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HNRNPA1P59 heterogeneous nuclear ribonucleoprotein A1 pseudogene 59 [ Homo sapiens (human) ]

Gene ID: 730246, updated on 12-Sep-2024

Summary

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Official Symbol
HNRNPA1P59provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein A1 pseudogene 59provided by HGNC
Primary source
HGNC:HGNC:48789
See related
AllianceGenome:HGNC:48789
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

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Location:
1q32.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (202911751..202912928)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (202174444..202175621)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (202880879..202882056)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene actin gamma 1 pseudogene 25 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:202853813-202854312 Neighboring gene RAB interacting factor Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1709 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2337 Neighboring gene kelch like family member 12 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2338 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:202897631-202898132 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:202898133-202898632 Neighboring gene Sharpr-MPRA regulatory region 11793 Neighboring gene adiponectin receptor 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1710 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1711 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1712 Neighboring gene cytochrome b5 reductase 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

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_022824.2 

    Range
    101..1278
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    202911751..202912928
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    202174444..202175621
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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