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HNRNPLP2 heterogeneous nuclear ribonucleoprotein L pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 644390, updated on 17-Aug-2024

Summary

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Official Symbol
HNRNPLP2provided by HGNC
Official Full Name
heterogeneous nuclear ribonucleoprotein L pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:48747
See related
AllianceGenome:HGNC:48747
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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See HNRNPLP2 in Genome Data Viewer
Location:
15q14
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (34488659..34490501, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (32294380..32296221, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (34780860..34782702, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene microRNA 1233-1 Neighboring gene golgin A8 family member A Neighboring gene amyloid beta precursor protein binding family A member 2 pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:34710454-34710954 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:34710955-34711455 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6285 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6286 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr15:34782687-34783188 Neighboring gene fascin actin-bundling protein 1 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6287 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6288 Neighboring gene dynamin 1 pseudogene 5

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)

General gene information

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Markers

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_029295.4 

    Range
    101..1943
    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_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    34488659..34490501 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    32294380..32296221 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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