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R3HDM2P2 R3H domain containing 2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100129694, updated on 10-Oct-2023

Summary

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Official Symbol
R3HDM2P2provided by HGNC
Official Full Name
R3H domain containing 2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:44057
See related
Ensembl:ENSG00000216817 AllianceGenome:HGNC:44057
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:
6q16.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (104017430..104019707, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (105192920..105195197, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (104465305..104467582, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377916 Neighboring gene small nucleolar RNA SNORA33 Neighboring gene Sharpr-MPRA regulatory region 11761 Neighboring gene NANOG hESC enhancer GRCh37_chr6:104245459-104245960 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_87382 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr6:104320451-104320998 Neighboring gene nucleophosmin 1 pseudogene 10 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr6:104565801-104567000 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr6:104571018-104571571 Neighboring gene uncharacterized LOC105377917

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_022319.2 

    Range
    101..2378
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    104017430..104019707 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    105192920..105195197 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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