ENSG00000144229


Homo sapiens

Features
Gene ID: ENSG00000144229
  
Biological name :THSD7B
  
Synonyms : Q9C0I4 / thrombospondin type 1 domain containing 7B / THSD7B
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: 1
Band: q22.1
Gene start: 136765545
Gene end: 137677717
  
Corresponding Affymetrix probe sets: 232327_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000387145
Ensembl peptide - ENSP00000473349
Ensembl peptide - ENSP00000413841
Ensembl peptide - ENSP00000272643
NCBI entrez gene - 80731     See in Manteia.
RefSeq - NM_001316349
RefSeq - XM_017005049
RefSeq Peptide - NP_001303278
swissprot - E7EM75
swissprot - Q9C0I4
swissprot - R4GMU2
swissprot - C9JKN6
Ensembl - ENSG00000144229
  
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
 thsd7baENSDARG00000095022Danio rerio
 thsd7bbENSDARG00000061497Danio rerio
 THSD7BENSGALG00000012362Gallus gallus
 Q6P4U0ENSMUSG00000042581Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9UPZ6 / THSD7A / thrombospondin type 1 domain containing 7AENSG0000000510850


Protein motifs (from Interpro)
Interpro ID Name
 IPR000884  Thrombospondin type-1 (TSP1) repeat
 IPR036383  Thrombospondin type-1 (TSP1) repeat superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA


Pathways (from Reactome)
Pathway description
Defective B3GALTL causes Peters-plus syndrome (PpS)
O-glycosylation of TSR domain-containing proteins


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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contact: otassy@igbmc.fr