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MED15P8 mediator complex subunit 15 pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 106480229, updated on 10-Dec-2024

Summary

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Official Symbol
MED15P8provided by HGNC
Official Full Name
mediator complex subunit 15 pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:48657
See related
AllianceGenome:HGNC:48657
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 MED15P8 in Genome Data Viewer
Location:
2q21.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (131200944..131202941, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (131634914..131636911, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (131958517..131960514, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene NEK2 pseudogene 4 Neighboring gene neurofibromin 1 pseudogene 8 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:131958317-131958818 Neighboring gene POTE ankyrin domain family member E Neighboring gene RNA, U6 small nuclear 127, pseudogene Neighboring gene uncharacterized LOC440910 Neighboring gene cytochrome P450 family 4 subfamily F member 31, 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)

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_043725.2 

    Range
    101..2098
    Download
    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
    131200944..131202941 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    131634914..131636911 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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