Incidental Mutation 'IGL02100:Rpl10a-ps2'
ID 279708
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rpl10a-ps2
Ensembl Gene ENSMUSG00000061988
Gene Name ribosomal protein L10A, pseudogene 2
Synonyms Gm5192
Accession Numbers
Essential gene? Not available question?
Stock # IGL02100
Quality Score
Status
Chromosome 13
Chromosomal Location 8990372-8991013 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 8990779 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139705 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021573] [ENSMUST00000187196]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000021573
SMART Domains Protein: ENSMUSP00000021573
Gene: ENSMUSG00000021148

DomainStartEndE-ValueType
Pfam:NUDIX 50 199 2e-19 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000071184
SMART Domains Protein: ENSMUSP00000071176
Gene: ENSMUSG00000061988

DomainStartEndE-ValueType
Pfam:Ribosomal_L1 11 210 3.7e-42 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104296
Predicted Effect probably benign
Transcript: ENSMUST00000187196
SMART Domains Protein: ENSMUSP00000139705
Gene: ENSMUSG00000021148

DomainStartEndE-ValueType
Pfam:NUDIX 50 200 7.9e-17 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acad9 A T 3: 36,136,029 (GRCm39) Q347L probably null Het
Acvr2a T C 2: 48,788,630 (GRCm39) probably benign Het
Ankrd28 T C 14: 31,449,582 (GRCm39) probably benign Het
Atp6v1b1 A G 6: 83,735,426 (GRCm39) Y498C probably damaging Het
Cdh3 G A 8: 107,270,322 (GRCm39) V400I probably benign Het
Chrnb1 G T 11: 69,684,281 (GRCm39) probably benign Het
Col1a2 A G 6: 4,524,177 (GRCm39) probably benign Het
Cyp2j7 A G 4: 96,124,793 (GRCm39) L35P probably damaging Het
Dennd2c G A 3: 103,060,991 (GRCm39) S561N probably damaging Het
Dennd4a A T 9: 64,816,988 (GRCm39) probably benign Het
Dnai4 A G 4: 102,907,346 (GRCm39) C647R probably damaging Het
Dynll1 A C 5: 115,436,852 (GRCm39) V58G probably damaging Het
Eif3a A T 19: 60,755,442 (GRCm39) probably benign Het
Ercc6 T C 14: 32,239,052 (GRCm39) S47P probably benign Het
Fam76b A G 9: 13,755,416 (GRCm39) probably benign Het
Gbp4 T A 5: 105,269,941 (GRCm39) probably benign Het
Gdi2 T C 13: 3,606,373 (GRCm39) F140L probably benign Het
Gm28043 T C 17: 29,910,400 (GRCm39) probably null Het
Gm5117 T A 8: 32,227,412 (GRCm39) noncoding transcript Het
Gstm6 G T 3: 107,849,653 (GRCm39) N85K probably benign Het
Hip1r C T 5: 124,137,006 (GRCm39) probably benign Het
Igf1r T C 7: 67,839,706 (GRCm39) I671T probably benign Het
Insrr T G 3: 87,718,927 (GRCm39) F961C probably damaging Het
Kbtbd8 T C 6: 95,099,663 (GRCm39) Y314H probably damaging Het
Kif26b C A 1: 178,743,512 (GRCm39) L756I probably damaging Het
Lcor G A 19: 41,547,193 (GRCm39) R259Q possibly damaging Het
Mad1l1 T A 5: 140,129,689 (GRCm39) S449C probably damaging Het
Map1a T G 2: 121,133,327 (GRCm39) L1381R probably damaging Het
Mdn1 G T 4: 32,715,708 (GRCm39) V1992L possibly damaging Het
Pigp G A 16: 94,165,626 (GRCm39) Q99* probably null Het
Pip4p2 T C 4: 14,893,536 (GRCm39) I133T probably benign Het
Rgs8 A T 1: 153,568,469 (GRCm39) probably null Het
Rnf170 T A 8: 26,614,012 (GRCm39) L36H probably damaging Het
Rpap1 T C 2: 119,599,807 (GRCm39) S1004G probably benign Het
Ryr2 T A 13: 11,752,759 (GRCm39) E1854V possibly damaging Het
Scn7a T G 2: 66,505,843 (GRCm39) *1682S probably null Het
Sema3d A G 5: 12,634,958 (GRCm39) T675A probably benign Het
Slc1a2 T C 2: 102,586,434 (GRCm39) F346S probably damaging Het
St14 G T 9: 31,011,426 (GRCm39) probably benign Het
Stard5 T C 7: 83,289,653 (GRCm39) V173A possibly damaging Het
Taf1b A G 12: 24,594,394 (GRCm39) Y309C possibly damaging Het
Tet1 T C 10: 62,648,507 (GRCm39) N1975S possibly damaging Het
Them5 T A 3: 94,251,782 (GRCm39) I131N probably damaging Het
Tnc A C 4: 63,918,398 (GRCm39) V1171G possibly damaging Het
Ttc12 C A 9: 49,351,482 (GRCm39) G672W probably damaging Het
Usp8 T C 2: 126,579,774 (GRCm39) probably benign Het
Utp4 A G 8: 107,624,807 (GRCm39) N92S probably benign Het
Was A T X: 7,956,554 (GRCm39) F38L possibly damaging Het
Other mutations in Rpl10a-ps2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00981:Rpl10a-ps2 APN 13 8,990,566 (GRCm39) unclassified probably benign
Posted On 2015-04-16