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GOLGA6FP golgin A6 family member F, pseudogene [ Homo sapiens (human) ]

Gene ID: 645752, updated on 13-May-2022

Summary

Official Symbol
GOLGA6FPprovided by HGNC
Official Full Name
golgin A6 family member F, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:49206
See related
AllianceGenome:HGNC:49206
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in testis (RPKM 4.3) and ovary (RPKM 0.2) See more
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Genomic context

See GOLGA6FP in Genome Data Viewer
Location:
15q24.3
Exon count:
18
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (77914217..77926846, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (75776440..75789072, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (78206559..78219188, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene chondroitin sulfate proteoglycan 4 pseudogene 13 Neighboring gene uncharacterized LOC124903533 Neighboring gene dynamin 1 pseudogene 9 Neighboring gene RNA, 7SL, cytoplasmic 214, pseudogene Neighboring gene Sharpr-MPRA regulatory region 89 Neighboring gene COMM domain containing 4 pseudogene 1 Neighboring gene ADAMTS7 pseudogene 3 Neighboring gene uncharacterized LOC91450

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Other Names

  • golgi autoantigen, golgin subfamily a, 6 pseudogene
  • golgin A6 family member A 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.

RNA

  1. NR_027024.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC104758

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    77914217..77926846 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    75776440..75789072 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)