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SUPT16HP1 SPT16 homolog, facilitates chromatin remodeling subunit pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 400011, updated on 23-Nov-2021

Summary

Official Symbol
SUPT16HP1provided by HGNC
Official Full Name
SPT16 homolog, facilitates chromatin remodeling subunit pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:31388
See related
Ensembl:ENSG00000256238
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
bcm670; SUPT16HP
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Genomic context

See SUPT16HP1 in Genome Data Viewer
Location:
12p12.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (16398875..16402509, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (16551809..16555443, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101928362 Neighboring gene solute carrier family 15 member 5 Neighboring gene microsomal glutathione S-transferase 1 Neighboring gene uncharacterized LOC107984494 Neighboring gene VISTA enhancer hs607 Neighboring gene GOT2 pseudogene 4

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_009707.3 

    Range
    101..3735
    Download
    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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    16398875..16402509 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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