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FAM169A-AS1 FAM169A antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 441086, updated on 23-Jul-2022

Summary

Official Symbol
FAM169A-AS1provided by HGNC
Official Full Name
FAM169A antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:56226
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
TP53LC02
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Genomic context

See FAM169A-AS1 in Genome Data Viewer
Location:
5q13.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (74865893..74867275)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (75346747..75348129)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (74161718..74163100)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene NSA2 ribosome biogenesis factor Neighboring gene RNA, U6 small nuclear 1330, pseudogene Neighboring gene family with sequence similarity 169 member A Neighboring gene ARPC1A pseudogene 3 Neighboring gene small nucleolar RNA SNORA40 Neighboring gene uncharacterized LOC105379039

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_134288.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC039003

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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    74865893..74867275
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    75346747..75348129
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)