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Symbol
Name
ID
Ifng
interferon gamma
MGI:107656
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Joint hemorrhage
Trismus
Sinusitis
Microcephaly
Interphalangeal joint erosions
Swan neck-like deformities of the fingers
Dupuytren contracture
Abnormality of the elbow
Limited elbow movement
Joint swelling
Limited shoulder movement
Joint hypermobility
Joint stiffness
Stiff interphalangeal joints
Abnormality of the skeletal system
Arthritis
Osteoarthritis
Rheumatoid arthritis
Polyarticular arthritis
Digital flexor tenosynovitis
Chordoma
Cerebral calcification
Disease(s) Associated with IFNG
ataxia telangiectasia
chronic granulomatous disease
factor VIII deficiency
graft-versus-host disease
rheumatoid arthritis
temporal arteritis
tuberous sclerosis 2
vesicoureteral reflux

Mouse Phenotypes
alveolar process atrophy
Availability Mouse Genotype
Ifngtm1Ts/Ifngtm1Ts

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
05/14/2024
MGI 6.23
The Jackson Laboratory