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GOLGA6L14P golgin A6 family like 14, pseudogene [ Homo sapiens (human) ]

Gene ID: 360027, updated on 10-Oct-2023

Summary

Official Symbol
GOLGA6L14Pprovided by HGNC
Official Full Name
golgin A6 family like 14, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:23961
See related
AllianceGenome:HGNC:23961
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

Location:
Yq11.23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (25492674..25495599, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (26305061..26307986, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (27638821..27641746, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene CSPG4 pseudogene 1 Y-linked Neighboring gene dynamin 1 pseudogene 48 Neighboring gene dynamin 1 pseudogene 26 Neighboring gene golgin A6 family like 16, pseudogene Neighboring gene AZFc P1.1b recombination region Neighboring gene chromodomain Y-linked 19 pseudogene

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_087939.1 

    Range
    101..3026
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    25492674..25495599 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    26305061..26307986 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)