Symbol Name ID |
Flna
filamin, alpha MGI:95556 |
Darker colors indicate more annotations |
Human Phenotypes | Long neck |
Short neck |
Abdominal distention |
Inguinal hernia |
Omphalocele |
Umbilical hernia |
Hernia |
Short stature |
Disproportionate tall stature |
Failure to thrive |
Postnatal growth retardation |
Disease(s) Associated with FLNA | |||||||||||
craniosynostosis | |||||||||||
Melnick-Needles syndrome | |||||||||||
mitral valve prolapse | |||||||||||
otopalatodigital syndrome type 1 | |||||||||||
otopalatodigital syndrome type 2 | |||||||||||
periventricular nodular heterotopia | |||||||||||
terminal osseous dysplasia | |||||||||||
X-linked chronic idiopathic intestinal pseudo-obstruction |
Mouse Phenotypes | failure of palatal shelf elevation |
abnormal palatal shelf fusion at midline |
cleft secondary palate |
omphalocele |
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Availability | Mouse Genotype | ||||
FlnaDilp2/Flna+ | |||||
FlnaDilp2/Y |
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 04/16/2024 MGI 6.23 |
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