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ANKRD20A19P ankyrin repeat domain 20 family member A19, pseudogene [ Homo sapiens (human) ]

Gene ID: 400110, updated on 13-May-2022

Summary

Official Symbol
ANKRD20A19Pprovided by HGNC
Official Full Name
ankyrin repeat domain 20 family member A19, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42737
See related
AllianceGenome:HGNC:42737
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Restricted expression toward testis (RPKM 3.4) See more
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Genomic context

See ANKRD20A19P in Genome Data Viewer
Location:
13q12.12
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (23907284..23949315, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (23113778..23156177, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (24481423..24523454, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene mitochondrial intermediate peptidase Neighboring gene MT-CO3 pseudogene 2 Neighboring gene C1q and TNF related 9B Neighboring gene prostate and testis expressed opposite C1QTNF9B and MIPEP Neighboring gene uncharacterized LOC105370115 Neighboring gene spermatogenesis associated 13 Neighboring gene Sharpr-MPRA regulatory region 9740

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

Phenotypes

EBI GWAS Catalog

Description
Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.
EBI GWAS Catalog

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.

RNA

  1. NR_073430.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AK127292, AL445985

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    23907284..23949315 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    23113778..23156177 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_207439.2: Suppressed sequence

    Description
    NM_207439.2: This RefSeq was permanently suppressed because currently there is insufficient support for the protein and the transcript, which is a nonsense-mediated mRNA decay (NMD) candidate.