Xp22.3

GPTKB entity

Statements (20)
Predicate Object
gptkbp:instanceOf chromosomal band
gptkbp:associatedWith gptkb:X-linked_ichthyosis
gptkb:Kallmann_syndrome
genetic disorders
Léri-Weill dyschondrosteosis
chondrodysplasia punctata
mental retardation syndromes
gptkbp:chromosomeArm p
gptkbp:containsGene gptkb:KAL1
STS
ARSE
NLGN4X
SHOX
gptkbp:genomicCoordinates NCBI GRCh38: 2,700,001-8,800,000
https://www.w3.org/2000/01/rdf-schema#label Xp22.3
gptkbp:locatedOn gptkb:X_chromosome
gptkbp:locatedOnChromosome gptkb:Xp22.3
22.3
gptkbp:bfsParent gptkb:KAL1
gptkbp:bfsLayer 7