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LOC100505797 (myosin heavy chain IB-like)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100505797
Atlas_Id 78082
Location 18q22.3  [Link to chromosome band 18q22]
Location_base_pair Starts at 72869040 and ends at 72881399 bp from pter ( according to hg38-Dec_2013)

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)-   -
Cards
Entrez_Gene (NCBI)LOC100505797  100505797  myosin heavy chain IB-like
Aliases
GeneCards (Weizmann)LOC100505797
Ensembl hg19 (Hinxton)ENSG00000263958 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263958 [Gene_View]  chr18:72869040-72881399 [Contig_View]  LOC100505797 [Vega]
ICGC DataPortalENSG00000263958
TCGA cBioPortalLOC100505797
AceView (NCBI)LOC100505797
Genatlas (Paris)LOC100505797
WikiGenes100505797
SOURCE (Princeton)LOC100505797
Genetics Home Reference (NIH)LOC100505797
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100505797  -     chr18:72869040-72881399 +  18q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100505797  -     18q22.3   [Description]    (hg19-Feb_2009)
EnsemblLOC100505797 - 18q22.3 [CytoView hg19]  LOC100505797 - 18q22.3 [CytoView hg38]
Mapping of homologs : NCBILOC100505797 [Mapview hg19]  LOC100505797 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW590150 BG182684 BX114234
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100505797
Cluster EST : UnigeneHs.145111 [ NCBI ]
CGAP (NCI)Hs.145111
Alternative Splicing GalleryENSG00000263958
Gene ExpressionLOC100505797 [ NCBI-GEO ]   LOC100505797 [ EBI - ARRAY_EXPRESS ]   LOC100505797 [ SEEK ]   LOC100505797 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100505797 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505797
GTEX Portal (Tissue expression)LOC100505797
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100505797
DMDM Disease mutations100505797
Blocks (Seattle)LOC100505797
Human Protein AtlasENSG00000263958
Protein Interaction databases
FunCoupENSG00000263958
BioGRIDLOC100505797
STRING (EMBL)LOC100505797
ZODIACLOC100505797
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100505797
BioCentury BCIQLOC100505797
ClinGenLOC100505797
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505797
Clinical trialLOC100505797
Miscellaneous
canSAR (ICR)LOC100505797 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100505797
EVEXLOC100505797
GoPubMedLOC100505797
iHOPLOC100505797
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 : Mon Sep 18 13:18:41 CEST 2017

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