Atlas of Genetics and Cytogenetics in Oncology and Haematology

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MYD88 (MYD88 innate immune signal transduction adaptor)


Alias (NCBI)IMD68
HGNC (Hugo) MYD88
HGNC Previous namemyeloid differentiation primary response gene (88)
 myeloid differentiation primary response 88
LocusID (NCBI) 4615
Atlas_Id 41476
Location 3p22.2  [Link to chromosome band 3p22]
Location_base_pair Starts at 38138661 and ends at 38143021 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
MYD88 (3p22.2) / ARHGEF10L (1p36.13)MYD88 (3p22.2) / INO80B (2p13.1)MYD88 (3p22.2) / MYLK (3q21.1)
NEURL1B (5q35.1) / MYD88 (3p22.2)


Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute



Other Leukemias implicated (Data extracted from papers in the Atlas) [ 6 ]
  B-cell Prolymphocytic Leukemia
Primary DLBCL of the central nervous system (CNS)
Gamma heavy chain disease
Ocular adnexal marginal zone lymphoma (OAMZL)
Primary Cutaneous B-Cell Lymphomas
Waldenstrom macroglobulinemia

External links

HGNC (Hugo)MYD88   7562
LRG (Locus Reference Genomic)LRG_157
Entrez_Gene (NCBI)MYD88    MYD88 innate immune signal transduction adaptor
AliasesIMD68; MYD88D
GeneCards (Weizmann)MYD88
Ensembl hg19 (Hinxton)ENSG00000172936 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000172936 [Gene_View]  ENSG00000172936 [Sequence]  chr3:38138661-38143021 [Contig_View]  MYD88 [Vega]
ICGC DataPortalENSG00000172936
TCGA cBioPortalMYD88
AceView (NCBI)MYD88
Genatlas (Paris)MYD88
SOURCE (Princeton)MYD88
Genetics Home Reference (NIH)MYD88
Genomic and cartography
GoldenPath hg38 (UCSC)MYD88  -     chr3:38138661-38143021 +  3p22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MYD88  -     3p22.2   [Description]    (hg19-Feb_2009)
GoldenPathMYD88 - 3p22.2 [CytoView hg19]  MYD88 - 3p22.2 [CytoView hg38]
Genome Data Viewer NCBIMYD88 [Mapview hg19]  
OMIM153600   602170   612260   
Gene and transcription
Genbank (Entrez)AB446470 AK097983 AK124685 AK296570 AK296716
RefSeq transcript (Entrez)NM_001172566 NM_001172567 NM_001172568 NM_001172569 NM_001365876 NM_001365877 NM_001374787 NM_001374788 NM_002468
Consensus coding sequences : CCDS (NCBI)MYD88
Gene ExpressionMYD88 [ NCBI-GEO ]   MYD88 [ EBI - ARRAY_EXPRESS ]   MYD88 [ SEEK ]   MYD88 [ MEM ]
Gene Expression Viewer (FireBrowse)MYD88 [ Firebrowse - Broad ]
GenevisibleExpression of MYD88 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)4615
GTEX Portal (Tissue expression)MYD88
Human Protein AtlasENSG00000172936-MYD88 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MYD88
Human Protein Atlas [tissue]ENSG00000172936-MYD88 [tissue]
Protein Interaction databases
Ontologies - Pathways
PubMed499 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:21:43 CEST 2021

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