ANKRD20A4-ANKRD20A20P ANKRD20A4-ANKRD20A20P readthrough [Homo sapiens (human)] - Gene

Summary

Gene symbol: ANKRD20A4-ANKRD20A20P
Gene description: ANKRD20A4-ANKRD20A20P readthrough
Gene type: ncRNA
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary: This locus represents naturally-occurring readthrough transcription between ankyrin repeat domain 20 family member A4 (ANKRD20A4) and ankyrin repeat domain 20 family member A20, pseudogene (ANKRD20A20P). Readthrough transcripts are expected to be candidates for nonsense-mediated decay (NMD) and are unlikely to be translated into functional proteins. [provided by RefSeq, Mar 2017]
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Genomic context

See ANKRD20A4-ANKRD20A20P in Genome Data Viewer

Location:: 9q13

Exon count:: 25

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	9	NC_000009.12 (64369394..64469242)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	9	NC_060933.1 (79641844..79748335)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	9	NC_000009.11 (69381812..69481660)

Chromosome 9 - NC_000009.12 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Expression

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See details

Project title: HPA RNA-seq normal tissues 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

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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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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Readthrough ANKRD20A4-ANKRD20A20P

Included genes: ANKRD20A4P, ANKRD20A20P

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.