U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from GEO Profiles

    • Showing Current items.

    MRTFA myocardin related transcription factor A [ Homo sapiens (human) ]

    Gene ID: 57591, updated on 27-Nov-2024

    Summary

    Official Symbol
    MRTFAprovided by HGNC
    Official Full Name
    myocardin related transcription factor Aprovided by HGNC
    Primary source
    HGNC:HGNC:14334
    See related
    Ensembl:ENSG00000196588 MIM:606078; AllianceGenome:HGNC:14334
    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
    MAL; MKL; BSAC; MKL1; MRTF-A
    Summary
    The protein encoded by this gene interacts with the transcription factor myocardin, a key regulator of smooth muscle cell differentiation. The encoded protein is predominantly nuclear and may help transduce signals from the cytoskeleton to the nucleus. This gene is involved in a specific translocation event that creates a fusion of this gene and the RNA-binding motif protein-15 gene. This translocation has been associated with acute megakaryocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
    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
    Ubiquitous expression in bone marrow (RPKM 14.0), testis (RPKM 9.1) and 25 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See MRTFA in Genome Data Viewer
    Location:
    22q13.1-q13.2
    Exon count:
    16
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (40410289..40636719, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (40880672..41108683, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (40806293..41032723, complement)

    Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene trinucleotide repeat containing adaptor 6B Neighboring gene uncharacterized LOC124905121 Neighboring gene MPRA-validated peak4496 silencer Neighboring gene ReSE screen-validated silencer GRCh37_chr22:40740204-40740376 Neighboring gene H3K27ac hESC enhancer GRCh37_chr22:40742019-40742532 Neighboring gene H3K27ac hESC enhancer GRCh37_chr22:40742533-40743046 Neighboring gene H3K27ac hESC enhancer GRCh37_chr22:40743047-40743559 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13769 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13770 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19084 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19085 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19086 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13771 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19087 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19088 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr22:40812395-40812894 Neighboring gene adenylosuccinate lyase Neighboring gene small G protein signaling modulator 3 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19092 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19091 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19089 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19090 Neighboring gene ReSE screen-validated silencer GRCh37_chr22:40851734-40851957 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19093 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:40867879-40868537 Neighboring gene H3K27ac hESC enhancer GRCh37_chr22:40894439-40894938 Neighboring gene H3K27ac hESC enhancer GRCh37_chr22:40906589-40907133 Neighboring gene MRTFA antisense RNA 1 Neighboring gene uncharacterized LOC105373037 Neighboring gene Sharpr-MPRA regulatory region 11047 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19095 Neighboring gene cytochrome c oxidase subunit 6B1 pseudogene 3 Neighboring gene Sharpr-MPRA regulatory region 12345 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13772 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19096 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr22:41033797-41034996 Neighboring gene ribosomal protein L4 pseudogene 6 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr22:41047623-41048822 Neighboring gene uncharacterized LOC124905122 Neighboring gene CRISPRi-validated cis-regulatory element chr22.2152 Neighboring gene uncharacterized LOC124905123 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr22:41060823-41061338 Neighboring gene glyceraldehyde 3 phosphate dehydrogenase pseudogene 37

    Genomic regions, transcripts, and products

    Expression

    • Project title: 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

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    Associated conditions

    Description Tests
    Immunodeficiency 66
    MedGen: C5394265 OMIM: 618847 GeneReviews: Not available
    not available

    EBI GWAS Catalog

    Description
    A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
    EBI GWAS Catalog
    A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
    EBI GWAS Catalog
    Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis.
    EBI GWAS Catalog
    Genome-wide association studies identify four ER negative-specific breast cancer risk loci.
    EBI GWAS Catalog
    Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk.
    EBI GWAS Catalog
    Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables actin binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables actin monomer binding ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables leucine zipper domain binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables transcription coactivator activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables transcription coactivator activity IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    enables transcription coactivator activity ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    Component Evidence Code Pubs
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytosol IDA
    Inferred from Direct Assay
    more info
     
    located_in cytosol TAS
    Traceable Author Statement
    more info
     
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
     
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
     
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    myocardin-related transcription factor A
    Names
    MKL/myocardin-like protein 1
    alternative protein MKL1
    basic, SAP and coiled-coil domain
    megakaryoblastic leukemia (translocation) 1
    megakaryoblastic leukemia 1 protein
    megakaryocytic acute leukemia 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.

