Display Settings:

Format

Send to:

Choose Destination

DEL17Q11.2 chromosome 17q11.2 deletion syndrome [ Homo sapiens (human) ]

Gene ID: 100852404, updated on 30-Jan-2015
Gene symbol
DEL17Q11.2
Gene description
chromosome 17q11.2 deletion syndrome
Primary source
MIM:613675
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
C17DELq11.2

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Other Names

  • NF1 microdeletion syndrome
  • neurofibromatosis 1 microdeletion syndrome

Property

  • phenotype only