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NOS2P1 nitric oxide synthase 2 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 645740, updated on 23-Nov-2021

Summary

Official Symbol
NOS2P1provided by HGNC
Official Full Name
nitric oxide synthase 2 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:7875
See related
MIM:600720
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
NOS2C
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Genomic context

See NOS2P1 in Genome Data Viewer
Location:
17q11.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (27651443..27664655, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (25978469..25991681, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene kinase suppressor of ras 1 Neighboring gene integral membrane protein 2B pseudogene 1 Neighboring gene galectin 9 Neighboring gene TBC1 domain family member 29, pseudogene pseudogene Neighboring gene carboxypeptidase D pseudogene 1

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

General gene information

Other Names

  • inducible nitric oxide synthase pseudogene
  • nitric oxide synthase 2C (pseudogene)

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_006943.4 

    Range
    101..13313
    Download
    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_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    27651443..27664655 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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