    Genomic

    1. NG_065810.1 RefSeqGene

      Range
      5001..231431
      Download
      GenBank, FASTA, Sequence Viewer (Graphics), LRG_1427

    mRNA and Protein(s)

    1. NM_001282660.2NP_001269589.1  myocardin-related transcription factor A isoform 1

      See identical proteins and their annotated locations for NP_001269589.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR, lacks a portion of the 5' coding region and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (1) has a shorter N-terminus, compared to isoform 5.
      Source sequence(s)
      AJ297257, BC115039, BG716386
      Consensus CDS
      CCDS14003.1
      UniProtKB/Swiss-Prot
      Q8TCL1, Q969V6, Q96SC5, Q96SC6, Q9P2B0
      UniProtKB/TrEMBL
      A0A087WU73
      Related
      ENSP00000385835.1, ENST00000407029.7
      Conserved Domains (2) summary
      smart00707
      Location:2449
      RPEL; Repeat in Drosophila CG10860, human KIAA0680 and C. elegans F26H9.2
      pfam02037
      Location:347380
      SAP; SAP domain
    2. NM_001282661.3NP_001269590.2  myocardin-related transcription factor A isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) lacks an alternate in-frame exon in the 5' coding region compared to variant 1. The encoded isoform (2) is shorter than isoform 5.
      Source sequence(s)
      BC021586, BC064620, BC115039, Z86090
      Consensus CDS
      CCDS74865.2
      UniProtKB/TrEMBL
      A0A087WU73, B0QY83
      Related
      ENSP00000385584.3, ENST00000402042.7
      Conserved Domains (3) summary
      smart00707
      Location:124149
      RPEL; Repeat in Drosophila CG10860, human KIAA0680 and C. elegans F26H9.2
      pfam02037
      Location:397430
      SAP; SAP domain
      cl28310
      Location:383525
      Rho; Transcription termination factor Rho [Transcription]
    3. NM_001282662.3NP_001269591.2  myocardin-related transcription factor A isoform 3

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) uses an alternate splice site in the 3' coding region, which results in a frameshift and an early stop codon compared to variant 1. The encoded isoform (3) has a shorter and distinct C-terminus compared to isoform 5.
      Source sequence(s)
      AF368061, BC115039, Z86090
      Consensus CDS
      CCDS74866.2
      UniProtKB/TrEMBL
      A0A087X287, A0A494BZX7, A4FUJ8
      Related
      ENSP00000498277.2, ENST00000651595.2
      Conserved Domains (2) summary
      smart00707
      Location:124149
      RPEL; Repeat in Drosophila CG10860, human KIAA0680 and C. elegans F26H9.2
      pfam02037
      Location:447480
      SAP; SAP domain
    4. NM_001318139.2NP_001305068.1  myocardin-related transcription factor A isoform 4

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5) differs in the 5' UTR and 5' coding region and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (1) has a shorter and distinct N-terminus, compared to isoform 5.
      Source sequence(s)
      HG764171
      Consensus CDS
      CCDS82720.1
      UniProtKB/TrEMBL
      A0A087WU73, W0Z7M9
      Related
      ENSP00000498671.1, ENST00000652095.2
      Conserved Domains (2) summary
      smart00707
      Location:5984
      RPEL; Repeat in Drosophila CG10860, human KIAA0680 and C. elegans F26H9.2
      pfam02037
      Location:382415
      SAP; SAP domain
    5. NM_020831.6NP_065882.2  myocardin-related transcription factor A isoform 5

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes the longest isoform (5).
      Source sequence(s)
      AL022238, AL031594, Z86090
      Consensus CDS
      CCDS93172.1
      UniProtKB/TrEMBL
      A0A087WU73, A0A499FIJ6
      Related
      ENSP00000347847.5, ENST00000355630.10
      Conserved Domains (3) summary
      smart00707
      Location:124149
      RPEL; Repeat in Drosophila CG10860, human KIAA0680 and C. elegans F26H9.2
      pfam02037
      Location:447480
      SAP; SAP domain
      cl28310
      Location:433575
      Rho; Transcription termination factor Rho [Transcription]

    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_000022.11 Reference GRCh38.p14 Primary Assembly

      Range
      40410289..40636719 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060946.1 Alternate T2T-CHM13v2.0

      Range
      40880672..41108683 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)