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MED28P5 mediator complex subunit 28 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 106479053, updated on 17-Sep-2024

Summary

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Official Symbol
MED28P5provided by HGNC
Official Full Name
mediator complex subunit 28 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:45082
See related
Ensembl:ENSG00000255205 AllianceGenome:HGNC:45082
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 MED28P5 in Genome Data Viewer
Location:
11q21
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (97000227..97000743, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (97006721..97007237, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (96871227..96871743, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2737 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancers GRCh37_chr11:96457069-96457656 and GRCh37_chr11:96457657-96458244 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:96463619-96464262 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:96464263-96464904 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:96479048-96479664 Neighboring gene AKTIP pseudogene 3 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:96609483-96610181 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:96647886-96648498 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:96835507-96836045 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:96836046-96836583 Neighboring gene uncharacterized LOC105369448 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr11:96916331-96916832 Neighboring gene long intergenic non-protein coding RNA 2553

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_044525.2 

    Range
    101..617
    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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    97000227..97000743 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    97006721..97007237 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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