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RN7SL607P RNA, 7SL, cytoplasmic 607, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481088, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL607Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 607, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46623
See related
Ensembl:ENSG00000278525 AllianceGenome:HGNC:46623
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 RN7SL607P in Genome Data Viewer
Location:
20p11.23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (20738433..20738731, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (20797139..20797437, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (20719076..20719374, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene Ral GTPase activating protein catalytic subunit alpha 2 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12711 Neighboring gene eukaryotic translation initiation factor 4E family member 2 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12712 Neighboring gene Sharpr-MPRA regulatory region 2040 Neighboring gene uncharacterized LOC105372555 Neighboring gene H3K27ac hESC enhancer GRCh37_chr20:20723796-20724502 Neighboring gene H3K27ac hESC enhancer GRCh37_chr20:20724503-20725209 Neighboring gene LLPH pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr20:20786234-20786734 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr20:20795309-20795885 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:20801574-20802363 Neighboring gene mitochondrial ribosomal protein S11 pseudogene 1 Neighboring gene long intergenic non-protein coding RNA 3083

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_044430.1 

    Range
    101..399
    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_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    20738433..20738731 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    20797139..20797437 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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