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RPL7AP45 ribosomal protein L7a pseudogene 45 [ Homo sapiens (human) ]

Gene ID: 100132678, updated on 10-Dec-2024

Summary

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Official Symbol
RPL7AP45provided by HGNC
Official Full Name
ribosomal protein L7a pseudogene 45provided by HGNC
Primary source
HGNC:HGNC:35935
See related
Ensembl:ENSG00000275160 AllianceGenome:HGNC:35935
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
RPL7A_15_979
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Genomic context

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See RPL7AP45 in Genome Data Viewer
Location:
9p11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (41479933..41480534)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (41814120..41814721, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (45562956..45563557)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene CDRT15 pseudogene 6 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28427 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19922 Neighboring gene uncharacterized LOC124900272 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28428 Neighboring gene uncharacterized LOC107984035 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28429 Neighboring gene uncharacterized LOC105376065 Neighboring gene uncharacterized LOC124900281

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Comparative analysis of processed ribosomal protein pseudogenes in four mammalian genomes. Balasubramanian S, et al. Genome Biol, 2009. PMID 19123937, Free PMC Article

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_021655.3 

    Range
    101..702
    Download
    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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    41479933..41480534
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    41814120..41814721 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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