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ARMH4 (armadillo like helical domain containing 4)

Identity

Alias (NCBI)C14orf37
UT2
c14_5376
HGNC (Hugo) ARMH4
LocusID (NCBI) 145407
Atlas_Id 80373
Location 14q23.1  [Link to chromosome band 14q23]
Location_base_pair Starts at 58116116 and ends at 58152213 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)
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



External links

 

Nomenclature
HGNC (Hugo)ARMH4   19846
Cards
Entrez_Gene (NCBI)ARMH4    armadillo like helical domain containing 4
AliasesC14orf37; UT2; c14_5376
GeneCards (Weizmann)ARMH4
Ensembl hg19 (Hinxton)ENSG00000139971 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000139971 [Gene_View]  ENSG00000139971 [Sequence]  chr14:58116116-58152213 [Contig_View]  ARMH4 [Vega]
ICGC DataPortalENSG00000139971
TCGA cBioPortalARMH4
AceView (NCBI)ARMH4
Genatlas (Paris)ARMH4
SOURCE (Princeton)ARMH4
Genetics Home Reference (NIH)ARMH4
Genomic and cartography
GoldenPath hg38 (UCSC)ARMH4  -     chr14:58116116-58152213 -  14q23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ARMH4  -     14q23.1   [Description]    (hg19-Feb_2009)
GoldenPathARMH4 - 14q23.1 [CytoView hg19]  ARMH4 - 14q23.1 [CytoView hg38]
ImmunoBaseENSG00000139971
Genome Data Viewer NCBIARMH4 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK292513 AK292605 AK294599 BC013707 BC031314
RefSeq transcript (Entrez)NM_001001872 NM_001320173
Consensus coding sequences : CCDS (NCBI)ARMH4
Gene ExpressionARMH4 [ NCBI-GEO ]   ARMH4 [ EBI - ARRAY_EXPRESS ]   ARMH4 [ SEEK ]   ARMH4 [ MEM ]
Gene Expression Viewer (FireBrowse)ARMH4 [ Firebrowse - Broad ]
GenevisibleExpression of ARMH4 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)145407
GTEX Portal (Tissue expression)ARMH4
Human Protein AtlasENSG00000139971-ARMH4 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ86TY3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ86TY3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ86TY3
PhosPhoSitePlusQ86TY3
Domains : Interpro (EBI)ARMH4   
Domain families : Pfam (Sanger)DUF4696 (PF15767)   
Domain families : Pfam (NCBI)pfam15767   
Conserved Domain (NCBI)ARMH4
SuperfamilyQ86TY3
AlphaFold pdb e-kbQ86TY3   
Human Protein Atlas [tissue]ENSG00000139971-ARMH4 [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q86TY3
IntAct (EBI)Q86TY3
BioGRIDARMH4
STRING (EMBL)ARMH4
ZODIACARMH4
Ontologies - Pathways
QuickGOQ86TY3
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkARMH4
Atlas of Cancer Signalling NetworkARMH4
Wikipedia pathwaysARMH4
Orthology - Evolution
OrthoDB145407
GeneTree (enSembl)ENSG00000139971
Phylogenetic Trees/Animal Genes : TreeFamARMH4
Homologs : HomoloGeneARMH4
Homology/Alignments : Family Browser (UCSC)ARMH4
Gene fusions - Rearrangements
Fusion : QuiverARMH4
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerARMH4 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ARMH4
dbVarARMH4
ClinVarARMH4
MonarchARMH4
1000_GenomesARMH4 
Exome Variant ServerARMH4
GNOMAD BrowserENSG00000139971
Varsome BrowserARMH4
ACMGARMH4 variants
VarityQ86TY3
Genomic Variants (DGV)ARMH4 [DGVbeta]
DECIPHERARMH4 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisARMH4 
Mutations
ICGC Data PortalARMH4 
TCGA Data PortalARMH4 
Broad Tumor PortalARMH4
OASIS PortalARMH4 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICARMH4  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DARMH4
Mutations and Diseases : HGMDARMH4
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaARMH4
DgiDB (Drug Gene Interaction Database)ARMH4
DoCM (Curated mutations)ARMH4
CIViC (Clinical Interpretations of Variants in Cancer)ARMH4
Cancer3DARMH4
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETARMH4
MedgenARMH4
Genetic Testing Registry ARMH4
NextProtQ86TY3 [Medical]
GENETestsARMH4
Target ValidationARMH4
Huge Navigator ARMH4 [HugePedia]
ClinGenARMH4
Clinical trials, drugs, therapy
MyCancerGenomeARMH4
Protein Interactions : CTDARMH4
Pharm GKB GenePA134941886
PharosQ86TY3
Clinical trialARMH4
Miscellaneous
canSAR (ICR)ARMH4
HarmonizomeARMH4
DataMed IndexARMH4
Probes
Litterature
PubMed11 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXARMH4
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 15:42:38 CEST 2021

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