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RPL21P39 ribosomal protein L21 pseudogene 39 [ Homo sapiens (human) ]

Gene ID: 389156, updated on 17-Sep-2024

Summary

Official Symbol
RPL21P39provided by HGNC
Official Full Name
ribosomal protein L21 pseudogene 39provided by HGNC
Primary source
HGNC:HGNC:36127
See related
Ensembl:ENSG00000239797 AllianceGenome:HGNC:36127
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RPL21_14_415
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Genomic context

See RPL21P39 in Genome Data Viewer
Location:
3q24
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (145824243..145824778, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (148579587..148580122, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (145542030..145542565, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105374144 Neighboring gene Sharpr-MPRA regulatory region 7261 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:145427323-145428144 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:145436788-145437383 Neighboring gene GM2A pseudogene 1 Neighboring gene NANOG hESC enhancer GRCh37_chr3:145533387-145533922 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_65040 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_65044 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:145621747-145622521 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:145645870-145646452 Neighboring gene uncharacterized LOC107986138 Neighboring gene lncRNA sorafenib resistance in renal cell carcinoma associated

Genomic regions, transcripts, and products

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_009665.2 

    Range
    101..636
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    145824243..145824778 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    148579587..148580122 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)