ENSG00000107890


Homo sapiens

Features
Gene ID: ENSG00000107890
  
Biological name :ANKRD26
  
Synonyms : ANKRD26 / ankyrin repeat domain 26 / Q9UPS8
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 10
Strand: -1
Band: p12.1
Gene start: 26991914
Gene end: 27100498
  
Corresponding Affymetrix probe sets: 205705_at (Human Genome U133 Plus 2.0 Array)   205706_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000405112
Ensembl peptide - ENSP00000365255
Ensembl peptide - ENSP00000394152
NCBI entrez gene - 22852     See in Manteia.
OMIM - 610855
RefSeq - XM_017015933
RefSeq - XM_017015928
RefSeq - XM_017015929
RefSeq - XM_017015930
RefSeq - XM_017015931
RefSeq - XM_017015932
RefSeq - NM_001256053
RefSeq - NM_014915
RefSeq - XM_006717423
RefSeq - XM_006717425
RefSeq - XM_011519416
RefSeq Peptide - NP_001242982
RefSeq Peptide - NP_055730
swissprot - H0Y4T9
swissprot - Q9UPS8
swissprot - E7ESJ3
Ensembl - ENSG00000107890
  
Related genetic diseases (OMIM): 188000 - Thrombocytopenia 2, 188000
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
 si:ch211-272n13.3ENSDARG00000099768Danio rerio
 ANKRD26ENSGALG00000009104Gallus gallus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
AC098850.3ENSG0000026630237
A2RUR9 / CCDC144A / coiled-coil domain containing 144AENSG0000017016036
A6QL64 / ANKRD36 / ankyrin repeat domain 36ENSG0000013597629
Q5JPF3 / ANKRD36C / ankyrin repeat domain 36CENSG0000017450129
Q8N2N9 / ANKRD36B / ankyrin repeat domain 36BENSG0000019691228
A2A2Z9 / ANKRD18B / ankyrin repeat domain 18BENSG0000023045328
Q9BXX2 / ANKRD30B / ankyrin repeat domain 30BENSG0000018077727
Q8IVF6 / ANKRD18A / ankyrin repeat domain 18AENSG0000018007127
A6NC57 / ANKRD62 / ankyrin repeat domain 62ENSG0000018162626
Q9BXX3 / ANKRD30A / ankyrin repeat domain 30AENSG0000014851325
Q5TYW2 / ANKRD20A1 / ankyrin repeat domain 20 family member A1ENSG0000026069122
Q4UJ75 / ANKRD20A4 / ankyrin repeat domain 20 family member A4ENSG0000017201422
Q5VUR7 / ANKRD20A3 / ankyrin repeat domain 20 family member A3ENSG0000027620322
Q5SQ80 / ANKRD20A2 / ankyrin repeat domain 20 family member A2ENSG0000018314822
Q5CZ79 / ANKRD20A8P / ankyrin repeat domain 20 family member A8, pseudogeneENSG0000022908922
POTEA / POTE ankyrin domain family member AENSG0000018887718
POTEE / Q6S8J3 / POTE ankyrin domain family member EENSG0000018821916
POTEF / A5A3E0 / POTE ankyrin domain family member FENSG0000019660416
POTEI / P0CG38 / POTE ankyrin domain family member IENSG0000019683416
H3BUK9 / POTEB2 / POTE ankyrin domain family member B2ENSG0000023003113


Protein motifs (from Interpro)
Interpro ID Name
 IPR002110  Ankyrin repeat
 IPR020683  Ankyrin repeat-containing domain
 IPR021885  Protein of unknown function DUF3496
 IPR036770  Ankyrin repeat-containing domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0045599 negative regulation of fat cell differentiation ISS
 cellular_componentGO:0005813 centrosome IDA
 molecular_functionGO:0005515 protein binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant 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 heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000978 Ecchymoses 
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 HP:0001873 Thrombocytopenia 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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