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ATD asphixiating thoracic dystrophy (chondroectodermal dysplasia-like syndrome) [ Homo sapiens (human) ]

Gene ID: 465, updated on 2-Oct-2019

Summary

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Gene symbol
ATD
Gene description
asphixiating thoracic dystrophy (chondroectodermal dysplasia-like syndrome)
Primary source
MIM:208500
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ATD1

Genomic context

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Location:
15q13

Bibliography

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Related articles in PubMed

  1. A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13. Morgan NV, et al. J Med Genet, 2003 Jun. PMID 12807964, Free PMC Article
  2. Del(12)(p11.21p12.2) associated with an asphyxiating thoracic dystrophy or chondroectodermal dysplasia-like syndrome. Nagai T, et al. Am J Med Genet, 1995 Jan 2. PMID 7702088

GeneRIFs: Gene References Into Functions

Phenotypes

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asphixiating thoracic dystrophy (chondroectodermal dysplasia-like syndrome)

General gene information

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Property

  • phenotype only

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Molecular Biology Databases