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KIND1 gene
Mutations associated with Kindler syndrome
Related
fermitin family homolog 1; kindlerin; kindlin syndrome protein; kindlin-1; Unc-112-related protein 1 (FERMT1, C20orf42, KIND1 URP1)
Kindler syndrome (hereditary acrokeratotic poikiloderma)
General
unclassified gene
Properties
TEMPLATE-FOR: messenger RNA
TEMPLATE-FOR: fermitin family homolog 1
LOCUS: human chromosome-20 P123
MOTIF: transcription factor binding site
transcriptional start site
exon
intron
transcriptional termination site
Database Correlations
OMIM 607900
MORBIDMAP 607900
References
OMIM :accession 607900