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MED15P5 mediator complex subunit 15 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 391436, updated on 27-Aug-2024

Summary

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Official Symbol
MED15P5provided by HGNC
Official Full Name
mediator complex subunit 15 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:48654
See related
Ensembl:ENSG00000236595 AllianceGenome:HGNC:48654
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:
2q21.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (130251502..130252737)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (130685398..130686633)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (131009075..131010310)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene ras homolog family member Q pseudogene 3 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11955 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16524 Neighboring gene NOC2 like nucleolar associated transcriptional repressor pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:131009389-131009890 Neighboring gene nuclear-encoded mitochondrial tRNA-Gln (TTG) 7-1 Neighboring gene MT-ND1 pseudogene 29

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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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_021585.1 

    Range
    101..1336
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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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    130251502..130252737
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_025791762.1 Reference GRCh38.p14 PATCHES

    Range
    428062..429297
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    130685398..130686633
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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