ENSG00000009765


Homo sapiens

Features
Gene ID: ENSG00000009765
  
Biological name :IYD
  
Synonyms : iodotyrosine deiodinase / IYD / Q6PHW0
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 6
Strand: 1
Band: q25.1
Gene start: 150368892
Gene end: 150405969
  
Corresponding Affymetrix probe sets: 231070_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000397342
Ensembl peptide - ENSP00000390081
Ensembl peptide - ENSP00000441276
Ensembl peptide - ENSP00000229447
Ensembl peptide - ENSP00000343763
Ensembl peptide - ENSP00000356304
Ensembl peptide - ENSP00000376084
Ensembl peptide - ENSP00000376085
NCBI entrez gene - 389434     See in Manteia.
OMIM - 612025
RefSeq - XM_006715479
RefSeq - NM_001164694
RefSeq - NM_001164695
RefSeq - NM_001318495
RefSeq - NM_203395
RefSeq - XM_006715478
RefSeq Peptide - NP_001158167
RefSeq Peptide - NP_001158166
RefSeq Peptide - NP_001305424
RefSeq Peptide - NP_981932
swissprot - H7C0X6
swissprot - F5H543
swissprot - C9JXJ9
swissprot - Q6PHW0
swissprot - F6VN83
Ensembl - ENSG00000009765
  
Related genetic diseases (OMIM): 274800 - Thyroid dyshormonogenesis 4, 274800
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:ch211-286f9.2ENSDARG00000076056Danio rerio
 IYDENSGALG00000012392Gallus gallus
 IydENSMUSG00000019762Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR000415  Nitroreductase-like
 IPR029479  Nitroreductase


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006570 tyrosine metabolic process IDA
 biological_processGO:0006590 thyroid hormone generation TAS
 biological_processGO:0042403 thyroid hormone metabolic process IDA
 biological_processGO:0055114 oxidation-reduction process IEA
 biological_processGO:0098869 cellular oxidant detoxification IEA
 cellular_componentGO:0005654 nucleoplasm IDA
 cellular_componentGO:0005886 plasma membrane IDA
 cellular_componentGO:0005887 integral component of plasma membrane IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0030659 cytoplasmic vesicle membrane IEA
 cellular_componentGO:0031410 cytoplasmic vesicle IEA
 molecular_functionGO:0004447 iodide peroxidase activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0010181 FMN binding IDA
 molecular_functionGO:0016491 oxidoreductase activity IEA


Pathways (from Reactome)
Pathway description
Thyroxine biosynthesis


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:0000158 Macroglossia "Increased length and width of the tongue." [pmid:19125428]
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 HP:0000239 Large fontanelles "In newborns, the two frontal bones, two parietal bones, and one occipital bone are joined by fibrous sutures, which form a small posterior fontanelle, and a larger, diamond-shaped anterior fontanelle. These regions allow for the skull to pass the birth canal and for later growth. The fontanelles gradually ossify, whereby the posterior fontanelle usually closes by eight weeks and the anterior fontanelle by the 9th to 16th month of age. Large fontanelles are diagnosed if the fontanelles are larger than age-dependent norms." [HPO:curators]
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 HP:0000280 Coarse facial features 
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 HP:0000821 Hypothyroidism 
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 HP:0000853 Goiter "An enlargement of the thyroid gland." [HPO:curators]
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 HP:0000952 Jaundice "Yellow pigmentation of the skin or sclera due to bilirubin, which in turn is the result of increased bilirubin concentration in the bloodstream." [HPO:curators]
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 HP:0001249 Mental retardation 
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 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]
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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:0001510 Growth retardation 
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 HP:0001537 Umbilical hernia "Protrusion of abdominal contents through a defect in the abdominal wall musculature around the umbilicus. Skin and subcutaneous tissue overlie the defect." [HPO:curators]
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 HP:0002019 Constipation 
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 HP:0003270 Abdominal distention "Enlargement or distention of the abdomen, which can be a secondary feature associated with a number of conditions such as bowel obstruction." [HPO:curators]
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0012378 Fatigue "A subjective feeling of tiredness characterized by a lack of energy and motivation." [HPO:probinson]
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 HP:0100786 Hypersomnia 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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contact: otassy@igbmc.fr