ENSG00000118495


Homo sapiens

Features
Gene ID: ENSG00000118495
  
Biological name :PLAGL1
  
Synonyms : PLAG1 like zinc finger 1 / PLAGL1 / Q9UM63
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 6
Strand: -1
Band: q24.2
Gene start: 143940300
Gene end: 144064599
  
Corresponding Affymetrix probe sets: 207002_s_at (Human Genome U133 Plus 2.0 Array)   207943_x_at (Human Genome U133 Plus 2.0 Array)   209318_x_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000485907
Ensembl peptide - ENSP00000400929
Ensembl peptide - ENSP00000486355
Ensembl peptide - ENSP00000487447
Ensembl peptide - ENSP00000486763
Ensembl peptide - ENSP00000486752
Ensembl peptide - ENSP00000486711
Ensembl peptide - ENSP00000486632
Ensembl peptide - ENSP00000346810
Ensembl peptide - ENSP00000353734
Ensembl peptide - ENSP00000356543
Ensembl peptide - ENSP00000356544
Ensembl peptide - ENSP00000376124
Ensembl peptide - ENSP00000392418
Ensembl peptide - ENSP00000395960
Ensembl peptide - ENSP00000400060
NCBI entrez gene - 5325     See in Manteia.
OMIM - 603044
RefSeq - NM_006718
RefSeq - NM_001080951
RefSeq - NM_001080952
RefSeq - NM_001080953
RefSeq - NM_001080954
RefSeq - NM_001080955
RefSeq - NM_001080956
RefSeq - NM_001289037
RefSeq - NM_001289038
RefSeq - NM_001289039
RefSeq - NM_001289040
RefSeq - NM_001289041
RefSeq - NM_001289042
RefSeq - NM_001289043
RefSeq - NM_001289044
RefSeq - NM_001289045
RefSeq - NM_001289046
RefSeq - NM_001289047
RefSeq - NM_001289048
RefSeq - NM_001289049
RefSeq - NM_001317156
RefSeq - NM_001317157
RefSeq - NM_001317158
RefSeq - NM_001317159
RefSeq - NM_001317160
RefSeq - NM_001317161
RefSeq - NM_001317162
RefSeq Peptide - NP_001304089
RefSeq Peptide - NP_001304091
RefSeq Peptide - NP_006709
RefSeq Peptide - NP_001275976
RefSeq Peptide - NP_001275977
RefSeq Peptide - NP_001275978
RefSeq Peptide - NP_001304085
RefSeq Peptide - NP_001304086
RefSeq Peptide - NP_001304087
RefSeq Peptide - NP_001304088
RefSeq Peptide - NP_001304090
RefSeq Peptide - NP_001074420
RefSeq Peptide - NP_001074421
RefSeq Peptide - NP_001074422
RefSeq Peptide - NP_001074423
RefSeq Peptide - NP_001074424
RefSeq Peptide - NP_001074425
RefSeq Peptide - NP_001275966
RefSeq Peptide - NP_001275967
RefSeq Peptide - NP_001275968
RefSeq Peptide - NP_001275969
RefSeq Peptide - NP_001275970
RefSeq Peptide - NP_001275971
RefSeq Peptide - NP_001275972
RefSeq Peptide - NP_001275973
RefSeq Peptide - NP_001275974
RefSeq Peptide - NP_001275975
swissprot - Q68DN7
swissprot - Q9UM63
swissprot - A0A0D9SEQ4
swissprot - A0A0D9SGF7
swissprot - A0A0D9SFM8
swissprot - A0A0D9SFI7
swissprot - A1YLA2
swissprot - A1YLA1
Ensembl - ENSG00000118495
  
Related genetic diseases (OMIM): 601410 - {Diabetes mellitus, transient neonatal}, 601410

This gene has been taged as a transcription factor by TFT
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
 PLAGL1ENSGALG00000013754Gallus gallus
 Plagl1ENSMUSG00000019817Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
PLAG1 / Q6DJT9 / PLAG1 zinc fingerENSG0000018169044
PLAGL2 / Q9UPG8 / PLAG1 like zinc finger 2ENSG0000012600337


