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FRAXA fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation) [ Homo sapiens (human) ]

Gene ID: 2477, discontinued on 12-Mar-2020

Summary

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Official Symbol
FRAXAprovided by HGNC
Official Full Name
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)provided by HGNC
Primary source
HGNC:HGNC:3945
Gene type
biological region
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FMR1
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Genomic context

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Location:
Xq27.3

Bibliography

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GeneRIFs: Gene References Into Functions

General gene information

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Other Names

  • fragile site, folic acid type, rare, fra(X)(q27.3), (macroorchidism, mental retardation)

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