ENSG00000135960


Homo sapiens

Features
Gene ID: ENSG00000135960
  
Biological name :EDAR
  
Synonyms : ectodysplasin A receptor / EDAR / Q9UNE0
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: -1
Band: q13
Gene start: 108894471
Gene end: 108989372
  
Corresponding Affymetrix probe sets: 220048_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000258443
Ensembl peptide - ENSP00000365839
Ensembl peptide - ENSP00000386371
NCBI entrez gene - 10913     See in Manteia.
OMIM - 604095
RefSeq - XM_011510503
RefSeq - NM_022336
RefSeq - XM_006712204
RefSeq - XM_011510502
RefSeq Peptide - NP_071731
swissprot - Q9UNE0
Ensembl - ENSG00000135960
  
Related genetic diseases (OMIM): 129490 - Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant, 129490
  224900 - Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive, 224900
  612630 - [Hair morphology 1, hair thickness], 612630
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
 edarENSDARG00000099088Danio rerio
 EDARENSGALG00000016809Gallus gallus
 EdarENSMUSG00000003227Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR011029  Death-like domain superfamily
 IPR034052  Tumor necrosis factor receptor EDAR, N-terminal


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001942 hair follicle development IEA
 biological_processGO:0006915 apoptotic process IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0008544 epidermis development TAS
 biological_processGO:0010628 positive regulation of gene expression IEA
 biological_processGO:0030154 cell differentiation IEA
 biological_processGO:0033209 tumor necrosis factor-mediated signaling pathway TAS
 biological_processGO:0042475 odontogenesis of dentin-containing tooth IEA
 biological_processGO:0043123 positive regulation of I-kappaB kinase/NF-kappaB signaling IBA
 biological_processGO:0043473 pigmentation IEA
 biological_processGO:0046330 positive regulation of JNK cascade IBA
 biological_processGO:0060662 salivary gland cavitation IEA
 cellular_componentGO:0005886 plasma membrane IBA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane NAS
 cellular_componentGO:0045177 apical part of cell IEA
 molecular_functionGO:0004888 transmembrane signaling receptor activity IDA
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
TNFs bind their physiological receptors


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:0000007 Autosomal recessive 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 homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000232 Everted lower lip 
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 HP:0000457 Flat nose 
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 HP:0000535 Sparse eyebrows 
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 HP:0000607 Periorbital wrinkles 
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 HP:0000653 Sparse eyelashes "Decreased density/number of eyelashes." [pmid:19125427]
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 HP:0000668 Hypodontia "Hypodontia describes a situation when there are fewer than the normal number of teeth, whereby 6 teeth or fewer teeth are missing (oligodontia refers to the condition of missing more than 6 teeth and the congenital absence of all teeth is called anodontia)." [HPO:curators]
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 HP:0000674 Anodontia "The congenital absence of all teeth." [HPO:curators]
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 HP:0000685 Hypoplastic teeth 
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 HP:0000691 Microdontia 
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 HP:0000958 Dry skin 
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 HP:0000963 Thin skin 
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 HP:0000964 Eczema "Eczema is a form of dermatitis. The term eczema is broadly applied to a range of persistent skin conditions and can be related to a number of underlying conditions. Manifestations of eczema can include dryness and recurring skin rashes with redness, skin edema, itching and dryness, crusting, flaking, blistering, cracking, oozing, or bleeding." [HPO:curators]
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 HP:0000966 Hypohidrosis "Abnormally diminished capacity to sweat." [HPO:curators]
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 HP:0000968 Ectodermal dysplasia 
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 HP:0000970 Anhidrosis "Inability to sweat." [HPO:curators]
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 HP:0001000 Abnormality of skin pigmentation 
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 HP:0001006 Hypotrichosis "Reduced or lacking hair growth." [HPO:curators]
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 HP:0001106 Periorbital hyperpigmentation 
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 HP:0001231 Abnormality of the fingernails "An abnormality of the `fingernails` (FMA:54327)." [HPO:probinson]
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 HP:0001425 Heterogeneous 
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 HP:0001596 Alopecia "Loss of hair from the head or body." [HPO:curators]
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 HP:0002007 Frontal bossing "The presence of an unusually prominent forehead." [HPO:curators]
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 HP:0002046 Intolerance to heat and fever 
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 HP:0002047 Malignant hyperthermia "Malignant hyperthermia is characterized by a rapid increase in temperature to 39-42 degrees C in response to inhalational anesthetics such as halothane or to muscle relaxants such as succinylcholine." [HPO:curators]
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 HP:0002164 Nail dysplasia 
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 HP:0002213 Fine hair 
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 HP:0002217 Slow-growing hair 
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 HP:0002231 Sparse body hair "Sparseness of the body hair." [HPO:probinson]
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 HP:0005280 Depressed nasal root and bridge 
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 HP:0006323 Premature deciduous tooth loss 
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 HP:0006482 Abnormality of dental morphology 
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 HP:0007607 Hypohidrotic ectodermal dysplasia 
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 HP:0008388 Abnormality of the toenails 
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 HP:0010803 Everted upper lip vermilion "Inner aspect of the upper lip vermilion (normally apposing the teeth) visible in a frontal view, i.e., the presence of an `everted` (PATO:0001597) `upper lip` (FMA:59817)." [HPO:probinson, pmid:19125428]
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 HP:0011220 Prominent forehead "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436]
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 HP:0012471 Thick vermilion border "Increased width of the "skin of vermilion border region of upper lip" (FMA:312645)." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000158813 EDA / Q92838 / ectodysplasin A  / reaction / complex
 ENSG00000186197 Q8WWZ3 / EDARADD / EDAR associated death domain  / reaction / complex






 

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