Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921528I07Rik |
A |
G |
9: 114,129,092 (GRCm39) |
|
noncoding transcript |
Het |
Acadsb |
A |
T |
7: 131,031,733 (GRCm39) |
T190S |
probably damaging |
Het |
Adamts17 |
G |
T |
7: 66,490,314 (GRCm39) |
G132V |
probably damaging |
Het |
Atosa |
A |
G |
9: 74,930,929 (GRCm39) |
I957M |
probably damaging |
Het |
Atp8b3 |
C |
T |
10: 80,359,681 (GRCm39) |
M984I |
probably benign |
Het |
Atp8b4 |
A |
T |
2: 126,256,379 (GRCm39) |
|
probably null |
Het |
Btbd18 |
T |
C |
2: 84,497,924 (GRCm39) |
Y521H |
probably damaging |
Het |
Casd1 |
A |
G |
6: 4,621,102 (GRCm39) |
N220S |
probably benign |
Het |
Ccdc112 |
T |
G |
18: 46,420,613 (GRCm39) |
E379A |
possibly damaging |
Het |
Ccdc88a |
T |
C |
11: 29,432,651 (GRCm39) |
I1219T |
probably benign |
Het |
Cntrl |
A |
T |
2: 35,063,123 (GRCm39) |
K1573M |
probably damaging |
Het |
Col14a1 |
A |
T |
15: 55,251,975 (GRCm39) |
I544F |
unknown |
Het |
Cyp20a1 |
A |
T |
1: 60,426,306 (GRCm39) |
Y416F |
probably damaging |
Het |
Dagla |
T |
C |
19: 10,247,096 (GRCm39) |
K132E |
probably damaging |
Het |
Dbn1 |
A |
T |
13: 55,624,042 (GRCm39) |
I350N |
possibly damaging |
Het |
Ddx41 |
A |
T |
13: 55,680,957 (GRCm39) |
V329E |
probably damaging |
Het |
Dhx32 |
A |
T |
7: 133,335,838 (GRCm39) |
Y272N |
probably damaging |
Het |
Fam114a1 |
C |
A |
5: 65,163,225 (GRCm39) |
P174Q |
probably benign |
Het |
Galnt3 |
C |
A |
2: 65,923,954 (GRCm39) |
R438L |
probably damaging |
Het |
Ghr |
T |
A |
15: 3,362,970 (GRCm39) |
L167F |
probably damaging |
Het |
Glod4 |
T |
A |
11: 76,134,397 (GRCm39) |
D25V |
probably damaging |
Het |
Gm9767 |
T |
C |
10: 25,954,756 (GRCm39) |
|
probably benign |
Het |
Golga4 |
T |
A |
9: 118,388,076 (GRCm39) |
S1733T |
probably benign |
Het |
Gsdme |
A |
T |
6: 50,206,333 (GRCm39) |
I170N |
probably damaging |
Het |
H2-M10.3 |
C |
T |
17: 36,678,722 (GRCm39) |
|
probably null |
Het |
Kmt2c |
T |
A |
5: 25,568,475 (GRCm39) |
K867M |
probably damaging |
Het |
Krt35 |
A |
G |
11: 99,985,453 (GRCm39) |
V196A |
possibly damaging |
Het |
Ltbp1 |
A |
T |
17: 75,671,492 (GRCm39) |
M1558L |
probably benign |
Het |
Mcam |
T |
G |
9: 44,052,640 (GRCm39) |
M623R |
possibly damaging |
Het |
Mrps26 |
A |
T |
2: 130,406,269 (GRCm39) |
Q134L |
probably benign |
Het |
Mxra8 |
T |
C |
4: 155,927,440 (GRCm39) |
|
probably null |
Het |
Or13a21 |
A |
G |
7: 139,999,123 (GRCm39) |
S188P |
probably damaging |
Het |
Or52n20 |
G |
A |
7: 104,320,046 (GRCm39) |
G46R |
probably damaging |
Het |
Orc4 |
G |
A |
2: 48,827,501 (GRCm39) |
P31S |
probably benign |
Het |
Pabir3 |
G |
A |
X: 52,382,376 (GRCm39) |
R94H |
possibly damaging |
Het |
Parg |
C |
A |
14: 31,931,592 (GRCm39) |
T404K |
probably damaging |
Het |
Parp8 |
C |
A |
13: 117,032,209 (GRCm39) |
L321F |
possibly damaging |
Het |
Piezo2 |
T |
C |
18: 63,205,951 (GRCm39) |
E1486G |
probably damaging |
Het |
Pign |
A |
T |
1: 105,525,391 (GRCm39) |
|
probably null |
Het |
Pik3r4 |
A |
G |
9: 105,549,924 (GRCm39) |
H1005R |
probably damaging |
Het |
Ppp6r1 |
A |
C |
7: 4,644,045 (GRCm39) |
|
probably null |
Het |
Ptdss2 |
A |
G |
7: 140,734,491 (GRCm39) |
T309A |
probably benign |
Het |
Ptprt |
T |
C |
2: 161,406,609 (GRCm39) |
