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ERC2-IT1 ERC2 intronic transcript 1 [ Homo sapiens (human) ]

Gene ID: 711, updated on 16-Jul-2021

Summary

Official Symbol
ERC2-IT1provided by HGNC
Official Full Name
ERC2 intronic transcript 1provided by HGNC
Primary source
HGNC:HGNC:1229
See related
Ensembl:ENSG00000281708
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
Po42; C1orf1; C3orf51
Summary
This gene is a putative tumor suppressor gene. [provided by RefSeq, Jul 2008]
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Genomic context

See ERC2-IT1 in Genome Data Viewer
Location:
3p14.3
Exon count:
1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (55657206..55659469, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (55691234..55693497, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene VISTA enhancer hs1472 Neighboring gene Wnt family member 5A Neighboring gene uncharacterized LOC105377100 Neighboring gene ELKS/RAB6-interacting/CAST family member 2 Neighboring gene microRNA 3938 Neighboring gene RN7SK pseudogene 45

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • ERC2 intronic transcript 1 (non-protein coding)

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_024615.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC025572
    Related
    ENST00000629461.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    55657206..55659469 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001213.1: Suppressed sequence

    Description
    NM_001213.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
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