943 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03073:Vmn1r170
|
APN |
7 |
23,306,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03151:Vmn1r170
|
APN |
7 |
23,306,002 (GRCm39) |
missense |
probably benign |
0.35 |
R0079:Vmn1r170
|
UTSW |
7 |
23,305,735 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0266:Vmn1r170
|
UTSW |
7 |
23,305,906 (GRCm39) |
missense |
probably benign |
0.00 |
R0980:Vmn1r170
|
UTSW |
7 |
23,305,759 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1345:Vmn1r170
|
UTSW |
7 |
23,305,787 (GRCm39) |
missense |
probably benign |
0.00 |
R1620:Vmn1r170
|
UTSW |
7 |
23,305,754 (GRCm39) |
missense |
probably benign |
0.30 |
R1713:Vmn1r170
|
UTSW |
7 |
23,306,288 (GRCm39) |
missense |
probably benign |
0.30 |
R1745:Vmn1r170
|
UTSW |
7 |
23,305,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R1974:Vmn1r170
|
UTSW |
7 |
23,305,906 (GRCm39) |
missense |
probably benign |
0.00 |
R2163:Vmn1r170
|
UTSW |
7 |
23,306,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R3812:Vmn1r170
|
UTSW |
7 |
23,305,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Vmn1r170
|
UTSW |
7 |
23,306,087 (GRCm39) |
missense |
probably benign |
0.25 |
R5309:Vmn1r170
|
UTSW |
7 |
23,305,880 (GRCm39) |
missense |
probably damaging |
0.97 |
R5378:Vmn1r170
|
UTSW |
7 |
23,305,963 (GRCm39) |
missense |
probably benign |
0.00 |
R5379:Vmn1r170
|
UTSW |
7 |
23,306,054 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5661:Vmn1r170
|
UTSW |
7 |
23,306,231 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5673:Vmn1r170
|
UTSW |
7 |
23,305,630 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6181:Vmn1r170
|
UTSW |
7 |
23,305,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R6192:Vmn1r170
|
UTSW |
7 |
23,305,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Vmn1r170
|
UTSW |
7 |
23,306,320 (GRCm39) |
missense |
not run |
|
R7667:Vmn1r170
|
UTSW |
7 |
23,306,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Vmn1r170
|
UTSW |
7 |
23,306,321 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8699:Vmn1r170
|
UTSW |
7 |
23,306,080 (GRCm39) |
nonsense |
probably null |
|
R8927:Vmn1r170
|
UTSW |
7 |
23,305,814 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8928:Vmn1r170
|
UTSW |
7 |
23,305,814 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9269:Vmn1r170
|
UTSW |
7 |
23,306,263 (GRCm39) |
missense |
probably benign |
0.02 |
R9569:Vmn1r170
|
UTSW |
7 |
23,306,294 (GRCm39) |
missense |
probably benign |
0.19 |
X0060:Vmn1r170
|
UTSW |
7 |
23,306,368 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Vmn1r170
|
UTSW |
7 |
23,305,835 (GRCm39) |
missense |
possibly damaging |
0.89 |
|