Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
G |
A |
7: 119,939,806 (GRCm39) |
V303I |
probably benign |
Het |
Abca4 |
G |
T |
3: 121,897,180 (GRCm39) |
V620L |
probably benign |
Het |
Ankk1 |
A |
T |
9: 49,329,995 (GRCm39) |
V320E |
possibly damaging |
Het |
Aoah |
G |
T |
13: 21,184,072 (GRCm39) |
A379S |
probably benign |
Het |
Apol7e |
A |
G |
15: 77,598,667 (GRCm39) |
D44G |
probably benign |
Het |
Atf2 |
T |
C |
2: 73,658,813 (GRCm39) |
|
probably null |
Het |
Cd209b |
T |
C |
8: 3,976,549 (GRCm39) |
|
probably null |
Het |
Chek1 |
G |
A |
9: 36,624,983 (GRCm39) |
S366L |
probably damaging |
Het |
Chpf2 |
T |
C |
5: 24,797,190 (GRCm39) |
L712P |
probably damaging |
Het |
Clmn |
C |
A |
12: 104,750,161 (GRCm39) |
|
probably null |
Het |
Cnksr3 |
T |
C |
10: 7,092,977 (GRCm39) |
D178G |
probably benign |
Het |
Cpox |
T |
C |
16: 58,495,780 (GRCm39) |
Y366H |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,538,056 (GRCm39) |
F3632S |
probably damaging |
Het |
Eif5b |
T |
A |
1: 38,076,388 (GRCm39) |
D645E |
probably damaging |
Het |
Emilin1 |
G |
A |
5: 31,075,966 (GRCm39) |
E736K |
probably damaging |
Het |
Gcnt4 |
G |
A |
13: 97,083,160 (GRCm39) |
R152Q |
probably benign |
Het |
Il6st |
T |
C |
13: 112,618,071 (GRCm39) |
S162P |
probably damaging |
Het |
Iqub |
T |
C |
6: 24,491,601 (GRCm39) |
K362E |
probably benign |
Het |
Kif22 |
G |
T |
7: 126,632,539 (GRCm39) |
P257Q |
possibly damaging |
Het |
Lhx2 |
T |
C |
2: 38,259,053 (GRCm39) |
V378A |
probably damaging |
Het |
Lipo3 |
A |
G |
19: 33,759,630 (GRCm39) |
V202A |
probably benign |
Het |
Lrp1b |
T |
A |
2: 40,553,738 (GRCm39) |
N366I |
unknown |
Het |
Mbip |
T |
C |
12: 56,382,662 (GRCm39) |
D268G |
probably damaging |
Het |
Mc5r |
A |
G |
18: 68,472,564 (GRCm39) |
M308V |
probably benign |
Het |
Mndal |
C |
A |
1: 173,690,070 (GRCm39) |
G420V |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,899,822 (GRCm39) |
N1442K |
probably damaging |
Het |
Ndufv1 |
A |
T |
19: 4,058,811 (GRCm39) |
|
probably null |
Het |
Ofcc1 |
A |
G |
13: 40,360,193 (GRCm39) |
S279P |
probably benign |
Het |
Or4k2 |
A |
T |
14: 50,424,326 (GRCm39) |
M116K |
possibly damaging |
Het |
Or6b2b |
T |
C |
1: 92,419,439 (GRCm39) |
I13V |
probably benign |
Het |
Pabpc1l |
A |
T |
2: 163,891,438 (GRCm39) |
H552L |
probably benign |
Het |
Pigr |
T |
A |
1: 130,774,341 (GRCm39) |
C440* |
probably null |
Het |
Pramel11 |
A |
G |
4: 143,623,490 (GRCm39) |
V228A |
probably benign |
Het |
Prss30 |
C |
T |
17: 24,191,820 (GRCm39) |
V271I |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,741,234 (GRCm39) |
|
probably null |
Het |
Qrich1 |
T |
A |
9: 108,410,807 (GRCm39) |
|
probably benign |
Het |
Rem1 |
C |
G |
2: 152,470,200 (GRCm39) |
A62G |
possibly damaging |
Het |
Rftn1 |
T |
C |
17: 50,354,354 (GRCm39) |
N58S |
probably damaging |
Het |
Rp9 |
G |
A |
9: 22,360,065 (GRCm39) |
|
probably benign |
Het |
Rrp1b |
G |
A |
17: 32,275,658 (GRCm39) |
V402I |
possibly damaging |
Het |
