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ADM2 (adrenomedullin 2)

Identity

Alias_symbol (synonym)AM2
FLJ21135
Other aliasdJ579N16.4
HGNC (Hugo) ADM2
LocusID (NCBI) 79924
Atlas_Id 51044
Location 22q13.33  [Link to chromosome band 22q13]
Location_base_pair Starts at 50920153 and ends at 50924866 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
ADM2 (22q13.33) / MIOX (22q13.33)

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)ADM2   28898
Cards
Entrez_Gene (NCBI)ADM2  79924  adrenomedullin 2
AliasesAM2; dJ579N16.4
GeneCards (Weizmann)ADM2
Ensembl hg19 (Hinxton)ENSG00000128165 [Gene_View]  chr22:50920153-50924866 [Contig_View]  ADM2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000128165 [Gene_View]  chr22:50920153-50924866 [Contig_View]  ADM2 [Vega]
ICGC DataPortalENSG00000128165
TCGA cBioPortalADM2
AceView (NCBI)ADM2
Genatlas (Paris)ADM2
WikiGenes79924
SOURCE (Princeton)ADM2
Genetics Home Reference (NIH)ADM2
Genomic and cartography
GoldenPath hg19 (UCSC)ADM2  -     chr22:50920153-50924866 +  22q13.33   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ADM2  -     22q13.33   [Description]    (hg38-Dec_2013)
EnsemblADM2 - 22q13.33 [CytoView hg19]  ADM2 - 22q13.33 [CytoView hg38]
Mapping of homologs : NCBIADM2 [Mapview hg19]  ADM2 [Mapview hg38]
OMIM608682   
Gene and transcription
Genbank (Entrez)AB121034 AB236970 AF529213 AK024788 AK090635
RefSeq transcript (Entrez)NM_001253845 NM_024866
RefSeq genomic (Entrez)NC_000022 NC_018933 NT_011526 NW_004929431
Consensus coding sequences : CCDS (NCBI)ADM2
Cluster EST : UnigeneHs.743540 [ NCBI ]
CGAP (NCI)Hs.743540
Alternative Splicing GalleryENSG00000128165
Gene ExpressionADM2 [ NCBI-GEO ]   ADM2 [ EBI - ARRAY_EXPRESS ]   ADM2 [ SEEK ]   ADM2 [ MEM ]
Gene Expression Viewer (FireBrowse)ADM2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)79924
GTEX Portal (Tissue expression)ADM2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ7Z4H4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ7Z4H4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ7Z4H4
Splice isoforms : SwissVarQ7Z4H4
PhosPhoSitePlusQ7Z4H4
Domains : Interpro (EBI)Calcitonin/adrenomedullin   
Domain families : Pfam (Sanger)Calc_CGRP_IAPP (PF00214)   
Domain families : Pfam (NCBI)pfam00214   
Conserved Domain (NCBI)ADM2
DMDM Disease mutations79924
Blocks (Seattle)ADM2
SuperfamilyQ7Z4H4
Human Protein AtlasENSG00000128165
Peptide AtlasQ7Z4H4
HPRD10563
IPIIPI00385109   IPI00550423   IPI00980929   
Protein Interaction databases
DIP (DOE-UCLA)Q7Z4H4
IntAct (EBI)Q7Z4H4
FunCoupENSG00000128165
BioGRIDADM2
STRING (EMBL)ADM2
ZODIACADM2
Ontologies - Pathways
QuickGOQ7Z4H4
Ontology : AmiGOangiogenesis  hormone activity  extracellular region  protein phosphorylation  adenylate cyclase-activating G-protein coupled receptor signaling pathway  digestion  feeding behavior  positive regulation of gene expression  protein complex binding  positive regulation of angiogenesis  negative regulation of blood pressure  
Ontology : EGO-EBIangiogenesis  hormone activity  extracellular region  protein phosphorylation  adenylate cyclase-activating G-protein coupled receptor signaling pathway  digestion  feeding behavior  positive regulation of gene expression  protein complex binding  positive regulation of angiogenesis  negative regulation of blood pressure  
NDEx NetworkADM2
Atlas of Cancer Signalling NetworkADM2
Wikipedia pathwaysADM2
Orthology - Evolution
OrthoDB79924
GeneTree (enSembl)ENSG00000128165
Phylogenetic Trees/Animal Genes : TreeFamADM2
HOVERGENQ7Z4H4
HOGENOMQ7Z4H4
Homologs : HomoloGeneADM2
Homology/Alignments : Family Browser (UCSC)ADM2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerADM2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ADM2
dbVarADM2
ClinVarADM2
1000_GenomesADM2 
Exome Variant ServerADM2
ExAC (Exome Aggregation Consortium)ADM2 (select the gene name)
Genetic variants : HAPMAP79924
Genomic Variants (DGV)ADM2 [DGVbeta]
DECIPHER (Syndromes)22:50920153-50924866  ENSG00000128165
CONAN: Copy Number AnalysisADM2 
Mutations
ICGC Data PortalADM2 
TCGA Data PortalADM2 
Broad Tumor PortalADM2
OASIS PortalADM2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICADM2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDADM2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ADM2
DgiDB (Drug Gene Interaction Database)ADM2
DoCM (Curated mutations)ADM2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ADM2 (select a term)
intoGenADM2
Cancer3DADM2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM608682   
Orphanet
MedgenADM2
Genetic Testing Registry ADM2
NextProtQ7Z4H4 [Medical]
TSGene79924
GENETestsADM2
Huge Navigator ADM2 [HugePedia]
snp3D : Map Gene to Disease79924
BioCentury BCIQADM2
ClinGenADM2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD79924
Chemical/Pharm GKB GenePA134898869
Clinical trialADM2
Miscellaneous
canSAR (ICR)ADM2 (select the gene name)
Probes
Litterature
PubMed39 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineADM2
EVEXADM2
GoPubMedADM2
iHOPADM2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:55:06 CET 2017

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