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KIAA0195 (KIAA0195)

Identity

Other aliasTMEM94
HGNC (Hugo) KIAA0195
LocusID (NCBI) 9772
Atlas_Id 64850
Location 17q25.1  [Link to chromosome band 17q25]
Location_base_pair Starts at 73452664 and ends at 73496533 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
KIAA0195 ICT1KIAA0195 NUP85KIAA0195 TTYH2

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)KIAA0195   28983
Cards
Entrez_Gene (NCBI)KIAA0195  9772  KIAA0195
AliasesTMEM94
GeneCards (Weizmann)KIAA0195
Ensembl hg19 (Hinxton)ENSG00000177728 [Gene_View]  chr17:73452664-73496533 [Contig_View]  KIAA0195 [Vega]
Ensembl hg38 (Hinxton)ENSG00000177728 [Gene_View]  chr17:73452664-73496533 [Contig_View]  KIAA0195 [Vega]
ICGC DataPortalENSG00000177728
TCGA cBioPortalKIAA0195
AceView (NCBI)KIAA0195
Genatlas (Paris)KIAA0195
WikiGenes9772
SOURCE (Princeton)KIAA0195
Genetics Home Reference (NIH)KIAA0195
Genomic and cartography
GoldenPath hg19 (UCSC)KIAA0195  -     chr17:73452664-73496533 +  17q25.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)KIAA0195  -     17q25.1   [Description]    (hg38-Dec_2013)
EnsemblKIAA0195 - 17q25.1 [CytoView hg19]  KIAA0195 - 17q25.1 [CytoView hg38]
Mapping of homologs : NCBIKIAA0195 [Mapview hg19]  KIAA0195 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF070545 AK094864 AK128508 AK294526 AK304819
RefSeq transcript (Entrez)NM_014738
RefSeq genomic (Entrez)NC_000017 NC_018928 NT_010783 NW_004929407
Consensus coding sequences : CCDS (NCBI)KIAA0195
Cluster EST : UnigeneHs.514474 [ NCBI ]
CGAP (NCI)Hs.514474
Alternative Splicing GalleryENSG00000177728
Gene ExpressionKIAA0195 [ NCBI-GEO ]   KIAA0195 [ EBI - ARRAY_EXPRESS ]   KIAA0195 [ SEEK ]   KIAA0195 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA0195 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)9772
GTEX Portal (Tissue expression)KIAA0195
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ12767   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ12767  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ12767
Splice isoforms : SwissVarQ12767
PhosPhoSitePlusQ12767
Domains : Interpro (EBI)ATPase_P-typ_cation-transptr_C    ATPase_P-typ_TM_dom   
Domain families : Pfam (Sanger)Cation_ATPase_C (PF00689)   
Domain families : Pfam (NCBI)pfam00689   
Conserved Domain (NCBI)KIAA0195
DMDM Disease mutations9772
Blocks (Seattle)KIAA0195
SuperfamilyQ12767
Human Protein AtlasENSG00000177728
Peptide AtlasQ12767
HPRD11068
IPIIPI00783211   IPI00431263   IPI01013882   
Protein Interaction databases
DIP (DOE-UCLA)Q12767
IntAct (EBI)Q12767
FunCoupENSG00000177728
BioGRIDKIAA0195
STRING (EMBL)KIAA0195
ZODIACKIAA0195
Ontologies - Pathways
QuickGOQ12767
Ontology : AmiGOnucleoplasm  integral component of membrane  
Ontology : EGO-EBInucleoplasm  integral component of membrane  
NDEx NetworkKIAA0195
Atlas of Cancer Signalling NetworkKIAA0195
Wikipedia pathwaysKIAA0195
Orthology - Evolution
OrthoDB9772
GeneTree (enSembl)ENSG00000177728
Phylogenetic Trees/Animal Genes : TreeFamKIAA0195
HOVERGENQ12767
HOGENOMQ12767
Homologs : HomoloGeneKIAA0195
Homology/Alignments : Family Browser (UCSC)KIAA0195
Gene fusions - Rearrangements
Fusion: TCGAKIAA0195 ICT1
Fusion: TCGAKIAA0195 NUP85
Fusion: TCGAKIAA0195 TTYH2
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA0195 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA0195
dbVarKIAA0195
ClinVarKIAA0195
1000_GenomesKIAA0195 
Exome Variant ServerKIAA0195
ExAC (Exome Aggregation Consortium)KIAA0195 (select the gene name)
Genetic variants : HAPMAP9772
Genomic Variants (DGV)KIAA0195 [DGVbeta]
DECIPHER (Syndromes)17:73452664-73496533  ENSG00000177728
CONAN: Copy Number AnalysisKIAA0195 
Mutations
ICGC Data PortalKIAA0195 
TCGA Data PortalKIAA0195 
Broad Tumor PortalKIAA0195
OASIS PortalKIAA0195 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA0195  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA0195
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 KIAA0195
DgiDB (Drug Gene Interaction Database)KIAA0195
DoCM (Curated mutations)KIAA0195 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA0195 (select a term)
intoGenKIAA0195
Cancer3DKIAA0195(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA0195
Genetic Testing Registry KIAA0195
NextProtQ12767 [Medical]
TSGene9772
GENETestsKIAA0195
Huge Navigator KIAA0195 [HugePedia]
snp3D : Map Gene to Disease9772
BioCentury BCIQKIAA0195
ClinGenKIAA0195
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD9772
Chemical/Pharm GKB GenePA142671623
Clinical trialKIAA0195
Miscellaneous
canSAR (ICR)KIAA0195 (select the gene name)
Probes
Litterature
PubMed14 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA0195
EVEXKIAA0195
GoPubMedKIAA0195
iHOPKIAA0195
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 12:09:39 CET 2017

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