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SEPTIN14P24 septin 14 pseudogene 24 [ Homo sapiens (human) ]

Gene ID: 106480345, updated on 10-Oct-2023

Summary

Official Symbol
SEPTIN14P24provided by HGNC
Official Full Name
septin 14 pseudogene 24provided by HGNC
Primary source
HGNC:HGNC:51710
See related
AllianceGenome:HGNC:51710
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
SEPT14P24
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Genomic context

Location:
7p11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (56360163..56360540, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (56518657..56519034, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (56427856..56428233, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene protein phosphatase 2 regulatory subunit B', epsilon pseudogene Neighboring gene RNA, U6 small nuclear 1335, pseudogene Neighboring gene putative uncharacterized protein FLJ44672 Neighboring gene capicua transcriptional repressor pseudogene 8

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.

Genomic

  1. NG_044627.2 

    Range
    101..478
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    GenBank, FASTA, Sequence Viewer (Graphics)

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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    56360163..56360540 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    56518657..56519034 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)