Incidental Mutation 'IGL02834:A530099J19Rik'
ID361574
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol A530099J19Rik
Ensembl Gene ENSMUSG00000047462
Gene NameRIKEN cDNA A530099J19 gene
Synonyms
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL02834
Quality Score
Status
Chromosome13
Chromosomal Location19727417-19732951 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to T at 19729875 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151029
SMART Domains Protein: ENSMUSP00000133733
Gene: ENSMUSG00000047462

DomainStartEndE-ValueType
Pfam:7tm_1 46 294 3.8e-7 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap10 A T 8: 77,365,100 L430Q probably damaging Het
Cc2d2a C T 5: 43,714,521 R900* probably null Het
Cd14 A G 18: 36,725,503 Y300H probably benign Het
Dgcr8 T A 16: 18,272,759 T584S probably benign Het
Epb41l5 C T 1: 119,623,955 G100D probably benign Het
Fat4 G A 3: 38,956,744 G1998R probably damaging Het
Fndc3b A T 3: 27,508,503 L279H probably damaging Het
Gabrr1 A G 4: 33,151,426 E114G probably damaging Het
Hrh2 A G 13: 54,215,000 R332G probably benign Het
Kif5a T C 10: 127,245,756 I180V probably benign Het
Lyg2 T A 1: 37,909,967 R105W probably damaging Het
Myc A G 15: 61,987,666 I64V probably damaging Het
Nrcam G A 12: 44,541,075 probably null Het
Ogdhl A G 14: 32,325,946 Y51C probably damaging Het
Olfr1339 C T 4: 118,734,606 L26F probably benign Het
Olfr631 T A 7: 103,929,394 C190* probably null Het
Pdlim3 A G 8: 45,917,532 R290G probably benign Het
Ppm1l G A 3: 69,549,343 A198T probably damaging Het
Prkd2 A G 7: 16,845,934 D119G probably damaging Het
Rapgef3 A T 15: 97,748,265 I820N probably damaging Het
Scnn1b A G 7: 121,912,062 Y324C probably damaging Het
Smc5 G A 19: 23,257,604 R289C probably benign Het
Vmn2r51 T A 7: 10,098,136 R508* probably null Het
Vps13c A T 9: 67,937,855 I2074L probably benign Het
Wdr64 T C 1: 175,805,849 probably benign Het
Ydjc C T 16: 17,147,289 P74L probably benign Het
Other mutations in A530099J19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03272:A530099J19Rik APN 13 19729537 exon noncoding transcript
R0383:A530099J19Rik UTSW 13 19729147 exon noncoding transcript
R0401:A530099J19Rik UTSW 13 19729494 exon noncoding transcript
R1564:A530099J19Rik UTSW 13 19729300 exon noncoding transcript
R1800:A530099J19Rik UTSW 13 19729679 exon noncoding transcript
R3964:A530099J19Rik UTSW 13 19729444 exon noncoding transcript
R3966:A530099J19Rik UTSW 13 19729444 exon noncoding transcript
R4091:A530099J19Rik UTSW 13 19729465 exon noncoding transcript
R4832:A530099J19Rik UTSW 13 19729670 exon noncoding transcript
R5671:A530099J19Rik UTSW 13 19729295 exon noncoding transcript
R5885:A530099J19Rik UTSW 13 19729349 exon noncoding transcript
R5932:A530099J19Rik UTSW 13 19729476 exon noncoding transcript
R5956:A530099J19Rik UTSW 13 19729130 exon noncoding transcript
X0026:A530099J19Rik UTSW 13 19729001 exon noncoding transcript
Z1088:A530099J19Rik UTSW 13 19729209 exon noncoding transcript
Posted On2015-12-18