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NTAN1P2 N-terminal asparagine amidase pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100420307, updated on 23-Nov-2021

Summary

Official Symbol
NTAN1P2provided by HGNC
Official Full Name
N-terminal asparagine amidase pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:45262
See related
Ensembl:ENSG00000250569
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 NTAN1P2 in Genome Data Viewer
Location:
8q21.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 8 NC_000008.11 (86481585..86483028, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (87493814..87495257, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene HNF4 motif-containing MPRA enhancer 29 Neighboring gene WWP1 antisense RNA 1 Neighboring gene WW domain containing E3 ubiquitin protein ligase 1 Neighboring gene regulator of microtubule dynamics 1 Neighboring gene solute carrier family 2 member 3 pseudogene 4 Neighboring gene copine 3

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_026048.3 

    Range
    101..1544
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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_000008.11 Reference GRCh38.p13 Primary Assembly

    Range
    86481585..86483028 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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