Incidental Mutation 'IGL01648:4930584F24Rik'
ID 102736
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930584F24Rik
Ensembl Gene ENSMUSG00000029044
Gene Name RIKEN cDNA 4930584F24 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # IGL01648
Quality Score
Status
Chromosome 5
Chromosomal Location 26665068-26698312 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 26695398 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: ENSMUST00000030910
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196508
Predicted Effect noncoding transcript
Transcript: ENSMUST00000197091
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198070
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 C T 10: 79,846,914 (GRCm39) S1664L probably damaging Het
Aebp1 G T 11: 5,820,607 (GRCm39) R499L possibly damaging Het
Agt C A 8: 125,291,145 (GRCm39) S54I probably benign Het
Chic2 T A 5: 75,187,860 (GRCm39) S67C probably damaging Het
Col12a1 T A 9: 79,508,451 (GRCm39) *3066Y probably null Het
Fan1 A G 7: 64,022,297 (GRCm39) S319P probably damaging Het
Fgd5 C T 6: 91,966,340 (GRCm39) Q700* probably null Het
Frem2 T A 3: 53,443,153 (GRCm39) H2537L possibly damaging Het
Lingo1 C A 9: 56,527,111 (GRCm39) A493S probably damaging Het
Med20 A G 17: 47,933,925 (GRCm39) H180R possibly damaging Het
Megf8 T C 7: 25,026,997 (GRCm39) C152R probably damaging Het
Mms22l T C 4: 24,502,805 (GRCm39) F59S probably damaging Het
Or4a39 A T 2: 89,236,535 (GRCm39) M296K probably damaging Het
Pgm5 T C 19: 24,801,715 (GRCm39) D171G probably damaging Het
Rbm47 A T 5: 66,182,321 (GRCm39) N437K possibly damaging Het
Tpra1 T A 6: 88,886,653 (GRCm39) probably benign Het
Tradd A G 8: 105,986,418 (GRCm39) L118S probably damaging Het
Trib1 G T 15: 59,526,350 (GRCm39) V307F probably benign Het
Vps50 T A 6: 3,498,545 (GRCm39) M8K probably benign Het
Xrcc6 A T 15: 81,909,835 (GRCm39) E238V probably damaging Het
Other mutations in 4930584F24Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02583:4930584F24Rik APN 5 26,684,717 (GRCm39) splice site noncoding transcript
R1484:4930584F24Rik UTSW 5 26,684,776 (GRCm39) exon noncoding transcript
R5030:4930584F24Rik UTSW 5 26,684,783 (GRCm39) exon noncoding transcript
R5444:4930584F24Rik UTSW 5 26,684,735 (GRCm39) exon noncoding transcript
Posted On 2014-01-21