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WWC2-AS2 WWC2 antisense RNA 2 [ Homo sapiens (human) ]

Gene ID: 152641, updated on 10-Oct-2023

Summary

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Official Symbol
WWC2-AS2provided by HGNC
Official Full Name
WWC2 antisense RNA 2provided by HGNC
Primary source
HGNC:HGNC:26390
See related
Ensembl:ENSG00000251359 AllianceGenome:HGNC:26390
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
C4orf38
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Genomic context

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Location:
4q35.1
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (183097021..183099199, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (186440563..186442741, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (184018174..184020352, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene CIBAR1 pseudogene 2 Neighboring gene uncharacterized LOC105377578 Neighboring gene Sharpr-MPRA regulatory region 3150 Neighboring gene Sharpr-MPRA regulatory region 10146 Neighboring gene Sharpr-MPRA regulatory region 13144 Neighboring gene Sharpr-MPRA regulatory region 7903 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:184043402-184043902 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:184043903-184044403 Neighboring gene WW and C2 domain containing 2 Neighboring gene uncharacterized LOC124900923 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:184103784-184104578 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:184104579-184105373 Neighboring gene WWC2 antisense RNA 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Complete sequencing and characterization of 21,243 full-length human cDNAs. Ota T, et al. Nat Genet, 2004 Jan. PMID 14702039
  2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

General gene information

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Markers

Other Names

  • WWC2 antisense RNA 2 (non-protein coding)

Clone Names

  • FLJ30277, FLJ30278, MGC161755, MGC161757

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_024008.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC019193, AK054839
    Related
    ENST00000578387.1

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    183097021..183099199 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    186440563..186442741 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_153008.3: Suppressed sequence

    Description
    NM_153008.3: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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