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SEPTIN7P3 septin 7 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 646913, updated on 10-Oct-2023

Summary

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Official Symbol
SEPTIN7P3provided by HGNC
Official Full Name
septin 7 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:38038
See related
Ensembl:ENSG00000226102 AllianceGenome:HGNC:38038
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
SEPT7P3
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Genomic context

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See SEPTIN7P3 in Genome Data Viewer
Location:
7p14.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (35946290..35974892)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (36087260..36115862)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (35985900..36014502)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 1085, pseudogene Neighboring gene zinc finger protein 383 pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:36007259-36007758 Neighboring gene protein phosphatase 1 regulatory inhibitor subunit 14B pseudogene 4 Neighboring gene uncharacterized LOC107986734 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18099 Neighboring gene Sharpr-MPRA regulatory region 2903 Neighboring gene uncharacterized LOC105375233 Neighboring gene uncharacterized LOC124901616

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. Human chromosome 7: DNA sequence and biology. Scherer SW, et al. Science, 2003 May 2. PMID 12690205, Free PMC Article

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)

See Variation Viewer (GRCh38)

General gene information

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Markers

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_008036.3 

    Range
    101..28703
    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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    35946290..35974892
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    36087260..36115862
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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