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HNRNPA1P14 heterogeneous nuclear ribonucleoprotein A1 pseudogene 14 [ Homo sapiens (human) ]

Gene ID: 100421351, updated on 10-Oct-2023

Summary

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Official Symbol
HNRNPA1P14provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein A1 pseudogene 14provided by HGNC
Primary source
HGNC:HGNC:39132
See related
AllianceGenome:HGNC:39132
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:
9q22.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (88410332..88411520, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (100564436..100565624, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (91025247..91026435, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902359 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr9:90993210-90994206 Neighboring gene uncharacterized LOC124902204 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:91002175-91003034 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20004 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:91010312-91010812 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:91010813-91011313 Neighboring gene spindlin 1 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:91033322-91034521 Neighboring gene NANOG hESC enhancer GRCh37_chr9:91044914-91045415 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr9:91058145-91058846 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28524 Neighboring gene ribosomal protein L21 pseudogene 85 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:91110399-91110940 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:91134584-91135288 Neighboring gene uncharacterized LOC105376134

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_023844.2 

    Range
    101..1289
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    88410332..88411520 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    100564436..100565624 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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