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ADCY10P1 ADCY10 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 221442, updated on 13-May-2022

Summary

Official Symbol
ADCY10P1provided by HGNC
Official Full Name
ADCY10 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:44143
See related
Ensembl:ENSG00000161912 AllianceGenome:HGNC:44143
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
Broad expression in testis (RPKM 4.2), ovary (RPKM 2.5) and 24 other tissues See more
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Genomic context

See ADCY10P1 in Genome Data Viewer
Location:
6p21.1
Exon count:
23
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (41101034..41140835)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (40929591..40969387)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (41068773..41108573)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene translocator protein 2 Neighboring gene apolipoprotein B mRNA editing enzyme catalytic subunit 2 Neighboring gene O-acyl-ADP-ribose deacylase 1 Neighboring gene nuclear transcription factor Y subunit alpha Neighboring gene triggering receptor expressed on myeloid cells like 1 Neighboring gene triggering receptor expressed on myeloid cells 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

  • adenylate cyclase 10, soluble pseudogene 1

Clone Names

  • FLJ46432

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_026938.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AI243114, AL133404, BX648193
    Related
    ENST00000567255.2

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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    41101034..41140835
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    40929591..40969387
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001010871.1: Suppressed sequence

    Description
    NM_001010871.1: This RefSeq was temporarily suppressed because the annotated coding region is incomplete and function of the locus is under review.