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LINC01444 (long intergenic non-protein coding RNA 1444)

Identity

Other alias-
HGNC (Hugo) LINC01444
LocusID (NCBI) 101927642
Atlas_Id 65999
Location 18p11.21  [Link to chromosome band 18p11]
Location_base_pair Starts at 14969606 and ends at 14970467 bp from pter ( according to hg19-Feb_2009)

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)LINC01444   50769
Cards
Entrez_Gene (NCBI)LINC01444  101927642  long intergenic non-protein coding RNA 1444
Aliases
GeneCards (Weizmann)LINC01444
Ensembl hg19 (Hinxton)ENSG00000264301 [Gene_View]  chr18:14969606-14970467 [Contig_View]  LINC01444 [Vega]
Ensembl hg38 (Hinxton)ENSG00000264301 [Gene_View]  chr18:14969606-14970467 [Contig_View]  LINC01444 [Vega]
ICGC DataPortalENSG00000264301
TCGA cBioPortalLINC01444
AceView (NCBI)LINC01444
Genatlas (Paris)LINC01444
WikiGenes101927642
SOURCE (Princeton)LINC01444
Genetics Home Reference (NIH)LINC01444
Genomic and cartography
GoldenPath hg19 (UCSC)LINC01444  -     chr18:14969606-14970467 -  18p11.21   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LINC01444  -     18p11.21   [Description]    (hg38-Dec_2013)
EnsemblLINC01444 - 18p11.21 [CytoView hg19]  LINC01444 - 18p11.21 [CytoView hg38]
Mapping of homologs : NCBILINC01444 [Mapview hg19]  LINC01444 [Mapview hg38]
Gene and transcription
Genbank (Entrez)CF995332 HG509814 HG509815
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000018 NC_018929 NT_010859 NW_004929409
Consensus coding sequences : CCDS (NCBI)LINC01444
Cluster EST : UnigeneHs.711242 [ NCBI ]
CGAP (NCI)Hs.711242
Alternative Splicing GalleryENSG00000264301
Gene ExpressionLINC01444 [ NCBI-GEO ]   LINC01444 [ EBI - ARRAY_EXPRESS ]   LINC01444 [ SEEK ]   LINC01444 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01444 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927642
GTEX Portal (Tissue expression)LINC01444
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01444
DMDM Disease mutations101927642
Blocks (Seattle)LINC01444
Human Protein AtlasENSG00000264301
Protein Interaction databases
FunCoupENSG00000264301
BioGRIDLINC01444
STRING (EMBL)LINC01444
ZODIACLINC01444
Ontologies - Pathways
Huge Navigator LINC01444 [HugePedia]
snp3D : Map Gene to Disease101927642
BioCentury BCIQLINC01444
ClinGenLINC01444
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927642
Clinical trialLINC01444
Miscellaneous
canSAR (ICR)LINC01444 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01444
EVEXLINC01444
GoPubMedLINC01444
iHOPLINC01444
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 Mar 14 12:13:56 CET 2017

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