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TXLNB (taxilin beta)

Identity

Alias (NCBI)C6orf198
LST001
MDP77
dJ522B19.2
HGNC (Hugo) TXLNB
HGNC Alias symbDKFZp451A175
MDP77
dJ522B19.2
HGNC Previous nameC6orf198
HGNC Previous namechromosome 6 open reading frame 198
LocusID (NCBI) 167838
Atlas_Id 75387
Location 6q24.1  [Link to chromosome band 6q24]
Location_base_pair Starts at 139240061 and ends at 139291998 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)
REV3L (6q21) / TXLNB (6q24.1)TXLNB (6q24.1) / CDC14A (1p21.2)

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)TXLNB   21617
Cards
Entrez_Gene (NCBI)TXLNB    taxilin beta
AliasesC6orf198; LST001; MDP77; dJ522B19.2
GeneCards (Weizmann)TXLNB
Ensembl hg19 (Hinxton)ENSG00000164440 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000164440 [Gene_View]  ENSG00000164440 [Sequence]  chr6:139240061-139291998 [Contig_View]  TXLNB [Vega]
ICGC DataPortalENSG00000164440
TCGA cBioPortalTXLNB
AceView (NCBI)TXLNB
Genatlas (Paris)TXLNB
SOURCE (Princeton)TXLNB
Genetics Home Reference (NIH)TXLNB
Genomic and cartography
GoldenPath hg38 (UCSC)TXLNB  -     chr6:139240061-139291998 -  6q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TXLNB  -     6q24.1   [Description]    (hg19-Feb_2009)
GoldenPathTXLNB - 6q24.1 [CytoView hg19]  TXLNB - 6q24.1 [CytoView hg38]
ImmunoBaseENSG00000164440
Genome Data Viewer NCBITXLNB [Mapview hg19]  
OMIM611438   
Gene and transcription
Genbank (Entrez)AB085905 AF111704 AK056970 AK314725 AL831988
RefSeq transcript (Entrez)NM_153235
Consensus coding sequences : CCDS (NCBI)TXLNB
Gene ExpressionTXLNB [ NCBI-GEO ]   TXLNB [ EBI - ARRAY_EXPRESS ]   TXLNB [ SEEK ]   TXLNB [ MEM ]
Gene Expression Viewer (FireBrowse)TXLNB [ Firebrowse - Broad ]
GenevisibleExpression of TXLNB in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)167838
GTEX Portal (Tissue expression)TXLNB
Human Protein AtlasENSG00000164440-TXLNB [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N3L3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N3L3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N3L3
PhosPhoSitePlusQ8N3L3
Domains : Interpro (EBI)Taxilin_fam   
Domain families : Pfam (Sanger)Taxilin (PF09728)   
Domain families : Pfam (NCBI)pfam09728   
Conserved Domain (NCBI)TXLNB
SuperfamilyQ8N3L3
AlphaFold pdb e-kbQ8N3L3   
Human Protein Atlas [tissue]ENSG00000164440-TXLNB [tissue]
HPRD10793
Protein Interaction databases
DIP (DOE-UCLA)Q8N3L3
IntAct (EBI)Q8N3L3
BioGRIDTXLNB
STRING (EMBL)TXLNB
ZODIACTXLNB
Ontologies - Pathways
QuickGOQ8N3L3
Ontology : AmiGOprotein binding  cytoplasm  syntaxin binding  
Ontology : EGO-EBIprotein binding  cytoplasm  syntaxin binding  
NDEx NetworkTXLNB
Atlas of Cancer Signalling NetworkTXLNB
Wikipedia pathwaysTXLNB
Orthology - Evolution
OrthoDB167838
GeneTree (enSembl)ENSG00000164440
Phylogenetic Trees/Animal Genes : TreeFamTXLNB
Homologs : HomoloGeneTXLNB
Homology/Alignments : Family Browser (UCSC)TXLNB
Gene fusions - Rearrangements
Fusion : QuiverTXLNB
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTXLNB [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TXLNB
dbVarTXLNB
ClinVarTXLNB
MonarchTXLNB
1000_GenomesTXLNB 
Exome Variant ServerTXLNB
GNOMAD BrowserENSG00000164440
Varsome BrowserTXLNB
ACMGTXLNB variants
VarityQ8N3L3
Genomic Variants (DGV)TXLNB [DGVbeta]
DECIPHERTXLNB [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTXLNB 
Mutations
ICGC Data PortalTXLNB 
TCGA Data PortalTXLNB 
Broad Tumor PortalTXLNB
OASIS PortalTXLNB [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTXLNB  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DTXLNB
Mutations and Diseases : HGMDTXLNB
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTXLNB
DgiDB (Drug Gene Interaction Database)TXLNB
DoCM (Curated mutations)TXLNB
CIViC (Clinical Interpretations of Variants in Cancer)TXLNB
Cancer3DTXLNB
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM611438   
Orphanet
DisGeNETTXLNB
MedgenTXLNB
Genetic Testing Registry TXLNB
NextProtQ8N3L3 [Medical]
GENETestsTXLNB
Target ValidationTXLNB
Huge Navigator TXLNB [HugePedia]
ClinGenTXLNB
Clinical trials, drugs, therapy
MyCancerGenomeTXLNB
Protein Interactions : CTDTXLNB
Pharm GKB GenePA134878600
PharosQ8N3L3
Clinical trialTXLNB
Miscellaneous
canSAR (ICR)TXLNB
HarmonizomeTXLNB
DataMed IndexTXLNB
Probes
Litterature
PubMed22 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTXLNB
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 16:27:37 CEST 2021

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