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RPL10P6 ribosomal protein L10 pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 285176, updated on 10-Oct-2023

Summary

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Official Symbol
RPL10P6provided by HGNC
Official Full Name
ribosomal protein L10 pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:52343
See related
Ensembl:ENSG00000230076 AllianceGenome:HGNC:52343
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See RPL10P6 in Genome Data Viewer
Location:
2q35
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (214847137..214847502)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (215332060..215332425)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (215711861..215712226)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17070 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17071 Neighboring gene BRCA1 associated RING domain 1 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:215667579-215668122 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17072 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17073 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12296 Neighboring gene small nucleolar RNA host gene 31 Neighboring gene small nucleolar RNA, H/ACA box 70I Neighboring gene NANOG hESC enhancer GRCh37_chr2:215769194-215769695 Neighboring gene ATP binding cassette subfamily A member 12 Neighboring gene uncharacterized LOC124906117 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:216028241-216028408 Neighboring gene uncharacterized LOC124907974

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_009924.2 

    Range
    101..466
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    214847137..214847502
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    215332060..215332425
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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