ENSG00000177374


Homo sapiens

Features
Gene ID: ENSG00000177374
  
Biological name :HIC1
  
Synonyms : HIC1 / HIC ZBTB transcriptional repressor 1 / Q14526
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 17
Strand: 1
Band: p13.3
Gene start: 2054154
Gene end: 2063241
  
Corresponding Affymetrix probe sets: 208461_at (Human Genome U133 Plus 2.0 Array)   230218_at (Human Genome U133 Plus 2.0 Array)   235887_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000476554
Ensembl peptide - ENSP00000314080
Ensembl peptide - ENSP00000382742
Ensembl peptide - ENSP00000460268
Ensembl peptide - ENSP00000477858
Ensembl peptide - ENSP00000461476
Ensembl peptide - ENSP00000467045
NCBI entrez gene - 3090     See in Manteia.
OMIM - 603825
RefSeq - NM_006497
RefSeq - NM_001098202
RefSeq Peptide - NP_001091672
RefSeq Peptide - NP_006488
swissprot - V9GYA4
swissprot - I3L388
swissprot - K7ENQ1
swissprot - Q14526
swissprot - Q70SM2
Ensembl - ENSG00000177374
  

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
 hic1ENSDARG00000055493Danio rerio
 HIC1ENSGALG00000042077Gallus gallus
 Hic1ENSMUSG00000043099Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
HIC2 / Q96JB3 / HIC ZBTB transcriptional repressor 2ENSG0000016963539
A1YPR0 / ZBTB7C / zinc finger and BTB domain containing 7CENSG0000018482817
Q99592 / ZBTB18 / zinc finger and BTB domain containing 18ENSG0000017945616
B2RXF5 / ZBTB42 / zinc finger and BTB domain containing 42ENSG0000017962716
O15156 / ZBTB7B / zinc finger and BTB domain containing 7BENSG0000016068516
ZBTB3 / Q9H5J0 / zinc finger and BTB domain containing 3ENSG0000018567016
O95365 / ZBTB7A / zinc finger and BTB domain containing 7AENSG0000017895116
ZBTB5 / O15062 / zinc finger and BTB domain containing 5ENSG0000016879515
Q86UZ6 / ZBTB46 / zinc finger and BTB domain containing 46ENSG0000013058415
Q96DT7 / ZBTB10 / zinc finger and BTB domain containing 10ENSG0000020518914
Q8NAP8 / ZBTB8B / zinc finger and BTB domain containing 8BENSG0000027327413
AL033529.1ENSG0000025455313
Q96BR9 / ZBTB8A / zinc finger and BTB domain containing 8AENSG0000016006213


Protein motifs (from Interpro)
Interpro ID Name
 IPR000210  BTB/POZ domain
 IPR011333  SKP1/BTB/POZ domain superfamily
 IPR013083  Zinc finger, RING/FYVE/PHD-type
 IPR013087  Zinc finger C2H2-type
 IPR028424  Hypermethylated in cancer 1 protein
 IPR036236  Zinc finger C2H2 superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000122 negative regulation of transcription by RNA polymerase II ISS
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated TAS
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0008630 intrinsic apoptotic signaling pathway in response to DNA damage IDA
 biological_processGO:0016055 Wnt signaling pathway IEA
 biological_processGO:0030178 negative regulation of Wnt signaling pathway IDA
 biological_processGO:0043517 positive regulation of DNA damage response, signal transduction by p53 class mediator ISS
 cellular_componentGO:0000785 chromatin ISS
 cellular_componentGO:0005622 intracellular IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm TAS
 cellular_componentGO:0005829 cytosol IDA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding NAS
 molecular_functionGO:0001227 transcriptional repressor activity, RNA polymerase II transcription regulatory region sequence-specific DNA binding IDA
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003700 DNA-binding transcription factor activity TAS
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0042826 histone deacetylase binding IDA
 molecular_functionGO:0043565 sequence-specific DNA binding IDA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
SUMOylation of transcription factors


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000112 Nephropathy "A nonspecific term referring to disease or damage of the kidneys." [HPO:curators]
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 HP:0000177 Abnormality of upper lip "An abnormality of the `upper lip` (FMA:59817)." [HPO:probinson]
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 HP:0000286 Epicanthus "An epicanthal fold is a semilunar fold of skin that extends from the upper eyelid across the medial canthal area to the lower eyelid." [HPO:curators]
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 HP:0000348 High forehead "An abnormally increased height of the forehead." [HPO:curators]
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 HP:0000463 Nares, anteverted "Anteriorly-facing nostrils viewed with the head in the Frankfurt horizontal and the eyes of the observer level with the eyes of the subject." [pmid:19152422]
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 HP:0000960 Sacral dimple "A subtype of `skin dimples` (HP:0010781) presenting as an indentation in the skin of the intergluteal cleft ." [HPO:probinson]
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001251 Ataxia "Ataxia is a nonspecific neurological sign and symptom consisting of gross lack of coordination of muscle movements. Ataxia is caused by dysfunction of one or more parts of the nervous system including the cerebellum, the sensory nervous system, the vestibular system, or the cerebral cortex." [HPO:curators]
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 HP:0001339 Lissencephaly "A congenital absence of the convolutions of the cerebral cortex and a poorly formed sylvian fissure." [HPO:curators]
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 HP:0001510 Growth retardation 
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 HP:0001539 Omphalocele 
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 HP:0001561 Polyhydramnios 
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 HP:0001626 Abnormality of the cardiovascular system "Any abnormality of the heart or vasculature." [HPO:curators]
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 HP:0002079 Hypoplasia of the corpus callosum "Underdevelopment of the corpus callosum." [HPO:curators]
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 HP:0002120 Cerebral cortical atrophy 
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 HP:0002353 EEG abnormalities "Abnormality observed by electroencephalogram (EEG), which is used to record of the brain s spontaneous electrical activity from multiple electrodes placed on the scalp." [HPO:curators]
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 HP:0003196 Nasal hypoplasia "Underdevelopment of the `nose` (FMA:46472)." [HPO:probinson]
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 HP:0004209 Clinodactyly of the 5th finger "Clinodactyly refers to a bending or curvature of the `fifth finger` (FMA:24949) in the radial direction (i.e., towards the 4th finger)." [HPO:curators]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000116030 SUMO1 / P63165 / small ubiquitin-like modifier 1  / complex / reaction
 ENSG00000103275 UBE2I / P63279 / ubiquitin conjugating enzyme E2 I  / reaction






 

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