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SEPTIN14P23 septin 14 pseudogene 23 [ Homo sapiens (human) ]

Gene ID: 107126290, updated on 10-Oct-2023

Summary

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Official Symbol
SEPTIN14P23provided by HGNC
Official Full Name
septin 14 pseudogene 23provided by HGNC
Primary source
HGNC:HGNC:51709
See related
Ensembl:ENSG00000228786 AllianceGenome:HGNC:51709
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
SEPT14P23; NCRNA00266D; LINC00266-4P; NCRNA00266Y2; NCRNA00266-4P
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Genomic context

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Location:
Yq11.23
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (25378300..25394719, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (26190682..26207100, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (27524447..27540866, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene RNA binding motif protein Y-linked family 2 member Y, pseudogene Neighboring gene ribosomal protein L41 pseudogene 6 Neighboring gene long intergenic non-protein coding RNA 265-3, pseudogene Neighboring gene capicua transcriptional repressor pseudogene 1 Neighboring gene golgin A6 family like 13, pseudogene Neighboring gene dynamin 1 pseudogene 27

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Toward a complete human genome sequence. Sanger Center, et al. Genome Res, 1998 Nov. PMID 9847074

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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Other Names

  • long intergenic non-protein coding RNA 266-4, pseudogene
  • non-protein coding RNA 266-4, pseudogene
  • non-protein coding RNA 266D

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_174182.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC006328
    Related
    ENST00000427373.5

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_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    25378300..25394719 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    26190682..26207100 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_029404.1: Suppressed sequence

    Description
    NG_029404.1: This RefSeq was removed because it is now thought that this gene is a transcribed pseudogene.

  2. NG_046625.2: Suppressed sequence

    Description
    NG_046625.2: This RefSeq was removed because it is now thought that this gene is a transcribed pseudogene.
Nucleotide Protein
Heading Accession and Version

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