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MED28P4 mediator complex subunit 28 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 100130359, updated on 17-Sep-2024

Summary

Official Symbol
MED28P4provided by HGNC
Official Full Name
mediator complex subunit 28 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:45081
See related
AllianceGenome:HGNC:45081
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

See MED28P4 in Genome Data Viewer
Location:
Xp11.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (45951602..45952342, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (45358979..45359719, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (45811037..45811777, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA SNORD77 Neighboring gene NANOG hESC enhancer GRCh37_chrX:45768669-45769204 Neighboring gene SRSF6 pseudogene 1 Neighboring gene keratin 18 pseudogene 68 Neighboring gene proliferating cell nuclear antigen pseudogene 3

Genomic regions, transcripts, and products

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_022594.2 

    Range
    101..841
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    45951602..45952342 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    45358979..45359719 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)