Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl2 |
T |
A |
3: 148,558,398 (GRCm39) |
T437S |
probably benign |
Het |
Akna |
A |
G |
4: 63,297,570 (GRCm39) |
F828S |
probably benign |
Het |
Alg9 |
G |
T |
9: 50,686,802 (GRCm39) |
A40S |
possibly damaging |
Het |
Alox8 |
T |
A |
11: 69,076,067 (GRCm39) |
H628L |
possibly damaging |
Het |
Aox3 |
T |
C |
1: 58,191,713 (GRCm39) |
W422R |
probably benign |
Het |
Atp13a4 |
T |
C |
16: 29,228,528 (GRCm39) |
D984G |
probably benign |
Het |
Bcam |
T |
C |
7: 19,494,307 (GRCm39) |
E363G |
possibly damaging |
Het |
Cadps2 |
C |
A |
6: 23,429,217 (GRCm39) |
V519F |
probably damaging |
Het |
Calca |
A |
G |
7: 114,234,396 (GRCm39) |
Y18H |
probably damaging |
Het |
Cd70 |
A |
G |
17: 57,453,364 (GRCm39) |
I100T |
probably damaging |
Het |
Cdk4 |
T |
A |
10: 126,900,520 (GRCm39) |
H95Q |
probably damaging |
Het |
Chchd1 |
T |
A |
14: 20,753,410 (GRCm39) |
N11K |
probably damaging |
Het |
Cma2 |
T |
A |
14: 56,210,272 (GRCm39) |
N52K |
probably damaging |
Het |
Cyp3a16 |
A |
G |
5: 145,373,267 (GRCm39) |
V500A |
probably benign |
Het |
Dicer1 |
A |
G |
12: 104,688,228 (GRCm39) |
|
probably null |
Het |
Dnajc13 |
A |
G |
9: 104,034,037 (GRCm39) |
S2206P |
probably benign |
Het |
Dtl |
T |
C |
1: 191,293,658 (GRCm39) |
|
probably null |
Het |
Fam186b |
T |
C |
15: 99,184,852 (GRCm39) |
T24A |
probably benign |
Het |
Fbxw21 |
A |
G |
9: 108,990,984 (GRCm39) |
V25A |
probably benign |
Het |
Gins1 |
T |
C |
2: 150,754,758 (GRCm39) |
S45P |
probably benign |
Het |
Gtpbp2 |
T |
A |
17: 46,476,869 (GRCm39) |
V349D |
probably damaging |
Het |
Hyal5 |
G |
T |
6: 24,876,792 (GRCm39) |
D222Y |
probably damaging |
Het |
Itgal |
A |
G |
7: 126,900,060 (GRCm39) |
|
probably null |
Het |
Klk14 |
A |
G |
7: 43,343,377 (GRCm39) |
|
probably null |
Het |
Lama1 |
T |
A |
17: 68,117,404 (GRCm39) |
L2518Q |
possibly damaging |
Het |
Lrrc2 |
G |
A |
9: 110,808,555 (GRCm39) |
G264D |
probably benign |
Het |
Ltbp4 |
A |
G |
7: 27,022,245 (GRCm39) |
S893P |
probably damaging |
Het |
Mast4 |
G |
A |
13: 102,875,771 (GRCm39) |
P1107L |
probably damaging |
Het |
Mbd1 |
T |
A |
18: 74,408,490 (GRCm39) |
|
probably null |
Het |
Naip2 |
A |
T |
13: 100,291,529 (GRCm39) |
D1136E |
probably benign |
Het |
Naip2 |
G |
A |
13: 100,291,537 (GRCm39) |
|
probably benign |
Het |
Ncan |
G |
A |
8: 70,562,848 (GRCm39) |
T470I |
probably benign |
Het |
Npy1r |
A |
T |
8: 67,156,813 (GRCm39) |
I78F |
probably damaging |
Het |
Or10q1b |
A |
T |
19: 13,682,889 (GRCm39) |
M233L |
probably benign |
Het |
Or8b52 |
G |
A |
9: 38,576,573 (GRCm39) |
T189M |
probably damaging |
Het |
Palb2 |
A |
T |
7: 121,710,061 (GRCm39) |
|
probably null |
Het |
Pax3 |
T |
C |
1: 78,080,121 (GRCm39) |
T422A |
probably benign |
Het |
Pebp1 |
A |
T |
5: 117,424,229 (GRCm39) |
D72E |
possibly damaging |
Het |
Pnliprp1 |
A |
T |
19: 58,728,901 (GRCm39) |
T363S |
probably benign |
Het |
Rbm44 |
G |
A |
1: 91,084,565 (GRCm39) |
|
probably null |
Het |
Rbm47 |
T |
A |
5: 66,182,358 (GRCm39) |
Y425F |
probably benign |
Het |
Robo3 |
G |
T |
9: 37,340,957 (GRCm39) |
A83E |
probably damaging |
Het |
Rrm1 |
A |
G |
7: 102,105,721 (GRCm39) |
Y279C |
probably damaging |
Het |
Rslcan18 |
A |
T |
13: 67,256,121 (GRCm39) |
|
probably benign |
Het |
Scara5 |
C |
A |
14: 65,968,314 (GRCm39) |
Q196K |
probably benign |
Het |
Setd1b |
C |
T |
5: 123,301,210 (GRCm39) |
|
probably benign |
Het |
Siah1a |
A |
G |
8: 87,451,869 (GRCm39) |
F205S |
probably damaging |
Het |
Smr2 |
AT |
