ENSG00000095787


Homo sapiens

Features
Gene ID: ENSG00000095787
  
Biological name :WAC
  
Synonyms : Q9BTA9 / WAC / WW domain containing adaptor with coiled-coil
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 10
Strand: 1
Band: p12.1
Gene start: 28532493
Gene end: 28623112
  
Corresponding Affymetrix probe sets: 217742_s_at (Human Genome U133 Plus 2.0 Array)   219679_s_at (Human Genome U133 Plus 2.0 Array)   222389_s_at (Human Genome U133 Plus 2.0 Array)   222390_at (Human Genome U133 Plus 2.0 Array)   230154_at (Human Genome U133 Plus 2.0 Array)   242427_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000400848
Ensembl peptide - ENSP00000486994
Ensembl peptide - ENSP00000434903
Ensembl peptide - ENSP00000415727
Ensembl peptide - ENSP00000415645
Ensembl peptide - ENSP00000404758
Ensembl peptide - ENSP00000404125
Ensembl peptide - ENSP00000311106
Ensembl peptide - ENSP00000346986
Ensembl peptide - ENSP00000364797
Ensembl peptide - ENSP00000364816
Ensembl peptide - ENSP00000395008
Ensembl peptide - ENSP00000399706
NCBI entrez gene - 51322     See in Manteia.
OMIM - 615049
RefSeq - XM_017016318
RefSeq - NM_016628
RefSeq - NM_100264
RefSeq - NM_100486
RefSeq - XM_011519491
RefSeq - XM_017016315
RefSeq - XM_017016316
RefSeq - XM_017016317
RefSeq Peptide - NP_567822
RefSeq Peptide - NP_567823
RefSeq Peptide - NP_057712
swissprot - C9JD58
swissprot - A0A0A0MRT2
swissprot - C9JVK6
swissprot - J3QT76
swissprot - J3QTA0
swissprot - Q9P1G8
swissprot - Q9BTA9
swissprot - E9PMZ7
swissprot - C9JMU2
Ensembl - ENSG00000095787
  
Related genetic diseases (OMIM): 616708 - Desanto-Shinawi syndrome, 616708
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
 wacaENSDARG00000012577Danio rerio
 WACENSGALG00000035281Gallus gallus
 WacENSMUSG00000024283Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR001202  WW domain
 IPR036020  WW domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006325 chromatin organization IEA
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0006974 cellular response to DNA damage stimulus IMP
 biological_processGO:0010390 histone monoubiquitination IMP
 biological_processGO:0016239 positive regulation of macroautophagy IMP
 biological_processGO:0016567 protein ubiquitination TAS
 biological_processGO:0032435 negative regulation of proteasomal ubiquitin-dependent protein catabolic process IMP
 biological_processGO:0044783 G1 DNA damage checkpoint IMP
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IMP
 biological_processGO:0071894 histone H2B conserved C-terminal lysine ubiquitination IMP
 cellular_componentGO:0005634 nucleus TAS
 cellular_componentGO:0005654 nucleoplasm TAS
 cellular_componentGO:0005681 spliceosomal complex IEA
 cellular_componentGO:0016607 nuclear speck IEA
 molecular_functionGO:0000993 RNA polymerase II core binding IDA
 molecular_functionGO:0003682 chromatin binding IDA
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
E3 ubiquitin ligases ubiquitinate target proteins


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:0000219 Thin upper lip 
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 HP:0000248 Brachycephaly "Brachycephaly refers to a short, wide head, which is often caused by premature closure of both coronal sutures." [HPO:curators]
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 HP:0000280 Coarse facial features 
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 HP:0000293 Full cheeks 
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 HP:0000316 Hypertelorism 
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 HP:0000337 Broad forehead "Abnormally large side-to-side distance of the forehead." [HPO:curators]
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 HP:0000358 Posteriorly rotated ears "A type of `abnormal location of the ears` (HP:0000357) in which the position of the ears is characterized by posterior rotation (the superior part of the ears is rotated towards the back of the head, and the inferior part of the ears towards the front)." [HPO:probinson]
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 HP:0000365 Hearing loss 
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 HP:0000377 Abnormal form of ears "Abnormal form of the out part of the ear (also referred to as the auricle or pinna)." [HPO:curators]
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 HP:0000407 Hearing loss, sensorineural "Hearing loss caused by damage or dysfunction of the auditory nerve (cranial nerve VIII)." [HPO:curators]
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 HP:0000414 Bulbous nose 
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 HP:0000470 Short neck 
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 HP:0000483 Astigmatism 
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 HP:0000486 Strabismus "Strabismus (also known as squint) is a condition in which the eyes are not properly aligned with each other." [HPO:curators]
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 HP:0000490 Deep set eyes 
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 HP:0000545 Myopia 
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 HP:0000574 Thick eyebrows 
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 HP:0000664 Synophrys "Fusion of the left and right `eyebrow` (FMA:54237)." [HPO:probinson]
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 HP:0000713 Agitation 
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 HP:0000718 Aggressive behavior "Aggressive behavior can denote verbal aggression, physical aggression against objects, physical aggression against people, and may also include aggression towards oneself." [HPO:curators]
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 HP:0000739 Anxiety 
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 HP:0000750 Impaired language development 
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 HP:0001007 Hirsutism "Abnormally increased hair growth." [HPO:curators]
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0002019 Constipation 
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 HP:0002079 Hypoplasia of the corpus callosum "Underdevelopment of the corpus callosum." [HPO:curators]
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 HP:0002360 Sleep disturbances "An abnormality of sleep including such phenomena as 1) insomnia/hypersomnia, 2) non-restorative sleep, 3) sleep schedule disorder, 4) excessive daytime somnolence, 5) sleep apnea, and 6) restlessness." [HPO:curators]
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 HP:0002714 Downturned corners of mouth "A morphological `abnormality of the mouth` (HP:0000153) in which the `angle of the mouth` (FMA:77269) is downturned." [HPO:probinson]
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 HP:0003186 Inverted nipples "The presence of nipples that instead of pointing outward are retracted inwards." [HPO:sdoelken]
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 HP:0003593 Early onset 
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 HP:0005280 Depressed nasal root and bridge 
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 HP:0007018 Attention deficit hyperactivity disorder "Attention deficit hyperactivity disorder (ADHD) manifests at age 2-3 years or by first grade at the latest. The main symptoms are distractibility, impulsivity, hyperactivity, and often trouble organizing tasks and projects, difficulty going to sleep, and social problems from being aggressive, loud, or impatient." [HPO:curators]
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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:0011800 Midface retrusion "Posterior positions and/or vertical shortening of the infraorbital and perialar regions, or increased concavity of the face and/or reduced nasolabial angle." [DDD:jclayton-smith]
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 HP:0011968 Feeding difficulties "Impaired ability to eat related to problems gathering food and getting ready to suck, chew, or swallow it." [ISCA:eriggs]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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