M987V |
probably damaging |
Het |
Rgs17 |
C |
A |
10: 5,868,192 (GRCm39) |
L9F |
probably benign |
Het |
Rock2 |
A |
G |
12: 17,027,738 (GRCm39) |
R168G |
probably damaging |
Het |
Rsph4a |
T |
A |
10: 33,787,623 (GRCm39) |
L593* |
probably null |
Het |
Scaf11 |
C |
A |
15: 96,322,719 (GRCm39) |
K108N |
probably damaging |
Het |
Sec23b |
T |
A |
2: 144,423,935 (GRCm39) |
M528K |
possibly damaging |
Het |
Shank2 |
G |
A |
7: 143,963,942 (GRCm39) |
D727N |
probably damaging |
Het |
Sipa1l2 |
T |
C |
8: 126,218,965 (GRCm39) |
D124G |
probably benign |
Het |
Spatc1 |
A |
T |
15: 76,176,685 (GRCm39) |
I479F |
probably damaging |
Het |
Tmem126b |
A |
G |
7: 90,118,316 (GRCm39) |
L188P |
probably damaging |
Het |
Tnrc6b |
T |
G |
15: 80,764,448 (GRCm39) |
L650W |
probably damaging |
Het |
|
Other mutations in Vmn2r62 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01726:Vmn2r62
|
APN |
7 |
42,414,526 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01900:Vmn2r62
|
APN |
7 |
42,438,495 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02551:Vmn2r62
|
APN |
7 |
42,437,930 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02799:Vmn2r62
|
UTSW |
7 |
42,437,396 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0144:Vmn2r62
|
UTSW |
7 |
42,438,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R1396:Vmn2r62
|
UTSW |
7 |
42,414,261 (GRCm39) |
missense |
probably damaging |
0.99 |
R1846:Vmn2r62
|
UTSW |
7 |
42,438,546 (GRCm39) |
missense |
probably damaging |
0.97 |
R3738:Vmn2r62
|
UTSW |
7 |
42,437,311 (GRCm39) |
missense |
probably benign |
0.00 |
R5138:Vmn2r62
|
UTSW |
7 |
42,414,240 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5381:Vmn2r62
|
UTSW |
7 |
42,437,219 (GRCm39) |
missense |
probably benign |
0.43 |
R6855:Vmn2r62
|
UTSW |
7 |
42,438,412 (GRCm39) |
missense |
probably benign |
0.00 |
R6872:Vmn2r62
|
UTSW |
7 |
42,438,412 (GRCm39) |
missense |
probably benign |
0.00 |
R6968:Vmn2r62
|
UTSW |
7 |
42,437,866 (GRCm39) |
missense |
probably benign |
0.18 |
R7030:Vmn2r62
|
UTSW |
7 |
42,438,473 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7067:Vmn2r62
|
UTSW |
7 |
42,414,302 (GRCm39) |
missense |
probably benign |
0.44 |
R7148:Vmn2r62
|
UTSW |
7 |
42,414,640 (GRCm39) |
missense |
probably benign |
0.02 |
R7305:Vmn2r62
|
UTSW |
7 |
42,414,235 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7493:Vmn2r62
|
UTSW |
7 |
42,437,316 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7583:Vmn2r62
|
UTSW |
7 |
42,437,466 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7593:Vmn2r62
|
UTSW |
7 |
42,437,213 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7851:Vmn2r62
|
UTSW |
7 |
42,438,539 (GRCm39) |
missense |
probably benign |
0.00 |
R7974:Vmn2r62
|
UTSW |
7 |
42,437,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Vmn2r62
|
UTSW |
7 |
42,414,031 (GRCm39) |
missense |
probably damaging |
0.98 |
R8085:Vmn2r62
|
UTSW |
7 |
42,437,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R8514:Vmn2r62
|
UTSW |
7 |
42,413,992 (GRCm39) |
missense |
probably benign |
0.00 |
R8935:Vmn2r62
|
UTSW |
7 |
42,437,791 (GRCm39) |
missense |
probably benign |
|
R9053:Vmn2r62
|
UTSW |
7 |
42,413,920 (GRCm39) |
missense |
|
|
|