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RN7SL644P RNA, 7SL, cytoplasmic 644, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481853, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL644Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 644, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46660
See related
Ensembl:ENSG00000264313 AllianceGenome:HGNC:46660
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 RN7SL644P in Genome Data Viewer
Location:
10q23.33
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (92659044..92659302)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (93538385..93538643)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (94418801..94419059)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene insulin degrading enzyme Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2617 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3770 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3771 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3772 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3773 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3774 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:94352873-94353624 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:94357207-94357722 Neighboring gene ribosomal protein L11 pseudogene 4 Neighboring gene kinesin family member 11 Neighboring gene uncharacterized LOC124902594 Neighboring gene eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 3

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_044406.1 

    Range
    101..359
    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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    92659044..92659302
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    93538385..93538643
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Other Literature Sources
Molecular Biology Databases