Incidental Mutation 'IGL03172:A530053G22Rik'
ID411862
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol A530053G22Rik
Ensembl Gene ENSMUSG00000046764
Gene NameRIKEN cDNA A530053G22 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.092) question?
Stock #IGL03172
Quality Score
Status
Chromosome6
Chromosomal Location60396349-60403698 bp(-) (GRCm38)
Type of Mutationintron
DNA Base Change (assembly) A to T at 60402062 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000060147
SMART Domains Protein: ENSMUSP00000053302
Gene: ENSMUSG00000046764

DomainStartEndE-ValueType
low complexity region 3 11 N/A INTRINSIC
PDB:1HQP|A 16 95 3e-10 PDB
SCOP:d1dzka_ 20 95 5e-12 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203367
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204370
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204579
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205153
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930111J21Rik1 T C 11: 48,948,176 H528R probably damaging Het
Aagab A G 9: 63,635,394 probably benign Het
Aknad1 A T 3: 108,781,203 I616F possibly damaging Het
Ap2a1 A C 7: 44,904,055 D629E probably benign Het
Apc2 C A 10: 80,313,386 Q1425K probably damaging Het
Asf1b A C 8: 83,967,913 H102P probably benign Het
Celf6 C T 9: 59,582,282 A90V probably damaging Het
Chrna2 A T 14: 66,142,239 Q9L probably benign Het
Csnk1g3 A G 18: 53,953,284 I420M possibly damaging Het
Eml3 T C 19: 8,939,179 probably benign Het
Epn3 T C 11: 94,491,630 N508S possibly damaging Het
Fam120a T C 13: 48,910,336 Y608C probably damaging Het
Fbn1 A C 2: 125,320,968 C2133G possibly damaging Het
Fhl5 A G 4: 25,211,309 F128L probably damaging Het
Fn1 T C 1: 71,641,262 N428S probably damaging Het
Fxr2 T C 11: 69,649,839 probably null Het
Gabrp T C 11: 33,554,388 Y309C probably damaging Het
Golga2 A G 2: 32,292,156 I50V probably benign Het
Ifi203 C T 1: 173,936,592 G105R possibly damaging Het
Itgav A T 2: 83,765,846 Q201L possibly damaging Het
Jade2 T C 11: 51,825,371 T336A probably damaging Het
Kdm4b A G 17: 56,401,649 D996G probably damaging Het
Me2 A G 18: 73,770,726 I557T probably benign Het
Memo1 A C 17: 74,245,001 L100R probably damaging Het
Mrps2 A G 2: 28,469,806 N225S probably damaging Het
Ndufa2 A G 18: 36,744,225 probably null Het
Olfr130 G T 17: 38,067,384 C71F probably damaging Het
Olfr832 G A 9: 18,945,461 S271N probably benign Het
Pak7 G T 2: 136,098,390 Y501* probably null Het
Pot1b A T 17: 55,695,206 F123I possibly damaging Het
Rev3l T C 10: 39,824,790 V1761A probably benign Het
Samd3 T A 10: 26,230,166 V14E probably damaging Het
Slc4a8 G A 15: 100,799,717 A605T probably benign Het
Smgc A T 15: 91,860,444 D333V probably damaging Het
Spata4 A G 8: 54,602,405 I147V probably benign Het
Ttc23l G A 15: 10,537,566 S206L probably benign Het
Vmn2r73 G A 7: 85,858,287 H606Y probably benign Het
Vsig8 A G 1: 172,560,349 N2S probably damaging Het
Wdr17 A C 8: 54,661,480 I667R probably damaging Het
Yif1b A G 7: 29,238,448 probably null Het
Zbtb5 A T 4: 44,994,003 H460Q possibly damaging Het
Zdhhc21 G A 4: 82,806,327 probably benign Het
Zfp944 A T 17: 22,340,037 H76Q probably damaging Het
Zkscan1 A G 5: 138,094,002 Q146R probably benign Het
Other mutations in A530053G22Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03193:A530053G22Rik APN 6 60402152 intron noncoding transcript
IGL03368:A530053G22Rik APN 6 60403545 splice site noncoding transcript
R0105:A530053G22Rik UTSW 6 60402152 intron noncoding transcript
R0105:A530053G22Rik UTSW 6 60402152 intron noncoding transcript
R4760:A530053G22Rik UTSW 6 60402101 intron noncoding transcript
Posted On2016-08-02