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

Gene ID: 108868751, updated on 13-Apr-2024

Summary

Official Symbol
GSC-DTprovided by HGNC
Official Full Name
GSC divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:53074
See related
AllianceGenome:HGNC:53074
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
DIGIT
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Genomic context

Location:
14q32.13
Exon count:
2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (94770642..94773607)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (89000706..89003671)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (95236979..95239944)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene ribosomal protein SA pseudogene 4 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_38793 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:95234013-95234551 Neighboring gene goosecoid homeobox Neighboring gene ribosomal protein L15 pseudogene 2 Neighboring gene uncharacterized LOC107984693

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

General gene information

Other Names

  • divergent to GSC, Induced by TGF-b family signaling
  • divergent to GSC, induced by TGF-beta family signaling

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IDA
Inferred from Direct Assay
more info
PubMed 
Process Evidence Code Pubs
involved_in endodermal cell differentiation IDA
Inferred from Direct Assay
more info
PubMed 

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_144432.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL121612

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    94770642..94773607
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    89000706..89003671
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)