Incidental Mutation 'IGL01072:Gm7275'
ID 52886
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7275
Ensembl Gene ENSMUSG00000067716
Gene Name predicted gene 7275
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.260) question?
Stock # IGL01072
Quality Score
Status
Chromosome 16
Chromosomal Location 47893360-47894545 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 47894519 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000085634 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088296]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000088296
SMART Domains Protein: ENSMUSP00000085634
Gene: ENSMUSG00000067716

DomainStartEndE-ValueType
Pfam:Peptidase_C48 67 246 1e-43 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ccdc65 A T 15: 98,606,277 (GRCm39) M1L unknown Het
Cyp3a44 T C 5: 145,728,438 (GRCm39) D262G probably benign Het
Dmbt1 C T 7: 130,687,098 (GRCm39) probably benign Het
Dnmt3l A G 10: 77,888,605 (GRCm39) N169S probably benign Het
Fbxw26 A T 9: 109,552,905 (GRCm39) F290I probably damaging Het
Foxj3 A G 4: 119,467,226 (GRCm39) M190V probably benign Het
Ly75 T A 2: 60,184,840 (GRCm39) D438V probably damaging Het
Lzts3 T C 2: 130,477,365 (GRCm39) E475G probably damaging Het
Mon2 A T 10: 122,846,444 (GRCm39) Y1375* probably null Het
Ndufc2 T A 7: 97,049,490 (GRCm39) V32D probably damaging Het
Nf2 A C 11: 4,739,713 (GRCm39) L431R probably null Het
Niban2 T C 2: 32,802,427 (GRCm39) probably benign Het
Ptpn9 C T 9: 56,943,987 (GRCm39) T287I possibly damaging Het
Rictor A G 15: 6,819,043 (GRCm39) D1422G probably damaging Het
Rpp40 C A 13: 36,086,017 (GRCm39) G115C probably damaging Het
Rps6ka5 A G 12: 100,540,157 (GRCm39) V522A probably benign Het
Scgb1b24 A T 7: 33,443,434 (GRCm39) D31V probably damaging Het
Trrap C A 5: 144,721,065 (GRCm39) probably benign Het
Vmn1r214 T C 13: 23,219,300 (GRCm39) Y265H possibly damaging Het
Other mutations in Gm7275
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01603:Gm7275 APN 16 47,893,942 (GRCm39) exon noncoding transcript
IGL01939:Gm7275 APN 16 47,893,946 (GRCm39) exon noncoding transcript
IGL02269:Gm7275 APN 16 47,894,185 (GRCm39) exon noncoding transcript
IGL02403:Gm7275 APN 16 47,893,991 (GRCm39) exon noncoding transcript
R0332:Gm7275 UTSW 16 47,894,132 (GRCm39) exon noncoding transcript
R1162:Gm7275 UTSW 16 47,894,395 (GRCm39) exon noncoding transcript
R1743:Gm7275 UTSW 16 47,894,120 (GRCm39) exon noncoding transcript
R3087:Gm7275 UTSW 16 47,894,098 (GRCm39) exon noncoding transcript
R4590:Gm7275 UTSW 16 47,893,982 (GRCm39) exon noncoding transcript
R5617:Gm7275 UTSW 16 47,894,527 (GRCm39) exon noncoding transcript
R5910:Gm7275 UTSW 16 47,893,826 (GRCm39) exon noncoding transcript
Posted On 2013-06-21