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    FRA16E fragile site, distamycin A type, rare, fra(16)(p12.1) [ Homo sapiens (human) ]

    Gene ID: 2464, updated on 10-Apr-2021

    Summary

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    Official Symbol
    FRA16Eprovided by HGNC
    Official Full Name
    fragile site, distamycin A type, rare, fra(16)(p12.1)provided by HGNC
    Primary source
    HGNC:HGNC:3861
    See related
    MIM:136570
    Gene type
    other
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    C16DELp12.1
    Annotation information
    not in current annotation release
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    Genomic context

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    Location:
    16p12.1

    Bibliography

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    Related articles in PubMed

    1. 16p12.2 Recurrent Deletion. Adam MP, et al. , 1993. PMID 25719193

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    Chromosome 16p12.1 deletion syndrome, 520kb
    MedGen: C3149276 OMIM: 136570 GeneReviews: 16p12.2 Recurrent Deletion
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