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KIAA1328 (KIAA1328)

Identity

Alias (NCBI)-
HGNC (Hugo) KIAA1328
HGNC Alias namehinderin
LocusID (NCBI) 57536
Atlas_Id 64882
Location 18q12.2  [Link to chromosome band 18q12]
Location_base_pair Starts at 36829127 and ends at 37225334 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
BBS5 (2q31.1) / KIAA1328 (18q12.2)CDH2 (18q12.1) / KIAA1328 (18q12.2)KIAA1328 (18q12.2) / DCC (18q21.2)

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)KIAA1328   29248
Cards
Entrez_Gene (NCBI)KIAA1328    KIAA1328
Aliases
GeneCards (Weizmann)KIAA1328
Ensembl hg19 (Hinxton)ENSG00000150477 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000150477 [Gene_View]  ENSG00000150477 [Sequence]  chr18:36829127-37225334 [Contig_View]  KIAA1328 [Vega]
ICGC DataPortalENSG00000150477
TCGA cBioPortalKIAA1328
AceView (NCBI)KIAA1328
Genatlas (Paris)KIAA1328
SOURCE (Princeton)KIAA1328
Genetics Home Reference (NIH)KIAA1328
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA1328  -     chr18:36829127-37225334 +  18q12.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA1328  -     18q12.2   [Description]    (hg19-Feb_2009)
GoldenPathKIAA1328 - 18q12.2 [CytoView hg19]  KIAA1328 - 18q12.2 [CytoView hg38]
ImmunoBaseENSG00000150477
Genome Data Viewer NCBIKIAA1328 [Mapview hg19]  
OMIM616480   
Gene and transcription
Genbank (Entrez)AB037749 AK130479 AK292288 AK304230 AL832625
RefSeq transcript (Entrez)NM_001322327 NM_001353918 NM_001353919 NM_001353920 NM_020776
Consensus coding sequences : CCDS (NCBI)KIAA1328
Gene ExpressionKIAA1328 [ NCBI-GEO ]   KIAA1328 [ EBI - ARRAY_EXPRESS ]   KIAA1328 [ SEEK ]   KIAA1328 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA1328 [ Firebrowse - Broad ]
GenevisibleExpression of KIAA1328 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57536
GTEX Portal (Tissue expression)KIAA1328
Human Protein AtlasENSG00000150477-KIAA1328 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ86T90   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ86T90  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ86T90
PhosPhoSitePlusQ86T90
Domains : Interpro (EBI)Hinderin   
Domain families : Pfam (Sanger)KIAA1328 (PF15369)   
Domain families : Pfam (NCBI)pfam15369   
Conserved Domain (NCBI)KIAA1328
SuperfamilyQ86T90
AlphaFold pdb e-kbQ86T90   
Human Protein Atlas [tissue]ENSG00000150477-KIAA1328 [tissue]
HPRD17211
Protein Interaction databases
DIP (DOE-UCLA)Q86T90
IntAct (EBI)Q86T90
BioGRIDKIAA1328
STRING (EMBL)KIAA1328
ZODIACKIAA1328
Ontologies - Pathways
QuickGOQ86T90
Ontology : AmiGOprotein binding  
Ontology : EGO-EBIprotein binding  
NDEx NetworkKIAA1328
Atlas of Cancer Signalling NetworkKIAA1328
Wikipedia pathwaysKIAA1328
Orthology - Evolution
OrthoDB57536
GeneTree (enSembl)ENSG00000150477
Phylogenetic Trees/Animal Genes : TreeFamKIAA1328
Homologs : HomoloGeneKIAA1328
Homology/Alignments : Family Browser (UCSC)KIAA1328
Gene fusions - Rearrangements
Fusion : QuiverKIAA1328
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA1328 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA1328
dbVarKIAA1328
ClinVarKIAA1328
MonarchKIAA1328
1000_GenomesKIAA1328 
Exome Variant ServerKIAA1328
GNOMAD BrowserENSG00000150477
Varsome BrowserKIAA1328
ACMGKIAA1328 variants
VarityQ86T90
Genomic Variants (DGV)KIAA1328 [DGVbeta]
DECIPHERKIAA1328 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKIAA1328 
Mutations
ICGC Data PortalKIAA1328 
TCGA Data PortalKIAA1328 
Broad Tumor PortalKIAA1328
OASIS PortalKIAA1328 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA1328  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DKIAA1328
Mutations and Diseases : HGMDKIAA1328
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaKIAA1328
DgiDB (Drug Gene Interaction Database)KIAA1328
DoCM (Curated mutations)KIAA1328
CIViC (Clinical Interpretations of Variants in Cancer)KIAA1328
Cancer3DKIAA1328
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM616480   
Orphanet
DisGeNETKIAA1328
MedgenKIAA1328
Genetic Testing Registry KIAA1328
NextProtQ86T90 [Medical]
GENETestsKIAA1328
Target ValidationKIAA1328
Huge Navigator KIAA1328 [HugePedia]
ClinGenKIAA1328
Clinical trials, drugs, therapy
MyCancerGenomeKIAA1328
Protein Interactions : CTDKIAA1328
Pharm GKB GenePA134875219
PharosQ86T90
Clinical trialKIAA1328
Miscellaneous
canSAR (ICR)KIAA1328
HarmonizomeKIAA1328
DataMed IndexKIAA1328
Probes
Litterature
PubMed15 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXKIAA1328
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:54:34 CEST 2021

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