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ST13P12 ST13, Hsp70 interacting protein pseudogene 12 [ Homo sapiens (human) ]

Gene ID: 100127911, updated on 17-Sep-2024

Summary

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Official Symbol
ST13P12provided by HGNC
Official Full Name
ST13, Hsp70 interacting protein pseudogene 12provided by HGNC
Primary source
HGNC:HGNC:38787
See related
Ensembl:ENSG00000248400 AllianceGenome:HGNC:38787
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 ST13P12 in Genome Data Viewer
Location:
5q14.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (82968810..82977347)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (83454627..83463165)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (82264629..82273166)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1338 Neighboring gene uncharacterized LOC107986430 Neighboring gene uncharacterized LOC105379051 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr5:82264875-82266074 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr5:82271083-82272282 Neighboring gene uncharacterized LOC105379052 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22739 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:82322441-82323288 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:82323395-82323896 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:82323897-82324396 Neighboring gene transmembrane protein 167A Neighboring gene small Cajal body-specific RNA 18

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 Variation Viewer (GRCh37.p13)

General gene information

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Other Names

  • suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 12

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_021887.2 

    Range
    101..8638
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    82968810..82977347
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    83454627..83463165
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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