Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd2 |
T |
C |
15: 91,074,896 (GRCm39) |
I306V |
probably damaging |
Het |
Actrt3 |
A |
T |
3: 30,652,316 (GRCm39) |
Y259* |
probably null |
Het |
Ankfy1 |
G |
A |
11: 72,645,285 (GRCm39) |
C788Y |
probably benign |
Het |
Ano1 |
T |
A |
7: 144,232,478 (GRCm39) |
M25L |
possibly damaging |
Het |
Apol10b |
A |
T |
15: 77,469,987 (GRCm39) |
D63E |
possibly damaging |
Het |
Atp6v1c1 |
C |
A |
15: 38,674,172 (GRCm39) |
S55* |
probably null |
Het |
C1s2 |
T |
G |
6: 124,606,960 (GRCm39) |
D296A |
probably damaging |
Het |
Cabs1 |
C |
T |
5: 88,127,613 (GRCm39) |
T88I |
possibly damaging |
Het |
Cadm4 |
G |
A |
7: 24,202,186 (GRCm39) |
V342M |
possibly damaging |
Het |
Cat |
T |
C |
2: 103,303,420 (GRCm39) |
E119G |
probably damaging |
Het |
Cdhr18 |
T |
C |
14: 13,868,002 (GRCm38) |
D229G |
probably benign |
Het |
Cdk5rap2 |
G |
A |
4: 70,199,719 (GRCm39) |
R802C |
probably damaging |
Het |
Clip1 |
A |
G |
5: 123,751,897 (GRCm39) |
|
probably benign |
Het |
Dhx57 |
T |
C |
17: 80,580,395 (GRCm39) |
N519S |
possibly damaging |
Het |
Dpep2 |
T |
C |
8: 106,712,831 (GRCm39) |
D260G |
probably damaging |
Het |
Edem1 |
T |
A |
6: 108,828,159 (GRCm39) |
|
probably null |
Het |
Epb41l4a |
A |
T |
18: 33,931,868 (GRCm39) |
|
probably null |
Het |
Esp1 |
T |
C |
17: 41,039,723 (GRCm39) |
S3P |
possibly damaging |
Het |
Fam111a |
A |
G |
19: 12,564,746 (GRCm39) |
Y165C |
probably damaging |
Het |
Fstl4 |
A |
G |
11: 53,059,031 (GRCm39) |
T497A |
probably benign |
Het |
Gstcd |
T |
C |
3: 132,787,834 (GRCm39) |
D288G |
probably damaging |
Het |
Hmcn2 |
T |
A |
2: 31,310,118 (GRCm39) |
L3264* |
probably null |
Het |
Hyal4 |
T |
A |
6: 24,766,089 (GRCm39) |
L481* |
probably null |
Het |
Ighv2-7 |
A |
G |
12: 113,771,055 (GRCm39) |
Y77H |
possibly damaging |
Het |
Jdp2 |
G |
T |
12: 85,685,614 (GRCm39) |
R125L |
probably benign |
Het |
Lrp1b |
A |
T |
2: 41,013,748 (GRCm39) |
|
probably null |
Het |
Lrp2 |
AC |
A |
2: 69,340,763 (GRCm39) |
|
probably null |
Het |
Marveld2 |
C |
T |
13: 100,733,886 (GRCm39) |
D250N |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,242,662 (GRCm39) |
S53P |
probably damaging |
Het |
Ms4a20 |
A |
G |
19: 11,083,114 (GRCm39) |
I102T |
possibly damaging |
Het |
Myo3b |
T |
C |
2: 70,143,707 (GRCm39) |
V1041A |
probably benign |
Het |
Nkpd1 |
T |
A |
7: 19,257,009 (GRCm39) |
F113I |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,923,490 (GRCm39) |
S6470P |
probably damaging |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or4a73 |
T |
C |
2: 89,420,661 (GRCm39) |
D266G |
possibly damaging |
Het |
Or9g4b |
C |
T |
2: 85,616,004 (GRCm39) |
R50C |
probably damaging |
Het |
Pdcd11 |
G |
T |
19: 47,108,722 (GRCm39) |
G1246V |
probably damaging |
Het |
Phc3 |
A |
T |
3: 30,996,714 (GRCm39) |
S219T |
probably damaging |
Het |
Plxnb1 |
C |
T |
9: 108,931,993 (GRCm39) |
|
probably null |
Het |
Polh |
T |
C |
17: 46,495,670 (GRCm39) |
D276G |
possibly damaging |
Het |
Polq |
T |
A |
16: 36,892,071 (GRCm39) |
V1991E |
probably damaging |
Het |
Polr2g |
G |
A |
19: 8,771,541 (GRCm39) |
R144C |
probably damaging |
Het |
Pramel16 |
G |
A |
4: 143,675,576 (GRCm39) |
H417Y |
possibly damaging |
Het |
Prex2 |
A |
C |
1: 11,207,001 (GRCm39) |
T520P |
possibly damaging |
Het |
Psg21 |
T |
A |
7: 18,386,279 (GRCm39) |
