Incidental Mutation 'IGL02386:4930555F03Rik'
ID 291543
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930555F03Rik
Ensembl Gene ENSMUSG00000031559
Gene Name RIKEN cDNA 4930555F03 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.106) question?
Stock # IGL02386
Quality Score
Status
Chromosome 8
Chromosomal Location 49823921-50002029 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to A at 49953472 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: ENSMUST00000033963
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126285
Predicted Effect noncoding transcript
Transcript: ENSMUST00000163925
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212179
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd17b T C 19: 21,658,263 (GRCm39) Y167H possibly damaging Het
Ablim1 T C 19: 57,123,086 (GRCm39) D167G probably damaging Het
Bpnt1 G T 1: 185,070,372 (GRCm39) K21N probably damaging Het
Cables2 A G 2: 179,903,431 (GRCm39) V251A probably benign Het
Cyp2b13 T C 7: 25,785,438 (GRCm39) L269P probably damaging Het
Dhodh A G 8: 110,321,396 (GRCm39) I330T probably damaging Het
Dnah5 T A 15: 28,340,527 (GRCm39) D2311E probably damaging Het
Dph1 T C 11: 75,074,428 (GRCm39) D128G probably benign Het
Dsg1c T A 18: 20,410,056 (GRCm39) I508N probably benign Het
Eftud2 T C 11: 102,742,580 (GRCm39) probably null Het
Fstl4 T A 11: 52,664,698 (GRCm39) H9Q probably benign Het
Glra3 A T 8: 56,542,063 (GRCm39) M269L probably benign Het
Gpatch8 C A 11: 102,398,983 (GRCm39) R83L unknown Het
Gss A G 2: 155,415,090 (GRCm39) V205A probably benign Het
Ifi30 A G 8: 71,217,405 (GRCm39) probably benign Het
Itch T A 2: 155,044,181 (GRCm39) Y495* probably null Het
Lilrb4a C T 10: 51,367,322 (GRCm39) Q22* probably null Het
Mest T C 6: 30,744,913 (GRCm39) F201S possibly damaging Het
Myh8 T A 11: 67,185,266 (GRCm39) I839N probably damaging Het
Myo7a C T 7: 97,724,319 (GRCm39) G1122E probably damaging Het
Ntan1 T A 16: 13,653,063 (GRCm39) M273K probably benign Het
Numa1 A G 7: 101,656,739 (GRCm39) K1548R probably benign Het
Obsl1 A G 1: 75,469,161 (GRCm39) V1260A probably damaging Het
Or4b12 T A 2: 90,096,295 (GRCm39) I160F probably damaging Het
Or4c10 T C 2: 89,760,888 (GRCm39) V245A probably damaging Het
Pde10a A G 17: 9,172,636 (GRCm39) S669G possibly damaging Het
Ppargc1b T C 18: 61,456,222 (GRCm39) D79G probably damaging Het
Rnf103 A G 6: 71,486,202 (GRCm39) T278A probably benign Het
Slc22a4 C A 11: 53,879,598 (GRCm39) probably benign Het
Snx25 A T 8: 46,494,386 (GRCm39) M833K possibly damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Susd2 A T 10: 75,475,929 (GRCm39) Y357N probably damaging Het
Syne4 C A 7: 30,015,659 (GRCm39) S91Y possibly damaging Het
Tgfbrap1 C A 1: 43,114,981 (GRCm39) G40C probably damaging Het
Tial1 A G 7: 128,050,069 (GRCm39) S94P probably damaging Het
Tle3 A G 9: 61,301,941 (GRCm39) T117A possibly damaging Het
Usp48 A C 4: 137,331,834 (GRCm39) R73S possibly damaging Het
Utrn G T 10: 12,297,352 (GRCm39) D685E possibly damaging Het
Other mutations in 4930555F03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0617:4930555F03Rik UTSW 8 49,953,527 (GRCm39) exon noncoding transcript
R0799:4930555F03Rik UTSW 8 49,948,474 (GRCm39) splice site noncoding transcript
R4163:4930555F03Rik UTSW 8 49,948,531 (GRCm39) intron noncoding transcript
Posted On 2015-04-16