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

Gene ID: 2464, updated on 17-Aug-2024

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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