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

INSYN2B (inhibitory synaptic factor family member 2B)

Identity

Other aliasC5orf57
FAM196B
HGNC (Hugo) INSYN2B
LocusID (NCBI) 100131897
Atlas_Id 80440
Location 5q35.1  [Link to chromosome band 5q35]
Location_base_pair Starts at 169861306 and ends at 169980757 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)INSYN2B   37271
Cards
Entrez_Gene (NCBI)INSYN2B  100131897  inhibitory synaptic factor family member 2B
AliasesC5orf57; FAM196B
GeneCards (Weizmann)INSYN2B
Ensembl hg19 (Hinxton)ENSG00000204767 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000204767 [Gene_View]  ENSG00000204767 [Sequence]  chr5:169861306-169980757 [Contig_View]  INSYN2B [Vega]
ICGC DataPortalENSG00000204767
TCGA cBioPortalINSYN2B
AceView (NCBI)INSYN2B
Genatlas (Paris)INSYN2B
WikiGenes100131897
SOURCE (Princeton)INSYN2B
Genetics Home Reference (NIH)INSYN2B
Genomic and cartography
GoldenPath hg38 (UCSC)INSYN2B  -     chr5:169861306-169980757 -  5q35.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)INSYN2B  -     5q35.1   [Description]    (hg19-Feb_2009)
GoldenPathINSYN2B - 5q35.1 [CytoView hg19]  INSYN2B - 5q35.1 [CytoView hg38]
ImmunoBaseENSG00000204767
Mapping of homologs : NCBIINSYN2B [Mapview hg19]  INSYN2B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI889725 AK055998
RefSeq transcript (Entrez)NM_001129891 NM_001346304
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)INSYN2B
Alternative Splicing GalleryENSG00000204767
Gene ExpressionINSYN2B [ NCBI-GEO ]   INSYN2B [ EBI - ARRAY_EXPRESS ]   INSYN2B [ SEEK ]   INSYN2B [ MEM ]
Gene Expression Viewer (FireBrowse)INSYN2B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100131897
GTEX Portal (Tissue expression)INSYN2B
Human Protein AtlasENSG00000204767-INSYN2B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)INSYN2B
DMDM Disease mutations100131897
Blocks (Seattle)INSYN2B
Human Protein Atlas [tissue]ENSG00000204767-INSYN2B [tissue]
IPIIPI00743011   
Protein Interaction databases
FunCoupENSG00000204767
BioGRIDINSYN2B
STRING (EMBL)INSYN2B
ZODIACINSYN2B
Ontologies - Pathways
Huge Navigator INSYN2B [HugePedia]
snp3D : Map Gene to Disease100131897
BioCentury BCIQINSYN2B
ClinGenINSYN2B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100131897
Chemical/Pharm GKB GenePA165660363
Clinical trialINSYN2B
Miscellaneous
canSAR (ICR)INSYN2B (select the gene name)
HarmonizomeINSYN2B
DataMed IndexINSYN2B
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineINSYN2B
EVEXINSYN2B
GoPubMedINSYN2B
iHOPINSYN2B
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 : Wed Mar 11 19:57:30 CET 2020

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.