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FAM138F family with sequence similarity 138 member F [ Homo sapiens (human) ]

Gene ID: 641702, updated on 12-Oct-2019

Summary

Official Symbol
FAM138Fprovided by HGNC
Official Full Name
family with sequence similarity 138 member Fprovided by HGNC
Primary source
HGNC:HGNC:33581
See related
Ensembl:ENSG00000282591
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
F379
Expression
Low expression observed in reference dataset See more

Genomic context

See FAM138F in Genome Data Viewer
Location:
19p13.3
Exon count:
3
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 19 NC_000019.10 (76220..77690, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (76220..77690, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene WASP family homolog 5, pseudogene Neighboring gene uncharacterized LOC105376912 Neighboring gene microRNA 1302-11 Neighboring gene olfactory receptor family 4 subfamily G member 3 pseudogene Neighboring gene olfactory receptor family 4 subfamily G member 1 pseudogene

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)

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_026820.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC008993
    Related
    ENST00000631376.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000019.10 Reference GRCh38.p13 Primary Assembly

    Range
    76220..77690 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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