Incidental Mutation 'IGL02583:4930584F24Rik'
ID 299436
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 # IGL02583
Quality Score
Status
Chromosome 5
Chromosomal Location 26665068-26698312 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to T at 26684717 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: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A430005L14Rik T A 4: 154,045,392 (GRCm39) D140E possibly damaging Het
Bod1l C T 5: 41,973,550 (GRCm39) probably null Het
Brms1 T A 19: 5,096,206 (GRCm39) V61D probably damaging Het
Card11 A T 5: 140,863,881 (GRCm39) N952K probably benign Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Cimap2 A T 4: 106,468,602 (GRCm39) probably benign Het
Col15a1 T C 4: 47,279,866 (GRCm39) V697A probably benign Het
Col7a1 A T 9: 108,791,297 (GRCm39) I1118F unknown Het
Cyfip2 T C 11: 46,140,585 (GRCm39) E746G possibly damaging Het
Dach1 A G 14: 98,065,830 (GRCm39) probably benign Het
Dock11 G T X: 35,270,370 (GRCm39) G1023W possibly damaging Het
Fbxo10 T C 4: 45,044,754 (GRCm39) D453G probably damaging Het
Fhad1 T C 4: 141,738,955 (GRCm39) probably benign Het
Gm17415 A G 1: 93,349,801 (GRCm39) probably benign Het
Gm4781 A T 10: 100,232,507 (GRCm39) noncoding transcript Het
Gpatch2 A C 1: 186,965,514 (GRCm39) probably null Het
Gpatch2 G T 1: 186,965,515 (GRCm39) probably null Het
Greb1 A G 12: 16,756,296 (GRCm39) probably benign Het
Greb1l A G 18: 10,542,362 (GRCm39) Y1319C probably damaging Het
Ice1 C T 13: 70,753,854 (GRCm39) R744H possibly damaging Het
Kcnq2 T A 2: 180,723,295 (GRCm39) S694C probably benign Het
Krt35 C A 11: 99,983,360 (GRCm39) V448L possibly damaging Het
Lmo7 A G 14: 102,171,360 (GRCm39) probably benign Het
Megf8 T C 7: 25,055,218 (GRCm39) S1984P probably benign Het
Nlrp1a T C 11: 71,014,227 (GRCm39) Q341R probably benign Het
Or1p1 T A 11: 74,180,330 (GRCm39) L286Q probably damaging Het
Or51a6 T C 7: 102,603,918 (GRCm39) T297A possibly damaging Het
Osr1 C T 12: 9,629,675 (GRCm39) H183Y probably damaging Het
Paf1 T C 7: 28,095,596 (GRCm39) V202A probably damaging Het
Pde10a A G 17: 9,200,462 (GRCm39) K1071E probably benign Het
Pwp2 T C 10: 78,016,917 (GRCm39) R268G probably benign Het
Rwdd1 T A 10: 33,877,669 (GRCm39) K178* probably null Het
Scn10a A T 9: 119,520,506 (GRCm39) probably benign Het
Sema3g A G 14: 30,943,476 (GRCm39) probably null Het
Slc22a6 C A 19: 8,600,980 (GRCm39) A391E possibly damaging Het
Slc41a3 G A 6: 90,621,153 (GRCm39) G372S probably damaging Het
Sqor G T 2: 122,641,690 (GRCm39) K3N probably damaging Het
Srl T C 16: 4,310,244 (GRCm39) Q495R possibly damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Stxbp3 G T 3: 108,708,187 (GRCm39) D371E probably damaging Het
Tnfrsf19 C A 14: 61,261,659 (GRCm39) V47F probably damaging Het
Usp11 A T X: 20,584,284 (GRCm39) E622V probably benign Het
Vmn1r52 T A 6: 90,156,126 (GRCm39) Y143* probably null Het
Zfp280d A G 9: 72,229,727 (GRCm39) probably benign Het
Zfp518a G A 19: 40,903,061 (GRCm39) G997R probably damaging Het
Zmat1 T C X: 133,874,021 (GRCm39) T457A probably damaging Het
Other mutations in 4930584F24Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01648:4930584F24Rik APN 5 26,695,398 (GRCm39) exon 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 2015-04-16