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RPL23AP37 ribosomal protein L23a pseudogene 37 [ Homo sapiens (human) ]

Gene ID: 130773, updated on 10-Oct-2023

Summary

Official Symbol
RPL23AP37provided by HGNC
Official Full Name
ribosomal protein L23a pseudogene 37provided by HGNC
Primary source
HGNC:HGNC:35664
See related
Ensembl:ENSG00000236148 AllianceGenome:HGNC:35664
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
RPL23A_5_234
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Genomic context

Location:
2p14
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (64347218..64347749, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (64354829..64355360, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (64574352..64574883, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105374769 Neighboring gene microRNA 4433b Neighboring gene microRNA 4433a Neighboring gene ATAC-STARR-seq lymphoblastoid active region 15892 Neighboring gene LGALSL divergent transcript Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:64631317-64631826 Neighboring gene uncharacterized LOC124907775 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11552 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11553 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11554 Neighboring gene galectin like

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Genetic variants associated with breast size also influence breast cancer risk.
EBI GWAS Catalog

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_011103.2 

    Range
    101..632
    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
    64347218..64347749 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    64354829..64355360 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)