Incidental Mutation 'IGL02027:Gm6576'
ID 184207
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6576
Ensembl Gene ENSMUSG00000090544
Gene Name predicted gene 6576
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock # IGL02027
Quality Score
Status
Chromosome 15
Chromosomal Location 27025386-27026207 bp(+) (GRCm38)
Type of Mutation exon
DNA Base Change (assembly) A to G at 27025866 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

DomainStartEndE-ValueType
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: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adipor1 A G 1: 134,431,185 T312A probably benign Het
Begain T G 12: 109,034,309 K384Q possibly damaging Het
C2cd6 T C 1: 59,060,604 I393V probably benign Het
Catsperz A G 19: 6,925,296 V5A probably benign Het
Cbx1 T A 11: 96,801,489 F67L probably damaging Het
Cerkl T C 2: 79,341,286 probably benign Het
Ctgf A G 10: 24,596,409 S117G probably damaging Het
Cubn G T 2: 13,287,594 D3259E probably damaging Het
Cyp2u1 A G 3: 131,297,951 Y307H probably damaging Het
Dcaf6 A C 1: 165,424,341 D71E probably damaging Het
Dclk3 A T 9: 111,467,843 K152* probably null Het
Fcgbp G A 7: 28,075,204 D68N probably damaging Het
Has2 T C 15: 56,668,171 T383A probably damaging Het
Htr1f T A 16: 64,926,321 K203* probably null Het
Il1f9 A T 2: 24,192,785 I191L probably benign Het
Iqgap3 T C 3: 88,087,342 I116T possibly damaging Het
Itga1 C T 13: 114,990,055 probably null Het
Kif5b T C 18: 6,209,089 D891G possibly damaging Het
Krt74 T C 15: 101,756,794 noncoding transcript Het
Lama3 A G 18: 12,516,513 K1776E probably damaging Het
Lats1 T C 10: 7,712,948 S1110P probably benign Het
Lipo3 T A 19: 33,580,519 K158* probably null Het
Lrrc9 T A 12: 72,470,334 probably benign Het
Met A G 6: 17,563,727 probably benign Het
Mmp13 A G 9: 7,272,955 Y105C probably damaging Het
Mtus1 T C 8: 40,993,601 E1151G probably damaging Het
Nov T C 15: 54,747,934 V155A probably damaging Het
Nptx1 T C 11: 119,544,596 D298G possibly damaging Het
Pdlim1 T C 19: 40,243,466 N156S probably benign Het
Pdzk1 A G 3: 96,854,673 probably benign Het
Pex5 A G 6: 124,398,888 S448P probably benign Het
Polr3e G T 7: 120,930,963 R124L probably damaging Het
Ppp2r2c C T 5: 36,952,472 R392C probably damaging Het
Prpf4b T C 13: 34,889,571 I543T probably benign Het
Prr27 A G 5: 87,843,443 S305G possibly damaging Het
Repin1 A G 6: 48,596,473 H56R probably damaging Het
Ryr2 A T 13: 11,597,112 L408H probably damaging Het
Sbf2 T A 7: 110,461,141 Q205H probably damaging Het
Sgo2b G A 8: 63,926,829 P990S probably benign Het
Slc33a1 G T 3: 63,948,141 P361Q probably damaging Het
Tmem98 T C 11: 80,815,657 probably benign Het
Ttc25 C T 11: 100,569,902 T495M probably damaging Het
Vmn1r16 T C 6: 57,323,059 T193A possibly damaging Het
Vmn1r5 T A 6: 56,985,655 I105K probably damaging Het
Zfp473 A T 7: 44,738,038 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
IGL02416:Gm6576 APN 15 27025987 exon noncoding transcript
IGL02670:Gm6576 APN 15 27025512 exon noncoding transcript
R0128:Gm6576 UTSW 15 27026000 exon noncoding transcript
Posted On 2014-05-07