ENSG00000131931


Homo sapiens

Features
Gene ID: ENSG00000131931
  
Biological name :THAP1
  
Synonyms : Q9NVV9 / THAP1 / THAP domain containing 1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 8
Strand: -1
Band: p11.21
Gene start: 42836674
Gene end: 42843325
  
Corresponding Affymetrix probe sets: 219292_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000254250
Ensembl peptide - ENSP00000433912
Ensembl peptide - ENSP00000344966
NCBI entrez gene - 55145     See in Manteia.
OMIM - 609520
RefSeq - NM_018105
RefSeq - NM_199003
RefSeq Peptide - NP_060575
RefSeq Peptide - NP_945354
swissprot - E9PIS9
swissprot - Q9NVV9
Ensembl - ENSG00000131931
  
Related genetic diseases (OMIM): 602629 - Dystonia 6, torsion, 602629

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
 thap1ENSDARG00000059020Danio rerio
 THAP1ENSGALG00000015385Gallus gallus
 Thap1ENSMUSG00000037214Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
THAP2 / Q9H0W7 / THAP domain containing 2ENSG0000017345132
THAP4 / Q8WY91 / THAP domain containing 4ENSG0000017694631
THAP3 / Q8WTV1 / THAP domain containing 3ENSG0000004198830
THAP5 / Q7Z6K1 / THAP domain containing 5ENSG0000017768324
THAP8 / Q8NA92 / THAP domain containing 8ENSG0000016127719
AC073612.1ENSG0000025806414


Protein motifs (from Interpro)
Interpro ID Name
 IPR006612  THAP-type zinc finger
 IPR026516  THAP domain-containing protein 1


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000122 negative regulation of transcription by RNA polymerase II IDA
 biological_processGO:0001935 endothelial cell proliferation IMP
 biological_processGO:0006351 transcription, DNA-templated IMP
 biological_processGO:0006355 regulation of transcription, DNA-templated IMP
 biological_processGO:0007049 cell cycle IEA
 biological_processGO:0007346 regulation of mitotic cell cycle IMP
 cellular_componentGO:0001650 fibrillar center IDA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IEA
 cellular_componentGO:0016605 PML body IEA
 cellular_componentGO:0043231 intracellular membrane-bounded organelle IDA
 molecular_functionGO:0000978 RNA polymerase II proximal promoter sequence-specific DNA binding IDA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding ISM
 molecular_functionGO:0001078 transcriptional repressor activity, RNA polymerase II proximal promoter sequence-specific DNA binding IC
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008270 zinc ion binding IDA
 molecular_functionGO:0042802 identical protein binding IPI
 molecular_functionGO:0042803 protein homodimerization activity IDA
 molecular_functionGO:0043565 sequence-specific DNA binding IMP
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
No match


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:0000234 Head abnormality 
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 HP:0000473 Torticollis 
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 HP:0000643 Blepharospasm "An involuntary recurrent spasm of both eyelids." [HPO:curators]
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 HP:0001260 Dysarthria "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators]
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 HP:0001304 Torsion dystonia 
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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:0001618 Dysphonia 
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 HP:0002356 Writer s cramp 
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 HP:0002451 Limb dystonia 
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 HP:0003829 Incomplete penetrance 
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 HP:0007325 Generalized dystonia 
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 HP:0012048 Oromandibular dystonia "A kind of focal dystonia characterized by forceful contractions of the face, jaw, and/or tongue causing difficulty in opening and closing the mouth and often affecting chewing and speech." [HPO:probinson]
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 HP:0012049 Laryngeal dystonia "A form of focal dystonia that affects the vocal cords, associated with involuntary contractions of the vocal cords causing interruptions of speech and affecting the voice quality and often leading to patterned, repeated breaks in speech." [HPO:probinson]
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 HP:0031008 Lingual dystonia "Involuntary protrusions, movements, spams and contortions of the tongue." [PMID:24808861]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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