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    slc40a1.S solute carrier family 40 (iron-regulated transporter), member 1 S homeolog [ Xenopus laevis (African clawed frog) ]

    Gene ID: 446661, updated on 27-Dec-2024

    Summary

    Official Symbol
    slc40a1.S
    Official Full Name
    solute carrier family 40 (iron-regulated transporter), member 1 S homeolog
    Primary source
    Xenbase:XB-GENE-6078185
    Locus tag
    XELAEV_18047408mg
    See related
    EnsemblRapid:ENSXLAG00005015177 AllianceGenome:Xenbase:XB-GENE-6078185
    Gene type
    protein coding
    RefSeq status
    MODEL
    Organism
    Xenopus laevis
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Amphibia; Batrachia; Anura; Pipoidea; Pipidae; Xenopodinae; Xenopus; Xenopus
    Also known as
    fpn1; mtp1; IREG1; slc11a3; slc39a1; slc40a1
    Summary
    Predicted to enable iron ion transmembrane transporter activity and metal ion binding activity. Predicted to act upstream of or within iron ion transmembrane transport. Predicted to be located in basolateral plasma membrane. Human ortholog(s) of this gene implicated in hemochromatosis type 4. Orthologous to human SLC40A1 (solute carrier family 40 member 1). [provided by Alliance of Genome Resources, Dec 2024]
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    Genomic context

    See slc40a1.S in Genome Data Viewer
    Location:
    chromosome: 9_10S
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    101 current Xenopus_laevis_v10.1 (GCF_017654675.1) 9_10S NC_054388.1 (82213415..82229157, complement)
    100 previous assembly Xenopus_laevis_v2 (GCF_001663975.1) 9_10S NC_030741.1 (75515096..75532485, complement)

    Chromosome 9_10S - NC_054388.1Genomic Context describing neighboring genes Neighboring gene WD repeat domain 75 S homeolog Neighboring gene solute carrier family 40 member 1 Neighboring gene ORMDL sphingolipid biosynthesis regulator 1 S homeolog Neighboring gene PMS1 homolog 1, mismatch repair system component S homeolog

    Genomic regions, transcripts, and products

    General gene information

    Clone Names

    • MGC82700

    Gene Ontology Provided by Xenbase

    Function Evidence Code Pubs
    enables iron ion transmembrane transporter activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables metal ion binding IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    acts_upstream_of_or_within iron ion transmembrane transport IEA
    Inferred from Electronic Annotation
    more info
     
    acts_upstream_of_or_within monoatomic ion transport IEA
    Inferred from Electronic Annotation
    more info
     
    acts_upstream_of_or_within transmembrane transport IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    located_in basolateral plasma membrane IEA
    Inferred from Electronic Annotation
    more info
     
    located_in membrane IEA
    Inferred from Electronic Annotation
    more info
     
    located_in plasma membrane IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    solute carrier family 40 (iron-regulated transporter), member 1 S homeolog; solute carrier family 40 member 1
    Names
    ferroportin 1
    ferroportin1

    NCBI Reference Sequences (RefSeq)

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    RefSeqs of Annotated Genomes: Xenopus laevis Annotation Release 101 details...Open this link in a new tab

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

    Reference Xenopus_laevis_v10.1 Primary Assembly

    Genomic

    1. NC_054388.1 Reference Xenopus_laevis_v10.1 Primary Assembly

      Range
      82213415..82229157 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_018237518.2XP_018093007.1  solute carrier family 40 member 1

      UniProtKB/TrEMBL
      A0A1L8EPZ2, A0A974H1W1, Q6DDN2
      Related
      ENSXLAP00005044517.1, ENSXLAT00005045597.1

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001093357.1: Suppressed sequence

      Description
      NM_001093357.1: This RefSeq was removed because it is a nonsense-mediated mRNA decay (NMD) candidate.