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

UNC93A (unc-93 homolog A)

Identity

Alias_namesunc93 (C.elegans) homolog A
Alias_symbol (synonym)dJ366N23.2
dJ366N23.1
Other aliasUnc-93A
HGNC (Hugo) UNC93A
LocusID (NCBI) 54346
Atlas_Id 42766
Location 6q27  [Link to chromosome band 6q27]
Location_base_pair Starts at 167291315 and ends at 167316014 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)
MLLT4 (6q27) / UNC93A (6q27)MLLT4 6q27 / UNC93A 6q27

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)UNC93A   12570
Cards
Entrez_Gene (NCBI)UNC93A  54346  unc-93 homolog A
AliasesUnc-93A; dJ366N23.1; dJ366N23.2
GeneCards (Weizmann)UNC93A
Ensembl hg19 (Hinxton)ENSG00000112494 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000112494 [Gene_View]  ENSG00000112494 [Sequence]  chr6:167291315-167316014 [Contig_View]  UNC93A [Vega]
ICGC DataPortalENSG00000112494
TCGA cBioPortalUNC93A
AceView (NCBI)UNC93A
Genatlas (Paris)UNC93A
WikiGenes54346
SOURCE (Princeton)UNC93A
Genetics Home Reference (NIH)UNC93A
Genomic and cartography
GoldenPath hg38 (UCSC)UNC93A  -     chr6:167291315-167316014 +  6q27   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)UNC93A  -     6q27   [Description]    (hg19-Feb_2009)
EnsemblUNC93A - 6q27 [CytoView hg19]  UNC93A - 6q27 [CytoView hg38]
Mapping of homologs : NCBIUNC93A [Mapview hg19]  UNC93A [Mapview hg38]
OMIM607995   
Gene and transcription
Genbank (Entrez)AJ422141 AJ508812 AK091987 BC098248 BC099718
RefSeq transcript (Entrez)NM_001143947 NM_018974
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)UNC93A
Cluster EST : UnigeneHs.567508 [ NCBI ]
CGAP (NCI)Hs.567508
Alternative Splicing GalleryENSG00000112494
Gene ExpressionUNC93A [ NCBI-GEO ]   UNC93A [ EBI - ARRAY_EXPRESS ]   UNC93A [ SEEK ]   UNC93A [ MEM ]
Gene Expression Viewer (FireBrowse)UNC93A [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)54346
GTEX Portal (Tissue expression)UNC93A
Human Protein AtlasENSG00000112494-UNC93A [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ86WB7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ86WB7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ86WB7
Splice isoforms : SwissVarQ86WB7
PhosPhoSitePlusQ86WB7
Domains : Interpro (EBI)Ion_channel_UNC-93    MFS_dom    MFS_trans_sf   
Domain families : Pfam (Sanger)UNC-93 (PF05978)   
Domain families : Pfam (NCBI)pfam05978   
Conserved Domain (NCBI)UNC93A
DMDM Disease mutations54346
Blocks (Seattle)UNC93A
SuperfamilyQ86WB7
Human Protein Atlas [tissue]ENSG00000112494-UNC93A [tissue]
Peptide AtlasQ86WB7
HPRD12148
IPIIPI00215932   IPI00607755   IPI00964160   
Protein Interaction databases
DIP (DOE-UCLA)Q86WB7
IntAct (EBI)Q86WB7
FunCoupENSG00000112494
BioGRIDUNC93A
STRING (EMBL)UNC93A
ZODIACUNC93A
Ontologies - Pathways
QuickGOQ86WB7
Ontology : AmiGOmolecular_function  plasma membrane  biological_process  integral component of membrane  
Ontology : EGO-EBImolecular_function  plasma membrane  biological_process  integral component of membrane  
NDEx NetworkUNC93A
Atlas of Cancer Signalling NetworkUNC93A
Wikipedia pathwaysUNC93A
Orthology - Evolution
OrthoDB54346
GeneTree (enSembl)ENSG00000112494
Phylogenetic Trees/Animal Genes : TreeFamUNC93A
HOVERGENQ86WB7
HOGENOMQ86WB7
Homologs : HomoloGeneUNC93A
Homology/Alignments : Family Browser (UCSC)UNC93A
Gene fusions - Rearrangements
Fusion PortalMLLT4 6q27 UNC93A 6q27 OV
Fusion : QuiverUNC93A
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerUNC93A [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)UNC93A
dbVarUNC93A
ClinVarUNC93A
1000_GenomesUNC93A 
Exome Variant ServerUNC93A
ExAC (Exome Aggregation Consortium)ENSG00000112494
GNOMAD BrowserENSG00000112494
Varsome BrowserUNC93A
Genetic variants : HAPMAP54346
Genomic Variants (DGV)UNC93A [DGVbeta]
DECIPHERUNC93A [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisUNC93A 
Mutations
ICGC Data PortalUNC93A 
TCGA Data PortalUNC93A 
Broad Tumor PortalUNC93A
OASIS PortalUNC93A [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICUNC93A  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDUNC93A
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 UNC93A
DgiDB (Drug Gene Interaction Database)UNC93A
DoCM (Curated mutations)UNC93A (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)UNC93A (select a term)
intoGenUNC93A
Cancer3DUNC93A(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607995   
Orphanet
DisGeNETUNC93A
MedgenUNC93A
Genetic Testing Registry UNC93A
NextProtQ86WB7 [Medical]
TSGene54346
GENETestsUNC93A
Target ValidationUNC93A
Huge Navigator UNC93A [HugePedia]
snp3D : Map Gene to Disease54346
BioCentury BCIQUNC93A
ClinGenUNC93A
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD54346
Chemical/Pharm GKB GenePA37207
Clinical trialUNC93A
Miscellaneous
canSAR (ICR)UNC93A (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineUNC93A
EVEXUNC93A
GoPubMedUNC93A
iHOPUNC93A
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 : Tue Nov 6 11:48:43 CET 2018

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.