ENSG00000205277


Homo sapiens

Features
Gene ID: ENSG00000205277
  
Biological name :MUC12
  
Synonyms : MUC12 / mucin 12, cell surface associated / Q9UKN1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 7
Strand: 1
Band: q22.1
Gene start: 100969623
Gene end: 101018949
  
Corresponding Affymetrix probe sets: 1557906_at (Human Genome U133 Plus 2.0 Array)   1557907_x_at (Human Genome U133 Plus 2.0 Array)   226654_at (Human Genome U133 Plus 2.0 Array)   231814_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000368755
Ensembl peptide - ENSP00000441929
Ensembl peptide - ENSP00000306919
NCBI entrez gene - 10071     See in Manteia.
OMIM - 604609
RefSeq - NM_001164462
RefSeq Peptide - NP_001157934
swissprot - H7BXN1
swissprot - Q9UKN1
Ensembl - ENSG00000205277
  
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 si:ch211-196f2.3ENSDARG00000105522Danio rerio


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
MUC17 / Q685J3 / mucin 17, cell surface associatedENSG0000016987614
MUC3A / Q02505 / mucin 3A, cell surface associatedENSG0000016989410


Protein motifs (from Interpro)
Interpro ID Name
 IPR000082  SEA domain
 IPR013032  EGF-like, conserved site
 IPR021157  Cytochrome c1, transmembrane anchor, C-terminal
 IPR036364  SEA domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001558 regulation of cell growth NAS
 biological_processGO:0002223 stimulatory C-type lectin receptor signaling pathway TAS
 biological_processGO:0016266 O-glycan processing TAS
 cellular_componentGO:0005796 Golgi lumen TAS
 cellular_componentGO:0005886 plasma membrane TAS
 cellular_componentGO:0005887 integral component of plasma membrane NAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0003674 molecular_function ND


Pathways (from Reactome)
Pathway description
Defective GALNT3 causes familial hyperphosphatemic tumoral calcinosis (HFTC)
Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS)
Defective GALNT12 causes colorectal cancer 1 (CRCS1)
Dectin-2 family
O-linked glycosylation of mucins
Termination of O-glycan biosynthesis


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
No match
  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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