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CHCHD2P1 coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100874506, updated on 10-Dec-2019

Summary

Official Symbol
CHCHD2P1provided by HGNC
Official Full Name
coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:39585
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 CHCHD2P1 in Genome Data Viewer
Location:
Xq25
Annotation release Status Assembly Chr Location
109.20191205 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (123785009..123785451)
105 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (122918859..122919301)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene mediator of cell motility 1 pseudogene 4 Neighboring gene RNA, U7 small nuclear 69 pseudogene Neighboring gene RNA, 7SL, cytoplasmic 190, pseudogene Neighboring gene X-linked inhibitor of apoptosis Neighboring gene RNA, U6 small nuclear 122, pseudogene

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_032323.1 

    Range
    101..543
    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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    123785009..123785451
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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