KEGG   DISEASE: Pan-Chung-Bellen syndrome
Entry
H02842                      Disease                                
Name
Pan-Chung-Bellen syndrome
Description
Pan-Chung-Bellen syndrome (PCBS) is a novel syndrome characterized by developmental delay, intellectual disability, and dysmorphic features. It has been reported that mutations in FRYL cause this syndrome. FRYL (FRY-like transcription coactivator) belongs to a Furry protein family that is evolutionarily conserved from yeast to humans. Although the functions of FRYL in mammals are largely unknown, Furry family proteins have diverse functions, including cell polarity maintenance, cell morphogenesis, arborization and tiling of dendrites, and transcriptional regulation.
Category
Congenital malformation
Brite
Human diseases in ICD-11 classification [BR:br08403]
 20 Developmental anomalies
  LD90  Conditions with disorders of intellectual development as a relevant clinical feature
   H02842  Pan-Chung-Bellen syndrome
Gene
FRYL [HSA:285527] [KO:K27804]
Other DBs
ICD-11: LD90.Y
OMIM: 621049
Reference
  Authors
Pan X, Tao AM, Lu S, Ma M, Hannan SB, Slaugh R, Drewes Williams S, O'Grady L, Kanca O, Person R, Carter MT, Platzer K, Schnabel F, Abou Jamra R, Roberts AE, Newburger JW, Revah-Politi A, Granadillo JL, Stegmann APA, Sinnema M, Accogli A, Salpietro V, Capra V, Ghaloul-Gonzalez L, Brueckner M, Simon MEH, Sweetser DA, Glinton KE, Kirk SE, Wangler MF, Yamamoto S, Chung WK, Bellen HJ
  Title
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features.
  Journal
Am J Hum Genet 111:742-760 (2024)
DOI:10.1016/j.ajhg.2024.02.007
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