Incidental Mutation 'IGL01751:Gvin3'
ID |
153124 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gvin3
|
Ensembl Gene |
ENSMUSG00000073902 |
Gene Name |
GTPase, very large interferon inducible, family member 3 |
Synonyms |
Gm1966 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.098)
|
Stock # |
IGL01751
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
106195950-106203242 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 106201516 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Isoleucine
at position 576
(N576I)
|
Gene Model |
predicted gene model for transcript(s):
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000098144
AA Change: N576I
PolyPhen 2
Score 0.800 (Sensitivity: 0.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000095748 Gene: ENSMUSG00000073902 AA Change: N576I
Domain | Start | End | E-Value | Type |
low complexity region
|
101 |
116 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000184540
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
A |
G |
5: 144,979,981 (GRCm39) |
|
probably null |
Het |
Abtb3 |
C |
A |
10: 85,490,366 (GRCm39) |
Q1011K |
probably damaging |
Het |
Aoc1l2 |
A |
T |
6: 48,907,522 (GRCm39) |
H174L |
possibly damaging |
Het |
Auts2 |
G |
T |
5: 131,501,198 (GRCm39) |
Q72K |
probably damaging |
Het |
Ccdc7b |
A |
T |
8: 129,863,049 (GRCm39) |
|
probably benign |
Het |
Frem3 |
A |
G |
8: 81,342,372 (GRCm39) |
E1555G |
probably benign |
Het |
Gm5263 |
T |
G |
1: 146,296,302 (GRCm39) |
|
noncoding transcript |
Het |
Gm5828 |
A |
G |
1: 16,840,208 (GRCm39) |
|
noncoding transcript |
Het |
Gm6605 |
T |
C |
7: 38,147,630 (GRCm39) |
|
noncoding transcript |
Het |
Hps3 |
T |
C |
3: 20,065,130 (GRCm39) |
D638G |
probably damaging |
Het |
Igdcc4 |
A |
T |
9: 65,039,014 (GRCm39) |
N887I |
probably damaging |
Het |
Itpkc |
G |
A |
7: 26,912,491 (GRCm39) |
|
probably benign |
Het |
Mfge8 |
A |
G |
7: 78,786,403 (GRCm39) |
|
probably null |
Het |
Mrc2 |
G |
T |
11: 105,216,560 (GRCm39) |
L116F |
probably benign |
Het |
Necab1 |
T |
C |
4: 14,978,171 (GRCm39) |
D226G |
probably damaging |
Het |
Neurod2 |
T |
C |
11: 98,218,201 (GRCm39) |
E321G |
possibly damaging |
Het |
Obp2b |
G |
T |
2: 25,627,760 (GRCm39) |
V59L |
possibly damaging |
Het |
Olr1 |
T |
C |
6: 129,465,811 (GRCm39) |
N65S |
possibly damaging |
Het |
Or14c39 |
A |
T |
7: 86,343,997 (GRCm39) |
Q111L |
probably benign |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or5d43 |
A |
T |
2: 88,104,977 (GRCm39) |
C139S |
possibly damaging |
Het |
Or8b48 |
C |
T |
9: 38,492,809 (GRCm39) |
P79S |
probably damaging |
Het |
Rock1 |
A |
G |
18: 10,079,113 (GRCm39) |
|
probably null |
Het |
Scn3a |
T |
A |
2: 65,291,596 (GRCm39) |
M1717L |
possibly damaging |
Het |
Smg7 |
T |
C |
1: 152,719,812 (GRCm39) |
D903G |
possibly damaging |
Het |
Tlr1 |
A |
T |
5: 65,083,290 (GRCm39) |
L429* |
probably null |
Het |
Ttll9 |
A |
T |
2: 152,825,025 (GRCm39) |
N68I |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,567,943 (GRCm39) |
V25904A |
possibly damaging |
Het |
Uaca |
G |
A |
9: 60,777,139 (GRCm39) |
V507M |
probably damaging |
Het |
Vmn1r195 |
G |
T |
13: 22,463,421 (GRCm39) |
C297F |
probably benign |
Het |
Zdhhc2 |
G |
A |
8: 40,926,042 (GRCm39) |
A346T |
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 |
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 |
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 |
|
|
Posted On |
2014-02-04 |