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fgfr2 gene
Gene abnormalities associated with Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome.
Related
acrocephalosyndactyly type I/II (Apert's syndrome, Apert-Crouzon syndrome, Vogt cephalodactyly)
fibroblast growth factor receptor 2; FGFR-2; keratinocyte growth factor receptor 2; CD332 (FGFR2, BEK, KGFR, KSAM)
General
unclassified gene
Properties
TEMPLATE-FOR: messenger RNA
TEMPLATE-FOR: FGF receptor-2
LOCUS: human chromosome-10 Q26
SIZE: entity length = 4.5 KB
MOTIF: transcription factor binding site
transcriptional start site
exon
intron
transcriptional termination site
Database Correlations
OMIM 176943
MORBIDMAP 176943
References
OMIM :accession 176943