Incidental Mutation 'IGL02355:Gvin-ps5'
ID 289636
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gvin-ps5
Ensembl Gene ENSMUSG00000095457
Gene Name GTPase, very large interferon inducible, pseudogene 5
Synonyms Gm21911, Gm8989
Accession Numbers
Essential gene? Probably non essential (E-score: 0.177) question?
Stock # IGL02355
Quality Score
Status
Chromosome 7
Chromosomal Location 105921603-105923735 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 105929480 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184782
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam3 C A 8: 25,187,207 (GRCm39) C428F probably damaging Het
Alas1 T C 9: 106,113,838 (GRCm39) Y469C probably damaging Het
Asxl1 C T 2: 153,243,706 (GRCm39) L1419F probably benign Het
Bcan C T 3: 87,901,449 (GRCm39) D418N possibly damaging Het
Cdc42bpg A G 19: 6,360,839 (GRCm39) D199G possibly damaging Het
Chst15 T C 7: 131,868,401 (GRCm39) N340D probably benign Het
Col12a1 T G 9: 79,537,993 (GRCm39) probably benign Het
Cyp2c67 T A 19: 39,631,849 (GRCm39) H116L probably benign Het
Cyp2c67 G A 19: 39,605,826 (GRCm39) R357* probably null Het
Ears2 T C 7: 121,643,773 (GRCm39) D395G probably benign Het
Fam227a A T 15: 79,528,139 (GRCm39) probably benign Het
Fap A G 2: 62,403,842 (GRCm39) V11A probably benign Het
Ganc A G 2: 120,264,238 (GRCm39) D397G probably damaging Het
Gjb6 C A 14: 57,361,752 (GRCm39) G170C possibly damaging Het
Gria2 A T 3: 80,614,244 (GRCm39) W599R probably damaging Het
Ighv1-64 A G 12: 115,471,236 (GRCm39) S94P probably benign Het
Kifc3 C T 8: 95,836,507 (GRCm39) A85T probably damaging Het
Lifr G A 15: 7,194,174 (GRCm39) probably null Het
Lonp2 T G 8: 87,350,874 (GRCm39) S21R probably benign Het
Nxpe3 A G 16: 55,710,949 (GRCm39) V30A probably benign Het
Olfml1 T C 7: 107,167,010 (GRCm39) V13A probably benign Het
Or10w1 T C 19: 13,632,597 (GRCm39) V268A probably benign Het
Or1af1 A G 2: 37,109,681 (GRCm39) Y60C probably damaging Het
Pcnt G A 10: 76,210,996 (GRCm39) Q2376* probably null Het
Pglyrp2 A G 17: 32,635,996 (GRCm39) L380P probably damaging Het
Plin3 A G 17: 56,593,636 (GRCm39) V26A probably benign Het
Potefam1 T C 2: 111,041,996 (GRCm39) probably benign Het
Pramel25 A G 4: 143,519,580 (GRCm39) S114G probably damaging Het
Rims1 A G 1: 22,522,288 (GRCm39) I470T probably damaging Het
Rora T C 9: 69,281,374 (GRCm39) Y329H probably damaging Het
Scnn1b G A 7: 121,516,770 (GRCm39) R503H probably damaging Het
Sec14l1 A G 11: 117,035,675 (GRCm39) D237G possibly damaging Het
Selplg A G 5: 113,957,467 (GRCm39) S280P probably benign Het
Serpina12 A G 12: 104,004,140 (GRCm39) L164P probably benign Het
Sik2 C T 9: 50,828,903 (GRCm39) W176* probably null Het
Slc2a1 T C 4: 118,993,612 (GRCm39) F483S possibly damaging Het
Speg A G 1: 75,400,559 (GRCm39) D2573G possibly damaging Het
Stil C T 4: 114,867,308 (GRCm39) S239L probably damaging Het
Tmem94 C A 11: 115,685,571 (GRCm39) S941R probably damaging Het
Tnfrsf11b T A 15: 54,115,778 (GRCm39) D273V probably damaging Het
Tns2 A G 15: 102,020,725 (GRCm39) T864A probably benign Het
Zfpm2 A G 15: 40,962,890 (GRCm39) H184R probably damaging Het
Other mutations in Gvin-ps5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01348:Gvin-ps5 APN 7 105,929,042 (GRCm39) missense unknown 0.00
IGL02005:Gvin-ps5 APN 7 105,928,627 (GRCm39) missense unknown 0.00
IGL02362:Gvin-ps5 APN 7 105,929,480 (GRCm39) exon noncoding transcript
IGL02608:Gvin-ps5 APN 7 105,928,876 (GRCm39) exon noncoding transcript
R1954:Gvin-ps5 UTSW 7 105,928,888 (GRCm39) missense probably damaging 1.00
R2141:Gvin-ps5 UTSW 7 105,929,163 (GRCm39) missense probably damaging 0.97
R3915:Gvin-ps5 UTSW 7 105,929,445 (GRCm39) missense probably benign 0.00
R4165:Gvin-ps5 UTSW 7 105,929,895 (GRCm39) exon noncoding transcript
R4989:Gvin-ps5 UTSW 7 105,928,664 (GRCm39) exon noncoding transcript
R5101:Gvin-ps5 UTSW 7 105,929,096 (GRCm39) exon noncoding transcript
R5807:Gvin-ps5 UTSW 7 105,929,430 (GRCm39) exon noncoding transcript
Posted On 2015-04-16