ENSG00000163374


Homo sapiens

Features
Gene ID: ENSG00000163374
  
Biological name :YY1AP1
  
Synonyms : Q9H869 / YY1AP1 / YY1 associated protein 1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 1
Strand: -1
Band: q22
Gene start: 155659443
Gene end: 155689000
  
Corresponding Affymetrix probe sets: 217836_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000385390
Ensembl peptide - ENSP00000384583
Ensembl peptide - ENSP00000385791
Ensembl peptide - ENSP00000413240
Ensembl peptide - ENSP00000409203
Ensembl peptide - ENSP00000390116
Ensembl peptide - ENSP00000295566
Ensembl peptide - ENSP00000311138
Ensembl peptide - ENSP00000316079
Ensembl peptide - ENSP00000346722
Ensembl peptide - ENSP00000347686
Ensembl peptide - ENSP00000352134
Ensembl peptide - ENSP00000354716
Ensembl peptide - ENSP00000355298
Ensembl peptide - ENSP00000357314
Ensembl peptide - ENSP00000357323
Ensembl peptide - ENSP00000357324
NCBI entrez gene - 55249     See in Manteia.
OMIM - 607860
RefSeq - NM_001198906
RefSeq - NM_001198899
RefSeq - NM_001198900
RefSeq - NM_001198901
RefSeq - NM_001198902
RefSeq - NM_001198903
RefSeq - NM_001198904
RefSeq - NM_001198905
RefSeq - NM_018253
RefSeq - NM_139118
RefSeq - NM_139119
RefSeq - NM_139121
RefSeq Peptide - NP_001185831
RefSeq Peptide - NP_001185832
RefSeq Peptide - NP_001185833
RefSeq Peptide - NP_001185834
RefSeq Peptide - NP_001185835
RefSeq Peptide - NP_060723
RefSeq Peptide - NP_620829
RefSeq Peptide - NP_001185830
RefSeq Peptide - NP_620830
RefSeq Peptide - NP_620832
RefSeq Peptide - NP_001185828
RefSeq Peptide - NP_001185829
swissprot - B0QZ55
swissprot - Q68CT8
swissprot - Q9H869
swissprot - B4DZQ4
swissprot - A3KFK1
swissprot - A3KFK2
swissprot - F8WD62
Ensembl - ENSG00000163374
  
Related genetic diseases (OMIM): 602531 - Grange syndrome, 602531
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
 gon4lENSDARG00000005867Danio rerio
 si:dkey-27c15.3ENSDARG00000056847Danio rerio
 ENSGALG00000014643Gallus gallus
 Gon4lENSMUSG00000054199Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
GON4L / Q3T8J9 / gon-4 likeENSG0000011658082


Protein motifs (from Interpro)
Interpro ID Name
 IPR033274  YY1-associated protein 1
 IPR033277  GON-4-like protein


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0008283 cell proliferation IMP
 biological_processGO:0030154 cell differentiation IMP
 biological_processGO:0030183 B cell differentiation IEA
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IEA
 biological_processGO:0051726 regulation of cell cycle IMP
 cellular_componentGO:0001650 fibrillar center IDA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IEA
 cellular_componentGO:0005730 nucleolus IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0031011 Ino80 complex IDA
 molecular_functionGO:0003714 transcription corepressor activity IEA
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
No match


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]
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 HP:0000822 Hypertension "High blood pressure." [HPO:curators]
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 HP:0001156 Brachydactyly 
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 HP:0001159 Syndactyly "Webbing or fusion of the fingers or toes, involving soft parts only or including bone structure. Bony fusions are revered to as "bony" Syndactyly if the fusion occurs in a radio-ulnar axis. Fusions of bones of the fingers or toes in a proximo-distal axis are refered to as "Symphalangism"." [HPO:curators]
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 HP:0001249 Mental retardation 
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 HP:0001328 Learning disability 
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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:0001643 Patent ductus arteriosus 
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 HP:0001647 Bicuspid aortic valve "The presence of a bicuspid `aortic valve` (FMA:7236)." [HPO:probinson]
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 HP:0001659 Aortic insufficiency "An insufficiency of the aortic valve, leading to regurgitation (backward flow) of blood from the aorta into the left ventricle." [HPO:curators]
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 HP:0001920 Renal artery stenosis 
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 HP:0002659 Increased susceptibility to fractures "An abnormally increased tendency to fractures of bones caused by an abnormal reduction in bone strength that is generally associated with an increased risk of fracture." [HPO:sdoelken]
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 HP:0002757 Recurrent fractures "The repeated occurence of bone fractures (implying an abnormally increased tendency for fracture)." [HPO:curators]
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 HP:0004279 Hypoplastic hand 
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 HP:0004325 Decreased body weight 
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 HP:0005145 Coronary artery stenosis 
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 HP:0006889 Mental retardation, borderline "Borderline intellectual retardation is defined as an intelligence quotient (IQ) in the range of 70-79." [HPO:curators]
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 HP:0100545 Arterial stenosis 
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 HP:0100817 Renovascular hypertension "The presence of `hypertension` (HP:0000822) related to stenosis of the `renal artery` (FMA:14751)." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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