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

Gene ID: 101927402, updated on 23-Nov-2021

Summary

Official Symbol
AFTPH-DTprovided by HGNC
Official Full Name
AFTPH divergent transcriptprovided by HGNC
Primary source
HGNC:HGNC:52788
See related
Ensembl:ENSG00000260101
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 AFTPH-DT in Genome Data Viewer
Location:
2p14
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (64522189..64524155, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (64749323..64751289, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene LGALSL divergent transcript Neighboring gene galectin like Neighboring gene Sharpr-MPRA regulatory region 8770 Neighboring gene long intergenic non-protein coding RNA 1805 Neighboring gene uncharacterized LOC105374773 Neighboring gene microRNA 4434 Neighboring gene aftiphilin Neighboring gene RNA, U6 small nuclear 100, pseudogene

Genomic regions, transcripts, and products

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_136167.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC008074, BC035180
    Related
    ENST00000561559.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    64522189..64524155 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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