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Symbol
Name
ID
Tinf2
Terf1 (TRF1)-interacting nuclear factor 2
MGI:107246
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Cerebral calcification
Cerebellar hypoplasia
Ataxia
Poor coordination
Delayed speech and language development
Progressive neurologic deterioration
Broad-based gait
Global developmental delay
Disease(s) Associated with TINF2
autosomal dominant dyskeratosis congenita 3
Revesz syndrome

Mouse Phenotypes
seizures
hydrocephaly
gliosis
Availability Mouse Genotype
Tinf2tm2.2Tdl/Tinf2+

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