U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from OMIM

    • Showing Current items.

    DEL16P13.3 Chromosome 16p13.3 deletion syndrome [ Homo sapiens (human) ]

    Gene ID: 100188814, updated on 16-Aug-2019

    Summary

    Go to the top of the page Help
    Gene symbol
    DEL16P13.3
    Gene description
    Chromosome 16p13.3 deletion syndrome
    Primary source
    MIM:610543
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    RSTSS

    Genomic context

    Go to the top of the page Help
    Location:
    16p13.3

    Bibliography

    Go to the top of the pageHelp

    GeneRIFs: Gene References Into Functions

    Phenotypes

    Go to the top of the page Help
    Chromosome 16p13.3 deletion syndrome

    General gene information

    Go to the top of the page Help

    Property

    • phenotype only

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

    Molecular Biology Databases