PSMC6P1 proteasome 26S subunit, ATPase, 6 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: PSMC6P1provided by HGNC
Official Full Name: proteasome 26S subunit, ATPase, 6 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:20634
See related: AllianceGenome:HGNC:20634
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: PSMC6P
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Genomic context

Location:: 8q12.1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	8	NC_000008.11 (56049679..56051216, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	8	NC_060932.1 (56426810..56428347, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	8	NC_000008.10 (56962238..56963775, complement)

Chromosome 8 - NC_000008.11 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?

PSMC6P amplification is associated with malignant mixed tumor of salivary gland
Title: Amplification of MGC2177, PLAG1, PSMC6P, and LYN in a malignant mixed tumor of salivary gland detected by cDNA microarray with tyramide signal amplification.

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

G43615 (e-PCR)
- UniSTS:95049

RH68060 (e-PCR)
- UniSTS:86604

RH80771 (e-PCR)
- UniSTS:89556

Other Names

proteasome (prosome, macropain) 26S subunit, ATPase, 6 pseudogene
proteasome 26S ATPase subunit 6 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.