Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,167,278 (GRCm39) |
|
probably null |
Het |
AU040320 |
T |
A |
4: 126,708,166 (GRCm39) |
S261T |
probably benign |
Het |
Banp |
T |
A |
8: 122,705,326 (GRCm39) |
C65* |
probably null |
Het |
Bloc1s5 |
T |
C |
13: 38,787,850 (GRCm39) |
D178G |
probably benign |
Het |
Cacna1c |
A |
G |
6: 118,575,727 (GRCm39) |
F1941L |
|
Het |
Ccdc121rt3 |
T |
C |
5: 112,503,063 (GRCm39) |
K214E |
probably benign |
Het |
Cd48 |
A |
G |
1: 171,523,348 (GRCm39) |
I64V |
probably damaging |
Het |
Cela3a |
A |
G |
4: 137,135,501 (GRCm39) |
S21P |
probably benign |
Het |
Cidec |
A |
G |
6: 113,411,415 (GRCm39) |
Y12H |
possibly damaging |
Het |
Col12a1 |
C |
G |
9: 79,588,803 (GRCm39) |
R1104T |
probably damaging |
Het |
Ctsf |
T |
G |
19: 4,906,567 (GRCm39) |
F165V |
probably damaging |
Het |
Cux2 |
T |
C |
5: 122,006,648 (GRCm39) |
D874G |
possibly damaging |
Het |
Dbnl |
C |
T |
11: 5,748,048 (GRCm39) |
L298F |
probably benign |
Het |
Dnah1 |
C |
A |
14: 31,032,866 (GRCm39) |
V390F |
probably benign |
Het |
Dnah17 |
T |
C |
11: 118,012,304 (GRCm39) |
D486G |
possibly damaging |
Het |
Dnah17 |
T |
C |
11: 117,916,466 (GRCm39) |
I4236V |
probably benign |
Het |
Dpp6 |
T |
A |
5: 27,857,274 (GRCm39) |
D406E |
probably benign |
Het |
Dsp |
C |
T |
13: 38,359,183 (GRCm39) |
A318V |
possibly damaging |
Het |
Duox1 |
T |
C |
2: 122,160,120 (GRCm39) |
L745P |
possibly damaging |
Het |
Ell |
C |
A |
8: 70,992,364 (GRCm39) |
A3E |
possibly damaging |
Het |
Fer1l5 |
T |
A |
1: 36,459,775 (GRCm39) |
L1832* |
probably null |
Het |
Filip1 |
G |
T |
9: 79,727,931 (GRCm39) |
N229K |
probably benign |
Het |
Flg |
A |
T |
3: 93,200,089 (GRCm39) |
H195L |
unknown |
Het |
Fndc7 |
G |
T |
3: 108,770,129 (GRCm39) |
P685H |
probably damaging |
Het |
Ggt1 |
A |
G |
10: 75,412,116 (GRCm39) |
N120S |
probably benign |
Het |
Gm4952 |
A |
T |
19: 12,604,428 (GRCm39) |
H280L |
probably benign |
Het |
Golim4 |
A |
T |
3: 75,794,091 (GRCm39) |
D551E |
probably damaging |
Het |
H3c13 |
C |
A |
3: 96,176,309 (GRCm39) |
Y100* |
probably null |
Het |
Hmbs |
A |
C |
9: 44,248,147 (GRCm39) |
|
probably null |
Het |
Ino80 |
T |
C |
2: 119,273,054 (GRCm39) |
D474G |
probably benign |
Het |
Ipo4 |
A |
C |
14: 55,869,787 (GRCm39) |
H343Q |
probably damaging |
Het |
Jade2 |
C |
T |
11: 51,707,744 (GRCm39) |
R823H |
probably damaging |
Het |
Jakmip1 |
C |
T |
5: 37,274,841 (GRCm39) |
T453I |
probably damaging |
Het |
Klk6 |
T |
C |
7: 43,478,689 (GRCm39) |
S199P |
probably damaging |
Het |
Ltn1 |
A |
T |
16: 87,223,166 (GRCm39) |
Y105N |
probably damaging |
Het |
Map3k19 |
G |
T |
1: 127,756,827 (GRCm39) |
T394N |
probably damaging |
Het |
Megf6 |
G |
A |
4: 154,354,927 (GRCm39) |
D1445N |
probably benign |
Het |
Mmp21 |
A |
G |
7: 133,280,791 (GRCm39) |
Y60H |
probably damaging |
Het |
Mylk4 |
C |
T |
13: 32,904,585 (GRCm39) |
|
probably null |
Het |
Nckipsd |
A |
T |
9: 108,691,216 (GRCm39) |
R38* |
probably null |
Het |
Nob1 |
G |
A |
8: 108,139,737 (GRCm39) |
R341* |
probably null |
Het |
Or11g25 |
A |
G |
14: 50,723,751 (GRCm39) |
T279A |
possibly damaging |
Het |
Or1e19 |
T |
A |
11: 73,324,175 (GRCm39) |
|
