ENSG00000165140


Homo sapiens

Features
Gene ID: ENSG00000165140
  
Biological name :FBP1
  
Synonyms : FBP1 / fructose-bisphosphatase 1 / P09467
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 9
Strand: -1
Band: q22.32
Gene start: 94603133
Gene end: 94640249
  
Corresponding Affymetrix probe sets: 209696_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000364475
Ensembl peptide - ENSP00000408025
Ensembl peptide - ENSP00000411619
NCBI entrez gene - 2203     See in Manteia.
OMIM - 611570
RefSeq - XM_006717005
RefSeq - NM_000507
RefSeq - NM_001127628
RefSeq Peptide - NP_001121100
RefSeq Peptide - NP_000498
swissprot - P09467
swissprot - Q5VZC3
Ensembl - ENSG00000165140
  
Related genetic diseases (OMIM): 229700 - Fructose-1,6-bisphosphatase deficiency, 229700
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
 FBP1ENSGALG00000012613Gallus gallus
 Fbp1ENSMUSG00000069805Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
FBP2 / O00757 / fructose-bisphosphatase 2ENSG0000013095776


Protein motifs (from Interpro)
Interpro ID Name
 IPR000146  Fructose-1,6-bisphosphatase class 1
 IPR020548  Fructose-1,6-bisphosphatase, active site
 IPR028343  Fructose-1,6-bisphosphatase
 IPR033391  Fructose-1-6-bisphosphatase class I, N-terminal


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000122 negative regulation of transcription by RNA polymerase II IMP
 biological_processGO:0005975 carbohydrate metabolic process IEA
 biological_processGO:0005986 sucrose biosynthetic process IBA
 biological_processGO:0006000 fructose metabolic process TAS
 biological_processGO:0006002 fructose 6-phosphate metabolic process IDA
 biological_processGO:0006094 gluconeogenesis TAS
 biological_processGO:0006111 regulation of gluconeogenesis IMP
 biological_processGO:0008152 metabolic process IEA
 biological_processGO:0016311 dephosphorylation IMP
 biological_processGO:0030308 negative regulation of cell growth IDA
 biological_processGO:0030388 fructose 1,6-bisphosphate metabolic process IBA
 biological_processGO:0035690 cellular response to drug IDA
 biological_processGO:0045820 negative regulation of glycolytic process IMP
 biological_processGO:0046580 negative regulation of Ras protein signal transduction IDA
 biological_processGO:0051289 protein homotetramerization IDA
 biological_processGO:0071286 cellular response to magnesium ion IDA
 cellular_componentGO:0005634 nucleus IMP
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005829 cytosol IBA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0001191 transcriptional repressor activity, RNA polymerase II transcription factor binding IMP
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0016208 AMP binding IDA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0016791 phosphatase activity IEA
 molecular_functionGO:0042132 fructose 1,6-bisphosphate 1-phosphatase activity TAS
 molecular_functionGO:0042578 phosphoric ester hydrolase activity IEA
 molecular_functionGO:0042802 identical protein binding IPI
 molecular_functionGO:0046872 metal ion binding IMP
 molecular_functionGO:0048029 monosaccharide binding ISS


Pathways (from Reactome)
Pathway description
Gluconeogenesis


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:0000737 Irritability 
Show

 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]
Show

 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]
Show

 HP:0001254 Lethargy 
Show

 HP:0001259 Coma 
Show

 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
Show

 HP:0001649 Tachycardia "A rapid heartrate that exceeds the range of the normal resting heartrate for age." [HPO:curators]
Show

 HP:0001942 Metabolic acidosis 
Show

 HP:0001943 Hypoglycemia "A lower than normal level of blood glucose." [HPO:curators]
Show

 HP:0001945 Fever 
Show

 HP:0001946 Ketosis 
Show

 HP:0002094 Dyspnea 
Show

 HP:0002104 Apnea "Lack of breathing with no movement of the respiratory muscles and no exchange of air in the lungs. This term refers to a disposition to have recurrent episodes of apnea rather than to a single event." [HPO:curators]
Show

 HP:0002240 Hepatomegaly "An abnormal enlargment of the liver." [HPO:curators]
Show

 HP:0002883 Hyperventilation 
Show

 HP:0040301 Increased urinary glycerol 
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000165140 FBP1 / P09467 / fructose-bisphosphatase 1  / complex






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr