Incidental Mutation 'IGL01910:Rpl23a-ps1'
ID 179774
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rpl23a-ps1
Ensembl Gene ENSMUSG00000070896
Gene Name ribosomal protein 23A, pseudogene 1
Synonyms Gm4851
Accession Numbers
Essential gene? Probably non essential (E-score: 0.229) question?
Stock # IGL01910
Quality Score
Status
Chromosome 1
Chromosomal Location 46020708-46021172 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 46020940 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: ENSMUST00000085632
SMART Domains Protein: ENSMUSP00000082772
Gene: ENSMUSG00000070896

DomainStartEndE-ValueType
Pfam:Ribosomal_L23eN 17 67 2.8e-28 PFAM
Pfam:Ribosomal_L23 78 149 3.1e-17 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000191295
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ammecr1l A G 18: 31,904,995 (GRCm39) M79V probably benign Het
Arhgap5 T A 12: 52,563,644 (GRCm39) V205E probably benign Het
BC061237 T C 14: 44,743,445 (GRCm39) probably benign Het
Calr T A 8: 85,571,598 (GRCm39) probably benign Het
Celsr1 T C 15: 85,814,096 (GRCm39) N1942S probably benign Het
Cfap100 T C 6: 90,386,606 (GRCm39) D373G probably damaging Het
Chst9 C A 18: 15,585,931 (GRCm39) A211S possibly damaging Het
Ephb1 T C 9: 101,879,056 (GRCm39) E478G probably benign Het
Fbrsl1 A T 5: 110,511,602 (GRCm39) V387D probably damaging Het
Fxyd5 T C 7: 30,734,643 (GRCm39) I161V probably damaging Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Hmx2 C T 7: 131,157,401 (GRCm39) R172C probably damaging Het
Itgam C T 7: 127,682,948 (GRCm39) A320V probably damaging Het
Macrod2 T A 2: 142,138,485 (GRCm39) N361K probably benign Het
Mbl1 T C 14: 40,875,703 (GRCm39) probably null Het
Nudt9 G A 5: 104,202,175 (GRCm39) G79R probably damaging Het
Ppan C T 9: 20,802,232 (GRCm39) R208C probably damaging Het
Slc17a1 A G 13: 24,062,440 (GRCm39) probably benign Het
Tep1 T C 14: 51,081,569 (GRCm39) T1269A probably benign Het
Vmn2r16 A T 5: 109,487,951 (GRCm39) N275Y probably damaging Het
Wdr93 T C 7: 79,421,321 (GRCm39) S405P probably damaging Het
Xcl1 T A 1: 164,759,458 (GRCm39) I81F probably damaging Het
Other mutations in Rpl23a-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01325:Rpl23a-ps1 APN 1 46,020,793 (GRCm39) unclassified noncoding transcript
IGL02473:Rpl23a-ps1 APN 1 46,020,951 (GRCm39) unclassified noncoding transcript
R0453:Rpl23a-ps1 UTSW 1 46,021,087 (GRCm39) unclassified noncoding transcript
Posted On 2014-05-07