ENSG00000142178


Homo sapiens

Features
Gene ID: ENSG00000142178
  
Biological name :SIK1
  
Synonyms : P57059 / salt inducible kinase 1 / SIK1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 21
Strand: -1
Band: q22.3
Gene start: 43414483
Gene end: 43427189
  
Corresponding Affymetrix probe sets: 208078_s_at (Human Genome U133 Plus 2.0 Array)   232470_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000270162
Ensembl peptide - ENSP00000495479
NCBI entrez gene - 150094     See in Manteia.
OMIM - 605705
RefSeq - XM_011529474
RefSeq - NM_173354
RefSeq Peptide - NP_775490
swissprot - P57059
Ensembl - ENSG00000142178
  
Related genetic diseases (OMIM): 616341 - Epileptic encephalopathy, early infantile, 30, 616341
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
 sik1ENSDARG00000058606Danio rerio
 SIK1ENSGALG00000041988Gallus gallus
 Sik1ENSMUSG00000024042Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
SIK1B / salt inducible kinase 1B (putative)ENSG00000275993100
SIK2 / Q9H0K1 / salt inducible kinase 2ENSG0000017014549
SIK3 / SIK family kinase 3ENSG0000016058438
MARK4 / Q96L34 / microtubule affinity regulating kinase 4ENSG0000000704729
MARK3 / P27448 / microtubule affinity regulating kinase 3ENSG0000007541329
MARK1 / Q9P0L2 / microtubule affinity regulating kinase 1ENSG0000011614128
MARK2 / Q7KZI7 / microtubule affinity regulating kinase 2ENSG0000007251828
SNRK / Q9NRH2 / SNF related kinaseENSG0000016378822
NIM1K / Q8IY84 / NIM1 serine/threonine protein kinaseENSG0000017745317


Protein motifs (from Interpro)
Interpro ID Name
 IPR000719  Protein kinase domain
 IPR008271  Serine/threonine-protein kinase, active site
 IPR011009  Protein kinase-like domain superfamily
 IPR015940  Ubiquitin-associated domain
 IPR017090  Serine/threonine-protein kinase, SIK1/2
 IPR017441  Protein kinase, ATP binding site
 IPR034672  Salt-Inducible kinase, catalytic domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0002028 regulation of sodium ion transport ISS
 biological_processGO:0006468 protein phosphorylation IEA
 biological_processGO:0007049 cell cycle IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0007346 regulation of mitotic cell cycle ISS
 biological_processGO:0010830 regulation of myotube differentiation ISS
 biological_processGO:0010868 negative regulation of triglyceride biosynthetic process ISS
 biological_processGO:0016310 phosphorylation IEA
 biological_processGO:0030154 cell differentiation IEA
 biological_processGO:0032792 negative regulation of CREB transcription factor activity ISS
 biological_processGO:0032870 cellular response to hormone stimulus IBA
 biological_processGO:0035556 intracellular signal transduction ISS
 biological_processGO:0043153 entrainment of circadian clock by photoperiod ISS
 biological_processGO:0045595 regulation of cell differentiation ISS
 biological_processGO:0045721 negative regulation of gluconeogenesis ISS
 biological_processGO:0046777 protein autophosphorylation IDA
 biological_processGO:0048511 rhythmic process IEA
 biological_processGO:0055007 cardiac muscle cell differentiation ISS
 biological_processGO:2000210 positive regulation of anoikis IMP
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005737 cytoplasm ISS
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0000287 magnesium ion binding ISS
 molecular_functionGO:0004672 protein kinase activity IEA
 molecular_functionGO:0004674 protein serine/threonine kinase activity IDA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0008140 cAMP response element binding protein binding ISS
 molecular_functionGO:0016301 kinase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0019901 protein kinase binding IPI
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0071889 14-3-3 protein binding IDA


Pathways (from Reactome)
Pathway description
Circadian Clock


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:0000733 Stereotyped, repetitive behaviour 
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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:0001254 Lethargy 
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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:0001298 Encephalopathy 
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 HP:0001336 Myoclonus "Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements." [HPO:curators]
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 HP:0001344 Absent speech development 
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 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
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 HP:0001522 Death in infancy 
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 HP:0002015 Dysphagia "Difficulty in swallowing." [HPO:curators]
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 HP:0002033 Poor suck "An inadequate sucking reflex, resulting in the difficult of newborns to be breast-fed." [HPO:curators]
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 HP:0002069 Generalized tonic-clonic seizures "Generalized tonic-clonic seizures are `generalized seizures` (HP:0002197) in which the patient suddenly loses conciousness, the eyes roll back, and the entire body musculature undergoes tonic contractions. In the clonic phase of the seizure, there are rhythmic contractions of the musculature alternating with relaxation of all muscle groups. Loss of sphincter control during the seizure is common. This form of seizure was formerly commonly called grand mal seizure." [HPO:curators]
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 HP:0002098 Respiratory distress 
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 HP:0002123 Myoclonic seizures "Myoclonic seizures are sudden, brief losses of consciousness and postural tone not associated with tonic muscular contractions. Myoclonic seizures may involve one body part or the entire body. In the latter case, the myoclonic seizure is accompanied by a violent fall but not by loss of consciousness." [HPO:curators]
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 HP:0002205 Recurrent respiratory infections 
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 HP:0002376 Developmental regression 
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 HP:0002521 Hypsarrhythmia "Hypsarrhythmia is abnormal interictal high amplitude waves and a background of irregular spikes demonstrated by electroencephalography (EEG)." [HPO:curators]
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 HP:0011121 Abnormality of skin morphology "Any morphological abnormality of the `skin` (FMA:7163)." [HPO:probinson]
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 HP:0011167 Focal tonic seizures "Seizures with sustained increase in muscle contraction in parts of the body lasting a few seconds to minutes." [HPO:jalbers]
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 HP:0011168 Eyelid myoclonias "Focal seizure with eyelid myoclonia, not eyelid myoclonias in the context of absence seizures." [HPO:ihelbig]
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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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 HP:0012469 Infantile spasms "Infantile spasms represent a subset of "epileptic spasms". Infantile Spasms are epileptic spasms starting in the first year of life (infancy)." [HPO:ihelbig]
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 HP:0200134 Epileptic encephalopathy 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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