Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apbb1ip |
T |
G |
2: 22,743,194 (GRCm39) |
I342S |
probably damaging |
Het |
Armh4 |
A |
T |
14: 50,005,923 (GRCm39) |
S591T |
probably damaging |
Het |
Atp6v1e1 |
T |
C |
6: 120,772,654 (GRCm39) |
|
probably benign |
Het |
Brwd1 |
A |
T |
16: 95,848,579 (GRCm39) |
C533* |
probably null |
Het |
Cacna2d4 |
A |
G |
6: 119,219,865 (GRCm39) |
S212G |
probably damaging |
Het |
Ccn5 |
A |
G |
2: 163,670,942 (GRCm39) |
R150G |
probably damaging |
Het |
Cit |
T |
C |
5: 116,011,902 (GRCm39) |
|
probably benign |
Het |
Clca3a1 |
C |
T |
3: 144,713,539 (GRCm39) |
M697I |
probably benign |
Het |
Cmklr1 |
T |
C |
5: 113,752,282 (GRCm39) |
T240A |
probably benign |
Het |
D630003M21Rik |
T |
C |
2: 158,059,276 (GRCm39) |
D208G |
probably benign |
Het |
Egr3 |
C |
A |
14: 70,316,732 (GRCm39) |
P143Q |
probably damaging |
Het |
Fbxw18 |
T |
A |
9: 109,530,675 (GRCm39) |
S41C |
probably damaging |
Het |
Focad |
T |
A |
4: 88,244,465 (GRCm39) |
I815N |
unknown |
Het |
Heatr5b |
T |
C |
17: 79,137,026 (GRCm39) |
T165A |
probably benign |
Het |
Iqub |
G |
T |
6: 24,505,627 (GRCm39) |
L94I |
probably benign |
Het |
Lrrc32 |
T |
C |
7: 98,147,583 (GRCm39) |
L121P |
probably damaging |
Het |
Mansc1 |
G |
A |
6: 134,594,289 (GRCm39) |
L118F |
probably damaging |
Het |
Mtor |
A |
G |
4: 148,615,214 (GRCm39) |
H1693R |
possibly damaging |
Het |
Muc5b |
A |
G |
7: 141,416,831 (GRCm39) |
Q3259R |
probably benign |
Het |
Nmnat2 |
A |
G |
1: 152,988,189 (GRCm39) |
S273G |
possibly damaging |
Het |
Npr2 |
T |
C |
4: 43,640,554 (GRCm39) |
C336R |
possibly damaging |
Het |
Or10al6 |
C |
T |
17: 38,083,122 (GRCm39) |
L193F |
probably damaging |
Het |
Or1f19 |
A |
G |
16: 3,410,848 (GRCm39) |
N196S |
possibly damaging |
Het |
Or1j11 |
A |
T |
2: 36,311,466 (GRCm39) |
I19F |
probably damaging |
Het |
Or56b1b |
A |
G |
7: 108,164,216 (GRCm39) |
V262A |
possibly damaging |
Het |
Or5aq1 |
A |
T |
2: 86,966,343 (GRCm39) |
Y107* |
probably null |
Het |
Or5d36 |
T |
C |
2: 87,901,468 (GRCm39) |
N86S |
possibly damaging |
Het |
Rad54l2 |
C |
T |
9: 106,579,971 (GRCm39) |
A967T |
probably damaging |
Het |
Rspo1 |
T |
C |
4: 124,898,829 (GRCm39) |
V50A |
possibly damaging |
Het |
Sar1b |
C |
T |
11: 51,682,274 (GRCm39) |
|
probably benign |
Het |
Scamp1 |
C |
T |
13: 94,340,530 (GRCm39) |
A280T |
probably damaging |
Het |
Spcs2 |
A |
G |
7: 99,488,911 (GRCm39) |
I251T |
probably benign |
Het |
Sspo |
G |
T |
6: 48,441,600 (GRCm39) |
|
probably null |
Het |
Tpm2 |
T |
A |
4: 43,518,251 (GRCm39) |
K251* |
probably null |
Het |
Ttn |
A |
G |
2: 76,571,250 (GRCm39) |
S26548P |
probably damaging |
Het |
Ugcg |
T |
G |
4: 59,213,865 (GRCm39) |
V149G |
possibly damaging |
Het |
Unc79 |
T |
A |
12: 103,045,177 (GRCm39) |
N784K |
probably damaging |
Het |
Vit |
A |
G |
17: 78,932,633 (GRCm39) |
D580G |
probably damaging |
Het |
Zbtb3 |
A |
G |
19: 8,781,680 (GRCm39) |
Y431C |
probably damaging |
Het |
Zfp608 |
T |
C |
18: 55,032,083 (GRCm39) |
D619G |
possibly damaging |
Het |
|
Other mutations in Vmn1r83 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01371:Vmn1r83
|
APN |
7 |
12,055,160 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01793:Vmn1r83
|
APN |
7 |
12,055,504 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02137:Vmn1r83
|
APN |
7 |
12,055,761 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03155:Vmn1r83
|
APN |
7 |
12,055,617 (GRCm39) |
missense |
probably benign |
|
IGL03182:Vmn1r83
|
APN |
7 |
12,055,617 (GRCm39) |
missense |
probably benign |
|
R0627:Vmn1r83
|
UTSW |
7 |
12,055,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R1511:Vmn1r83
|
UTSW |
7 |
12,055,197 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3882:Vmn1r83
|
UTSW |
7 |
12,055,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Vmn1r83
|
UTSW |
7 |
12,055,695 (GRCm39) |
missense |
probably benign |
0.00 |
R4678:Vmn1r83
|
UTSW |
7 |
12,055,697 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5580:Vmn1r83
|
UTSW |
7 |
12,055,800 (GRCm39) |
missense |
probably benign |
0.01 |
R6982:Vmn1r83
|
UTSW |
7 |
12,055,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R7440:Vmn1r83
|
UTSW |
7 |
12,055,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7476:Vmn1r83
|
UTSW |
7 |
12,055,542 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7522:Vmn1r83
|
UTSW |
7 |
12,055,505 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7759:Vmn1r83
|
UTSW |
7 |
12,055,360 (GRCm39) |
missense |
probably benign |
0.06 |
R8886:Vmn1r83
|
UTSW |
7 |
12,055,843 (GRCm39) |
missense |
probably benign |
0.10 |
R9077:Vmn1r83
|
UTSW |
7 |
12,055,571 (GRCm39) |
missense |
probably damaging |
1.00 |
|