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SETP8 SET pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 100128536, updated on 12-Oct-2019

Summary

Official Symbol
SETP8provided by HGNC
Official Full Name
SET pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:42927
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 SETP8 in Genome Data Viewer
Location:
Xq23
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (116963049..116963865)
105 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (116097017..116097644)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC100126447 Neighboring gene RNA, U6 small nuclear 1323, pseudogene Neighboring gene transcription elongation regulator 1 pseudogene Neighboring gene kelch like family member 13

Genomic regions, transcripts, and products

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_022693.2 

    Range
    101..917
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    116963049..116963865
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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