ENSG00000168955


Homo sapiens

Features
Gene ID: ENSG00000168955
  
Biological name :TM4SF20
  
Synonyms : Q53R12 / TM4SF20 / transmembrane 4 L six family member 20
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: -1
Band: q36.3
Gene start: 227362156
Gene end: 227381995
  
Corresponding Affymetrix probe sets: 220639_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000303028
Ensembl peptide - ENSP00000416565
NCBI entrez gene - 79853     See in Manteia.
OMIM - 615404
RefSeq - NM_024795
RefSeq - XM_011511876
RefSeq Peptide - NP_079071
swissprot - C9JES4
swissprot - Q53R12
Ensembl - ENSG00000168955
  
Related genetic diseases (OMIM): 615432 - {Specific language impairment 5}, 615432
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
 Q9CQY8ENSMUSG00000026149Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR008661  L6 membrane


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0045861 negative regulation of proteolysis IDA
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0005789 endoplasmic reticulum membrane IEA
 cellular_componentGO:0005886 plasma membrane IDA
 cellular_componentGO:0005925 focal adhesion IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IBA


Pathways (from Reactome)
Pathway description
No match


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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