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Symbol
Name
ID
Tctn2
tectonic family member 2
MGI:1915228
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Encephalocele
Decreased thyroid-stimulating hormone level
Increased circulating prolactin concentration
Pituitary hypothyroidism
Spasticity
Pachygyria
Polymicrogyria
Cerebellar hypoplasia
Ataxia
Dysmetria
Clumsiness
Absent speech
Lethargy
Hyperreflexia
Hyporeflexia
Gait disturbance
Attention deficit hyperactivity disorder
Depression
Neurodevelopmental delay
Global developmental delay
Disease(s) Associated with TCTN2
Joubert syndrome 24
Meckel syndrome 8

Mouse Phenotypes
abnormal embryonic neuroepithelium morphology
absent floor plate
open neural tube
exencephaly
Availability Mouse Genotype
Tctn2tm1.1Reit/Tctn2tm1.1Reit

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
01/12/2022
MGI 6.17
The Jackson Laboratory