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    SEMG1 semenogelin I [ Homo sapiens ]

    Gene ID: 6406, updated on 11-May-2012

    Summary

    Official Symbol
    SEMG1provided by HGNC
    Official Full Name
    semenogelin Iprovided by HGNC
    Primary source
    HGNC:10742
    See related
    Ensembl:ENSG00000124233; HPRD:01641; MIM:182140; Vega:OTTHUMG00000032565
    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
    SGI; SEMG; CT103; dJ172H20.2; FLJ78262; MGC14719
    Summary
    The protein encoded by this gene is the predominant protein in semen. The encoded secreted protein is involved in the formation of a gel matrix that encases ejaculated spermatozoa. The prostate-specific antigen (PSA) protease processes this protein into smaller peptides, with each possibly having a separate function. The proteolysis process breaks down the gel matrix and allows the spermatozoa to move more freely. [provided by RefSeq, Jul 2009]

    Genomic context

    Location :
    20q12-q13.2
    Sequence :
    Chromosome: 20; NC_000020.10 (43835638..43838414)
    See SEMG1 in Epigenomics, MapViewer

    Chromosome 20 - NC_000020.10Genomic Context describing neighboring genes Neighboring gene WAP four-disulfide core domain 12 Neighboring gene peptidase inhibitor 3, skin-derived Neighboring gene semenogelin II Neighboring gene secretory leukocyte peptidase inhibitor

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description
    P04279 P20151 KLK2    HPRD  PubMed  
    P04279 P07288 KLK3    HPRD  PubMed  
    P04279 P17252 PRKCA    HPRD  PubMed  
    P04279 Q02383 SEMG2    HPRD  PubMed  
    P04279 P22735 TGM1    HPRD  PubMed  
    P04279 Q9NRR5 UBQLN4    HPRD  PubMed  
    BioGRID:112306 BioGRID:112307 SEMG2    BioGRID  PubMed Affinity Capture-Western 
    BioGRID:112306 BioGRID:113164 UBC    BioGRID  PubMed Affinity Capture-MS; Reconstituted Complex 

    General gene information

    Markers

    Potential readthrough

    Included gene: SEMG2

    Pathways from BioSystems

    • Amyloids, organism-specific biosystem (from REACTOME)
      Amyloids, organism-specific biosystemAmyloid is a term used to describe typically extracellular deposits of aggregated proteins, sometimes known as plaques. Abnormal accumulation of amyloid is amyloidosis, a term associated with disease...
    • Disease, organism-specific biosystem (from REACTOME)
      Disease, organism-specific biosystemBiological processes are captured in Reactome by identifying the molecules (DNA, RNA, protein, small molecules) involved in them and describing the details of their interactions. From this molecular ...

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    structural molecule activity IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    insemination TAS
    Traceable Author Statement
    more info
    PubMed 
    sexual reproduction IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    extracellular region TAS
    Traceable Author Statement
    more info
     
    extracellular space TAS
    Traceable Author Statement
    more info
    PubMed 
    secretory granule IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    semenogelin-1
    Names
    semenogelin-1
    cancer/testis antigen 103
    semen coagulating protein

    NCBI Reference Sequences (RefSeq)

    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_003007.3NP_002998.1  semenogelin-1 preproprotein

      Status: REVIEWED

      Source sequence(s)
      AA687874, BC055416, DA874748, J04440
      Consensus CDS
      CCDS13345.1
      UniProtKB/Swiss-Prot
      P04279
      Related
      ENSP00000361867, OTTHUMP00000031098, ENST00000372781, OTTHUMT00000079416
      Conserved Domains (1) summary
      pfam05474
      Location:1462
      Blast Score: 1259
      Semenogelin; Semenogelin

    RefSeqs of Annotated Genomes: Build 37.3

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

    Reference GRCh37.p5 Primary Assembly

    Genomic

    1. NC_000020.10 Reference GRCh37.p5 Primary Assembly

      Range
      43835638..43838414
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate HuRef

    Genomic

    1. AC_000152.1 Alternate HuRef

      Range
      40577518..40580294
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_198139.1: Suppressed sequence

      Description
      NM_198139.1: This RefSeq was permanently suppressed because the transcript lacked a 180 nt repeat unit in the coding sequence compared to the reference genome sequence.

      Supplemental Content

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