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Ontology of Genes and Genomes
Last uploaded:
December 2, 2016
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Preferred Name | FRAXA | |
Synonyms |
FMR1 |
|
ID |
http://purl.obolibrary.org/obo/OGG_3000002477 |
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description |
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
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alternative term |
FMR1
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chromosome ID of gene |
X
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database_cross_reference |
HGNC:3945
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definition source |
WEB: http://www.ncbi.nlm.nih.gov/gene
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full name from nomenclature authority |
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
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gene map location |
Xq27.3
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has PubMed association |
PMID: 11121205; 11169559; 11273816; 11426454; 11807410; 11898618; 12612802; 12806492; 12871874; 14668200; 15277639; 15326620; 15335113; 15342126; 15546601; 15637705; 15834242; 15900569; 16201716; 16626328; 17383248; 18627041; 19028545; 21257332; 23307483
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label |
FRAXA
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modification date |
20140305
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NCBI GeneID |
2477
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nomenclature status |
Official from a nomenclature committee
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organism NCBITaxon ID |
9606
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prefixIRI |
OGG:3000002477
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prefLabel |
FRAXA
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symbol from nomenclature authority |
FRAXA
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term editor |
Bin Zhao, Yue Liu, Oliver He
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subClassOf |
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Create mapping
Mapping To | Ontology | Source |
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http://purl.bioontology.org/ontology/RCD/X78FC | RCD | LOOM |
http://purl.obolibrary.org/obo/OMIT_0032026 | OMIT | LOOM |
http://identifiers.org/hgnc/3945 | HGNC-NR | LOOM |
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0751156 | MEDLINEPLUS | LOOM |