probably benign |
Het |
Or5ac22 |
A |
G |
16: 59,134,997 (GRCm39) |
Y258H |
probably damaging |
Het |
Pcdh1 |
A |
G |
18: 38,336,569 (GRCm39) |
L22P |
unknown |
Het |
Pebp4 |
T |
A |
14: 70,297,056 (GRCm39) |
N198K |
probably benign |
Het |
Pkp4 |
T |
C |
2: 59,138,757 (GRCm39) |
S336P |
probably damaging |
Het |
Prr5l |
T |
A |
2: 101,547,442 (GRCm39) |
D361V |
probably benign |
Het |
Ralgapa1 |
C |
G |
12: 55,756,340 (GRCm39) |
V1086L |
probably damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,756,341 (GRCm39) |
Q1085H |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,705,219 (GRCm39) |
N2849S |
probably damaging |
Het |
Slc6a18 |
A |
T |
13: 73,820,915 (GRCm39) |
L223H |
probably damaging |
Het |
Sqstm1 |
T |
G |
11: 50,096,932 (GRCm39) |
|
probably null |
Het |
Syne1 |
T |
C |
10: 5,195,835 (GRCm39) |
E3945G |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,037,161 (GRCm39) |
Y3780C |
probably benign |
Het |
Tecpr1 |
A |
G |
5: 144,140,236 (GRCm39) |
Y840H |
probably damaging |
Het |
Tmem183a |
T |
C |
1: 134,288,539 (GRCm39) |
Q108R |
probably benign |
Het |
Tmtc1 |
A |
T |
6: 148,345,415 (GRCm39) |
C95S |
probably benign |
Het |
Trappc8 |
C |
T |
18: 20,958,119 (GRCm39) |
V1250I |
probably damaging |
Het |
Tshz1 |
A |
G |
18: 84,032,461 (GRCm39) |
V649A |
probably damaging |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Vmn2r63 |
A |
T |
7: 42,577,553 (GRCm39) |
H328Q |
possibly damaging |
Het |
Zeb1 |
T |
C |
18: 5,766,802 (GRCm39) |
S438P |
probably damaging |
Het |
|
Other mutations in Vmn1r123 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00927:Vmn1r123
|
APN |
7 |
20,896,216 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02330:Vmn1r123
|
APN |
7 |
20,896,969 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02742:Vmn1r123
|
APN |
7 |
20,896,968 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03240:Vmn1r123
|
APN |
7 |
20,896,282 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1173:Vmn1r123
|
UTSW |
7 |
20,896,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R6278:Vmn1r123
|
UTSW |
7 |
20,896,774 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6610:Vmn1r123
|
UTSW |
7 |
20,896,515 (GRCm39) |
missense |
probably benign |
0.00 |
R6679:Vmn1r123
|
UTSW |
7 |
20,896,868 (GRCm39) |
nonsense |
probably null |
|
R7241:Vmn1r123
|
UTSW |
7 |
20,896,537 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7642:Vmn1r123
|
UTSW |
7 |
20,896,795 (GRCm39) |
missense |
probably benign |
0.11 |
R7870:Vmn1r123
|
UTSW |
7 |
20,896,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7981:Vmn1r123
|
UTSW |
7 |
20,896,914 (GRCm39) |
missense |
probably damaging |
0.98 |
R8554:Vmn1r123
|
UTSW |
7 |
20,896,971 (GRCm39) |
missense |
probably benign |
|
R9079:Vmn1r123
|
UTSW |
7 |
20,896,979 (GRCm39) |
missense |
probably benign |
0.01 |
R9090:Vmn1r123
|
UTSW |
7 |
20,896,794 (GRCm39) |
missense |
probably benign |
|
R9271:Vmn1r123
|
UTSW |
7 |
20,896,794 (GRCm39) |
missense |
probably benign |
|
R9544:Vmn1r123
|
UTSW |
7 |
20,896,987 (GRCm39) |
missense |
probably benign |
0.30 |
R9779:Vmn1r123
|
UTSW |
7 |
20,896,111 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
|