MED14P1 mediator complex subunit 14 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: MED14P1provided by HGNC
Official Full Name: mediator complex subunit 14 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:2371
See related: Ensembl:ENSG00000233774 AllianceGenome:HGNC:2371
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: CRSP2P; MED14P; CXorf4P
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Genomic context

Location:: Yq11.221

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	Y	NC_000024.10 (12618985..12634401, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	Y	NC_060948.1 (13526797..13542212, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	Y	NC_000024.9 (14730917..14746332, complement)

Chromosome Y - NC_000024.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

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

DYS388 (e-PCR)
- UniSTS:57872

G66186 (e-PCR)
- UniSTS:230176

G66192 (e-PCR)
- UniSTS:230181

G49203 (e-PCR)
- UniSTS:163238

Other Names

cofactor required for Sp1 transcriptional activation, subunit 2, 150kDa pseudogene
cofactor required for Sp1 transcriptional activation, subunit 2, pseudogene

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.