ENSG00000126705


Homo sapiens

Features
Gene ID: ENSG00000126705
  
Biological name :AHDC1
  
Synonyms : AHDC1 / AT-hook DNA binding motif containing 1 / Q5TGY3
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 1
Strand: -1
Band: p35.3
Gene start: 27534035
Gene end: 27604431
  
Corresponding Affymetrix probe sets: 205002_at (Human Genome U133 Plus 2.0 Array)   229379_at (Human Genome U133 Plus 2.0 Array)   243793_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000363123
Ensembl peptide - ENSP00000495072
Ensembl peptide - ENSP00000495665
Ensembl peptide - ENSP00000247087
Ensembl peptide - ENSP00000494394
NCBI entrez gene - 27245     See in Manteia.
OMIM - 615790
RefSeq - XM_011541257
RefSeq - NM_001029882
RefSeq - XM_011541255
RefSeq - XM_011541256
RefSeq - XM_005245848
RefSeq - XM_005245849
RefSeq - XM_005245850
RefSeq - XM_005245851
RefSeq - XM_005245852
RefSeq Peptide - NP_001025053
swissprot - Q5TGY3
Ensembl - ENSG00000126705
  
Related genetic diseases (OMIM): 615829 - Xia-Gibbs syndrome, 615829
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
 ahdc1ENSDARG00000093453Danio rerio
 AHDC1ENSGALG00000042916Gallus gallus
 Ahdc1ENSMUSG00000037692Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR032757  Domain of unknown function DUF4683


Gene Ontology (GO)
TypeGO IDTermEv.Code
 molecular_functionGO:0003677 DNA 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:0000316 Hypertelorism 
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 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
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 HP:0000369 Low-set ears "Low-set ears are defined to be set below an arbitrary line drawn between the lateral canthus of the eye and the occipital protruberance." [HPO:curators]
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 HP:0000494 Downward slanting palpebral fissures 
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 HP:0000565 Esotropia 
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 HP:0000582 Upslanting palpebral fissures 
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 HP:0001249 Mental retardation 
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0001508 Failure to thrive 
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 HP:0001601 Laryngomalacia 
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 HP:0002079 Hypoplasia of the corpus callosum "Underdevelopment of the corpus callosum." [HPO:curators]
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 HP:0002870 Obstructive sleep apnea "A condition characterized by obstruction of the airway and by pauses in breathing during sleep occurring many times during the night. Obstructive sleep apnea is related to a relaxation of muscle tone (which normally occurs during sleep) leading to partial collapse of the soft tissues in the airway with resultant obstruction of the air flow." [HPO:curators]
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 HP:0005280 Depressed nasal root and bridge 
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 HP:0006951 Retrocerebellar cyst 
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 HP:0009879 Cortical gyral simplification "An abnormal reduction of the number and complexity of the pattern of gyrations of the cerebral cortex." [HPO:curators]
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 HP:0009909 Uplifted earlobes "An abnormal orientation of the earlobes such that they point out- and upward." [HPO:curators]
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 HP:0012448 Delayed myelination "`Delayed` (PATO:0000502) `myelination` (GO:0042552)." [ORCID:0000-0001-5208-3432]
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 HP:0025267 Snoring "Deep, noisy breathing during sleep accompanied by hoarse or harsh sounds caused by the vibration of respiratory structures (especially the soft palate) resulting in sound due to obstructed air movement during breathing while sleeping." []
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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