Slc25a33 |
A |
T |
4: 149,838,349 (GRCm39) |
Y108N |
probably benign |
Het |
Slc3a1 |
A |
G |
17: 85,340,008 (GRCm39) |
M189V |
probably damaging |
Het |
Slc44a1 |
A |
C |
4: 53,528,682 (GRCm39) |
K144T |
probably benign |
Het |
Tbc1d13 |
T |
A |
2: 30,027,393 (GRCm39) |
H100Q |
probably damaging |
Het |
Timm29 |
T |
C |
9: 21,504,749 (GRCm39) |
V139A |
probably damaging |
Het |
Tmem70 |
T |
C |
1: 16,735,556 (GRCm39) |
W9R |
possibly damaging |
Het |
Tspan1 |
A |
G |
4: 116,020,502 (GRCm39) |
|
probably null |
Het |
Unc13a |
T |
C |
8: 72,107,773 (GRCm39) |
|
probably null |
Het |
Uroc1 |
T |
C |
6: 90,323,738 (GRCm39) |
F395S |
probably damaging |
Het |
Uvrag |
A |
C |
7: 98,537,284 (GRCm39) |
L637R |
possibly damaging |
Het |
Zfp280d |
C |
T |
9: 72,238,224 (GRCm39) |
T528I |
probably benign |
Het |
Zfp526 |
C |
T |
7: 24,924,601 (GRCm39) |
Q287* |
probably null |
Het |
|
Other mutations in Vmn1r213 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0018:Vmn1r213
|
UTSW |
13 |
23,196,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Vmn1r213
|
UTSW |
13 |
23,195,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R0324:Vmn1r213
|
UTSW |
13 |
23,195,588 (GRCm39) |
intron |
probably benign |
|
R0389:Vmn1r213
|
UTSW |
13 |
23,195,932 (GRCm39) |
missense |
probably benign |
0.00 |
R0650:Vmn1r213
|
UTSW |
13 |
23,195,564 (GRCm39) |
intron |
probably benign |
|
R0652:Vmn1r213
|
UTSW |
13 |
23,195,564 (GRCm39) |
intron |
probably benign |
|
R1902:Vmn1r213
|
UTSW |
13 |
23,196,476 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1996:Vmn1r213
|
UTSW |
13 |
23,196,473 (GRCm39) |
missense |
probably benign |
0.02 |
R1997:Vmn1r213
|
UTSW |
13 |
23,196,473 (GRCm39) |
missense |
probably benign |
0.02 |
R4214:Vmn1r213
|
UTSW |
13 |
23,196,173 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4409:Vmn1r213
|
UTSW |
13 |
23,195,593 (GRCm39) |
intron |
probably benign |
|
R4650:Vmn1r213
|
UTSW |
13 |
23,196,422 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4685:Vmn1r213
|
UTSW |
13 |
23,195,800 (GRCm39) |
missense |
probably benign |
0.05 |
R4698:Vmn1r213
|
UTSW |
13 |
23,195,507 (GRCm39) |
intron |
probably benign |
|
R4799:Vmn1r213
|
UTSW |
13 |
23,196,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R4807:Vmn1r213
|
UTSW |
13 |
23,195,775 (GRCm39) |
nonsense |
probably null |
|
R7389:Vmn1r213
|
UTSW |
13 |
23,196,556 (GRCm39) |
missense |
probably benign |
0.18 |
R7414:Vmn1r213
|
UTSW |
13 |
23,195,446 (GRCm39) |
missense |
unknown |
|
R8054:Vmn1r213
|
UTSW |
13 |
23,195,910 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9069:Vmn1r213
|
UTSW |
13 |
23,196,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R9155:Vmn1r213
|
UTSW |
13 |
23,196,343 (GRCm39) |
nonsense |
probably null |
|
R9428:Vmn1r213
|
UTSW |
13 |
23,195,944 (GRCm39) |
missense |
|
|
R9469:Vmn1r213
|
UTSW |
13 |
23,196,101 (GRCm39) |
missense |
probably benign |
0.22 |
R9633:Vmn1r213
|
UTSW |
13 |
23,195,519 (GRCm39) |
missense |
unknown |
|
|