ENSG00000149256


Homo sapiens

Features
Gene ID: ENSG00000149256
  
Biological name :TENM4
  
Synonyms : Q6N022 / teneurin transmembrane protein 4 / TENM4
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 11
Strand: -1
Band: q14.1
Gene start: 78652831
Gene end: 79440948
  
Corresponding Affymetrix probe sets: 213273_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000432427
Ensembl peptide - ENSP00000433535
Ensembl peptide - ENSP00000432705
Ensembl peptide - ENSP00000278550
Ensembl peptide - ENSP00000431711
NCBI entrez gene - 26011     See in Manteia.
OMIM - 610084
RefSeq - XM_017017526
RefSeq - NM_001098816
RefSeq - XM_017017525
RefSeq Peptide - NP_001092286
swissprot - E9PPG4
swissprot - Q6N022
swissprot - H0YCJ4
swissprot - H0YCW4
Ensembl - ENSG00000149256
  
Related genetic diseases (OMIM): 616736 - Essential tremor, hereditary, 5, 616736
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
 tenm4ENSDARG00000105088Danio rerio
 Tenm4ENSMUSG00000048078Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
TENM3 / Q9P273 / teneurin transmembrane protein 3ENSG0000021833667
TENM1 / Q9UKZ4 / teneurin transmembrane protein 1ENSG0000000969463
TENM2 / Q9NT68 / teneurin transmembrane protein 2ENSG0000014593459
VWDE / Q8N2E2 / von Willebrand factor D and EGF domainsENSG000001465308
WIF1 / Q9Y5W5 / WNT inhibitory factor 1ENSG000001560763


Protein motifs (from Interpro)
Interpro ID Name
 IPR000742  EGF-like domain
 IPR006530  YD repeat
 IPR008969  Carboxypeptidase-like, regulatory domain superfamily
 IPR009471  Teneurin intracellular, N-terminal
 IPR011042  Six-bladed beta-propeller, TolB-like
 IPR013032  EGF-like, conserved site
 IPR013111  EGF-like domain, extracellular
 IPR022385  Rhs repeat-associated core
 IPR027688  Teneurin-1/4
 IPR028916  Tox-GHH domain
 IPR031325  RHS repeat


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000902 cell morphogenesis IBA
 biological_processGO:0001702 gastrulation with mouth forming second IEA
 biological_processGO:0007157 heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules IBA
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0030154 cell differentiation IEA
 biological_processGO:0031641 regulation of myelination IMP
 biological_processGO:0031643 positive regulation of myelination IEA
 biological_processGO:0032289 central nervous system myelin formation IEA
 biological_processGO:0048666 neuron development IEA
 biological_processGO:0048714 positive regulation of oligodendrocyte differentiation IEA
 biological_processGO:0060038 cardiac muscle cell proliferation IEA
 biological_processGO:0060912 cardiac cell fate specification IEA
 biological_processGO:0097264 self proteolysis IEA
 biological_processGO:2000543 positive regulation of gastrulation IEA
 cellular_componentGO:0005634 nucleus ISS
 cellular_componentGO:0005737 cytoplasm ISS
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0005887 integral component of plasma membrane IBA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0043005 neuron projection IEA
 molecular_functionGO:0042803 protein homodimerization activity IEA
 molecular_functionGO:0046982 protein heterodimerization activity IBA
 molecular_functionGO:0050839 cell adhesion molecule binding IBA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0002080 Intention tremor "An oscillatory cerebellar ataxia that tends to be absent when the limbs are inactive and during the first part of voluntary movement but worsening as the movement continues and greater precision is required (e.g., in touching a target such as the patient s nose or a physician s finger)." [HPO:curators]
Show

 HP:0002174 Postural tremor "A type of tremors that is triggered by holding a limb in a fixed position." [HPO:curators]
Show

 HP:0003677 Slow progression 
Show

 HP:0003828 Variable expressivity 
Show

 HP:0003831 Age-dependent penetrance 
Show

  


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






 

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