Protein motifs (from Interpro)
Interpro ID Name
 IPR013083  Zinc finger, RING/FYVE/PHD-type
 IPR013087  Zinc finger C2H2-type
 IPR027770  Zinc finger protein PLAGL1
 IPR036236  Zinc finger C2H2 superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0006357 regulation of transcription by RNA polymerase II IEA
 biological_processGO:0006366 transcription by RNA polymerase II IEA
 biological_processGO:0006915 apoptotic process TAS
 biological_processGO:0006977 DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest TAS
 biological_processGO:0007050 cell cycle arrest TAS
 biological_processGO:0030154 cell differentiation IBA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IDA
 cellular_componentGO:0005634 nucleus IBA
 cellular_componentGO:0005654 nucleoplasm TAS
 cellular_componentGO:0005794 Golgi apparatus IDA
 cellular_componentGO:0016604 nuclear body IDA
 cellular_componentGO:0043231 intracellular membrane-bounded organelle IDA
 molecular_functionGO:0000977 RNA polymerase II regulatory region sequence-specific DNA binding IEA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding NAS
 molecular_functionGO:0001228 transcriptional activator activity, RNA polymerase II transcription regulatory region sequence-specific DNA binding IDA
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003677 DNA binding IDA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000028 Cryptorchidism "Absence of one or both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis." [HPO:curators]
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 HP:0000065 Labial hypertrophy 
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 HP:0000124 Renal tubular dysfunction 
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 HP:0000158 Macroglossia "Increased length and width of the tongue." [pmid:19125428]
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 HP:0000212 Gingival hyperplasia 
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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:0000237 Small anterior fontanelle "Abnormally decreased size of the anterior fontanelle with respect to age-dependent norms." [HPO:curators]
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 HP:0000269 Prominent occiput 
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 HP:0000278 Retrognathia 
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 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
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 HP:0000363 Abnormality of ear lobes 
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 HP:0000365 Hearing loss 
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 HP:0000448 Prominent nose 
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 HP:0000586 Shallow orbits 
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 HP:0000826 Precocious puberty "The onset of secondary sexual characteristics before a normal age. Although it is difficult to define normal age ranges because of the marked variation with which puberty begins in normal children, precocious puberty can be defined as the onset of puberty before the age of 8 years in girls or 9 years in boys." [HPO:curators]
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 HP:0000857 Neonatal insulin-dependent diabetes mellitus 
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 HP:0001249 Mental retardation 
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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:0001259 Coma 
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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:0001270 Motor retardation 
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 HP:0001388 Joint laxity 
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 HP:0001488 Bilateral ptosis 
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 HP:0001508 Failure to thrive 
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 HP:0001511 Intrauterine growth retardation 
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 HP:0001537 Umbilical hernia "Protrusion of abdominal contents through a defect in the abdominal wall musculature around the umbilicus. Skin and subcutaneous tissue overlie the defect." [HPO:curators]
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 HP:0001562 Oligohydramnios 
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 HP:0001627 Cardiac abnormality "An abnormality of the `heart` (FMA:7088)." [HPO:probinson]
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 HP:0001629 Ventricular septal defect "A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum." [HPO:curators]
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 HP:0001640 Cardiomegaly 
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 HP:0001643 Patent ductus arteriosus 
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 HP:0001804 Hypoplastic fingernails "Underdeveloped fingernails." [HPO:curators]
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 HP:0001824 Weight loss 
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 HP:0001944 Dehydration 
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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: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:0002186 Apraxia "A defect in the understanding of complex motor commands and in the execution of certain learned movements, i.e., deficits in the cognitive components of learned movements." [HPO:curators]
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 HP:0002240 Hepatomegaly "An abnormal enlargment of the liver." [HPO:curators]
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 HP:0002570 Steatorrhea 
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 HP:0002643 Neonatal respiratory distress 
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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:0002804 Arthrogryposis multiplex congenita 
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 HP:0002919 Ketonuria 
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 HP:0003074 Hyperglycemia 
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 HP:0003076 Glycosuria "The excretion of abnormal amounts of glucose in the urine, generally resulting in osmotic diuresis." [HPO:curators]
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 HP:0005487 Prominent metopic suture "A prominent persistent frontal suture (metopic suture)." [HPO:curators]
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 HP:0005750 Contractures of lower limbs 
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 HP:0006476 Abnormality of the pancreatic islet cells "An abnormality of the islet of Langerhans, i.e., of the regions of the pancreas that contain its endocrine cells. These are the alpha cells, which produce glucogon, the beta cells, which produce insulin and amylin, the delta cells, which produce somatostatin, the PP cells, which produce pancreatic polypeptide, and the epsilon cells, which produce ghrelin." [HPO:curators]
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 HP:0008255 Transient neonatal diabetes mellitus 
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 HP:0008897 Growth retardation, progressive 
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 HP:0011106 Hypovolemia "An decrease in the amount of intravascular fluid, particularly in the volume of the circulating blood." [HPO:probinson]
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 HP:0100767 Abnormality of the placenta "An abnormality of the placenta, the organ that connects the developing fetus to the uterine wall to enable nutrient uptake, waste elimination, and gas exchange." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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