Format

Send to:

Choose Destination

FAM222A-AS1 FAM222A antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 84983, updated on 23-Nov-2021

Summary

Official Symbol
FAM222A-AS1provided by HGNC
Official Full Name
FAM222A antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:28223
See related
Ensembl:ENSG00000255650
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
Biased expression in testis (RPKM 3.4), fat (RPKM 1.4) and 8 other tissues See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See FAM222A-AS1 in Genome Data Viewer
Location:
12q24.11
Exon count:
4
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (109734209..109773487, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (110172014..110211292, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene metabolism of cobalamin associated B Neighboring gene mevalonate kinase Neighboring gene RN7SK pseudogene 250 Neighboring gene family with sequence similarity 222 member A Neighboring gene HNF1 motif-containing MPRA enhancer 206 Neighboring gene transient receptor potential cation channel subfamily V member 4 Neighboring gene uncharacterized LOC105369975 Neighboring gene microRNA 4497

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

General gene information

Markers

Other Names

  • FAM222A antisense RNA 1 (non-protein coding)

Clone Names

  • MGC14436

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_026661.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    BC007821, BQ684893, DA082338
    Related
    ENST00000541460.2
  2. NR_026662.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks an internal exon, compared to variant 1.
    Source sequence(s)
    BC007821, BQ684893
    Related
    ENST00000541723.5

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    109734209..109773487 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_032897.1: Suppressed sequence

    Description
    NM_032897.1: This RefSeq was permanently suppressed because it is now thought that this gene does not encode a protein.
Support Center