Online Mendelian Inheritance in Man

Last uploaded: August 28, 2024
Preferred Name

FRAGILE X MESSENGER RIBONUCLEOPROTEIN 1
Synonyms

FRAGILE SITE, FOLIC ACID TYPE, RARE, fraXq27.3

FRAGILE X TREMOR/ATAXIA SYNDROME

FRAGILE X MENTAL RETARDATION PROTEIN

FRAGILE X SYNDROME

FRAXA

FMR1

PREMATURE OVARIAN FAILURE 1

FMRP TRANSLATIONAL REGULATOR 1

FMRP

ID

http://purl.bioontology.org/ontology/OMIM/309550

altLabel

FRAGILE SITE, FOLIC ACID TYPE, RARE, fraXq27.3

FRAGILE X TREMOR/ATAXIA SYNDROME

FRAGILE X MENTAL RETARDATION PROTEIN

FRAGILE X SYNDROME

FRAXA

FMR1

PREMATURE OVARIAN FAILURE 1

FMRP TRANSLATIONAL REGULATOR 1

FMRP

cui

C1839780

C4552079

C1414806

C0016667

C1414649

Gene Locus

Xq27.3

Gene Symbol

FMR1

FRAXA

POF1

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/309550.0004

http://purl.bioontology.org/ontology/OMIM/309550.0001

http://purl.bioontology.org/ontology/OMIM/309550.0005

http://purl.bioontology.org/ontology/OMIM/309550.0002

http://purl.bioontology.org/ontology/OMIM/309550.0003

MIMTYPEMEANING

Gene with known sequence

notation

309550

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

FRAGILE X MESSENGER RIBONUCLEOPROTEIN 1

tui

T047

T028

Delete Subject Author Type Created
No notes to display
Create mapping