Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025G04Rik |
T |
A |
1: 151,769,150 (GRCm39) |
T121S |
possibly damaging |
Het |
4930503E14Rik |
T |
C |
14: 44,406,641 (GRCm39) |
E136G |
probably damaging |
Het |
Adgrg4 |
A |
G |
X: 56,005,320 (GRCm39) |
N2527S |
probably damaging |
Het |
Ak1 |
G |
A |
2: 32,519,593 (GRCm39) |
S7N |
probably benign |
Het |
Aktip |
A |
C |
8: 91,852,466 (GRCm39) |
I230R |
possibly damaging |
Het |
Alms1 |
A |
G |
6: 85,598,271 (GRCm39) |
I1032M |
probably damaging |
Het |
Asb4 |
T |
A |
6: 5,423,651 (GRCm39) |
V266E |
probably damaging |
Het |
Bace1 |
G |
A |
9: 45,765,962 (GRCm39) |
V130M |
probably damaging |
Het |
Bglap |
A |
T |
3: 88,291,744 (GRCm39) |
|
probably benign |
Het |
Brpf3 |
T |
C |
17: 29,040,233 (GRCm39) |
S885P |
probably benign |
Het |
Chd9 |
A |
T |
8: 91,750,202 (GRCm39) |
I1742F |
possibly damaging |
Het |
Col9a2 |
T |
A |
4: 120,909,586 (GRCm39) |
I415N |
probably damaging |
Het |
Cybc1 |
A |
T |
11: 121,115,528 (GRCm39) |
|
probably null |
Het |
Dnajc7 |
T |
C |
11: 100,492,607 (GRCm39) |
Y38C |
probably benign |
Het |
Dync2i2 |
A |
G |
2: 29,922,820 (GRCm39) |
L309P |
probably benign |
Het |
Enam |
A |
G |
5: 88,651,236 (GRCm39) |
Y840C |
probably damaging |
Het |
Etnppl |
T |
A |
3: 130,425,442 (GRCm39) |
C416S |
probably damaging |
Het |
Fgf20 |
A |
T |
8: 40,732,896 (GRCm39) |
S181T |
probably benign |
Het |
Fut8 |
T |
A |
12: 77,510,835 (GRCm39) |
Y421N |
probably damaging |
Het |
Gcn1 |
T |
G |
5: 115,737,147 (GRCm39) |
L1295R |
probably damaging |
Het |
Gm11437 |
A |
G |
11: 84,055,337 (GRCm39) |
V93A |
probably benign |
Het |
Gm9989 |
T |
C |
3: 81,829,549 (GRCm39) |
|
noncoding transcript |
Het |
Gsdmc4 |
A |
T |
15: 63,765,736 (GRCm39) |
|
probably null |
Het |
Ighv10-1 |
A |
T |
12: 114,442,643 (GRCm39) |
M114K |
probably benign |
Het |
Il22b |
T |
C |
10: 118,126,115 (GRCm39) |
I161V |
probably damaging |
Het |
Itfg2 |
T |
A |
6: 128,387,413 (GRCm39) |
|
probably benign |
Het |
Kirrel1 |
G |
A |
3: 86,995,774 (GRCm39) |
Q387* |
probably null |
Het |
Klk1 |
C |
T |
7: 43,876,968 (GRCm39) |
R24* |
probably null |
Het |
Klra7 |
T |
C |
6: 130,208,612 (GRCm39) |
|
probably null |
Het |
Ltn1 |
T |
C |
16: 87,213,118 (GRCm39) |
Y481C |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mrps2 |
A |
G |
2: 28,359,782 (GRCm39) |
N213S |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,569,869 (GRCm39) |
I310F |
possibly damaging |
Het |
Ntrk3 |
T |
A |
7: 78,167,185 (GRCm39) |
Y102F |
probably damaging |
Het |
Or8k24 |
A |
T |
2: 86,216,431 (GRCm39) |
C110* |
probably null |
Het |
Otof |
C |
T |
5: 30,556,635 (GRCm39) |
G282D |
probably damaging |
Het |
Pcdhb2 |
A |
T |
18: 37,430,367 (GRCm39) |
|
probably null |
Het |
Pign |
A |
T |
1: 105,515,703 (GRCm39) |
|
probably null |
Het |
Plekha6 |
G |
A |
1: 133,222,416 (GRCm39) |
E1001K |
probably benign |
Het |
Plxna2 |
C |
T |
1: 194,431,625 (GRCm39) |
S538F |
probably damaging |
Het |
Ppm1d |
A |
G |
11: 85,236,678 (GRCm39) |
T486A |
probably benign |
Het |
Pudp |
A |
G |
18: 50,701,329 (GRCm39) |
F135L |
probably benign |
Het |
Rd3l |
T |
G |
12: 111,945,945 (GRCm39) |
N178T |
probably benign |
Het |
Rel |
A |
C |
11: 23,703,215 (GRCm39) |
|
probably null |
Het |
Sf3a1 |
T |
A |
11: 4,117,824 (GRCm39) |
F195L |
probably damaging |
Het |
Slc30a1 |
G |
C |
1: 191,639,401 (GRCm39) |
A95P |
probably damaging |
Het |
Slc47a2 |
T |
C |
11: 61,194,773 (GRCm39) |
T469A |
probably benign |
Het |
Slc4a10 |
A |
T |
2: 61,876,989 (GRCm39) |
M1L |
probably benign |
Het |
Slc8a1 |
T |
A |
17: 81,955,703 (GRCm39) |
D445V |
probably damaging |
Het |
Slc9a7 |
C |
T |
X: 20,071,793 (GRCm39) |
G113R |
probably damaging |
Het |
Spata31e5 |
T |
A |
1: 28,816,712 (GRCm39) |
D440V |
probably damaging |
Het |
Spic |
T |
C |
10: 88,511,545 (GRCm39) |
H237R |
possibly damaging |
Het |
Stk26 |
A |
G |
X: 49,977,910 (GRCm39) |
E317G |
probably benign |
Het |
Tex10 |
A |
T |
4: 48,459,355 (GRCm39) |
Y506* |
probably null |
Het |
Trhde |
T |
A |
10: 114,280,585 (GRCm39) |
R848* |
probably null |
Het |
Trpc5 |
T |
A |
X: 143,202,594 (GRCm39) |
R545* |
probably null |
Het |
Usp24 |
C |
T |
4: 106,216,286 (GRCm39) |
T379M |
possibly damaging |
Het |
Zfp783 |
A |
T |
6: 47,922,499 (GRCm39) |
|
noncoding transcript |
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 |
R0016:Gvin3
|
UTSW |
7 |
106,202,453 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|
|