Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
C |
1: 71,333,959 (GRCm39) |
V1181G |
probably benign |
Het |
Adamts12 |
A |
T |
15: 11,217,915 (GRCm39) |
I291F |
probably damaging |
Het |
Aspm |
G |
C |
1: 139,407,282 (GRCm39) |
Q2056H |
probably benign |
Het |
C7 |
A |
T |
15: 5,076,406 (GRCm39) |
V122E |
probably benign |
Het |
Casp12 |
A |
T |
9: 5,352,844 (GRCm39) |
Q152L |
probably null |
Het |
Cdh16 |
T |
A |
8: 105,344,264 (GRCm39) |
T92S |
probably benign |
Het |
Chrd |
G |
C |
16: 20,553,058 (GRCm39) |
V162L |
possibly damaging |
Het |
Cpne8 |
A |
G |
15: 90,385,608 (GRCm39) |
|
probably benign |
Het |
Cspg4b |
T |
C |
13: 113,502,639 (GRCm39) |
Y115H |
probably damaging |
Het |
Cyp2j7 |
T |
A |
4: 96,090,384 (GRCm39) |
I347F |
probably damaging |
Het |
Cyp4a10 |
A |
T |
4: 115,378,304 (GRCm39) |
Q130L |
probably damaging |
Het |
Dach1 |
C |
T |
14: 98,406,184 (GRCm39) |
G188R |
probably damaging |
Het |
Dgkd |
T |
C |
1: 87,845,674 (GRCm39) |
S294P |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,882,290 (GRCm39) |
I621V |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,144,346 (GRCm39) |
|
probably benign |
Het |
Echdc1 |
A |
T |
10: 29,198,417 (GRCm39) |
|
probably benign |
Het |
Elovl3 |
T |
A |
19: 46,120,597 (GRCm39) |
F30Y |
probably damaging |
Het |
Fa2h |
T |
C |
8: 112,120,146 (GRCm39) |
Y80C |
probably damaging |
Het |
Fgd3 |
C |
T |
13: 49,450,085 (GRCm39) |
D55N |
probably benign |
Het |
Fhod1 |
T |
C |
8: 106,058,287 (GRCm39) |
E823G |
possibly damaging |
Het |
Gapvd1 |
A |
G |
2: 34,589,925 (GRCm39) |
|
probably benign |
Het |
Gm17067 |
A |
T |
7: 42,358,046 (GRCm39) |
I152K |
probably benign |
Het |
Kif27 |
A |
G |
13: 58,502,528 (GRCm39) |
V50A |
probably damaging |
Het |
Kpna2 |
T |
C |
11: 106,881,912 (GRCm39) |
T305A |
probably benign |
Het |
Krtap22-2 |
A |
G |
16: 88,807,407 (GRCm39) |
|
probably benign |
Het |
Lrp2bp |
T |
A |
8: 46,465,068 (GRCm39) |
F62L |
probably damaging |
Het |
Marf1 |
G |
A |
16: 13,970,129 (GRCm39) |
H197Y |
probably damaging |
Het |
Mob3b |
A |
G |
4: 35,083,947 (GRCm39) |
F81L |
probably benign |
Het |
Mon2 |
C |
T |
10: 122,871,451 (GRCm39) |
V389M |
probably damaging |
Het |
Myef2l |
A |
T |
3: 10,154,379 (GRCm39) |
M383L |
possibly damaging |
Het |
Myh8 |
A |
G |
11: 67,189,351 (GRCm39) |
K1176E |
probably damaging |
Het |
Naf1 |
T |
C |
8: 67,341,707 (GRCm39) |
|
probably benign |
Het |
Nckap1l |
A |
G |
15: 103,384,063 (GRCm39) |
T554A |
probably benign |
Het |
Oog3 |
A |
G |
4: 143,884,641 (GRCm39) |
Y432H |
probably damaging |
Het |
Paxbp1 |
A |
T |
16: 90,832,924 (GRCm39) |
|
probably benign |
Het |
Phf20 |
A |
T |
2: 156,109,114 (GRCm39) |
K154* |
probably null |
Het |
Pip4p1 |
C |
T |
14: 51,166,351 (GRCm39) |
R213Q |
probably damaging |
Het |
Plekhj1 |
T |
C |
10: 80,632,250 (GRCm39) |
D74G |
possibly damaging |
Het |
Plpp4 |
T |
C |
7: 128,925,148 (GRCm39) |
C128R |
probably damaging |
Het |
Rcan3 |
A |
T |
4: 135,145,689 (GRCm39) |
|
probably null |
Het |
Sh3rf1 |
T |
A |
8: 61,827,172 (GRCm39) |
M642K |
probably benign |
Het |
Slc7a1 |
A |
G |
5: 148,271,393 (GRCm39) |
V522A |
probably benign |
Het |
Sorbs1 |
A |
G |
19: 40,303,182 (GRCm39) |
|
probably benign |
Het |
Spry2 |
C |
T |
14: 106,130,731 (GRCm39) |
V152M |
probably benign |
Het |
Srgap2 |
A |
G |
1: 131,277,200 (GRCm39) |
M349T |
possibly damaging |
Het |
Stag3 |
A |
G |
5: 138,289,643 (GRCm39) |
H271R |
possibly damaging |
Het |
Stat4 |
T |
C |
1: 52,107,939 (GRCm39) |
V136A |
probably benign |
Het |
Stc2 |
A |
T |
11: 31,310,177 (GRCm39) |
D286E |
probably benign |
Het |
Stk31 |
T |
C |
6: 49,414,311 (GRCm39) |
Y482H |
probably damaging |
Het |
Tasor2 |
A |
C |
13: 3,635,170 (GRCm39) |
|
probably null |
