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TIMM29 (translocase of inner mitochondrial membrane 29)

Identity

Other aliasC19orf52
HGNC (Hugo) TIMM29
LocusID (NCBI) 90580
Atlas_Id 78697
Location 19p13.2  [Link to chromosome band 19p13]
Location_base_pair Starts at 11039424 and ends at 11040916 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


External links

Nomenclature
HGNC (Hugo)TIMM29   25152
Cards
Entrez_Gene (NCBI)TIMM29  90580  translocase of inner mitochondrial membrane 29
AliasesC19orf52
GeneCards (Weizmann)TIMM29
Ensembl hg19 (Hinxton) [Gene_View]  chr19:11039424-11040916 [Contig_View]  TIMM29 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr19:11039424-11040916 [Contig_View]  TIMM29 [Vega]
TCGA cBioPortalTIMM29
AceView (NCBI)TIMM29
Genatlas (Paris)TIMM29
WikiGenes90580
SOURCE (Princeton)TIMM29
Genetics Home Reference (NIH)TIMM29
Genomic and cartography
GoldenPath hg19 (UCSC)TIMM29  -     chr19:11039424-11040916 +  19p13.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)TIMM29  -     19p13.2   [Description]    (hg38-Dec_2013)
EnsemblTIMM29 - 19p13.2 [CytoView hg19]  TIMM29 - 19p13.2 [CytoView hg38]
Mapping of homologs : NCBITIMM29 [Mapview hg19]  TIMM29 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC005075 BC007244 BC011833
RefSeq transcript (Entrez)NM_138358
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TIMM29
Cluster EST : UnigeneHs.164026 [ NCBI ]
CGAP (NCI)Hs.164026
Gene ExpressionTIMM29 [ NCBI-GEO ]   TIMM29 [ EBI - ARRAY_EXPRESS ]   TIMM29 [ SEEK ]   TIMM29 [ MEM ]
Gene Expression Viewer (FireBrowse)TIMM29 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)90580
GTEX Portal (Tissue expression)TIMM29
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9BSF4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9BSF4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9BSF4
Splice isoforms : SwissVarQ9BSF4
PhosPhoSitePlusQ9BSF4
Domains : Interpro (EBI)DUF2366   
Domain families : Pfam (Sanger)DUF2366 (PF10171)   
Domain families : Pfam (NCBI)pfam10171   
Conserved Domain (NCBI)TIMM29
DMDM Disease mutations90580
Blocks (Seattle)TIMM29
SuperfamilyQ9BSF4
Peptide AtlasQ9BSF4
HPRD14275
IPIIPI00157215   
Protein Interaction databases
DIP (DOE-UCLA)Q9BSF4
IntAct (EBI)Q9BSF4
BioGRIDTIMM29
STRING (EMBL)TIMM29
ZODIACTIMM29
Ontologies - Pathways
QuickGOQ9BSF4
Ontology : AmiGOprotein binding  mitochondrial inner membrane  mitochondrial inner membrane protein insertion complex  
Ontology : EGO-EBIprotein binding  mitochondrial inner membrane  mitochondrial inner membrane protein insertion complex  
NDEx NetworkTIMM29
Atlas of Cancer Signalling NetworkTIMM29
Wikipedia pathwaysTIMM29
Orthology - Evolution
OrthoDB90580
Phylogenetic Trees/Animal Genes : TreeFamTIMM29
HOVERGENQ9BSF4
HOGENOMQ9BSF4
Homologs : HomoloGeneTIMM29
Homology/Alignments : Family Browser (UCSC)TIMM29
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTIMM29 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TIMM29
dbVarTIMM29
ClinVarTIMM29
1000_GenomesTIMM29 
Exome Variant ServerTIMM29
ExAC (Exome Aggregation Consortium)TIMM29 (select the gene name)
Genetic variants : HAPMAP90580
Genomic Variants (DGV)TIMM29 [DGVbeta]
DECIPHER (Syndromes)19:11039424-11040916  
CONAN: Copy Number AnalysisTIMM29 
Mutations
ICGC Data PortalTIMM29 
TCGA Data PortalTIMM29 
Broad Tumor PortalTIMM29
OASIS PortalTIMM29 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDTIMM29
BioMutasearch TIMM29
DgiDB (Drug Gene Interaction Database)TIMM29
DoCM (Curated mutations)TIMM29 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TIMM29 (select a term)
intoGenTIMM29
Cancer3DTIMM29(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTIMM29
Genetic Testing Registry TIMM29
NextProtQ9BSF4 [Medical]
TSGene90580
GENETestsTIMM29
Huge Navigator TIMM29 [HugePedia]
snp3D : Map Gene to Disease90580
BioCentury BCIQTIMM29
ClinGenTIMM29
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD90580
Chemical/Pharm GKB GenePA147358399
Clinical trialTIMM29
Miscellaneous
canSAR (ICR)TIMM29 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTIMM29
EVEXTIMM29
GoPubMedTIMM29
iHOPTIMM29
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 12:48:09 CET 2017

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