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RPL23AP97 ribosomal protein L23a pseudogene 97 [ Homo sapiens (human) ]

Gene ID: 102723647, updated on 22-Oct-2024

Summary

Official Symbol
RPL23AP97provided by HGNC
Official Full Name
ribosomal protein L23a pseudogene 97provided by HGNC
Primary source
HGNC:HGNC:51632
See related
Ensembl:ENSG00000260615 AllianceGenome:HGNC:51632
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

See RPL23AP97 in Genome Data Viewer
Location:
13q34
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (114346156..114346686)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (113555196..113555726)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 (PATCHES) NW_003571051.1 (26490..27020)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5563 Neighboring gene chromosome alignment maintaining phosphoprotein 1 Neighboring gene long intergenic non-protein coding RNA 1054 Neighboring gene uncharacterized LOC112268113

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_242255.1 

    Range
    101..631
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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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    114346156..114346686
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    113555196..113555726
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)