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FEM1AP3 fem-1 homolog A pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 643859, updated on 10-Oct-2023

Summary

Official Symbol
FEM1AP3provided by HGNC
Official Full Name
fem-1 homolog A pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:39831
See related
Ensembl:ENSG00000217770 AllianceGenome:HGNC:39831
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:
6q21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (112365735..112367267, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (113549147..113550679, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (112686937..112688469, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:112683751-112684250 Neighboring gene ribosomal protein SA pseudogene 45 Neighboring gene keratin 18 pseudogene 65 Neighboring gene uncharacterized LOC101927664 Neighboring gene small nucleolar RNA U13

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_022321.2 

    Range
    101..1633
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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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    112365735..112367267 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    113549147..113550679 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)