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    SCARF1 scavenger receptor class F member 1 [ Homo sapiens (human) ]

    Gene ID: 8578, updated on 10-Dec-2024

    Summary

    Official Symbol
    SCARF1provided by HGNC
    Official Full Name
    scavenger receptor class F member 1provided by HGNC
    Primary source
    HGNC:HGNC:16820
    See related
    Ensembl:ENSG00000074660 MIM:607873; AllianceGenome:HGNC:16820
    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
    SREC; SREC1; SREC-I
    Summary
    The protein encoded by this gene is a scavenger receptor that is expressed in endothelial cells. It regulates the uptake of chemically modified low density lipoproteins, including acetylated low density lipoprotein (Ac-LDL), and it may be involved in atherogenesis. This gene is regulated by the transcription factors ZNF444/EZF-2 and SP1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]
    Expression
    Broad expression in spleen (RPKM 18.4), lung (RPKM 9.9) and 22 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See SCARF1 in Genome Data Viewer
    Location:
    17p13.3
    Exon count:
    11
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (1633858..1645732, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (1522663..1534522, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (1537152..1549026, complement)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene solute carrier family 43 member 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:1509837-1510602 Neighboring gene RNA, 7SL, cytoplasmic 105, pseudogene Neighboring gene small nucleolar RNA U13 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:1530301-1530838 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:1530839-1531376 Neighboring gene Sharpr-MPRA regulatory region 224 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:1554397-1554907 Neighboring gene Rab interacting lysosomal protein Neighboring gene pre-mRNA processing factor 8

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    Related articles in PubMed

    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

    Clone Names

    • KIAA0149, MGC47738

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables low-density lipoprotein particle binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables low-density lipoprotein particle binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables scavenger receptor activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables scavenger receptor activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables transmembrane signaling receptor activity TAS
    Traceable Author Statement
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in cholesterol catabolic process IC
    Inferred by Curator
    more info
    PubMed 
    involved_in dendrite development IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in neuron remodeling IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in neuron remodeling ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in positive regulation of axon regeneration ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in positive regulation of neuron projection development IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in positive regulation of neuron projection development ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in receptor-mediated endocytosis TAS
    Traceable Author Statement
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in endocytic vesicle membrane TAS
    Traceable Author Statement
    more info
     
    is_active_in membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in plasma membrane TAS
    Traceable Author Statement
    more info
     

    General protein information

    Preferred Names
    scavenger receptor class F member 1
    Names
    acetyl LDL receptor
    scavenger receptor expressed by endothelial cells 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_003693.4NP_003684.2  scavenger receptor class F member 1 isoform 1 precursor

      See identical proteins and their annotated locations for NP_003684.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes the longer isoform (1).
      Source sequence(s)
      AC130343, AK291810, CA434049
      Consensus CDS
      CCDS11007.1
      UniProtKB/Swiss-Prot
      A8MQ05, O43701, Q14162, Q8NHD2, Q8NHD3, Q8NHD4, Q8NHD5
      UniProtKB/TrEMBL
      A8K6Z5
      Related
      ENSP00000263071.4, ENST00000263071.9
      Conserved Domains (1) summary
      pfam16019
      Location:100135
      CSRNP_N; Cysteine/serine-rich nuclear protein N-terminus
    2. NM_145350.3NP_663325.1  scavenger receptor class F member 1 isoform 3 precursor

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) uses an alternate splice site which results in a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (3, also known as SREC-3) has a distinct and shorter C-terminus, compared to isoform 1.
      Source sequence(s)
      AB052948, AC130343, CA434049
      Consensus CDS
      CCDS45564.1
      UniProtKB/Swiss-Prot
      Q14162
      Related
      ENSP00000458174.1, ENST00000571272.5
      Conserved Domains (1) summary
      pfam16019
      Location:100135
      CSRNP_N; Cysteine/serine-rich nuclear protein N-terminus

    RNA

    1. NR_028075.3 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) uses an alternate splice site in the central region, 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)
      AB052947, AC130343, CA434049, DC429327
      Related
      ENST00000434376.6
    2. NR_102409.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (6) uses an alternate splice site in the 5'-most exon, 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)
      AC130343, AK310174, CA434049, DC429327

    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_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      1633858..1645732 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_187611.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      63886..75760 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      1522663..1534522 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_145352.2: Suppressed sequence

      Description
      NM_145352.2: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
    2. NR_028076.1: Suppressed sequence

      Description
      NR_028076.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript, which retains an intron.