Incidental Mutation 'IGL03272:A530099J19Rik'
ID415304
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 #IGL03272
Quality Score
Status
Chromosome13
Chromosomal Location19727417-19732951 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to T at 19729537 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: 24 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp2 C T 2: 91,204,233 probably benign Het
B4galnt3 T C 6: 120,216,306 D413G probably damaging Het
Chd2 T C 7: 73,453,166 D1357G possibly damaging Het
Dsg1b T C 18: 20,397,389 L367P probably benign Het
Emsy A T 7: 98,593,762 F1057I probably damaging Het
Fam171a2 A T 11: 102,444,118 F64L possibly damaging Het
Fat4 T C 3: 39,009,703 S4603P probably benign Het
Fyco1 T C 9: 123,829,603 T503A probably benign Het
Gpr179 T C 11: 97,336,593 T1579A possibly damaging Het
Itgae T C 11: 73,133,854 probably null Het
Lrriq3 A T 3: 155,101,058 I115F probably damaging Het
Mmrn1 A G 6: 60,988,435 D1149G probably damaging Het
Mylk A C 16: 34,979,189 K1650Q probably benign Het
Nrap T C 19: 56,345,568 probably benign Het
Olfr193 A C 16: 59,110,556 V18G probably benign Het
Ovgp1 T A 3: 105,981,325 D332E probably damaging Het
Pou2f1 A T 1: 165,896,480 I296K possibly damaging Het
Psd4 A G 2: 24,405,680 probably benign Het
Satb2 T C 1: 56,845,643 Q433R probably damaging Het
Serpinb9f A T 13: 33,327,916 N134I probably damaging Het
Slc6a3 A G 13: 73,540,929 N124S probably damaging Het
Spta1 A G 1: 174,214,144 N1360S probably benign Het
Strc G A 2: 121,371,751 T1212I probably damaging Het
Tmtc3 T C 10: 100,457,080 K472R probably benign Het
Other mutations in A530099J19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02834:A530099J19Rik APN 13 19729875 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 On2016-08-02