Incidental Mutation 'IGL02075:4931429P17Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4931429P17Rik
Ensembl Gene ENSMUSG00000047324
Gene NameRIKEN cDNA 4931429P17 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.111) question?
Stock #IGL02075
Quality Score
Chromosomal Location47960330-48018608 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to G at 47960748 bp
Amino Acid Change
Predicted Effect noncoding transcript
Transcript: ENSMUST00000061899
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 24 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcd4 A T 12: 84,608,804 probably null Het
Agrn A T 4: 156,170,210 M1548K probably benign Het
Als2 A G 1: 59,207,786 S565P probably damaging Het
Atm T C 9: 53,527,237 I126M probably damaging Het
Btbd9 G A 17: 30,274,936 R494* probably null Het
Coro1c G T 5: 113,844,393 R461S probably damaging Het
Gm13023 T A 4: 143,795,032 F406Y probably benign Het
Gtf2h1 A G 7: 46,801,741 K19E probably damaging Het
Kcnc1 A G 7: 46,427,973 T400A probably damaging Het
Kcnh5 T C 12: 75,087,605 Y390C probably benign Het
Ly75 G T 2: 60,352,356 S534R probably damaging Het
Mapk15 A G 15: 75,994,888 E38G probably benign Het
Olfr1501 T A 19: 13,838,466 T236S probably damaging Het
Otof A T 5: 30,370,726 N1924K probably benign Het
Plekhm2 T A 4: 141,628,306 H861L probably benign Het
Rufy4 A T 1: 74,129,359 K100N probably damaging Het
Sptbn1 T C 11: 30,138,496 E879G probably damaging Het
Stab2 T C 10: 86,967,650 N345S possibly damaging Het
Tacc2 C T 7: 130,728,852 P1996S probably benign Het
Tfcp2 A G 15: 100,513,180 probably benign Het
Trpm8 A G 1: 88,325,488 T100A probably damaging Het
Trrap A G 5: 144,828,494 T2507A probably benign Het
Vmn2r118 T C 17: 55,610,517 T332A probably benign Het
Zfp189 T A 4: 49,522,445 D27E probably damaging Het
Other mutations in 4931429P17Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01690:4931429P17Rik APN 13 47960970 exon noncoding transcript
R0323:4931429P17Rik UTSW 13 47961017 splice site noncoding transcript
R1630:4931429P17Rik UTSW 13 47960725 exon noncoding transcript
R1707:4931429P17Rik UTSW 13 47961005 exon noncoding transcript
Posted On2014-05-07