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ANAPC15P2 ANAPC15 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 117751731, updated on 10-Oct-2023

Summary

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Official Symbol
ANAPC15P2provided by HGNC
Official Full Name
ANAPC15 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:54889
See related
Ensembl:ENSG00000232601
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

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Location:
3q26.31
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (174302937..174303283, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (177089880..177090226, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (174020727..174021073, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene neuroligin 1 Neighboring gene NLGN1 antisense RNA 1 Neighboring gene RN7SK pseudogene 234 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:173929552-173930052 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:173948692-173949418 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:173949419-173950143 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:173950144-173950869 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:173950870-173951594 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:173982710-173983249 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:173983250-173983788 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:174130757-174131368 Neighboring gene uncharacterized LOC105374226 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr3:174156710-174157909 Neighboring gene ribosomal protein L8 pseudogene 4

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

General gene information

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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_079071.1 

    Range
    101..447
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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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    174302937..174303283 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    177089880..177090226 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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