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HTC2 hypertrichosis 2 (generalized, congenital) [ Homo sapiens (human) ]

Gene ID: 3342, updated on 2-Oct-2019

Summary

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Gene symbol
HTC2
Gene description
hypertrichosis 2 (generalized, congenital)
Primary source
MIM:307150
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CGH; HCG; CXINSq27.1

Genomic context

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Location:
Xq27.1

Bibliography

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Related articles in PubMed

  1. Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait. Tadin-Strapps M, et al. Clin Genet, 2003 May. PMID 12752576
  2. X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3. Zhu H, et al. Am J Hum Genet, 2011 Jun 10. PMID 21636067, Free PMC Article
  3. Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis. DeStefano GM, et al. Proc Natl Acad Sci U S A, 2013 May 7. PMID 23603273, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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hypertrichosis 2 (generalized, congenital)

General gene information

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Other Names

  • hypertrichosis 2 (generalised, congenital)

Property

  • phenotype only

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