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KIAA1107 (KIAA1107)

Identity

Other alias-
HGNC (Hugo) KIAA1107
LocusID (NCBI) 23285
Atlas_Id 64871
Location 1p22.1  [Link to chromosome band 1p22]
Location_base_pair Starts at 92168858 and ends at 92184725 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)KIAA1107   29192
Cards
Entrez_Gene (NCBI)KIAA1107  23285  KIAA1107
Aliases
GeneCards (Weizmann)KIAA1107
Ensembl hg19 (Hinxton)ENSG00000069712 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000069712 [Gene_View]  chr1:92168858-92184725 [Contig_View]  KIAA1107 [Vega]
ICGC DataPortalENSG00000069712
TCGA cBioPortalKIAA1107
AceView (NCBI)KIAA1107
Genatlas (Paris)KIAA1107
WikiGenes23285
SOURCE (Princeton)KIAA1107
Genetics Home Reference (NIH)KIAA1107
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA1107  -     chr1:92168858-92184725 +  1p22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA1107  -     1p22.1   [Description]    (hg19-Feb_2009)
EnsemblKIAA1107 - 1p22.1 [CytoView hg19]  KIAA1107 - 1p22.1 [CytoView hg38]
Mapping of homologs : NCBIKIAA1107 [Mapview hg19]  KIAA1107 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB029030 AF017090 AK302496 BC037317 BC047628
RefSeq transcript (Entrez)NM_015237
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KIAA1107
Cluster EST : UnigeneHs.21554 [ NCBI ]
CGAP (NCI)Hs.21554
Alternative Splicing GalleryENSG00000069712
Gene ExpressionKIAA1107 [ NCBI-GEO ]   KIAA1107 [ EBI - ARRAY_EXPRESS ]   KIAA1107 [ SEEK ]   KIAA1107 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA1107 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)23285
GTEX Portal (Tissue expression)KIAA1107
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9UPP5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9UPP5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9UPP5
Splice isoforms : SwissVarQ9UPP5
PhosPhoSitePlusQ9UPP5
Domains : Interpro (EBI)DUF4596   
Domain families : Pfam (Sanger)DUF4596 (PF15363)   
Domain families : Pfam (NCBI)pfam15363   
Conserved Domain (NCBI)KIAA1107
DMDM Disease mutations23285
Blocks (Seattle)KIAA1107
SuperfamilyQ9UPP5
Human Protein AtlasENSG00000069712
Peptide AtlasQ9UPP5
IPIIPI00298902   IPI00885110   
Protein Interaction databases
DIP (DOE-UCLA)Q9UPP5
IntAct (EBI)Q9UPP5
FunCoupENSG00000069712
BioGRIDKIAA1107
STRING (EMBL)KIAA1107
ZODIACKIAA1107
Ontologies - Pathways
QuickGOQ9UPP5
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkKIAA1107
Atlas of Cancer Signalling NetworkKIAA1107
Wikipedia pathwaysKIAA1107
Orthology - Evolution
OrthoDB23285
GeneTree (enSembl)ENSG00000069712
Phylogenetic Trees/Animal Genes : TreeFamKIAA1107
HOVERGENQ9UPP5
HOGENOMQ9UPP5
Homologs : HomoloGeneKIAA1107
Homology/Alignments : Family Browser (UCSC)KIAA1107
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA1107 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA1107
dbVarKIAA1107
ClinVarKIAA1107
1000_GenomesKIAA1107 
Exome Variant ServerKIAA1107
ExAC (Exome Aggregation Consortium)KIAA1107 (select the gene name)
Genetic variants : HAPMAP23285
Genomic Variants (DGV)KIAA1107 [DGVbeta]
DECIPHERKIAA1107 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKIAA1107 
Mutations
ICGC Data PortalKIAA1107 
TCGA Data PortalKIAA1107 
Broad Tumor PortalKIAA1107
OASIS PortalKIAA1107 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA1107  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA1107
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 KIAA1107
DgiDB (Drug Gene Interaction Database)KIAA1107
DoCM (Curated mutations)KIAA1107 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA1107 (select a term)
intoGenKIAA1107
Cancer3DKIAA1107(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA1107
Genetic Testing Registry KIAA1107
NextProtQ9UPP5 [Medical]
TSGene23285
GENETestsKIAA1107
Target ValidationKIAA1107
Huge Navigator KIAA1107 [HugePedia]
snp3D : Map Gene to Disease23285
BioCentury BCIQKIAA1107
ClinGenKIAA1107
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD23285
Chemical/Pharm GKB GenePA142671620
Clinical trialKIAA1107
Miscellaneous
canSAR (ICR)KIAA1107 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA1107
EVEXKIAA1107
GoPubMedKIAA1107
iHOPKIAA1107
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:11:49 CEST 2017

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