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ANKRD62P1 ankyrin repeat domain 62 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 107080639, updated on 10-Oct-2023

Summary

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Official Symbol
ANKRD62P1provided by HGNC
Official Full Name
ankyrin repeat domain 62 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:42363
See related
Ensembl:ENSG00000259271 AllianceGenome:HGNC:42363
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:
22q11.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (16671665..16679598, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (17348218..17356148, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (17152555..17160488, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene TPTE pseudogene 1 Neighboring gene ANKRD62P1-PARP4P3 readthrough, transcribed pseudogene Neighboring gene solute carrier family 25 member 15 pseudogene 5 Neighboring gene MPRA-validated peak4438 silencer Neighboring gene poly(ADP-ribose) polymerase family member 4 pseudogene 3 Neighboring gene ReSE screen-validated silencer GRCh37_chr22:17177994-17178151 Neighboring gene von Willebrand factor pseudogene 1 Neighboring gene long intergenic non-protein coding RNA 1665

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 studies and variants in dbVar

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_046683.1 

    Range
    101..8034
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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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    16671665..16679598 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    17348218..17356148 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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