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    ECSCR endothelial cell surface expressed chemotaxis and apoptosis regulator [ Homo sapiens (human) ]

    Gene ID: 641700, updated on 10-Dec-2024

    Summary

    Official Symbol
    ECSCRprovided by HGNC
    Official Full Name
    endothelial cell surface expressed chemotaxis and apoptosis regulatorprovided by HGNC
    Primary source
    HGNC:HGNC:35454
    See related
    Ensembl:ENSG00000249751 MIM:615736; AllianceGenome:HGNC:35454
    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
    ARIA; ECSM2
    Summary
    The protein encoded by this gene is primarily found in endothelial cells and blood vessels, where it is involved in cell shape changes and EGF-induced cell migration. It can enhance the activation of vascular endothelial growth factor receptor-2/kinase insert domain receptor and also promote the proteolysis of internalized kinase insert domain receptor. This gene may play a role in angiogenesis-related diseases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
    Annotation information
    Note: This gene aligns across a gap in the GRCh38 reference genome assembly, and therefore, the 5' end of this gene was annotated on NT_029289.12 and the 3' end was annotated on NT_034772.7 in NCBI's Homo sapiens Annotation Release 106. [17 Jun 2014]
    Annotation category: suggests misassembly
    Expression
    Broad expression in placenta (RPKM 24.9), lung (RPKM 23.6) and 22 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See ECSCR in Genome Data Viewer
    Location:
    5q31.2
    Exon count:
    11
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (139448560..139462743, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (139974387..139987818, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (138784249..138842328, complement)

    Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene DnaJ heat shock protein family (Hsp40) member C18 Neighboring gene uncharacterized LOC124901082 Neighboring gene NANOG hESC enhancer GRCh37_chr5:138755520-138756025 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16412 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:138773284-138773784 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16413 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:138775085-138775584 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23232 Neighboring gene RNA, U5B small nuclear 4, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23233 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:138840510-138841099 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:138841100-138841688 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:138842278-138842865 Neighboring gene Sharpr-MPRA regulatory region 4960 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:138852141-138852662 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:138854227-138854748 Neighboring gene small integral membrane protein 33 Neighboring gene Sharpr-MPRA regulatory region 11914 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23234 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 23235 Neighboring gene stimulator of interferon response cGAMP interactor 1

    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

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Component Evidence Code Pubs
    is_active_in cytosol IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in cytosol IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in intracellular membrane-bounded organelle IDA
    Inferred from Direct Assay
    more info
     
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
     
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in plasma membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    endothelial cell-specific chemotaxis regulator
    Names
    apoptosis regulator through modulating IAP expression
    endothelial cell-specific molecule 2

    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_001077693.4NP_001071161.1  endothelial cell-specific chemotaxis regulator isoform 1 precursor

      See identical proteins and their annotated locations for NP_001071161.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes the longer isoform (1).
      Source sequence(s)
      AI699314, EU025066
      Consensus CDS
      CCDS75317.1
      UniProtKB/Swiss-Prot
      B4E3H7, C3RSF2, Q19T08
      Related
      ENSP00000479243.1, ENST00000618155.3
      Conserved Domains (1) summary
      pfam15820
      Location:101203
      ECSCR; Endothelial cell-specific chemotaxis regulator
    2. NM_001293739.2NP_001280668.1  endothelial cell-specific chemotaxis regulator isoform 2 precursor

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) uses an alternate splice site in the 3' terminal exon, compared to variant 1, resulting in an isoform (2) that has a distinct C-terminus and is 1 aa shorter than isoform 1.
      Source sequence(s)
      AC142391, AC188049, AI699314, BI834795, EU025066
      UniProtKB/Swiss-Prot
      Q19T08
      Conserved Domains (1) summary
      pfam15820
      Location:101203
      ECSCR; Endothelial cell-specific chemotaxis regulator

    RNA

    1. NR_121659.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) contains an additional internal exon and uses an alternate splice site in the 3' terminal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      ABBA01026462, AC142391, AI699314, BF526332, EU025066

    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_000005.10 Reference GRCh38.p14 Primary Assembly

      Range
      139448560..139462743 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_021159996.1 Reference GRCh38.p14 PATCHES

      Range
      39089..52538 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060929.1 Alternate T2T-CHM13v2.0

      Range
      139974387..139987818 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)