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RN7SL300P RNA, 7SL, cytoplasmic 300, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481004, updated on 4-Mar-2025

Summary

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Official Symbol
RN7SL300Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 300, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46316
See related
Ensembl:ENSG00000265813 AllianceGenome:HGNC:46316
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

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See RN7SL300P in Genome Data Viewer
Location:
3q25.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (153199700..153200017, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (155970269..155970586, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (152917489..152917806, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124909451 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:152877821-152878352 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:152878353-152878882 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:152879114-152879682 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14830 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14831 Neighboring gene uncharacterized LOC105374164 Neighboring gene RAP2B, member of RAS oncogene family Neighboring gene NANOG hESC enhancer GRCh37_chr3:152943874-152944499 Neighboring gene MPRA-validated peak4867 silencer Neighboring gene Sharpr-MPRA regulatory region 1900 Neighboring gene Sharpr-MPRA regulatory region 4515 Neighboring gene long intergenic non-protein coding RNA 3109 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20717 Neighboring gene long intergenic non-protein coding RNA 2006 Neighboring gene long intergenic non-protein coding RNA 2083

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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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)

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_043779.1 

    Range
    101..418
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    153199700..153200017 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    155970269..155970586 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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