Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MYADML2 (myeloid associated differentiation marker like 2)

Identity

Alias_symbol (synonym)LOC255275
Other alias-
HGNC (Hugo) MYADML2
LocusID (NCBI) 255275
Atlas_Id 70597
Location 17q25.3  [Link to chromosome band 17q25]
Location_base_pair Starts at 81939645 and ends at 81947233 bp from pter ( according to hg38-Dec_2013)

Note

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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)MYADML2   34548
Cards
Entrez_Gene (NCBI)MYADML2  255275  myeloid associated differentiation marker like 2
Aliases
GeneCards (Weizmann)MYADML2
Ensembl hg19 (Hinxton)ENSG00000185105 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000185105 [Gene_View]  chr17:81939645-81947233 [Contig_View]  MYADML2 [Vega]
ICGC DataPortalENSG00000185105
TCGA cBioPortalMYADML2
AceView (NCBI)MYADML2
Genatlas (Paris)MYADML2
WikiGenes255275
SOURCE (Princeton)MYADML2
Genetics Home Reference (NIH)MYADML2
Genomic and cartography
GoldenPath hg38 (UCSC)MYADML2  -     chr17:81939645-81947233 -  17q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MYADML2  -     17q25.3   [Description]    (hg19-Feb_2009)
EnsemblMYADML2 - 17q25.3 [CytoView hg19]  MYADML2 - 17q25.3 [CytoView hg38]
Mapping of homologs : NCBIMYADML2 [Mapview hg19]  MYADML2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC029306 BM674638
RefSeq transcript (Entrez)NM_001145113
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MYADML2
Cluster EST : UnigeneHs.729645 [ NCBI ]
CGAP (NCI)Hs.729645
Alternative Splicing GalleryENSG00000185105
Gene ExpressionMYADML2 [ NCBI-GEO ]   MYADML2 [ EBI - ARRAY_EXPRESS ]   MYADML2 [ SEEK ]   MYADML2 [ MEM ]
Gene Expression Viewer (FireBrowse)MYADML2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)255275
GTEX Portal (Tissue expression)MYADML2
Protein : pattern, domain, 3D structure
UniProt/SwissProtA6NDP7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA6NDP7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA6NDP7
Splice isoforms : SwissVarA6NDP7
PhosPhoSitePlusA6NDP7
Domaine pattern : Prosite (Expaxy)MARVEL (PS51225)   
Domains : Interpro (EBI)Marvel   
Domain families : Pfam (Sanger)MARVEL (PF01284)   
Domain families : Pfam (NCBI)pfam01284   
Conserved Domain (NCBI)MYADML2
DMDM Disease mutations255275
Blocks (Seattle)MYADML2
SuperfamilyA6NDP7
Human Protein AtlasENSG00000185105
Peptide AtlasA6NDP7
IPIIPI00161380   
Protein Interaction databases
DIP (DOE-UCLA)A6NDP7
IntAct (EBI)A6NDP7
FunCoupENSG00000185105
BioGRIDMYADML2
STRING (EMBL)MYADML2
ZODIACMYADML2
Ontologies - Pathways
QuickGOA6NDP7
Ontology : AmiGOcytoplasm  integral component of membrane  
Ontology : EGO-EBIcytoplasm  integral component of membrane  
NDEx NetworkMYADML2
Atlas of Cancer Signalling NetworkMYADML2
Wikipedia pathwaysMYADML2
Orthology - Evolution
OrthoDB255275
GeneTree (enSembl)ENSG00000185105
Phylogenetic Trees/Animal Genes : TreeFamMYADML2
HOVERGENA6NDP7
HOGENOMA6NDP7
Homologs : HomoloGeneMYADML2
Homology/Alignments : Family Browser (UCSC)MYADML2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMYADML2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MYADML2
dbVarMYADML2
ClinVarMYADML2
1000_GenomesMYADML2 
Exome Variant ServerMYADML2
ExAC (Exome Aggregation Consortium)MYADML2 (select the gene name)
Genetic variants : HAPMAP255275
Genomic Variants (DGV)MYADML2 [DGVbeta]
DECIPHERMYADML2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMYADML2 
Mutations
ICGC Data PortalMYADML2 
TCGA Data PortalMYADML2 
Broad Tumor PortalMYADML2
OASIS PortalMYADML2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMYADML2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMYADML2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MYADML2
DgiDB (Drug Gene Interaction Database)MYADML2
DoCM (Curated mutations)MYADML2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MYADML2 (select a term)
intoGenMYADML2
Cancer3DMYADML2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMYADML2
Genetic Testing Registry MYADML2
NextProtA6NDP7 [Medical]
TSGene255275
GENETestsMYADML2
Target ValidationMYADML2
Huge Navigator MYADML2 [HugePedia]
snp3D : Map Gene to Disease255275
BioCentury BCIQMYADML2
ClinGenMYADML2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD255275
Chemical/Pharm GKB GenePA164723246
Clinical trialMYADML2
Miscellaneous
canSAR (ICR)MYADML2 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMYADML2
EVEXMYADML2
GoPubMedMYADML2
iHOPMYADML2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed May 31 15:31:59 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.