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FAM111A-DT FAM111A divergent transcript [ Homo sapiens (human) ]

Gene ID: 101927204, updated on 11-Jun-2021

Summary

Official Symbol
FAM111A-DTprovided by HGNC
Official Full Name
FAM111A divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:53752
See related
Ensembl:ENSG00000245571
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
Ubiquitous expression in prostate (RPKM 3.6), thyroid (RPKM 2.3) and 23 other tissues See more
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Genomic context

See FAM111A-DT in Genome Data Viewer
Location:
11q12.1
Exon count:
4
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (59133972..59142808, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (58901445..58910281, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369315 Neighboring gene glycine-N-acyltransferase like 1B Neighboring gene FAM111 trypsin like peptidase B Neighboring gene protein kinase cAMP-dependent type II regulatory subunit beta pseudogene Neighboring gene FAM111 trypsin like peptidase A Neighboring gene Sharpr-MPRA regulatory region 11967 Neighboring gene deltex E3 ubiquitin ligase 4

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_110184.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AP001258, BC028022
    Related
    ENST00000658798.1

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_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    59133972..59142808 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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