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EGLN3P1 egl-9 family hypoxia-inducible factor 3 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100420503, updated on 25-Jan-2022

Summary

Official Symbol
EGLN3P1provided by HGNC
Official Full Name
egl-9 family hypoxia-inducible factor 3 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:49857
See related
AllianceGenome:HGNC:49857
Gene type
pseudo
RefSeq status
INFERRED
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 EGLN3P1 in Genome Data Viewer
Location:
12p12.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (15971818..15972802, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (16124752..16125736, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC102724146 Neighboring gene mitochondrial ribosomal protein S7 pseudogene 2 Neighboring gene serine/threonine kinase receptor associated protein Neighboring gene deoxyribose-phosphate aldolase Neighboring gene VISTA enhancer hs798 Neighboring gene uncharacterized LOC101928362 Neighboring gene solute carrier family 15 member 5

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_023986.2 

    Range
    1..985
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    GenBank, FASTA, Sequence Viewer (Graphics)

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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    15971818..15972802 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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