Incidental Mutation 'IGL02670:Gm6576'
ID 302891
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6576
Ensembl Gene ENSMUSG00000090544
Gene Name predicted gene 6576
Accession Numbers
Essential gene? Not available question?
Stock # IGL02670
Quality Score
Chromosome 15
Chromosomal Location 27025386-27026207 bp(+) (GRCm38)
Type of Mutation exon
DNA Base Change (assembly) A to C at 27025512 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000126334 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000169678]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000169678
SMART Domains Protein: ENSMUSP00000126334
Gene: ENSMUSG00000090544

low complexity region 1 12 N/A INTRINSIC
low complexity region 14 35 N/A INTRINSIC
Pfam:Ribosomal_S5 84 148 1.4e-30 PFAM
Pfam:Ribosomal_S5_C 167 238 3.6e-28 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik C T 3: 36,967,305 (GRCm38) Q2193* probably null Het
Asb1 T C 1: 91,546,918 (GRCm38) probably benign Het
Cnot6 G A 11: 49,685,114 (GRCm38) Q178* probably null Het
Col5a1 C T 2: 27,974,715 (GRCm38) A737V unknown Het
Cyp27b1 T C 10: 127,050,358 (GRCm38) S303P probably benign Het
Dnah5 T C 15: 28,409,296 (GRCm38) L3620P probably damaging Het
Dock7 A T 4: 98,966,286 (GRCm38) probably null Het
Fam161b T C 12: 84,357,594 (GRCm38) D104G probably benign Het
Fam8a1 A G 13: 46,673,604 (GRCm38) M284V possibly damaging Het
Fkbp3 T A 12: 65,069,103 (GRCm38) K65* probably null Het
Gatb A G 3: 85,613,551 (GRCm38) probably null Het
Gm572 A T 4: 148,651,228 (GRCm38) H38L probably benign Het
L2hgdh G A 12: 69,692,480 (GRCm38) R406W possibly damaging Het
Lmo7 A T 14: 101,880,980 (GRCm38) T214S probably damaging Het
Map3k12 T C 15: 102,503,546 (GRCm38) H361R probably benign Het
Mios T C 6: 8,235,378 (GRCm38) probably benign Het
Mta1 T C 12: 113,130,121 (GRCm38) L315P probably damaging Het
Pask A C 1: 93,310,818 (GRCm38) V1315G probably damaging Het
Pias4 A T 10: 81,164,070 (GRCm38) C50S probably damaging Het
Rgs11 G A 17: 26,207,631 (GRCm38) V279I probably benign Het
Sgk1 T A 10: 21,928,546 (GRCm38) C92S probably benign Het
Slc2a13 C T 15: 91,497,509 (GRCm38) G259E probably damaging Het
Slc5a4b A G 10: 76,075,100 (GRCm38) C301R probably damaging Het
Sstr4 G T 2: 148,396,533 (GRCm38) G355* probably null Het
Tnrc6a T A 7: 123,171,312 (GRCm38) L775Q possibly damaging Het
Vmn1r218 A G 13: 23,137,004 (GRCm38) I94V probably benign Het
Xpa A G 4: 46,185,682 (GRCm38) F99L probably benign Het
Other mutations in Gm6576
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00232:Gm6576 APN 15 27,025,798 (GRCm38) exon noncoding transcript
IGL01325:Gm6576 APN 15 27,025,884 (GRCm38) exon noncoding transcript
IGL02027:Gm6576 APN 15 27,025,866 (GRCm38) exon noncoding transcript
IGL02416:Gm6576 APN 15 27,025,987 (GRCm38) exon noncoding transcript
R0128:Gm6576 UTSW 15 27,026,000 (GRCm38) exon noncoding transcript
Posted On 2015-04-16