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SOCS5P5 suppressor of cytokine signaling 5 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 643884, updated on 10-Oct-2023

Summary

Official Symbol
SOCS5P5provided by HGNC
Official Full Name
suppressor of cytokine signaling 5 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:44601
See related
Ensembl:ENSG00000216904 AllianceGenome:HGNC:44601
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

Location:
6q21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (113222151..113224269)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (114405513..114407631)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (113543353..113545471)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377956 Neighboring gene uncharacterized LOC105377953 Neighboring gene uncharacterized LOC105377955 Neighboring gene uncharacterized LOC107986637 Neighboring gene uncharacterized LOC124901497 Neighboring gene long intergenic non-protein coding RNA 2518

Genomic regions, transcripts, and products

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_022369.2 

    Range
    101..2219
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    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
    113222151..113224269
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    114405513..114407631
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)