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
Is this an 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 Q2193* probably null Het
Asb1 T C 1: 91,546,918 probably benign Het
Cnot6 G A 11: 49,685,114 Q178* probably null Het
Col5a1 C T 2: 27,974,715 A737V unknown Het
Cyp27b1 T C 10: 127,050,358 S303P probably benign Het
Dnah5 T C 15: 28,409,296 L3620P probably damaging Het
Dock7 A T 4: 98,966,286 probably null Het
Fam161b T C 12: 84,357,594 D104G probably benign Het
Fam8a1 A G 13: 46,673,604 M284V possibly damaging Het
Fkbp3 T A 12: 65,069,103 K65* probably null Het
Gatb A G 3: 85,613,551 probably null Het
Gm572 A T 4: 148,651,228 H38L probably benign Het
L2hgdh G A 12: 69,692,480 R406W possibly damaging Het
Lmo7 A T 14: 101,880,980 T214S probably damaging Het
Map3k12 T C 15: 102,503,546 H361R probably benign Het
Mios T C 6: 8,235,378 probably benign Het
Mta1 T C 12: 113,130,121 L315P probably damaging Het
Pask A C 1: 93,310,818 V1315G probably damaging Het
Pias4 A T 10: 81,164,070 C50S probably damaging Het
Rgs11 G A 17: 26,207,631 V279I probably benign Het
Sgk1 T A 10: 21,928,546 C92S probably benign Het
Slc2a13 C T 15: 91,497,509 G259E probably damaging Het
Slc5a4b A G 10: 76,075,100 C301R probably damaging Het
Sstr4 G T 2: 148,396,533 G355* probably null Het
Tnrc6a T A 7: 123,171,312 L775Q possibly damaging Het
Vmn1r218 A G 13: 23,137,004 I94V probably benign Het
Xpa A G 4: 46,185,682 F99L probably benign Het
Other mutations in Gm6576
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00232:Gm6576 APN 15 27025798 exon noncoding transcript
IGL01325:Gm6576 APN 15 27025884 exon noncoding transcript
IGL02027:Gm6576 APN 15 27025866 exon noncoding transcript
IGL02416:Gm6576 APN 15 27025987 exon noncoding transcript
R0128:Gm6576 UTSW 15 27026000 exon noncoding transcript
Posted On 2015-04-16