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RPL7AP36 ribosomal protein L7a pseudogene 36 [ Homo sapiens (human) ]

Gene ID: 728179, updated on 17-Jun-2024

Summary

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Official Symbol
RPL7AP36provided by HGNC
Official Full Name
ribosomal protein L7a pseudogene 36provided by HGNC
Primary source
HGNC:HGNC:36356
See related
Ensembl:ENSG00000216368 AllianceGenome:HGNC:36356
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_9_655
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Genomic context

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See RPL7AP36 in Genome Data Viewer
Location:
6p24.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (10118434..10119312)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (9986801..9987679)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (10118667..10119545)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901484 Neighboring gene orofacial cleft 1 candidate 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16898 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:9810687-9811203 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:9811204-9811719 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:9971388-9971998 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:9971999-9972609 Neighboring gene uncharacterized LOC105374919 Neighboring gene MPRA-validated peak5651 silencer Neighboring gene uncharacterized LOC124900218 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:10134047-10134548 Neighboring gene uncharacterized LOC105374918 Neighboring gene ribosomal protein L21 pseudogene 62

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_010595.2 

    Range
    101..979
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    10118434..10119312
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    9986801..9987679
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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