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NCF4-AS1 NCF4 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 107985578, updated on 13-May-2022

Summary

Official Symbol
NCF4-AS1provided by HGNC
Official Full Name
NCF4 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:40393
See related
Ensembl:ENSG00000183822 AllianceGenome:HGNC:40393
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

See NCF4-AS1 in Genome Data Viewer
Location:
22q12.3
Exon count:
2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (36847372..36870443, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (37303227..37329452, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (37243415..37266485, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene CACNG2 divergent transcript Neighboring gene intraflagellar transport 27 Neighboring gene parvalbumin Neighboring gene neutrophil cytosolic factor 4 Neighboring gene uncharacterized LOC105373022 Neighboring gene uncharacterized LOC105373023 Neighboring gene colony stimulating factor 2 receptor subunit beta

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

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_147197.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    DA828142, KF511456, Z82185
    Related
    ENST00000619915.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    36847372..36870443 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NT_187631.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    68159..94394 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    37303227..37329452 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)