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ST13P9 ST13, Hsp70 interacting protein pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 390301, updated on 10-Oct-2023

Summary

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Official Symbol
ST13P9provided by HGNC
Official Full Name
ST13, Hsp70 interacting protein pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:38744
See related
Ensembl:ENSG00000256070 AllianceGenome:HGNC:38744
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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Location:
12p11.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (33454274..33455655)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (33325492..33326873)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (33607209..33608590)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene argininosuccinate synthetase 1 pseudogene 14 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:33333175-33334374 Neighboring gene ReSE screen-validated silencer GRCh37_chr12:33467193-33467363 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:33591665-33592481 Neighboring gene synaptotagmin 10 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:33673977-33674537 Neighboring gene CRISPRi-validated cis-regulatory element chr12.1007 Neighboring gene RNA, U6 small nuclear 400, pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:33802829-33803428 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:33823144-33823925 Neighboring gene uncharacterized LOC105369726

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)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 9

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_021711.2 

    Range
    101..1482
    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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    33454274..33455655
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    33325492..33326873
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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