Metazoan complexes |
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Emili & Marcotte labs |
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Details of NME1 gene in Homo sapiens
IDs | |||||||||
---|---|---|---|---|---|---|---|---|---|
Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| NME1 | NDPKA,NM23 | P15531 | NDKA_HUMAN | 4830 | ENSG00000239672 | Nucleoside diphosphate kinase A | SPROT |
Phenotypes
Abdominal distention, Abdominal pain, Abdominal symptom, Abnormal axial skeleton morphology, Abnormal bleeding, Abnormality of blood and blood-forming tissues, Abnormality of body weight, Abnormality of cardiovascular system physiology, Abnormality of central motor function, Abnormality of coordination, Abnormality of erythrocytes, Abnormality of eye movement, Abnormality of metabolism/homeostasis, Abnormality of movement, Abnormality of muscle physiology, Abnormality of skeletal morphology, Abnormality of skeletal physiology, Abnormality of temperature regulation, Abnormality of the abdomen, Abnormality of the anterior segment of the eye, Abnormality of the autonomic nervous system, Abnormality of the cardiovascular system, Abnormality of the central nervous system, Abnormality of the cerebellum, Abnormality of the eye, Abnormality of the hindbrain, Abnormality of the integument, Abnormality of the iris, Abnormality of the metencephalon, Abnormality of the musculature, Abnormality of the nervous system, Abnormality of the pupil, Abnormality of the skeletal system, Abnormality of the skin, Abnormality of the spinal cord, Abnormality of the thorax, Abnormality of the uvea, All, Anemia, Ataxia, Autosomal dominant inheritance, Bone pain, Bruising susceptibility, Decreased body weight, Diarrhea, Failure to thrive, Fever, Ganglioneuroblastoma, Ganglioneuroma, Generalized abnormality of skin, Growth abnormality, Heterogeneous, Horner syndrome, Hypertension, Incomplete penetrance, Involuntary movements, Localized skin lesion, Malignant neoplasm of the central nervous system, Miosis, Mode of inheritance, Morphological abnormality of the central nervous system, Myoclonus, Neoplasm, Neoplasm by anatomical site, Neoplasm of the central nervous system, Neoplasm of the nervous system, Neuroblastic tumors, Neuroblastoma, Onset, Onset and clinical course, Opsoclonus, Phenotypic abnormality, Phenotypic variability, Ptosis, Skin nodule, Skin papules, Spinal cord compression, Subcutaneous hemorrhage, Vascular skin abnormality, Weight loss.
Orthologs in other species | |||||||||
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M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
Nme1 | --- | --- | --- |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
---|---|---|---|---|---|---|---|---|---|
PRDX5 | NME1 | 0.989340131 | PRDX5 | NME1 | cpx74 | no | yes | no | Known |
FUBP1 | NME1 | 0.103995746 | FUBP1 | NME1 | cpx74 | no | no | no | Novel |