Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano4 |
A |
G |
10: 88,870,961 (GRCm39) |
Y238H |
probably damaging |
Het |
Apol7a |
T |
C |
15: 77,274,055 (GRCm39) |
|
probably benign |
Het |
Cacna1d |
A |
T |
14: 29,773,699 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,541,023 (GRCm39) |
V2368A |
probably damaging |
Het |
Creb3l4 |
A |
G |
3: 90,150,138 (GRCm39) |
M1T |
probably null |
Het |
Dpys |
T |
C |
15: 39,710,045 (GRCm39) |
D128G |
probably damaging |
Het |
Ero1b |
A |
G |
13: 12,616,623 (GRCm39) |
|
probably null |
Het |
Fcgbpl1 |
T |
C |
7: 27,854,743 (GRCm39) |
C1790R |
probably damaging |
Het |
Fcgr4 |
A |
G |
1: 170,853,358 (GRCm39) |
S188G |
possibly damaging |
Het |
Fry |
A |
G |
5: 150,346,252 (GRCm39) |
D1587G |
probably benign |
Het |
Gm43638 |
T |
A |
5: 87,634,473 (GRCm39) |
R45* |
probably null |
Het |
Gm7647 |
T |
A |
5: 95,111,746 (GRCm39) |
C152S |
probably benign |
Het |
Golga3 |
T |
G |
5: 110,335,583 (GRCm39) |
M299R |
probably benign |
Het |
Iqub |
A |
T |
6: 24,501,005 (GRCm39) |
|
probably benign |
Het |
Irak3 |
A |
T |
10: 119,978,695 (GRCm39) |
Y493* |
probably null |
Het |
Jakmip1 |
G |
T |
5: 37,242,750 (GRCm39) |
E13* |
probably null |
Het |
Morc3 |
G |
A |
16: 93,659,534 (GRCm39) |
C446Y |
probably damaging |
Het |
Mroh2b |
G |
A |
15: 4,971,024 (GRCm39) |
D1010N |
probably damaging |
Het |
Or14c44 |
A |
G |
7: 86,061,998 (GRCm39) |
T184A |
probably damaging |
Het |
Or2y16 |
T |
A |
11: 49,335,201 (GRCm39) |
N174K |
probably damaging |
Het |
Or5m9 |
A |
T |
2: 85,876,996 (GRCm39) |
M57L |
possibly damaging |
Het |
Pkhd1 |
G |
A |
1: 20,593,482 (GRCm39) |
H1544Y |
possibly damaging |
Het |
Rps2-ps10 |
C |
T |
18: 61,392,896 (GRCm39) |
|
probably benign |
Het |
Smco1 |
T |
C |
16: 32,092,887 (GRCm39) |
V186A |
probably damaging |
Het |
Snx1 |
C |
T |
9: 66,001,713 (GRCm39) |
E314K |
possibly damaging |
Het |
Timd2 |
T |
C |
11: 46,567,170 (GRCm39) |
Y255C |
probably benign |
Het |
Tnc |
A |
T |
4: 63,935,571 (GRCm39) |
I455K |
probably benign |
Het |
Tsc22d1 |
A |
G |
14: 76,656,181 (GRCm39) |
I31V |
possibly damaging |
Het |
Tyk2 |
A |
G |
9: 21,031,996 (GRCm39) |
S360P |
probably benign |
Het |
Uroc1 |
G |
T |
6: 90,335,883 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn1r122 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01322:Vmn1r122
|
APN |
7 |
20,868,036 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01397:Vmn1r122
|
APN |
7 |
20,867,707 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02894:Vmn1r122
|
APN |
7 |
20,867,649 (GRCm39) |
missense |
probably benign |
|
R1837:Vmn1r122
|
UTSW |
7 |
20,867,291 (GRCm39) |
missense |
probably benign |
0.34 |
R3040:Vmn1r122
|
UTSW |
7 |
20,867,371 (GRCm39) |
missense |
probably benign |
|
R4111:Vmn1r122
|
UTSW |
7 |
20,867,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R4868:Vmn1r122
|
UTSW |
7 |
20,867,227 (GRCm39) |
missense |
probably benign |
0.01 |
R5239:Vmn1r122
|
UTSW |
7 |
20,868,023 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6851:Vmn1r122
|
UTSW |
7 |
20,867,845 (GRCm39) |
missense |
probably benign |
|
R7010:Vmn1r122
|
UTSW |
7 |
20,867,896 (GRCm39) |
missense |
probably damaging |
0.97 |
R7184:Vmn1r122
|
UTSW |
7 |
20,867,820 (GRCm39) |
missense |
probably benign |
0.14 |
R7922:Vmn1r122
|
UTSW |
7 |
20,867,587 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8539:Vmn1r122
|
UTSW |
7 |
20,867,281 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9344:Vmn1r122
|
UTSW |
7 |
20,867,271 (GRCm39) |
missense |
probably benign |
0.07 |
|