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ST13P20 ST13, Hsp70 interacting protein pseudogene 20 [ Homo sapiens (human) ]

Gene ID: 729828, updated on 23-Nov-2021

Summary

Official Symbol
ST13P20provided by HGNC
Official Full Name
ST13, Hsp70 interacting protein pseudogene 20provided by HGNC
Primary source
HGNC:HGNC:38863
See related
Ensembl:ENSG00000215875
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

See ST13P20 in Genome Data Viewer
Location:
1p31.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (81721612..81723258)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (82187297..82188943)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene adhesion G protein-coupled receptor L2 Neighboring gene uncharacterized LOC101927434 Neighboring gene ribosomal protein S20 pseudogene 7 Neighboring gene uncharacterized LOC105378814 Neighboring gene uncharacterized LOC107985396 Neighboring gene VISTA enhancer hs442

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 20

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_022788.2 

    Range
    101..1747
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    81721612..81723258
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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