T236S |
possibly damaging |
Het |
Ptpru |
A |
T |
4: 131,520,836 (GRCm39) |
S761R |
probably benign |
Het |
Rapgef6 |
G |
A |
11: 54,510,842 (GRCm39) |
R253Q |
probably damaging |
Het |
Rc3h2 |
C |
T |
2: 37,279,658 (GRCm39) |
V524I |
probably benign |
Het |
Sde2 |
T |
C |
1: 180,685,784 (GRCm39) |
V112A |
probably damaging |
Het |
Septin7 |
T |
C |
9: 25,205,100 (GRCm39) |
|
probably null |
Het |
Spef2 |
A |
G |
15: 9,727,618 (GRCm39) |
V155A |
possibly damaging |
Het |
St7 |
T |
C |
6: 17,819,333 (GRCm39) |
|
probably null |
Het |
Tmcc3 |
A |
T |
10: 94,418,249 (GRCm39) |
Y339F |
probably damaging |
Het |
Tmed6 |
T |
C |
8: 107,792,083 (GRCm39) |
E54G |
probably damaging |
Het |
Tnks1bp1 |
C |
T |
2: 84,889,624 (GRCm39) |
|
probably benign |
Het |
Trim43c |
T |
C |
9: 88,722,600 (GRCm39) |
L82P |
possibly damaging |
Het |
Txndc2 |
T |
C |
17: 65,945,466 (GRCm39) |
D237G |
probably benign |
Het |
Vmn1r91 |
T |
A |
7: 19,835,404 (GRCm39) |
C108S |
possibly damaging |
Het |
Vtn |
A |
T |
11: 78,390,836 (GRCm39) |
D165V |
probably damaging |
Het |
Wdr3 |
A |
T |
3: 100,068,468 (GRCm39) |
S13R |
probably damaging |
Het |
Zdhhc16 |
A |
G |
19: 41,926,198 (GRCm39) |
Y31C |
probably benign |
Het |
Zfp39 |
A |
T |
11: 58,781,887 (GRCm39) |
W292R |
probably benign |
Het |
Zfp612 |
A |
T |
8: 110,816,606 (GRCm39) |
L604F |
probably damaging |
Het |
|
Other mutations in Cavin2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00926:Cavin2
|
APN |
1 |
51,340,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:Cavin2
|
APN |
1 |
51,328,570 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1649:Cavin2
|
UTSW |
1 |
51,339,939 (GRCm39) |
missense |
probably benign |
0.09 |
R1676:Cavin2
|
UTSW |
1 |
51,340,330 (GRCm39) |
missense |
probably benign |
0.05 |
R1966:Cavin2
|
UTSW |
1 |
51,328,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R3038:Cavin2
|
UTSW |
1 |
51,340,416 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3440:Cavin2
|
UTSW |
1 |
51,340,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R4128:Cavin2
|
UTSW |
1 |
51,340,581 (GRCm39) |
makesense |
probably null |
|
R4524:Cavin2
|
UTSW |
1 |
51,340,229 (GRCm39) |
missense |
probably benign |
0.25 |
R4660:Cavin2
|
UTSW |
1 |
51,340,510 (GRCm39) |
missense |
probably benign |
0.00 |
R4662:Cavin2
|
UTSW |
1 |
51,340,510 (GRCm39) |
missense |
probably benign |
0.00 |
R5091:Cavin2
|
UTSW |
1 |
51,340,398 (GRCm39) |
missense |
probably benign |
0.01 |
R5296:Cavin2
|
UTSW |
1 |
51,329,029 (GRCm39) |
critical splice donor site |
probably null |
|
R5844:Cavin2
|
UTSW |
1 |
51,328,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R6141:Cavin2
|
UTSW |
1 |
51,340,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6252:Cavin2
|
UTSW |
1 |
51,328,828 (GRCm39) |
missense |
probably benign |
0.30 |
R7128:Cavin2
|
UTSW |
1 |
51,328,579 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7583:Cavin2
|
UTSW |
1 |
51,328,777 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8051:Cavin2
|
UTSW |
1 |
51,340,283 (GRCm39) |
missense |
probably benign |
|
R9573:Cavin2
|
UTSW |
1 |
51,328,795 (GRCm39) |
missense |
probably damaging |
0.99 |
X0028:Cavin2
|
UTSW |
1 |
51,340,261 (GRCm39) |
missense |
probably benign |
0.07 |
Z1176:Cavin2
|
UTSW |
1 |
51,340,315 (GRCm39) |
missense |
probably damaging |
0.96 |
|