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ANKRD20A13P ankyrin repeat domain 20 family member A13, pseudogene [ Homo sapiens (human) ]

Gene ID: 100132733, updated on 10-Oct-2023

Summary

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Official Symbol
ANKRD20A13Pprovided by HGNC
Official Full Name
ankyrin repeat domain 20 family member A13, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:43604
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:
1q21.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 Unlocalized Scaffold NT_187361.1 (91421..95499, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (127837530..127841608)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (143209182..143213260, complement)

NT_187361.1Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379854 Neighboring gene uncharacterized LOC101060632 Neighboring gene sorting nexin 18 pseudogene 19 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:143201417-143201917 Neighboring gene uncharacterized LOC124905319 Neighboring gene basic salivary proline-rich protein 1-like Neighboring gene OCT4 hESC enhancer GRCh37_chr1:143283469-143283970 Neighboring gene sorting nexin 18 pseudogene 21

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)

See Variation Viewer (GRCh38)

General gene information

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Markers

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_029281.2 

    Range
    101..4179
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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. NT_187361.1 Reference GRCh38.p14 Primary Assembly

    Range
    91421..95499 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    127837530..127841608
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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