Het |
Ticrr |
C |
T |
7: 79,343,540 (GRCm39) |
P1135L |
probably benign |
Het |
Trim27 |
A |
T |
13: 21,375,399 (GRCm39) |
E310V |
probably benign |
Het |
Uvrag |
T |
C |
7: 98,641,188 (GRCm39) |
K284R |
probably benign |
Het |
Vmn1r78 |
A |
C |
7: 11,887,279 (GRCm39) |
S297R |
probably benign |
Het |
Xylt2 |
A |
G |
11: 94,560,466 (GRCm39) |
S270P |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,676,810 (GRCm39) |
M2620T |
probably benign |
Het |
Zkscan2 |
C |
A |
7: 123,099,219 (GRCm39) |
|
probably benign |
Het |
Zwint |
T |
C |
10: 72,493,030 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Gvin3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01400:Gvin3
|
APN |
7 |
106,201,242 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01410:Gvin3
|
APN |
7 |
106,202,258 (GRCm39) |
exon |
noncoding transcript |
|
IGL01415:Gvin3
|
APN |
7 |
106,202,258 (GRCm39) |
exon |
noncoding transcript |
|
IGL01538:Gvin3
|
APN |
7 |
106,201,744 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01751:Gvin3
|
APN |
7 |
106,201,516 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01916:Gvin3
|
APN |
7 |
106,201,033 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02171:Gvin3
|
APN |
7 |
106,200,548 (GRCm39) |
exon |
noncoding transcript |
|
IGL02550:Gvin3
|
APN |
7 |
106,200,846 (GRCm39) |
exon |
noncoding transcript |
|
H8562:Gvin3
|
UTSW |
7 |
106,202,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R0178:Gvin3
|
UTSW |
7 |
106,201,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R0420:Gvin3
|
UTSW |
7 |
106,203,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Gvin3
|
UTSW |
7 |
106,202,093 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1378:Gvin3
|
UTSW |
7 |
106,201,373 (GRCm39) |
missense |
probably damaging |
0.97 |
R1506:Gvin3
|
UTSW |
7 |
106,200,788 (GRCm39) |
missense |
probably benign |
0.08 |
R1628:Gvin3
|
UTSW |
7 |
106,202,476 (GRCm39) |
nonsense |
probably null |
|
R1834:Gvin3
|
UTSW |
7 |
106,202,983 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1888:Gvin3
|
UTSW |
7 |
106,196,630 (GRCm39) |
exon |
noncoding transcript |
|
R2145:Gvin3
|
UTSW |
7 |
106,202,215 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4056:Gvin3
|
UTSW |
7 |
106,203,216 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4067:Gvin3
|
UTSW |
7 |
106,198,772 (GRCm39) |
exon |
noncoding transcript |
|
R4631:Gvin3
|
UTSW |
7 |
106,198,730 (GRCm39) |
exon |
noncoding transcript |
|
R4817:Gvin3
|
UTSW |
7 |
106,200,437 (GRCm39) |
exon |
noncoding transcript |
|
R4900:Gvin3
|
UTSW |
7 |
106,197,793 (GRCm39) |
exon |
noncoding transcript |
|
R4970:Gvin3
|
UTSW |
7 |
106,199,864 (GRCm39) |
exon |
noncoding transcript |
|
R5009:Gvin3
|
UTSW |
7 |
106,200,767 (GRCm39) |
exon |
noncoding transcript |
|
R5050:Gvin3
|
UTSW |
7 |
106,196,179 (GRCm39) |
exon |
noncoding transcript |
|
R5086:Gvin3
|
UTSW |
7 |
106,197,234 (GRCm39) |
exon |
noncoding transcript |
|
R5090:Gvin3
|
UTSW |
7 |
106,200,109 (GRCm39) |
exon |
noncoding transcript |
|
R5168:Gvin3
|
UTSW |
7 |
106,196,054 (GRCm39) |
exon |
noncoding transcript |
|
R5260:Gvin3
|
UTSW |
7 |
106,198,411 (GRCm39) |
exon |
noncoding transcript |
|
R5331:Gvin3
|
UTSW |
7 |
106,197,958 (GRCm39) |
exon |
noncoding transcript |
|
R5389:Gvin3
|
UTSW |
7 |
106,197,442 (GRCm39) |
exon |
noncoding transcript |
|
R5433:Gvin3
|
UTSW |
7 |
106,199,314 (GRCm39) |
exon |
noncoding transcript |
|
R5488:Gvin3
|
UTSW |
7 |
106,200,797 (GRCm39) |
exon |
noncoding transcript |
|
R5489:Gvin3
|
UTSW |
7 |
106,200,797 (GRCm39) |
exon |
noncoding transcript |
|
R5504:Gvin3
|
UTSW |
7 |
106,201,951 (GRCm39) |
exon |
noncoding transcript |
|
R5956:Gvin3
|
UTSW |
7 |
106,200,677 (GRCm39) |
exon |
noncoding transcript |
|
|