Format

Send to:

Choose Destination

NCLP2 nucleolin pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100379142, updated on 12-Oct-2019

Summary

Official Symbol
NCLP2provided by HGNC
Official Full Name
nucleolin pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:35473
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
bA85L21.1

Genomic context

See NCLP2 in Genome Data Viewer
Location:
Xq26.3
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (135075012..135076007, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (134209166..134210627, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC112268301 Neighboring gene retrotransposon Gag like 8A Neighboring gene small integral membrane protein 10 like 2B Neighboring gene embryonic testis differentiation homolog B

Genomic regions, transcripts, and products

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_016573.2 

    Range
    101..1096
    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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    135075012..135076007 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center