Format

Send to:

Choose Destination

HIF1AP1 HIF1AP pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100874523, updated on 12-Oct-2019

Summary

Official Symbol
HIF1AP1provided by HGNC
Official Full Name
HIF1AP pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:43016
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See HIF1AP1 in Genome Data Viewer
Location:
14q24.3
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (75116426..75116608, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (75583129..75583311, complement)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene acylphosphatase 1 Neighboring gene zinc finger C2HC-type containing 1C Neighboring gene NIMA related kinase 9 Neighboring gene transmembrane p24 trafficking protein 10 Neighboring gene RNA, U4atac small nuclear 14, pseudogene

Genomic regions, transcripts, and products

General gene information

Other Names

  • hypoxia inducible factor 1 alpha subunit pseudogene 1
  • hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) pseudogene 1

NCBI Reference Sequences (RefSeq)

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_032553.1 

    Range
    101..283
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    75116426..75116608 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center