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HTC1 hypertrichosis 1 (universalis, congenital) [ Homo sapiens (human) ]

Gene ID: 3341, updated on 24-Jun-2020

Summary

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Gene symbol
HTC1
Gene description
hypertrichosis 1 (universalis, congenital)
Primary source
MIM:145701
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
8q22

Bibliography

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Related articles in PubMed

  1. Diagnosis of Ambras syndrome: comments on complex cytogenetic rearrangement of chromosome 8q in a case of Ambras syndrome. Baumeister FA. Am J Med Genet, 2002 Apr 15. PMID 11932999
  2. A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22). Balducci R, et al. Clin Genet, 1998 Jun. PMID 9712536

GeneRIFs: Gene References Into Functions

Phenotypes

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hypertrichosis 1 (universalis, congenital)

General gene information

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Other Names

  • Ambras syndrome
  • hypertrichosis universalis (universalis, congenital)

Property

  • phenotype only

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