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MANBAL (mannosidase beta like)

Identity

Alias_namesmannosidase, beta A, lysosomal-like
mannosidase beta A like
Alias_symbol (synonym)dJ1141E15.2
Other alias-
HGNC (Hugo) MANBAL
LocusID (NCBI) 63905
Atlas_Id 68782
Location 20q11.23  [Link to chromosome band 20q11]
Location_base_pair Starts at 37289648 and ends at 37317260 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
CIZ1 (9q34.11) / MANBAL (20q11.23)

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)MANBAL   15799
Cards
Entrez_Gene (NCBI)MANBAL  63905  mannosidase beta like
Aliases
GeneCards (Weizmann)MANBAL
Ensembl hg19 (Hinxton)ENSG00000101363 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000101363 [Gene_View]  chr20:37289648-37317260 [Contig_View]  MANBAL [Vega]
ICGC DataPortalENSG00000101363
TCGA cBioPortalMANBAL
AceView (NCBI)MANBAL
Genatlas (Paris)MANBAL
WikiGenes63905
SOURCE (Princeton)MANBAL
Genetics Home Reference (NIH)MANBAL
Genomic and cartography
GoldenPath hg38 (UCSC)MANBAL  -     chr20:37289648-37317260 +  20q11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MANBAL  -     20q11.23   [Description]    (hg19-Feb_2009)
EnsemblMANBAL - 20q11.23 [CytoView hg19]  MANBAL - 20q11.23 [CytoView hg38]
Mapping of homologs : NCBIMANBAL [Mapview hg19]  MANBAL [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK026708 AK292971 AV753915 BC014672 BC016822
RefSeq transcript (Entrez)NM_001003897 NM_022077
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MANBAL
Cluster EST : UnigeneHs.6126 [ NCBI ]
CGAP (NCI)Hs.6126
Alternative Splicing GalleryENSG00000101363
Gene ExpressionMANBAL [ NCBI-GEO ]   MANBAL [ EBI - ARRAY_EXPRESS ]   MANBAL [ SEEK ]   MANBAL [ MEM ]
Gene Expression Viewer (FireBrowse)MANBAL [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)63905
GTEX Portal (Tissue expression)MANBAL
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9NQG1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9NQG1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9NQG1
Splice isoforms : SwissVarQ9NQG1
PhosPhoSitePlusQ9NQG1
Domains : Interpro (EBI)UPF0239   
Domain families : Pfam (Sanger)UPF0239 (PF06783)   
Domain families : Pfam (NCBI)pfam06783   
Conserved Domain (NCBI)MANBAL
DMDM Disease mutations63905
Blocks (Seattle)MANBAL
SuperfamilyQ9NQG1
Human Protein AtlasENSG00000101363
Peptide AtlasQ9NQG1
HPRD14356
IPIIPI00004988   IPI00794377   
Protein Interaction databases
DIP (DOE-UCLA)Q9NQG1
IntAct (EBI)Q9NQG1
FunCoupENSG00000101363
BioGRIDMANBAL
STRING (EMBL)MANBAL
ZODIACMANBAL
Ontologies - Pathways
QuickGOQ9NQG1
Ontology : AmiGOprotein binding  integral component of membrane  
Ontology : EGO-EBIprotein binding  integral component of membrane  
NDEx NetworkMANBAL
Atlas of Cancer Signalling NetworkMANBAL
Wikipedia pathwaysMANBAL
Orthology - Evolution
OrthoDB63905
GeneTree (enSembl)ENSG00000101363
Phylogenetic Trees/Animal Genes : TreeFamMANBAL
HOVERGENQ9NQG1
HOGENOMQ9NQG1
Homologs : HomoloGeneMANBAL
Homology/Alignments : Family Browser (UCSC)MANBAL
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMANBAL [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MANBAL
dbVarMANBAL
ClinVarMANBAL
1000_GenomesMANBAL 
Exome Variant ServerMANBAL
ExAC (Exome Aggregation Consortium)MANBAL (select the gene name)
Genetic variants : HAPMAP63905
Genomic Variants (DGV)MANBAL [DGVbeta]
DECIPHERMANBAL [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMANBAL 
Mutations
ICGC Data PortalMANBAL 
TCGA Data PortalMANBAL 
Broad Tumor PortalMANBAL
OASIS PortalMANBAL [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMANBAL  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMANBAL
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MANBAL
DgiDB (Drug Gene Interaction Database)MANBAL
DoCM (Curated mutations)MANBAL (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MANBAL (select a term)
intoGenMANBAL
Cancer3DMANBAL(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMANBAL
Genetic Testing Registry MANBAL
NextProtQ9NQG1 [Medical]
TSGene63905
GENETestsMANBAL
Huge Navigator MANBAL [HugePedia]
snp3D : Map Gene to Disease63905
BioCentury BCIQMANBAL
ClinGenMANBAL
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD63905
Chemical/Pharm GKB GenePA30578
Clinical trialMANBAL
Miscellaneous
canSAR (ICR)MANBAL (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMANBAL
EVEXMANBAL
GoPubMedMANBAL
iHOPMANBAL
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 11:37:48 CEST 2017

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