Incidental Mutation 'IGL02075:4931429P17Rik'
ID 185972
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4931429P17Rik
Ensembl Gene ENSMUSG00000047324
Gene Name RIKEN cDNA 4931429P17 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # IGL02075
Quality Score
Status
Chromosome 13
Chromosomal Location 48113806-48172084 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 48114224 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
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: 84,655,578 (GRCm39) probably null Het
Agrn A T 4: 156,254,667 (GRCm39) M1548K probably benign Het
Als2 A G 1: 59,246,945 (GRCm39) S565P probably damaging Het
Atm T C 9: 53,438,537 (GRCm39) I126M probably damaging Het
Btbd9 G A 17: 30,493,910 (GRCm39) R494* probably null Het
Coro1c G T 5: 113,982,454 (GRCm39) R461S probably damaging Het
Gtf2h1 A G 7: 46,451,165 (GRCm39) K19E probably damaging Het
Kcnc1 A G 7: 46,077,397 (GRCm39) T400A probably damaging Het
Kcnh5 T C 12: 75,134,379 (GRCm39) Y390C probably benign Het
Ly75 G T 2: 60,182,700 (GRCm39) S534R probably damaging Het
Mapk15 A G 15: 75,866,737 (GRCm39) E38G probably benign Het
Or9i2 T A 19: 13,815,830 (GRCm39) T236S probably damaging Het
Otof A T 5: 30,528,070 (GRCm39) N1924K probably benign Het
Plekhm2 T A 4: 141,355,617 (GRCm39) H861L probably benign Het
Pramel25 T A 4: 143,521,602 (GRCm39) F406Y probably benign Het
Rufy4 A T 1: 74,168,518 (GRCm39) K100N probably damaging Het
Sptbn1 T C 11: 30,088,496 (GRCm39) E879G probably damaging Het
Stab2 T C 10: 86,803,514 (GRCm39) N345S possibly damaging Het
Tacc2 C T 7: 130,330,582 (GRCm39) P1996S probably benign Het
Tfcp2 A G 15: 100,411,061 (GRCm39) probably benign Het
Trpm8 A G 1: 88,253,210 (GRCm39) T100A probably damaging Het
Trrap A G 5: 144,765,304 (GRCm39) T2507A probably benign Het
Vmn2r118 T C 17: 55,917,517 (GRCm39) T332A probably benign Het
Zfp189 T A 4: 49,522,445 (GRCm39) D27E probably damaging Het
Other mutations in 4931429P17Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01690:4931429P17Rik APN 13 48,114,446 (GRCm39) exon noncoding transcript
R0323:4931429P17Rik UTSW 13 48,114,493 (GRCm39) splice site noncoding transcript
R1630:4931429P17Rik UTSW 13 48,114,201 (GRCm39) exon noncoding transcript
R1707:4931429P17Rik UTSW 13 48,114,481 (GRCm39) exon noncoding transcript
Posted On 2014-05-07