|
Symbol Name ID |
Trim32
tripartite motif-containing 32 MGI:1917057 |
| Darker colors indicate more annotations |
| Human Phenotypes | Facial palsy |
Abnormality of the sense of smell |
Aganglionic megacolon |
Photophobia |
Spasticity |
Ataxia |
Abnormality of speech or vocalization |
Delayed speech and language development |
Nasal dysarthria |
Depression |
Emotional lability |
Anxiety |
Atypical behavior |
Autism |
Cognitive impairment |
Short attention span |
Intellectual disability |
Areflexia |
Hyporeflexia |
Gait disturbance |
Loss of ambulation |
Waddling gait |
Neurodevelopmental delay |
Specific learning disability |
Seizure |
Paresthesia |
| Disease(s) Associated with TRIM32 | ||||||||||||||||||||||||||
| autosomal recessive limb-girdle muscular dystrophy type 2H | ||||||||||||||||||||||||||
| Bardet-Biedl syndrome |
| Mouse Phenotypes | abnormal axon morphology |
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| Availability | Mouse Genotype | |
| Trim32Gt(BGA355)Byg/Trim32Gt(BGA355)Byg | ||
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 |
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