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    MAL mal, T cell differentiation protein [ Homo sapiens (human) ]

    Gene ID: 4118, updated on 10-Dec-2024

    Summary

    Official Symbol
    MALprovided by HGNC
    Official Full Name
    mal, T cell differentiation proteinprovided by HGNC
    Primary source
    HGNC:HGNC:6817
    See related
    Ensembl:ENSG00000172005 MIM:188860; AllianceGenome:HGNC:6817
    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
    HLD28; MVP17; VIP17
    Summary
    The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012]
    Annotation information
    Note: MAL (Gene ID: 4118), TIRAP (Gene ID: 114609), and MKL1 (Gene ID: 57591) share the MAL symbol/alias in common. MAL is a widely used alternative name for TIR domain containing adaptor protein (TIRAP) and megakaryoblastic leukemia (translocation) 1 (MKL1). [23 May 2018]
    Expression
    Biased expression in esophagus (RPKM 937.0) and kidney (RPKM 115.6) See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See MAL in Genome Data Viewer
    Location:
    2q11.1
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (95025708..95053992)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (95532209..95560493)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (95691453..95719737)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105373487 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:95660342-95660890 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:95660891-95661438 Neighboring gene RNA, 7SL, cytoplasmic 575, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16180 Neighboring gene MAL antisense RNA 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:95687830-95688330 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11737 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:95691837-95692560 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:95697485-95698400 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11738 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:95709333-95709988 Neighboring gene uncharacterized LOC124906047 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:95713447-95713986 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16181 Neighboring gene uncharacterized LOC124907857 Neighboring gene uncharacterized LOC105373488 Neighboring gene NANOG hESC enhancer GRCh37_chr2:95753198-95753763 Neighboring gene mitochondrial ribosomal protein S5 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11739

    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?

    HIV-1 interactions

    Protein interactions

    Protein Gene Interaction Pubs
    Nef nef HIV-1 Nef interacts with MAL-dependent pathway to enhance exosome release PubMed

    Go to the HIV-1, Human Interaction Database

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables lipid binding TAS
    Traceable Author Statement
    more info
    PubMed 
    enables peptidase activator activity involved in apoptotic process NAS
    Non-traceable Author Statement
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables structural constituent of myelin sheath IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables structural constituent of myelin sheath IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in Schmidt-Lanterman incisure IEA
    Inferred from Electronic Annotation
    more info
     
    located_in apical plasma membrane TAS
    Traceable Author Statement
    more info
    PubMed 
    located_in endoplasmic reticulum IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in hinge region between urothelial plaques of apical plasma membrane IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in membrane raft IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in plasma membrane raft IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    myelin and lymphocyte protein
    Names
    T-lymphocyte maturation-associated protein

    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_002371.4NP_002362.1  myelin and lymphocyte protein isoform a

      See identical proteins and their annotated locations for NP_002362.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (a) includes both alternatively spliced exons 2 and 3, resulting in the longest isoform (a).
      Source sequence(s)
      BC000458, DT215613, X76678
      Consensus CDS
      CCDS2006.1
      UniProtKB/Swiss-Prot
      P21145, Q6FH77
      Related
      ENSP00000310880.4, ENST00000309988.9
      Conserved Domains (1) summary
      pfam01284
      Location:19145
      MARVEL; Membrane-associating domain
    2. NM_022438.3NP_071883.1  myelin and lymphocyte protein isoform b

      See identical proteins and their annotated locations for NP_071883.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (b) includes alternatively spliced exon 2 but is missing exon 3, resulting in isoform b which is shorter than the predominant isoform (a).
      Source sequence(s)
      BC000458, DT215613, X76679
      Consensus CDS
      CCDS2007.1
      UniProtKB/Swiss-Prot
      P21145
      Related
      ENSP00000306568.4, ENST00000353004.7
    3. NM_022439.3NP_071884.1  myelin and lymphocyte protein isoform c

      See identical proteins and their annotated locations for NP_071884.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (c) is missing alternatively spliced exon 2 but includes exon 3, resulting in isoform c which is shorter than the predominant isoform (a).
      Source sequence(s)
      BC000458, DT215613, X76680
      Consensus CDS
      CCDS2008.1
      UniProtKB/Swiss-Prot
      P21145
      Related
      ENSP00000304924.3, ENST00000354078.7
      Conserved Domains (1) summary
      cl04571
      Location:3189
      MARVEL; Membrane-associating domain
    4. NM_022440.3NP_071885.1  myelin and lymphocyte protein isoform d

      See identical proteins and their annotated locations for NP_071885.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (d) is missing alternatively spliced exons 2 and 3, resulting in the shortest isoform (d).
      Source sequence(s)
      BC000458, DT215613, X76681
      Consensus CDS
      CCDS2009.1
      UniProtKB/Swiss-Prot
      P21145
      Related
      ENSP00000322860.3, ENST00000349807.3

    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_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      95025708..95053992
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      95532209..95560493
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)