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    MTCL3 MTCL family member 3 [ Homo sapiens (human) ]

    Gene ID: 387104, updated on 2-Nov-2024

    Summary

    Official Symbol
    MTCL3provided by HGNC
    Official Full Name
    MTCL family member 3provided by HGNC
    Primary source
    HGNC:HGNC:21494
    See related
    Ensembl:ENSG00000214338 AllianceGenome:HGNC:21494
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    SOGA3; C6orf174; dJ403A15.3
    Summary
    Predicted to be involved in regulation of autophagy. Predicted to be located in extracellular space and membrane. [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Biased expression in brain (RPKM 11.8), fat (RPKM 5.6) and 13 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See MTCL3 in Genome Data Viewer
    Location:
    6q22.33
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (127472974..127519335, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (128661901..128708261, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (127794119..127840480, complement)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene SOGA3-KIAA0408 readthrough Neighboring gene KIAA0408 Neighboring gene uncharacterized LOC124901399 Neighboring gene Sharpr-MPRA regulatory region 7566 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr6:127802337-127803536 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 25041 Neighboring gene uncharacterized LOC107986642 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:127835952-127836476 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17529 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17530 Neighboring gene chromosome 6 open reading frame 58 Neighboring gene uncharacterized LOC105377995

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Readthrough SOGA3-KIAA0408

    Readthrough gene: SOGA3-KIAA0408, Included gene: KIAA0408

    Gene Ontology Provided by GOA

    Process Evidence Code Pubs
    involved_in regulation of autophagy IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    located_in extracellular space IEA
    Inferred from Electronic Annotation
    more info
     
    located_in membrane IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    microtubule cross-linking factor 3
    Names
    SOGA family member 3
    protein SOGA3

    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_001400265.1NP_001387194.1  microtubule cross-linking factor 3 precursor

      Status: VALIDATED

      Source sequence(s)
      AL096711, AL583806
      Consensus CDS
      CCDS43505.1
      UniProtKB/Swiss-Prot
      Q5TF21
      Related
      ENSP00000434570.1, ENST00000525778.6

    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_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      127472974..127519335 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      128661901..128708261 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001012279.3: Suppressed sequence

      Description
      NM_001012279.3: This RefSeq was removed because currently there is insufficient support for the transcript.
    2. NM_001395923.1: Suppressed sequence

      Description
      NM_001395923.1: This RefSeq was removed because currently there is insufficient support for the transcript.
    3. NM_001395924.1: Suppressed sequence

      Description
      NM_001395924.1: This RefSeq was removed because currently there is insufficient support for the transcript.
    4. NM_001395925.1: Suppressed sequence

      Description
      NM_001395925.1: This RefSeq was removed because currently there is insufficient support for the transcript.
    5. NM_001395926.1: Suppressed sequence

      Description
      NM_001395926.1: This RefSeq was removed because currently there is insufficient support for the transcript.
    6. NM_001395928.1: Suppressed sequence

      Description
      NM_001395928.1: This RefSeq was removed because currently there is insufficient support for the transcript.
    7. NM_001395929.1: Suppressed sequence

      Description
      NM_001395929.1: This RefSeq was removed because currently there is insufficient support for the transcript.