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SEPTIN14P10 septin 14 pseudogene 10 [ Homo sapiens (human) ]

Gene ID: 107105352, updated on 10-Oct-2023

Summary

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Official Symbol
SEPTIN14P10provided by HGNC
Official Full Name
septin 14 pseudogene 10provided by HGNC
Primary source
HGNC:HGNC:51697
See related
AllianceGenome:HGNC:51697
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
SEPT14P10
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Genomic context

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Location:
10p11.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (38457679..38460266)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (38501689..38504276)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (38746607..38749194)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101929540 Neighboring gene long intergenic non-protein coding RNA 999 Neighboring gene capicua transcriptional repressor pseudogene 9 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr10:38815532-38816393 Neighboring gene NANOG hESC enhancer GRCh37_chr10:38876229-38876730 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr10:38877019-38877912 Neighboring gene NANOG hESC enhancer GRCh37_chr10:38888420-38888921 Neighboring gene ATP binding cassette subfamily D member 1 pseudogene 2 Neighboring gene poly(A) binding protein cytoplasmic 1 pseudogene 12

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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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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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_046611.2 

    Range
    101..2688
    Download
    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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    38457679..38460266
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021160000.1 Reference GRCh38.p14 PATCHES

    Range
    94507..97094
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    38501689..38504276
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Other Literature Sources
Molecular Biology Databases