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Symbol
Name
ID
Flna
filamin, alpha
MGI:95556
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Widow's peak
Low anterior hairline
Frontal bossing
Prominent occiput
Biparietal narrowing
Brachycephaly
Brachyturricephaly
Craniosynostosis
Coronal craniosynostosis
Bicoronal synostosis
Unicoronal synostosis
Left unicoronal synostosis
Right unicoronal synostosis
Lambdoidal craniosynostosis
Pansynostosis
Sagittal craniosynostosis
Dolichocephaly
Scaphocephaly
Thickened calvaria
Trigonocephaly
Turricephaly
Oxycephaly
Micrognathia
Increased size of the mandible
Antegonial notching of mandible
Obtuse angle of mandible
Retrognathia
Hypoplasia of the maxilla
Absent frontal sinuses
Hypoplastic frontal sinuses
Malar flattening
Large foramen magnum
Shallow orbits
Flat sella turcica
Vertical clivus
Sclerosis of skull base
Thick skull base
Microcephaly
Progressive microcephaly
Macrocephaly
Metopic synostosis
Delayed cranial suture closure
Delayed closure of the anterior fontanelle
Wormian bones
Wide anterior fontanel
Large fontanelles
Encephalocele
Abnormal facial shape
Coarse facial features
Flat face
Broad face
Small face
Preauricular pit
Midface retrusion
Pointed chin
Short chin
Broad forehead
Frontal hirsutism
Prominent forehead
Thick lower lip vermilion
Long philtrum
Smooth philtrum
Thick vermilion border
Accessory oral frenulum
Cleft soft palate
Cleft palate
High palate
High, narrow palate
Narrow palate
Glossoptosis
Narrow mouth
Supernumerary tooth
Anodontia
Oligodontia
Selective tooth agenesis
Delayed eruption of teeth
Multiple impacted teeth
Persistence of primary teeth
Hypoplasia of teeth
Tooth malposition
Dental malocclusion
Pierre-Robin sequence
Anteverted nares
Depressed nasal tip
Depressed nasal bridge
Wide nasal bridge
Short nose
Downslanted palpebral fissures
Upslanted palpebral fissure
Epicanthus
Telecanthus
Prominent supraorbital ridges
Disease(s) Associated with FLNA
craniosynostosis
frontometaphyseal dysplasia 1
Melnick-Needles syndrome
mitral valve prolapse
otopalatodigital syndrome type 1
otopalatodigital syndrome type 2
periventricular nodular heterotopia
terminal osseous dysplasia
X-linked cardiac valvular dysplasia
X-linked chronic idiopathic intestinal pseudo-obstruction

Mouse Phenotypes
failure of palatal shelf elevation
abnormal palatal shelf fusion at midline
cleft secondary palate
Availability Mouse Genotype
FlnaDilp2/Flna+
FlnaDilp2/Y

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory