ENSG00000102383


Homo sapiens

Features
Gene ID: ENSG00000102383
  
Biological name :ZDHHC15
  
Synonyms : Q96MV8 / ZDHHC15 / zinc finger DHHC-type containing 15
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: X
Strand: -1
Band: q13.3
Gene start: 75368427
Gene end: 75523502
  
Corresponding Affymetrix probe sets: 1552557_a_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000362465
Ensembl peptide - ENSP00000445420
NCBI entrez gene - 158866     See in Manteia.
OMIM - 300576
RefSeq - XM_017029298
RefSeq - NM_001146256
RefSeq - NM_144969
RefSeq - XM_006724624
RefSeq - XM_017029296
RefSeq - XM_017029297
RefSeq Peptide - NP_659406
RefSeq Peptide - NP_001139728
swissprot - Q96MV8
Ensembl - ENSG00000102383
  
Related genetic diseases (OMIM): 300577 - ?Mental retardation, X-linked 91, 300577
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
 zdhhc15bENSDARG00000071872Danio rerio
 ZDHHC15ENSGALG00000007800Gallus gallus
 Q8BGJ0ENSMUSG00000033906Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9UIJ5 / ZDHHC2 / zinc finger DHHC-type containing 2ENSG0000010421958
Q5W0Z9 / ZDHHC20 / zinc finger DHHC-type containing 20ENSG0000018077655
Q9NYG2 / ZDHHC3 / zinc finger DHHC-type containing 3ENSG0000016381222
Q9NXF8 / ZDHHC7 / zinc finger DHHC-type containing 7ENSG0000015378621
Q8IVQ6 / ZDHHC21 / zinc finger DHHC-type containing 21ENSG0000017589318
Q8IYP9 / ZDHHC23 / zinc finger DHHC-type containing 23ENSG0000018430716


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


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0016188 synaptic vesicle maturation IBA
 biological_processGO:0018345 protein palmitoylation IDA
 biological_processGO:0045184 establishment of protein localization IEA
 cellular_componentGO:0005794 Golgi apparatus IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0016409 palmitoyltransferase activity IDA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0016746 transferase activity, transferring acyl groups IEA
 molecular_functionGO:0019706 protein-cysteine S-palmitoyltransferase activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 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:0000286 Epicanthus "An epicanthal fold is a semilunar fold of skin that extends from the upper eyelid across the medial canthal area to the lower eyelid." [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:0001256 Mental retardation, mild "Mild mental retardation is defined as an intelligence quotient (IQ) in the range of 50-69." [HPO:curators]
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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:0001344 Absent speech development 
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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:0001423 X-linked dominant inheritance "A mode of inheritance that is observed for dominant traits related to a gene encoded on the X chromosome. In the context of medical genetics, X-linked dominant disorders tend to manifest very severely in affected males. The severity of manifestation in females may depend on the degree of skewed X inactivation." [HPO:curators]
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 HP:0001513 Obesity "A status with BODY WEIGHT that is grossly above the acceptable or desirable weight, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY)." [MeSH:D009765]
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 HP:0001572 Macrodontia "Increased size of one or more teeth." [HPO:curators]
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 HP:0001773 Short, broad feet "Abnormally short and wide feet." [HPO:curators]
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 HP:0001999 Facial dysmorphism 
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 HP:0002162 Low posterior hairline 
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 HP:0002967 Cubitus valgus 
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 HP:0003196 Nasal hypoplasia "Underdevelopment of the `nose` (FMA:46472)." [HPO:probinson]
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 HP:0006829 Severe muscular hypotonia "A severe degree of muscular hypotonia characterized by markedly reduced muscle tone." [HPO:curators]
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 HP:0009237 Hypoplastic/small 5th finger "Hypoplastic/small 5th (little) finger." [HPO:curators]
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 HP:0200055 Small hands 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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