ATT |
5: 88,256,683 (GRCm39) |
|
probably null |
Het |
Ssu72 |
A |
G |
4: 155,815,814 (GRCm39) |
D86G |
probably benign |
Het |
St7 |
G |
T |
6: 17,886,110 (GRCm39) |
K357N |
probably damaging |
Het |
Sv2b |
G |
A |
7: 74,797,425 (GRCm39) |
T323I |
probably damaging |
Het |
Syt1 |
T |
C |
10: 108,340,361 (GRCm39) |
N319S |
probably benign |
Het |
Tanc1 |
T |
A |
2: 59,621,995 (GRCm39) |
F371L |
probably damaging |
Het |
Tcf20 |
C |
A |
15: 82,739,693 (GRCm39) |
G586V |
probably benign |
Het |
Tg |
T |
C |
15: 66,601,534 (GRCm39) |
|
probably null |
Het |
Tyk2 |
A |
T |
9: 21,026,758 (GRCm39) |
N620K |
probably benign |
Het |
Ube2j1 |
T |
A |
4: 33,045,116 (GRCm39) |
S130T |
probably benign |
Het |
Ubr2 |
G |
T |
17: 47,243,418 (GRCm39) |
P1696H |
probably damaging |
Het |
Ubr5 |
A |
T |
15: 38,041,085 (GRCm39) |
D266E |
probably damaging |
Het |
Vmn2r104 |
A |
T |
17: 20,262,477 (GRCm39) |
W218R |
probably damaging |
Het |
Vmn2r83 |
T |
A |
10: 79,314,956 (GRCm39) |
N401K |
probably damaging |
Het |
Vwf |
A |
G |
6: 125,632,214 (GRCm39) |
E82G |
unknown |
Het |
Vwf |
T |
A |
6: 125,640,534 (GRCm39) |
Y2323* |
probably null |
Het |
Wdr76 |
T |
G |
2: 121,359,402 (GRCm39) |
V329G |
probably damaging |
Het |
Zan |
A |
G |
5: 137,460,214 (GRCm39) |
C1226R |
unknown |
Het |
Zbtb16 |
G |
T |
9: 48,743,572 (GRCm39) |
Q247K |
probably damaging |
Het |
Zfp541 |
T |
C |
7: 15,812,640 (GRCm39) |
V431A |
possibly damaging |
Het |
|
Other mutations in Vipr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00691:Vipr2
|
APN |
12 |
116,102,368 (GRCm39) |
splice site |
probably null |
|
IGL02233:Vipr2
|
APN |
12 |
116,058,356 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02691:Vipr2
|
APN |
12 |
116,099,849 (GRCm39) |
missense |
probably benign |
0.11 |
PIT4377001:Vipr2
|
UTSW |
12 |
116,058,418 (GRCm39) |
missense |
probably benign |
0.01 |
R0135:Vipr2
|
UTSW |
12 |
116,106,447 (GRCm39) |
missense |
probably benign |
0.00 |
R0207:Vipr2
|
UTSW |
12 |
116,106,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R1389:Vipr2
|
UTSW |
12 |
116,100,950 (GRCm39) |
missense |
probably benign |
0.01 |
R1560:Vipr2
|
UTSW |
12 |
116,058,401 (GRCm39) |
missense |
probably benign |
0.18 |
R1696:Vipr2
|
UTSW |
12 |
116,102,777 (GRCm39) |
missense |
probably benign |
0.13 |
R1970:Vipr2
|
UTSW |
12 |
116,099,826 (GRCm39) |
missense |
probably benign |
0.01 |
R2010:Vipr2
|
UTSW |
12 |
116,086,430 (GRCm39) |
critical splice donor site |
probably null |
|
R3873:Vipr2
|
UTSW |
12 |
116,099,724 (GRCm39) |
unclassified |
probably benign |
|
R4713:Vipr2
|
UTSW |
12 |
116,043,751 (GRCm39) |
missense |
probably benign |
0.00 |
R4953:Vipr2
|
UTSW |
12 |
116,107,876 (GRCm39) |
missense |
probably benign |
0.07 |
R6041:Vipr2
|
UTSW |
12 |
116,106,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Vipr2
|
UTSW |
12 |
116,086,363 (GRCm39) |
nonsense |
probably null |
|
R6902:Vipr2
|
UTSW |
12 |
116,102,819 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6946:Vipr2
|
UTSW |
12 |
116,102,819 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7763:Vipr2
|
UTSW |
12 |
116,086,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R9339:Vipr2
|
UTSW |
12 |
116,058,344 (GRCm39) |
missense |
probably damaging |
0.96 |
R9523:Vipr2
|
UTSW |
12 |
116,093,788 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Vipr2
|
UTSW |
12 |
116,106,565 (GRCm39) |
splice site |
probably null |
|
X0067:Vipr2
|
UTSW |
12 |
116,102,792 (GRCm39) |
missense |
probably damaging |
1.00 |
|