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FAM27E5 family with sequence similarity E5 [ Homo sapiens (human) ]

Gene ID: 284123, updated on 11-Jun-2021

Summary

Official Symbol
FAM27E5provided by HGNC
Official Full Name
family with sequence similarity E5provided by HGNC
Primary source
HGNC:HGNC:32410
See related
Ensembl:ENSG00000178130
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
FAM27L
Expression
Low expression observed in reference dataset See more
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Genomic context

See FAM27E5 in Genome Data Viewer
Location:
17p11.2
Exon count:
2
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (22298764..22299893)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (21825370..21826499)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2002 Neighboring gene uncharacterized LOC105371597 Neighboring gene FERM domain containing kindlin 3 pseudogene Neighboring gene uncharacterized LOC105377824 Neighboring gene uncharacterized LOC107987246

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

Phenotypes

Associated conditions

Description Tests
A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia.
GeneReviews: Not available

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_028336.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC138761, BC031617
    Related
    ENST00000426869.3

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    22298764..22299893
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_203392.2: Suppressed sequence

    Description
    NM_203392.2: This RefSeq was permanently suppressed because it is now thought that this gene does not encode a protein.
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