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ST13P15 ST13, Hsp70 interacting protein pseudogene 15 [ Homo sapiens (human) ]

Gene ID: 100422603, updated on 10-Dec-2019

Summary

Official Symbol
ST13P15provided by HGNC
Official Full Name
ST13, Hsp70 interacting protein pseudogene 15provided by HGNC
Primary source
HGNC:HGNC:38850
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See ST13P15 in Genome Data Viewer
Location:
3q24
Annotation release Status Assembly Chr Location
109.20191205 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (143517083..143518313, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (143235965..143237071, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene solute carrier family 9 member A9 Neighboring gene SLC9A9 antisense RNA 1 Neighboring gene glyceraldehyde 3 phosphate dehydrogenase pseudogene 47 Neighboring gene ubiquitin domain containing 2 pseudogene Neighboring gene uncharacterized LOC102724120

Genomic regions, transcripts, and products

General gene information

Other Names

  • suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 15

NCBI Reference Sequences (RefSeq)

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_025637.2 

    Range
    101..1331
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    143517083..143518313 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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