Incidental Mutation 'IGL01461:E330020D12Rik'
ID 87996
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol E330020D12Rik
Ensembl Gene ENSMUSG00000073538
Gene Name Riken cDNA E330020D12 gene
Synonyms Gm6648
Accession Numbers
Essential gene? Probably non essential (E-score: 0.081) question?
Stock # IGL01461
Quality Score
Status
Chromosome 1
Chromosomal Location 153280573-153289981 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 153284105 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000097535
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186785
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188717
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210408I21Rik T C 13: 77,429,214 (GRCm39) F767S probably benign Het
Abca13 A G 11: 9,353,834 (GRCm39) T3719A probably damaging Het
Apob A T 12: 8,051,884 (GRCm39) M1137L probably benign Het
Brd9 C T 13: 74,099,717 (GRCm39) Q445* probably null Het
Cdh23 T C 10: 60,244,926 (GRCm39) T990A possibly damaging Het
Cenpf A G 1: 189,389,293 (GRCm39) L1513S probably damaging Het
Col27a1 A G 4: 63,142,480 (GRCm39) K56R probably damaging Het
Cryaa A G 17: 31,900,000 (GRCm39) Y118C probably damaging Het
Dtl T C 1: 191,278,729 (GRCm39) T378A possibly damaging Het
F7 A G 8: 13,082,245 (GRCm39) D145G possibly damaging Het
Flvcr2 A G 12: 85,849,905 (GRCm39) probably benign Het
Hltf A T 3: 20,154,103 (GRCm39) K680* probably null Het
Ing1 T G 8: 11,611,453 (GRCm39) F22V probably benign Het
Ipo5 A G 14: 121,165,945 (GRCm39) D330G probably damaging Het
Itgax G T 7: 127,734,190 (GRCm39) D321Y probably damaging Het
Kel A C 6: 41,678,845 (GRCm39) probably null Het
Marchf10 T C 11: 105,280,431 (GRCm39) K618R probably damaging Het
Mast4 T A 13: 102,890,576 (GRCm39) M925L probably damaging Het
Miga1 C T 3: 152,040,934 (GRCm39) E78K probably damaging Het
Or4c106 G T 2: 88,682,669 (GRCm39) C125F probably damaging Het
Or7e165 T A 9: 19,695,245 (GRCm39) probably null Het
Pkdrej T C 15: 85,704,575 (GRCm39) I454V possibly damaging Het
Poglut2 T C 1: 44,150,094 (GRCm39) Q365R probably damaging Het
Prpf6 C A 2: 181,273,304 (GRCm39) T283N probably benign Het
R3hdm1 A G 1: 128,106,643 (GRCm39) H197R probably damaging Het
Resf1 T C 6: 149,233,013 (GRCm39) probably benign Het
Smpd4 A C 16: 17,439,370 (GRCm39) Q7P probably damaging Het
Vmn2r84 A T 10: 130,227,094 (GRCm39) I248K possibly damaging Het
Other mutations in E330020D12Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1500:E330020D12Rik UTSW 1 153,284,125 (GRCm39) exon noncoding transcript
R2850:E330020D12Rik UTSW 1 153,282,336 (GRCm39) exon noncoding transcript
Posted On 2013-11-18