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FCHO2-DT FCHO2 divergent transcript [ Homo sapiens (human) ]

Gene ID: 118597832, updated on 10-Oct-2023

Summary

Official Symbol
FCHO2-DTprovided by HGNC
Official Full Name
FCHO2 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:55232
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

Location:
5q13.2
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (72936535..72955884, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (73417615..73436967, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene transportin 1 Neighboring gene ribosomal protein L35a pseudogene 13 Neighboring gene microRNA 4804 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16086 Neighboring gene FCH and mu domain containing endocytic adaptor 2 Neighboring gene CTDNEP1 pseudogene 2 Neighboring gene CHP1 pseudogene 1

Genomic regions, transcripts, and products

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.

RNA

  1. NR_186391.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC008972
  2. NR_186392.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC008972

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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    72936535..72955884 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    73417615..73436967 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)