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) question?
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

DomainStartEndE-ValueType
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
GeneRefVarChr/LocMutationPredicted EffectZygosity
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
AlleleSourceChrCoordTypePredicted EffectPPH 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