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ERMN (ermin)

Identity

Alias (NCBI)JN
KIAA1189
HGNC (Hugo) ERMN
HGNC Alias symbJN
ERMIN
HGNC Alias namejuxtanodin
HGNC Previous nameKIAA1189
HGNC Previous nameKIAA1189
 ermin, ERM-like protein
LocusID (NCBI) 57471
Atlas_Id 62897
Location 2q24.1  [Link to chromosome band 2q24]
Location_base_pair Starts at 157318631 and ends at 157325824 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)
ERMN (2q24.1) / SEPT8 (5q31.1)TAF1D (11q21) / ERMN (2q24.1)

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)ERMN   29208
Cards
Entrez_Gene (NCBI)ERMN    ermin
AliasesJN; KIAA1189
GeneCards (Weizmann)ERMN
Ensembl hg19 (Hinxton)ENSG00000136541 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000136541 [Gene_View]  ENSG00000136541 [Sequence]  chr2:157318631-157325824 [Contig_View]  ERMN [Vega]
ICGC DataPortalENSG00000136541
TCGA cBioPortalERMN
AceView (NCBI)ERMN
Genatlas (Paris)ERMN
SOURCE (Princeton)ERMN
Genetics Home Reference (NIH)ERMN
Genomic and cartography
GoldenPath hg38 (UCSC)ERMN  -     chr2:157318631-157325824 -  2q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ERMN  -     2q24.1   [Description]    (hg19-Feb_2009)
GoldenPathERMN - 2q24.1 [CytoView hg19]  ERMN - 2q24.1 [CytoView hg38]
ImmunoBaseENSG00000136541
Genome Data Viewer NCBIERMN [Mapview hg19]  
OMIM610072   
Gene and transcription
Genbank (Entrez)AA736604 AB033015 AI207881 AK295051 AK295844
RefSeq transcript (Entrez)NM_001009959 NM_001304344 NM_001304345 NM_001304346 NM_020711
Consensus coding sequences : CCDS (NCBI)ERMN
Gene ExpressionERMN [ NCBI-GEO ]   ERMN [ EBI - ARRAY_EXPRESS ]   ERMN [ SEEK ]   ERMN [ MEM ]
Gene Expression Viewer (FireBrowse)ERMN [ Firebrowse - Broad ]
GenevisibleExpression of ERMN in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57471
GTEX Portal (Tissue expression)ERMN
Human Protein AtlasENSG00000136541-ERMN [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8TAM6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8TAM6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8TAM6
PhosPhoSitePlusQ8TAM6
Domains : Interpro (EBI)Moesin_tail_sf   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)ERMN
SuperfamilyQ8TAM6
AlphaFold pdb e-kbQ8TAM6   
Human Protein Atlas [tissue]ENSG00000136541-ERMN [tissue]
HPRD13838
Protein Interaction databases
DIP (DOE-UCLA)Q8TAM6
IntAct (EBI)Q8TAM6
BioGRIDERMN
STRING (EMBL)ERMN
ZODIACERMN
Ontologies - Pathways
QuickGOQ8TAM6
Ontology : AmiGOmorphogenesis of a branching structure  protein binding  cytoplasm  cytoskeleton  cell cortex  cell cortex  actin filament organization  actin filament organization  regulation of cell shape  regulation of cell shape  filopodium  regulation of cell projection organization  regulation of cell projection organization  internode region of axon  internode region of axon  paranode region of axon  paranode region of axon  neuronal cell body  myelin sheath  actin filament binding  extracellular exosome  
Ontology : EGO-EBImorphogenesis of a branching structure  protein binding  cytoplasm  cytoskeleton  cell cortex  cell cortex  actin filament organization  actin filament organization  regulation of cell shape  regulation of cell shape  filopodium  regulation of cell projection organization  regulation of cell projection organization  internode region of axon  internode region of axon  paranode region of axon  paranode region of axon  neuronal cell body  myelin sheath  actin filament binding  extracellular exosome  
NDEx NetworkERMN
Atlas of Cancer Signalling NetworkERMN
Wikipedia pathwaysERMN
Orthology - Evolution
OrthoDB57471
GeneTree (enSembl)ENSG00000136541
Phylogenetic Trees/Animal Genes : TreeFamERMN
Homologs : HomoloGeneERMN
Homology/Alignments : Family Browser (UCSC)ERMN
Gene fusions - Rearrangements
Fusion : QuiverERMN
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerERMN [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ERMN
dbVarERMN
ClinVarERMN
MonarchERMN
1000_GenomesERMN 
Exome Variant ServerERMN
GNOMAD BrowserENSG00000136541
Varsome BrowserERMN
ACMGERMN variants
VarityQ8TAM6
Genomic Variants (DGV)ERMN [DGVbeta]
DECIPHERERMN [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisERMN 
Mutations
ICGC Data PortalERMN 
TCGA Data PortalERMN 
Broad Tumor PortalERMN
OASIS PortalERMN [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICERMN  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DERMN
Mutations and Diseases : HGMDERMN
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaERMN
DgiDB (Drug Gene Interaction Database)ERMN
DoCM (Curated mutations)ERMN
CIViC (Clinical Interpretations of Variants in Cancer)ERMN
Cancer3DERMN
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM610072   
Orphanet
DisGeNETERMN
MedgenERMN
Genetic Testing Registry ERMN
NextProtQ8TAM6 [Medical]
GENETestsERMN
Target ValidationERMN
Huge Navigator ERMN [HugePedia]
ClinGenERMN
Clinical trials, drugs, therapy
MyCancerGenomeERMN
Protein Interactions : CTDERMN
Pharm GKB GenePA162385355
PharosQ8TAM6
Clinical trialERMN
Miscellaneous
canSAR (ICR)ERMN
HarmonizomeERMN
DataMed IndexERMN
Probes
Litterature
PubMed18 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXERMN
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 15:49:06 CEST 2021

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