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NMNAT1P1 NMNAT1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 326607, updated on 17-Sep-2024

Summary

Official Symbol
NMNAT1P1provided by HGNC
Official Full Name
NMNAT1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:20024
See related
AllianceGenome:HGNC:20024
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
NMNATP
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Genomic context

See NMNAT1P1 in Genome Data Viewer
Location:
14q31.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (81032474..81032979)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (75244682..75245187)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (81498818..81499323)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene thyroid stimulating hormone receptor Neighboring gene GPRASP3 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5983 Neighboring gene uncharacterized LOC101928462 Neighboring gene ribosomal protein L17 pseudogene 3 Neighboring gene ReSE screen-validated silencer GRCh37_chr14:81507651-81507772 Neighboring gene uncharacterized LOC105370594 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8823 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8824 Neighboring gene general transcription factor IIA subunit 1 Neighboring gene small nucleolar RNA, H/ACA box 79

Genomic regions, transcripts, and products

General gene information

Other Names

  • nicotinamide nucleotide adenylyltransferase 1 pseudogene
  • nicotinamide nucleotide adenylyltransferase 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_002596.4 

    Range
    101..606
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    81032474..81032979
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    75244682..75245187
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)