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KIAA1755 (KIAA1755)

Identity

Alias_symbol (synonym)RP5-1054A22.3
Other alias-
HGNC (Hugo) KIAA1755
LocusID (NCBI) 85449
Atlas_Id 64901
Location 20q11.23  [Link to chromosome band 20q11]
Location_base_pair Starts at 36838907 and ends at 36889174 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
KIAA1755 (20q11.23) / HS6ST2 (Xq26.2)UQCC1 (20q11.22) / KIAA1755 (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)KIAA1755   29372
Cards
Entrez_Gene (NCBI)KIAA1755  85449  KIAA1755
Aliases
GeneCards (Weizmann)KIAA1755
Ensembl hg19 (Hinxton)ENSG00000149633 [Gene_View]  chr20:36838907-36889174 [Contig_View]  KIAA1755 [Vega]
Ensembl hg38 (Hinxton)ENSG00000149633 [Gene_View]  chr20:36838907-36889174 [Contig_View]  KIAA1755 [Vega]
ICGC DataPortalENSG00000149633
TCGA cBioPortalKIAA1755
AceView (NCBI)KIAA1755
Genatlas (Paris)KIAA1755
WikiGenes85449
SOURCE (Princeton)KIAA1755
Genetics Home Reference (NIH)KIAA1755
Genomic and cartography
GoldenPath hg19 (UCSC)KIAA1755  -     chr20:36838907-36889174 -  20q11.23   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)KIAA1755  -     20q11.23   [Description]    (hg38-Dec_2013)
EnsemblKIAA1755 - 20q11.23 [CytoView hg19]  KIAA1755 - 20q11.23 [CytoView hg38]
Mapping of homologs : NCBIKIAA1755 [Mapview hg19]  KIAA1755 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB051542 AK096202 BC011516 BC029137 BC033704
RefSeq transcript (Entrez)NM_001029864
RefSeq genomic (Entrez)NC_000020 NC_018931 NT_011362 NW_004929418
Consensus coding sequences : CCDS (NCBI)KIAA1755
Cluster EST : UnigeneHs.472690 [ NCBI ]
CGAP (NCI)Hs.472690
Alternative Splicing GalleryENSG00000149633
Gene ExpressionKIAA1755 [ NCBI-GEO ]   KIAA1755 [ EBI - ARRAY_EXPRESS ]   KIAA1755 [ SEEK ]   KIAA1755 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA1755 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)85449
GTEX Portal (Tissue expression)KIAA1755
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5JYT7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5JYT7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5JYT7
Splice isoforms : SwissVarQ5JYT7
PhosPhoSitePlusQ5JYT7
Domains : Interpro (EBI)CRAL-TRIO_dom   
Domain families : Pfam (Sanger)CRAL_TRIO_2 (PF13716)   
Domain families : Pfam (NCBI)pfam13716   
Conserved Domain (NCBI)KIAA1755
DMDM Disease mutations85449
Blocks (Seattle)KIAA1755
SuperfamilyQ5JYT7
Human Protein AtlasENSG00000149633
Peptide AtlasQ5JYT7
IPIIPI00304549   IPI00552934   
Protein Interaction databases
DIP (DOE-UCLA)Q5JYT7
IntAct (EBI)Q5JYT7
FunCoupENSG00000149633
BioGRIDKIAA1755
STRING (EMBL)KIAA1755
ZODIACKIAA1755
Ontologies - Pathways
QuickGOQ5JYT7
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkKIAA1755
Atlas of Cancer Signalling NetworkKIAA1755
Wikipedia pathwaysKIAA1755
Orthology - Evolution
OrthoDB85449
GeneTree (enSembl)ENSG00000149633
Phylogenetic Trees/Animal Genes : TreeFamKIAA1755
HOVERGENQ5JYT7
HOGENOMQ5JYT7
Homologs : HomoloGeneKIAA1755
Homology/Alignments : Family Browser (UCSC)KIAA1755
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA1755 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA1755
dbVarKIAA1755
ClinVarKIAA1755
1000_GenomesKIAA1755 
Exome Variant ServerKIAA1755
ExAC (Exome Aggregation Consortium)KIAA1755 (select the gene name)
Genetic variants : HAPMAP85449
Genomic Variants (DGV)KIAA1755 [DGVbeta]
DECIPHER (Syndromes)20:36838907-36889174  ENSG00000149633
CONAN: Copy Number AnalysisKIAA1755 
Mutations
ICGC Data PortalKIAA1755 
TCGA Data PortalKIAA1755 
Broad Tumor PortalKIAA1755
OASIS PortalKIAA1755 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA1755  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA1755
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch KIAA1755
DgiDB (Drug Gene Interaction Database)KIAA1755
DoCM (Curated mutations)KIAA1755 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA1755 (select a term)
intoGenKIAA1755
Cancer3DKIAA1755(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA1755
Genetic Testing Registry KIAA1755
NextProtQ5JYT7 [Medical]
TSGene85449
GENETestsKIAA1755
Huge Navigator KIAA1755 [HugePedia]
snp3D : Map Gene to Disease85449
BioCentury BCIQKIAA1755
ClinGenKIAA1755
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD85449
Chemical/Pharm GKB GenePA162393181
Clinical trialKIAA1755
Miscellaneous
canSAR (ICR)KIAA1755 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA1755
EVEXKIAA1755
GoPubMedKIAA1755
iHOPKIAA1755
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:09:49 CET 2017

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