Format

Send to:

Choose Destination

ANKRD20A9P ankyrin repeat domain 20 family member A9, pseudogene [ Homo sapiens (human) ]

Gene ID: 284232, updated on 23-Nov-2021

Summary

Official Symbol
ANKRD20A9Pprovided by HGNC
Official Full Name
ankyrin repeat domain 20 family member A9, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42023
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See ANKRD20A9P in Genome Data Viewer
Location:
13q11
Exon count:
22
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 13 NC_000013.11 (18811143..18871967, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (19385283..19446107, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 328-2, pseudogene Neighboring gene sorting nexin 18 pseudogene 26 Neighboring gene ras homolog family member T1 pseudogene 3 Neighboring gene RNA, U6 small nuclear 55, pseudogene Neighboring gene RNA, U6 small nuclear 76, pseudogene Neighboring gene sorting nexin 19 pseudogene 2

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Other Names

  • ankyrin repeat domain 20 family, member A2 pseudogene
  • coiled-coil domain containing 29-like

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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.

RNA

  1. NR_138091.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL391382

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p13 Primary Assembly

    Range
    18811143..18871967 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_1

Genomic

  1. NT_187594.1 Reference GRCh38.p13 ALT_REF_LOCI_1

    Range
    112793..173617 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_011431.1: Suppressed sequence

    Description
    NG_011431.1: This RefSeq was removed because it is now thought that this gene is transcribed.
  2. NR_027995.1: Suppressed sequence

    Description
    NR_027995.1: This RefSeq was removed because currently there is insufficient support for the transcript.
Support Center