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Details of RANBP2 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| RANBP2 | NUP358 | P49792 | RBP2_HUMAN | 5903
| Q53TE2
| Q59FH7 | Encephalopathy |
Phenotypes
Abnormal bleeding, Abnormality of blood and blood-forming tissues, Abnormality of central motor function, Abnormality of fluid regulation, Abnormality of higher mental function, Abnormality of metabolism/homeostasis, Abnormality of pyramidal motor function, Abnormality of the central nervous system, Abnormality of the cerebrospinal fluid, Abnormality of the cerebrum, Abnormality of the forebrain, Abnormality of the glial cells, Abnormality of the immune system, Abnormality of the lung, Abnormality of the nervous system, Abnormality of the respiratory system, Age of onset, All, Autosomal dominant inheritance, Cerebral edema, Cognitive impairment, Coma, Edema, Encephalopathy, Gliosis, Hypertonia, Increased CSF protein, Infantile onset, Intellectual disability, Mode of inheritance, Morphological abnormality of the central nervous system, Onset, Onset and clinical course, Phenotypic abnormality, Pneumonia, Reduced consciousness/confusion, Respiratory tract infection, Seizures, Spastic tetraplegia, Spasticity.
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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