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NHIP neuronal hypoxia inducible, placenta associated [ Homo sapiens (human) ]

Gene ID: 105373085, updated on 28-Apr-2022

Summary

Official Symbol
NHIPprovided by HGNC
Official Full Name
neuronal hypoxia inducible, placenta associatedprovided by HGNC
Primary source
HGNC:HGNC:55561
See related
Ensembl:ENSG00000286381
Gene type
ncRNA
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

See NHIP in Genome Data Viewer
Location:
22q13.32
Exon count:
3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (49047480..49052385, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (49548357..49556872, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1310 Neighboring gene Sharpr-MPRA regulatory region 10948 Neighboring gene uncharacterized LOC105373086 Neighboring gene ribosomal protein L35 pseudogene 8

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    49047480..49052385 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_001755599.2 RNA Sequence

  2. XR_001755600.3 RNA Sequence

    Related
    ENST00000669789.1
  3. XR_001755598.3 RNA Sequence

    Related
    ENST00000657875.1
  4. XR_007068147.1 RNA Sequence

  5. XR_007068146.1 RNA Sequence

  6. XR_938332.3 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    49548357..49556872 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007090739.1 RNA Sequence

  2. XR_007090738.1 RNA Sequence

  3. XR_007090742.1 RNA Sequence

  4. XR_007090741.1 RNA Sequence

  5. XR_007090737.1 RNA Sequence

  6. XR_007090740.1 RNA Sequence