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RNASEH1P3 ribonuclease H1 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 199827, updated on 17-Sep-2024

Summary

Official Symbol
RNASEH1P3provided by HGNC
Official Full Name
ribonuclease H1 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:18716
See related
AllianceGenome:HGNC:18716
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 RNASEH1P3 in Genome Data Viewer
Location:
1q32.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (210303676..210304818)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (209542362..209543504)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (210477021..210478163)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 1241 Neighboring gene ST13, Hsp70 interacting protein pseudogene 19 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:210473593-210474427 Neighboring gene long intergenic non-protein coding RNA 2602 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:210484426-210485625 Neighboring gene uncharacterized LOC124904502 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_3009 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1779 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2478 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_3018 Neighboring gene uncharacterized LOC124904503 Neighboring gene hedgehog acyltransferase

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_001567.3 

    Range
    101..1243
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    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
    210303676..210304818
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_011332687.1 Reference GRCh38.p14 PATCHES

    Range
    83418..84560
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    209542362..209543504
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    GenBank, FASTA, Sequence Viewer (Graphics)