ENSG00000188706


Homo sapiens

Features
Gene ID: ENSG00000188706
  
Biological name :ZDHHC9
  
Synonyms : Q9Y397 / ZDHHC9 / zinc finger DHHC-type containing 9
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: X
Strand: -1
Band: q26.1
Gene start: 129803288
Gene end: 129843909
  
Corresponding Affymetrix probe sets: 222451_s_at (Human Genome U133 Plus 2.0 Array)   235015_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000349689
Ensembl peptide - ENSP00000360103
Ensembl peptide - ENSP00000383991
Ensembl peptide - ENSP00000406165
NCBI entrez gene - 51114     See in Manteia.
OMIM - 300646
RefSeq - NM_001008222
RefSeq - NM_016032
RefSeq Peptide - NP_001008223
RefSeq Peptide - NP_057116
swissprot - Q9Y397
swissprot - H0Y6K6
swissprot - Q5JYE8
Ensembl - ENSG00000188706
  
Related genetic diseases (OMIM): 300799 - Mental retardation, X-linked syndromic, Raymond type, 300799
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
 zdhhc9ENSDARG00000060515Danio rerio
 ZDHHC9ENSGALG00000031551Gallus gallus
 P59268ENSMUSG00000036985Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q8IZN3 / ZDHHC14 / zinc finger DHHC-type containing 14ENSG0000017504858
Q9NUE0 / ZDHHC18 / zinc finger DHHC-type containing 18ENSG0000020416051
Q9ULC8 / ZDHHC8 / zinc finger DHHC-type containing 8ENSG0000009990435
Q9C0B5 / ZDHHC5 / zinc finger DHHC-type containing 5ENSG0000015659935
Q8WVZ1 / ZDHHC19 / zinc finger DHHC-type containing 19ENSG0000016395821
Q8WTX9 / ZDHHC1 / zinc finger DHHC-type containing 1ENSG0000015971419
Q9H8X9 / ZDHHC11 / zinc finger DHHC-type containing 11ENSG0000018881816
P0C7U3 / ZDHHC11B / zinc finger DHHC-type containing 11BENSG0000020607716


Protein motifs (from Interpro)
Interpro ID Name
 IPR001594  Palmitoyltransferase, DHHC domain
 IPR030292  Palmitoyltransferase ZDHHC9


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0018230 peptidyl-L-cysteine S-palmitoylation IDA
 biological_processGO:0018345 protein palmitoylation IDA
 cellular_componentGO:0000139 Golgi membrane IEA
 cellular_componentGO:0002178 palmitoyltransferase complex IDA
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0005789 endoplasmic reticulum membrane IEA
 cellular_componentGO:0005794 Golgi apparatus IEA
 cellular_componentGO:0005829 cytosol IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0031228 intrinsic component of Golgi membrane IDA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0016409 palmitoyltransferase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0016746 transferase activity, transferring acyl groups IEA
 molecular_functionGO:0019706 protein-cysteine S-palmitoyltransferase activity IEA
 molecular_functionGO:0043849 Ras palmitoyltransferase activity IDA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000053 Macroorchidism "The presence of abnormally large testes." [HPO:curators]
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 HP:0000218 High palate "Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective)." [pmid:19125428]
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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:0000256 Macrocephaly "The presence of an abnormally large `skull` (FMA:46565)." [HPO:probinson]
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 HP:0000275 Narrow face 
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 HP:0000322 Short philtrum 
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 HP:0000327 Hypoplasia of the maxilla "Underdevelopment of the `Maxilla` (FMA:9711)." [HPO:probinson]
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 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
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 HP:0000348 High forehead "An abnormally increased height of the forehead." [HPO:curators]
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 HP:0000369 Low-set ears "Low-set ears are defined to be set below an arbitrary line drawn between the lateral canthus of the eye and the occipital protruberance." [HPO:curators]
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 HP:0000411 Protruding ears 
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 HP:0000426 Prominent nasal bridge 
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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:0000678 Dental overcrowding 
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 HP:0000708 Behavioural/Psychiatric Abnormality 
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 HP:0000709 Psychosis "A condition characterized by changes of personality and thought patterns often accompanied by hallucinations and delusional beliefs." [HPO:curators]
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 HP:0000738 Hallucinations 
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 HP:0000767 Pectus excavatum "A defect of the chest wall characterized by a depression of the sternum, giving the chest ("pectus") a caved-in ("excavatum") appearance." [HPO:curators]
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 HP:0000768 Pectus carinatum "A deformity of the chest caused by overgrowth of the ribs and characterized by protrusion of the sternum." [HPO:curators]
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 HP:0001156 Brachydactyly 
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 HP:0001166 Arachnodactyly "Abnormally long and slender fingers ("spider fingers")." [HPO:curators]
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 HP:0001249 Mental retardation 
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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:0001252 Muscular hypotonia "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators]
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 HP:0001417 X-linked inheritance "A mode of inheritance that is observed for traits related to a gene encoded on the X chromosome." [HPO:curators]
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 HP:0001519 Dolichostenomelia "A tall and slim body build with increased arm span to height ratio (>1.05) and a reduced upper-to-lower segment ratio (<0.85), i.e., unusually long arms and legs. The extremities as well as the hands and feet are unusually slim." [HPO:curators]
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 HP:0001611 Nasal speech 
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 HP:0001631 Atrial septal defect "Atrial septal defect (ASD) is a congenital heart defect that enables blood flow between the left and right atria via the interatrial septum. The three common types of ASD are sinus venosus defects, ostium secundum defects, and ostium primum defects." [HPO:curators]
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 HP:0001763 Pes planus "A condition in which the arch of the foot is flat, with the entire sole of the foot being in near-complete contact with the ground." [HPO:curators]
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 HP:0002167 Neurological speech impairment 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0005692 Joint hyperflexibility 
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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:0007370 Aplasia/Hypoplasia of the corpus callosum "Absence or underdevelopment of the corpus callosum." [HPO:curators]
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 HP:0009183 Joint contractures of the 5th finger "Chronic loss of joint motion in the 5th finger due to structural changes in non-bony tissue. The term camptodactyly of the 5th finger is used if the distal and/or proximal interphalangeal joints are affected." [HPO:curators]
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 HP:0100490 Camptodactyly (hands) "Contractures of one ore more joints of the fingers." [HPO:sdoelken]
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 HP:0100753 Schizophrenia "A mental disorder characterized by a disintegration of thought processes and of emotional responsiveness. It most commonly manifests as auditory hallucinations, paranoid or bizarre delusions, or disorganized speech and thinking, and it is accompanied by significant social or occupational dysfunction. The onset of symptoms typically occurs in young adulthood, with a global lifetime prevalence of about 0.3-0.7%." [HPO:sdoelken]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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