ENSG00000134759


Homo sapiens

Features
Gene ID: ENSG00000134759
  
Biological name :ELP2
  
Synonyms : elongator acetyltransferase complex subunit 2 / ELP2 / Q6IA86
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 18
Strand: 1
Band: q12.2
Gene start: 36129444
Gene end: 36180556
  
Corresponding Affymetrix probe sets: 230178_s_at (Human Genome U133 Plus 2.0 Array)   231713_s_at (Human Genome U133 Plus 2.0 Array)   235623_at (Human Genome U133 Plus 2.0 Array)   238709_at (Human Genome U133 Plus 2.0 Array)   243735_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000468091
Ensembl peptide - ENSP00000257191
Ensembl peptide - ENSP00000316051
Ensembl peptide - ENSP00000350967
Ensembl peptide - ENSP00000391202
Ensembl peptide - ENSP00000443555
Ensembl peptide - ENSP00000443800
Ensembl peptide - ENSP00000414851
Ensembl peptide - ENSP00000438533
Ensembl peptide - ENSP00000440426
Ensembl peptide - ENSP00000440516
Ensembl peptide - ENSP00000440651
Ensembl peptide - ENSP00000440774
NCBI entrez gene - 55250     See in Manteia.
OMIM - 616054
RefSeq - NM_001242875
RefSeq - NM_001242877
RefSeq - NM_001242878
RefSeq - NM_001242879
RefSeq - NM_018255
RefSeq - NM_001242876
RefSeq Peptide - NP_001229804
RefSeq Peptide - NP_001229806
RefSeq Peptide - NP_001229807
RefSeq Peptide - NP_001229808
RefSeq Peptide - NP_060725
RefSeq Peptide - NP_001229805
swissprot - Q6IA86
swissprot - F5GWY6
swissprot - F5GX79
swissprot - F5GYE9
swissprot - H0YFW0
swissprot - K7ER35
Ensembl - ENSG00000134759
  
Related genetic diseases (OMIM): 617270 - Mental retardation, autosomal recessive 58, 617270
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
 elp2ENSDARG00000017199Danio rerio
 ELP2ENSGALG00000039034Gallus gallus
 Elp2ENSMUSG00000024271Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR001680  WD40 repeat
 IPR011043  Galactose oxidase/kelch, beta-propeller
 IPR011047  Quinoprotein alcohol dehydrogenase-like superfamily
 IPR015943  WD40/YVTN repeat-like-containing domain superfamily
 IPR017986  WD40-repeat-containing domain
 IPR036322  WD40-repeat-containing domain superfamily
 IPR037289  Elongator complex protein 2


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0002098 tRNA wobble uridine modification IEA
 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 TAS
 biological_processGO:0006368 transcription elongation from RNA polymerase II promoter TAS
 biological_processGO:0046425 regulation of JAK-STAT cascade IEA
 cellular_componentGO:0000123 histone acetyltransferase complex IDA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005737 cytoplasm NAS
 cellular_componentGO:0005829 cytosol IDA
 cellular_componentGO:0008023 transcription elongation factor complex IDA
 cellular_componentGO:0033588 Elongator holoenzyme complex IEA
 molecular_functionGO:0000993 RNA polymerase II core binding IDA
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0019901 protein kinase binding IEA


Pathways (from Reactome)
Pathway description
HATs acetylate histones


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive 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 homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
Show

 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:0000733 Stereotyped, repetitive behaviour 
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 HP:0000750 Impaired language development 
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 HP:0001249 Mental retardation 
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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:0001264 Spastic diplegia "Spasticity (neuromuscular hypertonia) primarily in the muscles of the legs, hips, and pelvis." [HPO:curators]
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 HP:0001266 Choreoathetosis 
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 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
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 HP:0002421 Poor head control 
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 HP:0003577 Onset at birth 
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 HP:0003676 Progressive disorder 
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0008936 Muscular hypotonia of the trunk "Muscular hypotonia (abnormally low muscle tone) affecting the musculature of the trunk." [HPO:curators]
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 HP:0011856 Pica "An appetite for and the persistent ingestion of non-food substances such as clay. In order to diagnose pica, this behavior must have persisted over a period of at least one month." [HPO:probinson]
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 HP:0100716 Autoagression "Aggression towards oneself." [HPO:sdoelken]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000134014 ELP3 / Q9H9T3 / elongator acetyltransferase complex subunit 3  / complex
 ENSG00000163832 ELP6 / Q0PNE2 / elongator acetyltransferase complex subunit 6  / complex
 ENSG00000070061 ELP1 / O95163 / elongator complex protein 1  / complex
 ENSG00000170291 ELP5 / Q8TE02 / elongator acetyltransferase complex subunit 5  / complex
 ENSG00000109911 ELP4 / Q96EB1 / elongator acetyltransferase complex subunit 4  / complex
 ENSG00000276180 P62805 / HIST1H4I / histone cluster 1 H4 family member i  / reaction






 

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