Incidental Mutation 'IGL00981:Rpl10a-ps2'
ID 306652
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 # IGL00981
Quality Score
Status
Chromosome 13
Chromosomal Location 8990372-8991013 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 8990566 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: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930503L19Rik G A 18: 70,586,404 (GRCm39) Q478* probably null Het
Armh4 A T 14: 50,010,447 (GRCm39) L420Q probably damaging Het
Atp7b T C 8: 22,517,543 (GRCm39) probably null Het
Bcan T A 3: 87,905,139 (GRCm39) I2F possibly damaging Het
Boc A G 16: 44,312,164 (GRCm39) S633P probably damaging Het
C2cd6 A G 1: 59,117,104 (GRCm39) S130P probably damaging Het
Cacna1a T C 8: 85,275,182 (GRCm39) F490L probably damaging Het
Carm1 T A 9: 21,498,490 (GRCm39) D469E possibly damaging Het
Cdyl A T 13: 36,000,096 (GRCm39) S126C probably damaging Het
Ceacam5 A T 7: 17,479,458 (GRCm39) I192F probably benign Het
Cyp2b19 C T 7: 26,462,886 (GRCm39) T256I possibly damaging Het
Dlgap5 C T 14: 47,635,925 (GRCm39) E515K probably damaging Het
Eif3a A T 19: 60,755,049 (GRCm39) D1044E unknown Het
Eif3i T A 4: 129,488,862 (GRCm39) Y125F probably benign Het
Gnai1 T G 5: 18,472,045 (GRCm39) N346T probably benign Het
Kcnd1 C T X: 7,702,672 (GRCm39) T629I probably benign Het
Mcc A T 18: 44,582,416 (GRCm39) N578K probably damaging Het
Ncoa6 C T 2: 155,248,099 (GRCm39) R1735Q probably damaging Het
Nlrp4d A T 7: 10,116,021 (GRCm39) noncoding transcript Het
Nsun5 A T 5: 135,404,249 (GRCm39) Q352L possibly damaging Het
Or14j6 G A 17: 38,215,072 (GRCm39) V212M probably benign Het
Or2d2b C A 7: 106,705,268 (GRCm39) E267* probably null Het
Or2d2b T A 7: 106,705,269 (GRCm39) K266N probably benign Het
Or8g18 A G 9: 39,148,901 (GRCm39) V276A probably benign Het
Pkdrej C T 15: 85,703,857 (GRCm39) G693D probably damaging Het
Spink1 C T 18: 43,870,159 (GRCm39) probably null Het
Sqle T C 15: 59,198,468 (GRCm39) V464A probably damaging Het
Trav6-4 A T 14: 53,692,153 (GRCm39) T84S probably damaging Het
Trim33 T A 3: 103,259,311 (GRCm39) probably benign Het
Txlng T C X: 161,567,368 (GRCm39) M319V probably benign Het
Wee1 A T 7: 109,738,876 (GRCm39) E582D probably damaging Het
Other mutations in Rpl10a-ps2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02100:Rpl10a-ps2 APN 13 8,990,779 (GRCm39) unclassified probably benign
Posted On 2015-04-16