Incidental Mutation 'IGL02476:Rpl34'
ID 294971
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rpl34
Ensembl Gene ENSMUSG00000062006
Gene Name ribosomal protein L34
Synonyms 1100001I22Rik
Accession Numbers
Essential gene? Probably essential (E-score: 0.929) question?
Stock # IGL02476
Quality Score
Status
Chromosome 3
Chromosomal Location 130520480-130524047 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 130520613 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000143752 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062601] [ENSMUST00000079085] [ENSMUST00000133802] [ENSMUST00000196202] [ENSMUST00000200517]
AlphaFold Q9D1R9
Predicted Effect probably benign
Transcript: ENSMUST00000062601
SMART Domains Protein: ENSMUSP00000086614
Gene: ENSMUSG00000062006

DomainStartEndE-ValueType
Pfam:Ribosomal_L34e 1 96 2.9e-40 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000079085
SMART Domains Protein: ENSMUSP00000078092
Gene: ENSMUSG00000062006

DomainStartEndE-ValueType
Pfam:Ribosomal_L34e 1 96 2.9e-40 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000133802
SMART Domains Protein: ENSMUSP00000142951
Gene: ENSMUSG00000062006

DomainStartEndE-ValueType
Pfam:Ribosomal_L34e 1 90 3.2e-34 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135691
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196074
Predicted Effect probably benign
Transcript: ENSMUST00000196202
SMART Domains Protein: ENSMUSP00000142486
Gene: ENSMUSG00000062006

DomainStartEndE-ValueType
Pfam:Ribosomal_L34e 1 96 2.9e-40 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199001
Predicted Effect noncoding transcript
Transcript: ENSMUST00000200321
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199911
Predicted Effect probably benign
Transcript: ENSMUST00000200517
SMART Domains Protein: ENSMUSP00000143752
Gene: ENSMUSG00000062006

DomainStartEndE-ValueType
Pfam:Ribosomal_L34e 1 60 3.6e-23 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aamp T A 1: 74,320,683 (GRCm39) probably benign Het
Birc6 A G 17: 75,003,386 (GRCm39) E4752G possibly damaging Het
Chd1 C T 17: 15,954,535 (GRCm39) P468S probably damaging Het
Cnot3 A G 7: 3,661,067 (GRCm39) D556G probably benign Het
Csnk1d A G 11: 120,863,338 (GRCm39) Y201H probably damaging Het
Dhtkd1 A G 2: 5,935,717 (GRCm39) S132P possibly damaging Het
Dhx58 G T 11: 100,593,090 (GRCm39) Q206K probably benign Het
Dio1 C A 4: 107,149,574 (GRCm39) V195F probably damaging Het
Dio3 T C 12: 110,245,916 (GRCm39) V84A probably benign Het
Dnai4 T A 4: 102,944,545 (GRCm39) I3L possibly damaging Het
Extl3 T C 14: 65,314,693 (GRCm39) K163R probably benign Het
Fat2 A T 11: 55,201,950 (GRCm39) S375T probably damaging Het
Fbrs A G 7: 127,086,841 (GRCm39) D73G probably damaging Het
Fnip1 A G 11: 54,390,393 (GRCm39) probably benign Het
Frmpd4 A G X: 166,280,851 (GRCm39) V343A probably damaging Het
Gcc1 T C 6: 28,420,468 (GRCm39) D283G probably benign Het
Ghr T C 15: 3,349,528 (GRCm39) D550G probably damaging Het
Glycam1 G A 15: 103,471,307 (GRCm39) probably benign Het
Gpatch8 A G 11: 102,369,417 (GRCm39) S1374P probably damaging Het
Grm1 A T 10: 10,565,197 (GRCm39) M1037K probably benign Het
Gtpbp3 T C 8: 71,945,242 (GRCm39) L438P probably damaging Het
Ifi205 G T 1: 173,842,627 (GRCm39) N356K probably damaging Het
Ifi206 A G 1: 173,309,132 (GRCm39) L288P probably benign Het
Ift57 T C 16: 49,584,252 (GRCm39) V291A probably benign Het
Kif13a A C 13: 46,938,772 (GRCm39) C166G probably damaging Het
Lypd6 A G 2: 50,080,740 (GRCm39) T143A possibly damaging Het
Mtus2 G A 5: 148,014,748 (GRCm39) A514T probably benign Het
Neu2 T C 1: 87,524,674 (GRCm39) W220R probably damaging Het
Notch3 T C 17: 32,377,612 (GRCm39) S155G possibly damaging Het
Nrxn2 A G 19: 6,505,015 (GRCm39) E286G probably damaging Het
Onecut3 A G 10: 80,349,724 (GRCm39) E406G probably benign Het
Oog2 T A 4: 143,921,799 (GRCm39) D236E probably benign Het
Pck1 A G 2: 173,000,075 (GRCm39) H502R probably benign Het
Pld1 A G 3: 28,102,188 (GRCm39) Y313C probably damaging Het
Rhox3f A T X: 36,763,192 (GRCm39) probably benign Het
Sema4c T C 1: 36,595,031 (GRCm39) K31E probably damaging Het
Septin11 T C 5: 93,296,443 (GRCm39) probably null Het
Slc4a9 T A 18: 36,668,498 (GRCm39) probably null Het
Snrnp200 T A 2: 127,059,408 (GRCm39) S434T probably benign Het
Snx13 A T 12: 35,136,940 (GRCm39) I134F probably damaging Het
Syt2 T C 1: 134,675,369 (GRCm39) S407P probably benign Het
Tbc1d19 T C 5: 54,046,755 (GRCm39) probably null Het
Tbc1d32 G T 10: 56,074,638 (GRCm39) Q192K possibly damaging Het
Ubr4 T A 4: 139,148,560 (GRCm39) C1681* probably null Het
Vmn1r43 T A 6: 89,847,043 (GRCm39) I148F possibly damaging Het
Vwa8 T C 14: 79,162,781 (GRCm39) V187A possibly damaging Het
Other mutations in Rpl34
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6192:Rpl34 UTSW 3 130,522,716 (GRCm39) missense probably benign 0.01
R6516:Rpl34 UTSW 3 130,522,716 (GRCm39) missense probably benign 0.01
R6796:Rpl34 UTSW 3 130,522,926 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16