Incidental Mutation 'IGL02114:1700084J12Rik'
ID 280296
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700084J12Rik
Ensembl Gene ENSMUSG00000058101
Gene Name RIKEN cDNA 1700084J12 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02114
Quality Score
Status
Chromosome 15
Chromosomal Location 33405355-33406085 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) C to A at 33405844 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000154400 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042167] [ENSMUST00000228916]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000042167
SMART Domains Protein: ENSMUSP00000039046
Gene: ENSMUSG00000039007

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
low complexity region 186 199 N/A INTRINSIC
Pfam:Peptidase_M28 268 457 5.9e-29 PFAM
Pfam:Peptidase_M20 284 457 1.6e-8 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000079057
SMART Domains Protein: ENSMUSP00000130018
Gene: ENSMUSG00000058101

DomainStartEndE-ValueType
Pfam:Ribosomal_L30 14 64 9.6e-15 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187707
Predicted Effect probably benign
Transcript: ENSMUST00000228916
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akap3 T C 6: 126,842,959 (GRCm39) V526A probably damaging Het
Ano6 C A 15: 95,841,341 (GRCm39) S479R probably damaging Het
Aqp8 C A 7: 123,063,419 (GRCm39) H90N probably damaging Het
Arih1 A T 9: 59,333,452 (GRCm39) C229S probably damaging Het
Col6a6 C A 9: 105,644,398 (GRCm39) probably null Het
Cp A G 3: 20,020,511 (GRCm39) E168G probably benign Het
Creb5 C T 6: 53,581,443 (GRCm39) probably benign Het
Cstdc3 T A 16: 36,131,617 (GRCm39) Y42* probably null Het
Cyp2c66 C A 19: 39,159,519 (GRCm39) probably benign Het
Dcpp2 C A 17: 24,119,609 (GRCm39) A141D possibly damaging Het
Dnah5 A G 15: 28,397,270 (GRCm39) D3321G probably damaging Het
Ecsit T C 9: 21,989,440 (GRCm39) probably benign Het
Gabra1 T C 11: 42,026,402 (GRCm39) I297V probably damaging Het
Gja8 T C 3: 96,827,341 (GRCm39) K107R probably benign Het
Gm16686 A T 4: 88,673,739 (GRCm39) L30Q probably null Het
Hbp1 T C 12: 31,980,674 (GRCm39) probably benign Het
Inhbc T C 10: 127,205,971 (GRCm39) I99V probably benign Het
Kcne3 T A 7: 99,833,697 (GRCm39) probably benign Het
Larp1 T C 11: 57,947,881 (GRCm39) Y926H probably damaging Het
Lhfpl5 G T 17: 28,795,149 (GRCm39) A59S possibly damaging Het
Mov10 T A 3: 104,702,634 (GRCm39) probably benign Het
Myl12b A T 17: 71,284,164 (GRCm39) N21K possibly damaging Het
Ncoa7 A T 10: 30,538,360 (GRCm39) V675E probably damaging Het
Nt5c1b T C 12: 10,425,444 (GRCm39) I255T probably damaging Het
Numa1 T A 7: 101,661,083 (GRCm39) probably benign Het
Or13c3 T A 4: 52,856,144 (GRCm39) Y123F probably damaging Het
Otop2 A T 11: 115,217,806 (GRCm39) D214V possibly damaging Het
Plec C A 15: 76,057,748 (GRCm39) G3928V probably damaging Het
Prkcz T C 4: 155,356,047 (GRCm39) E176G probably damaging Het
Qdpr G A 5: 45,592,018 (GRCm39) T106I possibly damaging Het
R3hdm2 T G 10: 127,319,978 (GRCm39) M481R probably damaging Het
Setdb2 C T 14: 59,639,764 (GRCm39) R709Q probably damaging Het
Skic2 C T 17: 35,060,092 (GRCm39) V145M probably damaging Het
Slx4ip T A 2: 136,842,120 (GRCm39) V15D probably damaging Het
Stat4 T C 1: 52,142,024 (GRCm39) S624P probably damaging Het
Tecpr2 T A 12: 110,935,321 (GRCm39) L1380Q probably damaging Het
Traf2 T C 2: 25,415,004 (GRCm39) I286V possibly damaging Het
Vmn2r30 T C 7: 7,340,408 (GRCm39) I29V possibly damaging Het
Wdr43 A G 17: 71,959,843 (GRCm39) Q561R probably benign Het
Zfp607b T A 7: 27,403,150 (GRCm39) F535L probably benign Het
Other mutations in 1700084J12Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01448:1700084J12Rik APN 15 33,405,779 (GRCm39) intron probably benign
Posted On 2015-04-16