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loading...| Preferred Name |
FRAXA |
| ID |
http://purl.obolibrary.org/obo/OGG_3000002477 |
| description |
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation) |
| alternative term |
FMR1 |
| chromosome ID of gene |
X |
| database_cross_reference |
HGNC:3945 |
| definition source | |
| full name from nomenclature authority |
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation) |
| gene map location |
Xq27.3 |
| 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 |
| label |
FRAXA |
| modification date |
20140305 |
| NCBI GeneID |
2477 |
| nomenclature status |
Official from a nomenclature committee |
| organism NCBITaxon ID |
9606 |
| prefixIRI |
OGG:3000002477 |
| prefLabel |
FRAXA |
| symbol from nomenclature authority |
FRAXA |
| term editor |
Bin Zhao, Yue Liu, Oliver He |
| subClassOf |
Create New Mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MEDLINEPLUS/C0751156 | MedlinePlus Health Topics / MedlinePlus网站健康主题 | LOOM |