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RN7SL205P RNA, 7SL, cytoplasmic 205, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479297, updated on 17-Sep-2024

Summary

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Official Symbol
RN7SL205Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 205, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46221
See related
Ensembl:ENSG00000241392 AllianceGenome:HGNC:46221
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 RN7SL205P in Genome Data Viewer
Location:
4q28.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (131720260..131720543, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (135024076..135024359, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (132641415..132641698, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377423 Neighboring gene long intergenic non-protein coding RNA 2377 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21903 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21904 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr4:132486813-132488012 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21905 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:132651396-132651896 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:132651897-132652397 Neighboring gene ReSE screen-validated silencer GRCh37_chr4:132653436-132653587 Neighboring gene uncharacterized LOC124900860 Neighboring gene uncharacterized LOC124900859

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_044433.1 

    Range
    101..384
    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    131720260..131720543 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    135024076..135024359 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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