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    ASIC3 acid sensing ion channel subunit 3 [ Homo sapiens (human) ]

    Gene ID: 9311, updated on 10-Dec-2024

    Summary

    Official Symbol
    ASIC3provided by HGNC
    Official Full Name
    acid sensing ion channel subunit 3provided by HGNC
    Primary source
    HGNC:HGNC:101
    See related
    Ensembl:ENSG00000213199 MIM:611741; AllianceGenome:HGNC:101
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ACCN3; TNaC1; DRASIC; SLNAC1
    Summary
    This gene encodes a member of the degenerin/epithelial sodium channel (DEG/ENaC) superfamily. The members of this family are amiloride-sensitive sodium channels that contain intracellular N and C termini, two hydrophobic transmembrane regions, and a large extracellular loop, which has many cysteine residues with conserved spacing. The member encoded by this gene is an acid sensor and may play an important role in the detection of lasting pH changes. In addition, a heteromeric association between this member and acid-sensing (proton-gated) ion channel 2 has been observed as proton-gated channels sensitive to gadolinium. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2012]
    Expression
    Broad expression in testis (RPKM 3.0), brain (RPKM 2.0) and 20 other tissues See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See ASIC3 in Genome Data Viewer
    Location:
    7q36.1
    Exon count:
    11
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (151048292..151052756)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (152221380..152225844)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (150745379..150749843)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901777 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:150722492-150723096 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr7:150723702-150724305 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr7:150724306-150724910 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:150725516-150726120 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:150726121-150726724 Neighboring gene ATP binding cassette subfamily B member 8 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:150736215-150736999 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:150737000-150737783 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:150747130-150747768 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18791 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:150748624-150749202 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:150750636-150751136 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:150754255-150754788 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26847 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26848 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26849 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26850 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18792 Neighboring gene cyclin dependent kinase 5 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18793 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:150757470-150758377 Neighboring gene uncharacterized LOC128092247 Neighboring gene solute carrier family 4 member 2

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Potential readthrough

    Included gene: ABCB8

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables enterobactin transmembrane transporter activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables ligand-gated sodium channel activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables monoatomic cation channel activity TAS
    Traceable Author Statement
    more info
    PubMed 
    enables sodium channel activity TAS
    Traceable Author Statement
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in perinuclear region of cytoplasm IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in plasma membrane TAS
    Traceable Author Statement
    more info
     

    General protein information

    Preferred Names
    acid-sensing ion channel 3
    Names
    acid sensing (proton gated) ion channel 3
    amiloride-sensitive cation channel 3, testis
    modulatory subunit of ASIC2a
    neuronal amiloride-sensitive cation channel 3
    proton-gated cation channel subunit
    testis sodium channel 1

    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.

    mRNA and Protein(s)

    1. NM_004769.4NP_004760.1  acid-sensing ion channel 3 isoform a

      See identical proteins and their annotated locations for NP_004760.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) uses an alternate splice site in the 3' coding region, compared to variant 2. The resulting protein (isoform a) has a shorter and distinct C-terminus, compared to isoform b.
      Source sequence(s)
      AF095897, AK313926
      Consensus CDS
      CCDS5916.1
      UniProtKB/Swiss-Prot
      B2R9V0, O60263, O75906, Q59FN9, Q9UER8, Q9UHC3, Q9UHC4
      UniProtKB/TrEMBL
      A0A090N7X8
      Related
      ENSP00000344838.5, ENST00000349064.10
      Conserved Domains (1) summary
      cl02990
      Location:20514
      ASC; Amiloride-sensitive sodium channel
    2. NM_020321.3NP_064717.1  acid-sensing ion channel 3 isoform b

      See identical proteins and their annotated locations for NP_064717.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) represents the longest transcript and encodes the longest isoform (b).
      Source sequence(s)
      AC010973, AF195025, AI580095, AK313926
      Consensus CDS
      CCDS5915.1
      UniProtKB/TrEMBL
      A0A090N8Q1
      Related
      ENSP00000297512.8, ENST00000297512.12
      Conserved Domains (1) summary
      cl02990
      Location:20534
      ASC; Amiloride-sensitive sodium channel
    3. NM_020322.3NP_064718.1  acid-sensing ion channel 3 isoform c

      See identical proteins and their annotated locations for NP_064718.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) lacks an exon and uses an alternate splice site in the 3' coding region, compared to variant 2. The resulting protein (isoform c) has a shorter and distinct C-terminus, compared to isoform b.
      Source sequence(s)
      AC010973, AF095897, AI580095, AK313926
      Consensus CDS
      CCDS5914.1
      UniProtKB/TrEMBL
      A0A090N8Z6
      Related
      ENSP00000350600.4, ENST00000357922.8
      Conserved Domains (1) summary
      cl02990
      Location:20523
      ASC; Amiloride-sensitive sodium channel

    RNA

    1. NR_046401.1 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) lacks an alternate internal exon and uses an alternate splice site, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AB209421, AC010973, AI580095, AK313926
      Related
      ENST00000377904.8

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      151048292..151052756
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      152221380..152225844
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)