Incidental Mutation 'IGL00971:Gvin-ps3'
ID 306623
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gvin-ps3
Ensembl Gene ENSMUSG00000095649
Gene Name GTPase, very large interferon inducible, pseudogene 3
Synonyms Gm8979, Gm21884
Accession Numbers
Essential gene? Probably non essential (E-score: 0.133) question?
Stock # IGL00971
Quality Score
Status
Chromosome 7
Chromosomal Location 105674938-105678355 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to A at 105681008 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: ENSMUST00000176647
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183386
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930596D02Rik C T 14: 35,532,170 (GRCm39) C135Y possibly damaging Het
Afdn T A 17: 14,072,575 (GRCm39) probably benign Het
Akap10 A G 11: 61,795,622 (GRCm39) V347A possibly damaging Het
Ankrd11 A G 8: 123,622,092 (GRCm39) S587P probably damaging Het
Ces1g T C 8: 94,029,660 (GRCm39) Y524C probably damaging Het
Cimip2b A G 4: 43,428,377 (GRCm39) L51P probably damaging Het
Cubn T C 2: 13,283,219 (GRCm39) N3573S possibly damaging Het
Cyp1a1 G T 9: 57,607,990 (GRCm39) C206F probably damaging Het
Fbxo30 T C 10: 11,166,042 (GRCm39) Y255H probably benign Het
Ggnbp2 T C 11: 84,731,230 (GRCm39) I295V possibly damaging Het
Gpatch8 A G 11: 102,370,743 (GRCm39) Y932H unknown Het
Heatr6 C T 11: 83,650,135 (GRCm39) P197L probably damaging Het
Helb T C 10: 119,930,168 (GRCm39) D737G possibly damaging Het
Helz A T 11: 107,554,479 (GRCm39) I1226F possibly damaging Het
Ipo11 A T 13: 106,993,277 (GRCm39) I749N probably damaging Het
Ipo13 T C 4: 117,771,564 (GRCm39) E2G possibly damaging Het
Jam3 A C 9: 27,013,188 (GRCm39) D127E probably damaging Het
Kif16b G T 2: 142,553,664 (GRCm39) Q1045K probably benign Het
Kin T C 2: 10,095,159 (GRCm39) W121R possibly damaging Het
Man1b1 T G 2: 25,233,337 (GRCm39) S237A possibly damaging Het
Mmel1 C T 4: 154,972,289 (GRCm39) probably benign Het
Morn4 T C 19: 42,064,559 (GRCm39) N143S possibly damaging Het
Nlrp4b A G 7: 10,448,882 (GRCm39) T362A possibly damaging Het
Ntpcr C T 8: 126,474,501 (GRCm39) T153M probably damaging Het
Or13p10 T A 4: 118,523,475 (GRCm39) F254I probably damaging Het
Pdzd2 A G 15: 12,374,804 (GRCm39) L1777P probably benign Het
Postn A G 3: 54,276,697 (GRCm39) N192S possibly damaging Het
Prkar1a A T 11: 109,551,877 (GRCm39) Y122F probably benign Het
Serpinb7 A G 1: 107,355,976 (GRCm39) probably benign Het
Setd3 A T 12: 108,126,496 (GRCm39) I121N probably damaging Het
Slamf7 T A 1: 171,466,810 (GRCm39) I132L probably benign Het
Syt4 T C 18: 31,580,227 (GRCm39) probably benign Het
Tesc G A 5: 118,194,504 (GRCm39) probably null Het
Tsc1 C A 2: 28,560,952 (GRCm39) S270* probably null Het
Wap C A 11: 6,586,808 (GRCm39) C97F probably damaging Het
Zfp451 A G 1: 33,822,234 (GRCm39) S155P probably benign Het
Zfp469 A G 8: 122,996,472 (GRCm39) probably benign Het
Zfp51 C T 17: 21,683,844 (GRCm39) T153M probably benign Het
Zfp579 A G 7: 4,996,390 (GRCm39) I507T probably damaging Het
Other mutations in Gvin-ps3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01125:Gvin-ps3 APN 7 105,682,021 (GRCm39) missense unknown 0.00
IGL01392:Gvin-ps3 APN 7 105,682,962 (GRCm39) missense probably benign 0.01
R1184:Gvin-ps3 UTSW 7 105,683,159 (GRCm39) missense probably benign 0.03
R1411:Gvin-ps3 UTSW 7 105,682,686 (GRCm39) missense probably benign 0.39
R2198:Gvin-ps3 UTSW 7 105,682,758 (GRCm39) missense probably benign 0.00
R2311:Gvin-ps3 UTSW 7 105,682,797 (GRCm39) missense probably damaging 0.99
R2380:Gvin-ps3 UTSW 7 105,681,374 (GRCm39) missense possibly damaging 0.86
R3825:Gvin-ps3 UTSW 7 105,682,780 (GRCm39) missense possibly damaging 0.92
R4397:Gvin-ps3 UTSW 7 105,682,130 (GRCm39) exon noncoding transcript
R4693:Gvin-ps3 UTSW 7 105,681,585 (GRCm39) exon noncoding transcript
R4787:Gvin-ps3 UTSW 7 105,681,041 (GRCm39) exon noncoding transcript
R4840:Gvin-ps3 UTSW 7 105,680,627 (GRCm39) exon noncoding transcript
R4972:Gvin-ps3 UTSW 7 105,682,521 (GRCm39) exon noncoding transcript
R5221:Gvin-ps3 UTSW 7 105,683,181 (GRCm39) exon noncoding transcript
R5296:Gvin-ps3 UTSW 7 105,681,055 (GRCm39) exon noncoding transcript
Posted On 2015-04-16