ENSG00000164512


Homo sapiens

Features
Gene ID: ENSG00000164512
  
Biological name :ANKRD55
  
Synonyms : ANKRD55 / ankyrin repeat domain 55 / Q3KP44
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 5
Strand: -1
Band: q11.2
Gene start: 56099678
Gene end: 56233359
  
Corresponding Affymetrix probe sets: 220112_at (Human Genome U133 Plus 2.0 Array)   240456_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000423507
Ensembl peptide - ENSP00000429421
Ensembl peptide - ENSP00000424230
Ensembl peptide - ENSP00000342295
NCBI entrez gene - 79722     See in Manteia.
OMIM - 615189
RefSeq - XM_011543646
RefSeq - XM_017009852
RefSeq - XM_017009853
RefSeq - NM_024669
RefSeq Peptide - NP_078945
swissprot - Q3KP44
swissprot - D6R9N4
swissprot - D6RBD3
Ensembl - ENSG00000164512
  
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
 ankrd55ENSDARG00000099182Danio rerio
 ANKRD55ENSGALG00000014717Gallus gallus
 Q8BLD6ENSMUSG00000049985Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR002110  Ankyrin repeat
 IPR020683  Ankyrin repeat-containing domain
 IPR036770  Ankyrin repeat-containing domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 molecular_functionGO:0005515 protein binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000689 Dental malocclusion "Dental malocclusion refers to an abnormality of the occlusion, or alignment, of the teeth and the way the upper and lower teeth fit together, resulting in overcrowding of teeth or in abnormal bite patterns." [HPO:curators]
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 HP:0001094 Iridocyclitis 
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 HP:0001373 Joint dislocation "Displacement or malalignment of joints." [HPO:curators]
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 HP:0001376 Decreased mobility of joints 
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 HP:0001386 Joint swelling 
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 HP:0002186 Apraxia "A defect in the understanding of complex motor commands and in the execution of certain learned movements, i.e., deficits in the cognitive components of learned movements." [HPO:curators]
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 HP:0002829 Arthralgia 
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 HP:0003493 Antinuclear antibody positive 
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 HP:0003565 Elevated erythrocyte sedimentation rate 
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 HP:0005681 Rheumatoid arthritis, juvenile 
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 HP:0005764 Polyarticular arthritis 
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 HP:0011227 Elevated C-reactive protein level "An abnormal elevation of the C-reactive protein level in serum." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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