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RCC2P2 regulator of chromosome condensation 2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100421075, updated on 10-Oct-2023

Summary

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Official Symbol
RCC2P2provided by HGNC
Official Full Name
regulator of chromosome condensation 2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:38419
See related
Ensembl:ENSG00000237997 AllianceGenome:HGNC:38419
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:
Yq11.223
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (19986588..19987873, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (20893125..20894410, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (22148474..22149759, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377224 Neighboring gene lysine demethylase 5D Neighboring gene zinc finger protein 886, pseudogene Neighboring gene BRD4-independent group 4 enhancer GRCh37_chrY:22253264-22254463 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chrY:22277369-22278568 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chrY:22280323-22281522 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chrY:22299473-22300672 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chrY:22316202-22317401 Neighboring gene MED14-independent group 3 enhancer GRCh37_chrY:22339850-22341049 Neighboring gene zinc finger protein 884, pseudogene

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_021918.1 

    Range
    101..1386
    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_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    19986588..19987873 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    20893125..20894410 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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