ENSG00000169567


Homo sapiens

Features
Gene ID: ENSG00000169567
  
Biological name :HINT1
  
Synonyms : HINT1 / histidine triad nucleotide binding protein 1 / P49773
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 5
Strand: -1
Band: q23.3
Gene start: 131159027
Gene end: 131171735
  
Corresponding Affymetrix probe sets: 1555960_at (Human Genome U133 Plus 2.0 Array)   1555961_a_at (Human Genome U133 Plus 2.0 Array)   200093_s_at (Human Genome U133 Plus 2.0 Array)   207721_x_at (Human Genome U133 Plus 2.0 Array)   208826_x_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000424974
Ensembl peptide - ENSP00000430909
Ensembl peptide - ENSP00000427499
Ensembl peptide - ENSP00000427008
Ensembl peptide - ENSP00000426860
Ensembl peptide - ENSP00000425260
Ensembl peptide - ENSP00000304229
Ensembl peptide - ENSP00000421608
Ensembl peptide - ENSP00000422444
NCBI entrez gene - 3094     See in Manteia.
OMIM - 601314
RefSeq - NM_005340
RefSeq - XM_017009410
RefSeq Peptide - NP_005331
swissprot - D6REP8
swissprot - P49773
swissprot - H0YC49
swissprot - D6RE99
swissprot - D6RD60
swissprot - D6RC06
Ensembl - ENSG00000169567
  
Related genetic diseases (OMIM): 137200 - Neuromyotonia and axonal neuropathy, autosomal recessive, 137200
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
 hint1ENSDARG00000103824Danio rerio
 HINT1ZENSGALG00000000428Gallus gallus
 Hint1ENSMUSG00000020267Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
HINT2 / Q9BX68 / histidine triad nucleotide binding protein 2ENSG0000013713359


Protein motifs (from Interpro)
Interpro ID Name
 IPR001310  Histidine triad (HIT) protein
 IPR011146  HIT-like domain
 IPR019808  Histidine triad, conserved site
 IPR036265  HIT-like superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IMP
 biological_processGO:0006915 apoptotic process IEA
 biological_processGO:0007165 signal transduction TAS
 biological_processGO:0009154 purine ribonucleotide catabolic process IDA
 biological_processGO:0050850 positive regulation of calcium-mediated signaling IEA
 biological_processGO:0072332 intrinsic apoptotic signaling pathway by p53 class mediator IMP
 cellular_componentGO:0000118 histone deacetylase complex IDA
 cellular_componentGO:0005634 nucleus TAS
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol IDA
 cellular_componentGO:0005856 cytoskeleton TAS
 cellular_componentGO:0005886 plasma membrane IDA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0005080 protein kinase C binding TAS
 molecular_functionGO:0016787 hydrolase activity IEA


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:0000975 Hyperhidrosis "An abnormally increased perspiration." [HPO:probinson]
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 HP:0001760 Abnormality of the feet "An abnormality of the feet (foot deformity) is a disorder of the foot that can either be congenital or acquired. Such deformities can include hammer toe, club foot deformity, flat feet, pes cavus, Congenital vertical talus (rocker bottom foot) & etc." [HPO:curators]
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 HP:0002380 Fasciculations "Fasciculations are observed as small, local, involuntary muscle contractions (twitching) visible under the skin. Fasciculations result from increased irritability of an axon (which in turn is often a manifestation of disease of a motor neuron). This leads to sporadic discharges of all the muscle fibers controlled by the axon in isolation from other motor units." [HPO:curators]
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 HP:0002411 Myokymia 
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 HP:0002486 Myotonia "Myotonia is characterized by an abnormally slow relaxation of the muscles after voluntary contraction or electrical stimulation. During physical examination, myotonia may be elicited by asking the patient to make a tight fist and then quickly open the hand." [HPO:curators]
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 HP:0002936 Distal sensory impairment 
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 HP:0003202 Amyotrophy "The presence of muscular atrophy (which is also known as amyotrophy)." [HPO:curators]
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 HP:0003236 Elevated serum creatine phosphokinase 
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 HP:0003390 Sensory axonal neuropathy "An axonal neuropathy of peripheral sensory nerves." [HPO:curators]
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 HP:0003394 Muscle cramps 
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 HP:0003552 Muscle stiffness 
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 HP:0003676 Progressive disorder 
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 HP:0009027 Foot dorsiflexor weakness 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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