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ADAM3A ADAM metallopeptidase domain 3A (pseudogene) [ Homo sapiens (human) ]

Gene ID: 1587, updated on 23-Nov-2021

Summary

Official Symbol
ADAM3Aprovided by HGNC
Official Full Name
ADAM metallopeptidase domain 3A (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:209
See related
Ensembl:ENSG00000197475
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ADAM3; CYRN1; tMDCI
Expression
Restricted expression toward testis (RPKM 9.1) See more
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Genomic context

See ADAM3A in Genome Data Viewer
Location:
8p11.22
Exon count:
22
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 8 NC_000008.11 (39451045..39522989, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (39308564..39380508, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene lysine acetyltransferase 2B pseudogene Neighboring gene ADAM metallopeptidase domain 5 (pseudogene) Neighboring gene ADAM metallopeptidase domain 3A-like Neighboring gene ADAM metallopeptidase domain 18

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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

General gene information

Markers

Other Names

  • a disintegrin and metalloproteinase domain 3a (cyritestin 1)
  • cyritestin 1

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_001569.3 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks an alternate internal exon, compared to variant 4.
    Source sequence(s)
    AC106011, AJ005372, BG717260, HY234081, X89654
    Related
    ENST00000495171.6
  2. NR_024106.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) lacks an alternate internal exon, compared to variant 4.
    Source sequence(s)
    AC106011, AK308250, BG717260, HY234081, X89655
    Related
    ENST00000481351.6
  3. NR_024107.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) uses an alternate internal splice site, compared to variant 4.
    Source sequence(s)
    AC106011, AC123767, BC025386, BG717260, HY234081, X89654
    Related
    ENST00000460383.6
  4. NR_073423.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (4) represents the longest variant.
    Source sequence(s)
    AC106011, AC123767, BC025386, BG717260, HY234081, X89657
    Related
    ENST00000490268.6

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_000008.11 Reference GRCh38.p13 Primary Assembly

    Range
    39451045..39522989 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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