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FMNL1-DT FMNL1 divergent transcript [ Homo sapiens (human) ]

Gene ID: 339192, updated on 13-May-2022

Summary

Official Symbol
FMNL1-DTprovided by HGNC
Official Full Name
FMNL1 divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:55311
See related
Ensembl:ENSG00000267121 AllianceGenome:HGNC:55311
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See FMNL1-DT in Genome Data Viewer
Location:
17q21.31
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (45190931..45221765, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (46044557..46075484, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (43268298..43299132, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105371795 Neighboring gene HEXIM P-TEFb complex subunit 2 Neighboring gene Sharpr-MPRA regulatory region 8248 Neighboring gene formin like 1 Neighboring gene EF-hand calcium-binding domain-containing protein 3-like Neighboring gene MAP3K14 antisense RNA 1 Neighboring gene spermatogenesis associated 32

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_147507.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC008105
    Related
    ENST00000586376.5

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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    45190931..45221765 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    46044557..46075484 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)