Incidental Mutation 'IGL00392:0610011F06Rik'
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ID5766
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 0610011F06Rik
Ensembl Gene ENSMUSG00000025731
Gene NameRIKEN cDNA 0610011F06 gene
Synonyms
Accession Numbers
Stock #IGL00392
Quality Score
Status
Chromosome17
Chromosomal Location25875464-25886007 bp(+) (GRCm38)
Type of Mutationcritical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to C at 25876124 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000026827 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026827]
Predicted Effect probably null
Transcript: ENSMUST00000026827
SMART Domains Protein: ENSMUSP00000026827
Gene: ENSMUSG00000025731

DomainStartEndE-ValueType
Pfam:DUF938 1 203 7.4e-95 PFAM
Pfam:Methyltransf_25 31 133 1.1e-7 PFAM
SMART Domains
(Predicted Sequence)

DomainStartEndE-ValueType
Pfam:DUF938 1 78 1.1e-26 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130011E15Rik T G 19: 45,940,488 H389P probably benign Het
Alpk3 T C 7: 81,078,009 Y296H possibly damaging Het
Brca2 A G 5: 150,541,240 T1490A probably benign Het
Btaf1 A T 19: 37,009,702 D1732V probably damaging Het
Capzb T C 4: 139,288,947 probably benign Het
Cc2d2a A G 5: 43,724,380 probably benign Het
Ccdc173 T C 2: 69,771,984 H361R possibly damaging Het
Cdh22 A G 2: 165,112,601 Y667H probably damaging Het
Celsr1 T A 15: 85,931,345 Q1823L probably benign Het
Cntrl T C 2: 35,137,814 Het
Dhx15 A T 5: 52,157,582 probably benign Het
Dip2c A T 13: 9,493,108 D30V possibly damaging Het
Dyrk2 T C 10: 118,859,844 D503G probably damaging Het
Enpp1 T A 10: 24,645,427 I801F possibly damaging Het
Fnbp4 A C 2: 90,751,622 probably benign Het
Klk1b5 T A 7: 44,216,504 W2R probably benign Het
Lama2 T C 10: 27,188,265 K1240R probably benign Het
Lrrc16a G A 13: 24,094,491 T575I probably damaging Het
Matn2 A G 15: 34,402,856 N409S probably benign Het
Mep1b A T 18: 21,084,186 K121* probably null Het
Myh7 T C 14: 54,987,388 E⇒G probably damaging Het
Nfkbie G A 17: 45,560,213 probably null Het
Nlrc4 T C 17: 74,446,534 R285G probably damaging Het
Pax8 T C 2: 24,443,132 Y66C probably damaging Het
Plxna2 A G 1: 194,800,568 D1523G probably damaging Het
Pou2f1 A G 1: 165,896,590 probably benign Het
Prom1 A G 5: 44,007,021 probably null Het
Ptk6 T C 2: 181,195,818 D436G probably benign Het
Robo4 T A 9: 37,408,229 F644I probably damaging Het
Sec24c C A 14: 20,693,203 S1040R possibly damaging Het
Sgcb G T 5: 73,635,678 N⇒K possibly damaging Het
Smarcd2 T C 11: 106,265,904 D268G probably damaging Het
Unc13b C T 4: 43,240,285 R769W possibly damaging Het
Zfpl1 C A 19: 6,081,107 R285L probably damaging Het
Other mutations in 0610011F06Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4985:0610011F06Rik UTSW 17 25876776 makesense probably null
R5813:0610011F06Rik UTSW 17 25876021 missense probably damaging 1.00
Posted OnApr 20, 2012