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FAM182B family with sequence similarity 182 member B [ Homo sapiens (human) ]

Gene ID: 728882, updated on 25-Jan-2022

Summary

Official Symbol
FAM182Bprovided by HGNC
Official Full Name
family with sequence similarity 182 member Bprovided by HGNC
Primary source
HGNC:HGNC:34503
See related
AllianceGenome:HGNC:34503
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 brain (RPKM 1.3), skin (RPKM 0.8) and 12 other tissues See more
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Genomic context

See FAM182B in Genome Data Viewer
Location:
20p11.1
Exon count:
7
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 20 NC_000020.11 (25763452..25801291, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (25744088..25781927, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985400 Neighboring gene vomeronasal 1 receptor 108 pseudogene Neighboring gene uncharacterized LOC105372582 Neighboring gene BSND pseudogene 1 Neighboring gene uncharacterized LOC101926935 Neighboring gene BSND pseudogene 2 Neighboring gene CFTR pseudogene 1

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_026714.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AL390198
  2. NR_027061.3 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL390198

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_000020.11 Reference GRCh38.p13 Primary Assembly

    Range
    25763452..25801291 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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