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FRA18C fragile site, aphidicolin type, common, fra(18)(q22.2) [ Homo sapiens (human) ]

Gene ID: 116710, updated on 17-Aug-2024

Summary

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Official Symbol
FRA18Cprovided by HGNC
Official Full Name
fragile site, aphidicolin type, common, fra(18)(q22.2)provided by HGNC
Primary source
HGNC:HGNC:16929
Gene type
other
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Annotation information
not in current annotation release
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Genomic context

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Location:
18q22.2

Bibliography

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Related articles in PubMed

  1. FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage. Debacker K, et al. J Med Genet, 2007 May. PMID 17475918, Free PMC Article

GeneRIFs: Gene References Into Functions

General gene information

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Other Names

  • fragile site, folic acid type, rare, fra(18)(q22.1)

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