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FAM24B (family with sequence similarity 24 member B)

Identity

Alias (NCBI)-
HGNC (Hugo) FAM24B
HGNC Alias symbMGC45962
AC073585.2
HGNC Previous namefamily with sequence similarity 24, member B
LocusID (NCBI) 196792
Atlas_Id 63176
Location 10q26.13  [Link to chromosome band 10q26]
Location_base_pair Starts at 122849078 and ends at 122879581 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)
SHTN1 (10q25.3) / FAM24B (10q26.13)

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)FAM24B   23475
Cards
Entrez_Gene (NCBI)FAM24B    family with sequence similarity 24 member B
Aliases
GeneCards (Weizmann)FAM24B
Ensembl hg19 (Hinxton)ENSG00000213185 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000213185 [Gene_View]  ENSG00000213185 [Sequence]  chr10:122849078-122879581 [Contig_View]  FAM24B [Vega]
ICGC DataPortalENSG00000213185
TCGA cBioPortalFAM24B
AceView (NCBI)FAM24B
Genatlas (Paris)FAM24B
SOURCE (Princeton)FAM24B
Genetics Home Reference (NIH)FAM24B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM24B  -     chr10:122849078-122879581 -  10q26.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM24B  -     10q26.13   [Description]    (hg19-Feb_2009)
GoldenPathFAM24B - 10q26.13 [CytoView hg19]  FAM24B - 10q26.13 [CytoView hg38]
ImmunoBaseENSG00000213185
Genome Data Viewer NCBIFAM24B [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AL832386 AL832795 AV762334 BC031343 BG490871
RefSeq transcript (Entrez)NM_001204364 NM_152644
Consensus coding sequences : CCDS (NCBI)FAM24B
Gene ExpressionFAM24B [ NCBI-GEO ]   FAM24B [ EBI - ARRAY_EXPRESS ]   FAM24B [ SEEK ]   FAM24B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM24B [ Firebrowse - Broad ]
GenevisibleExpression of FAM24B in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)196792
GTEX Portal (Tissue expression)FAM24B
Human Protein AtlasENSG00000213185-FAM24B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N5W8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N5W8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N5W8
PhosPhoSitePlusQ8N5W8
Domains : Interpro (EBI)FAM24   
Domain families : Pfam (Sanger)FAM24 (PF15193)   
Domain families : Pfam (NCBI)pfam15193   
Conserved Domain (NCBI)FAM24B
SuperfamilyQ8N5W8
AlphaFold pdb e-kbQ8N5W8   
Human Protein Atlas [tissue]ENSG00000213185-FAM24B [tissue]
HPRD13299
Protein Interaction databases
DIP (DOE-UCLA)Q8N5W8
IntAct (EBI)Q8N5W8
BioGRIDFAM24B
STRING (EMBL)FAM24B
ZODIACFAM24B
Ontologies - Pathways
QuickGOQ8N5W8
Ontology : AmiGOprotein binding  extracellular region  
Ontology : EGO-EBIprotein binding  extracellular region  
NDEx NetworkFAM24B
Atlas of Cancer Signalling NetworkFAM24B
Wikipedia pathwaysFAM24B
Orthology - Evolution
OrthoDB196792
GeneTree (enSembl)ENSG00000213185
Phylogenetic Trees/Animal Genes : TreeFamFAM24B
Homologs : HomoloGeneFAM24B
Homology/Alignments : Family Browser (UCSC)FAM24B
Gene fusions - Rearrangements
Fusion : QuiverFAM24B
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM24B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM24B
dbVarFAM24B
ClinVarFAM24B
MonarchFAM24B
1000_GenomesFAM24B 
Exome Variant ServerFAM24B
GNOMAD BrowserENSG00000213185
Varsome BrowserFAM24B
ACMGFAM24B variants
VarityQ8N5W8
Genomic Variants (DGV)FAM24B [DGVbeta]
DECIPHERFAM24B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM24B 
Mutations
ICGC Data PortalFAM24B 
TCGA Data PortalFAM24B 
Broad Tumor PortalFAM24B
OASIS PortalFAM24B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM24B  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DFAM24B
Mutations and Diseases : HGMDFAM24B
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaFAM24B
DgiDB (Drug Gene Interaction Database)FAM24B
DoCM (Curated mutations)FAM24B
CIViC (Clinical Interpretations of Variants in Cancer)FAM24B
Cancer3DFAM24B
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETFAM24B
MedgenFAM24B
Genetic Testing Registry FAM24B
NextProtQ8N5W8 [Medical]
GENETestsFAM24B
Target ValidationFAM24B
Huge Navigator FAM24B [HugePedia]
ClinGenFAM24B
Clinical trials, drugs, therapy
MyCancerGenomeFAM24B
Protein Interactions : CTDFAM24B
Pharm GKB GenePA134880209
PharosQ8N5W8
Clinical trialFAM24B
Miscellaneous
canSAR (ICR)FAM24B
HarmonizomeFAM24B
DataMed IndexFAM24B
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXFAM24B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Mon Oct 4 15:50:01 CEST 2021

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