Details of MSH6 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| MSH6 | GTBP | P52701 | MSH6_HUMAN | 2956
| Q8TCX4
| Q9BTB5 | Mismatch repair c |
Phenotypes
Abnormality of blood and blood-forming tissues, Abnormality of cellular immune system, Abnormality of leukocytes, Abnormality of skin morphology, Abnormality of skin pigmentation, Abnormality of the abdomen, Abnormality of the astrocytes, Abnormality of the central nervous system, Abnormality of the glial cells, Abnormality of the immune system, Abnormality of the integument, Abnormality of the nervous system, Abnormality of the skin, All, Astrocytoma, Autosomal recessive inheritance, Axillary freckling, Basal cell carcinoma, Cafe-au-lait spot, Ependymoma, Freckling, Generalized abnormality of skin, Glioma, Hematological neoplasm, Hypermelanotic macule, Hyperpigmentation of the skin, Irregular hyperpigmentation, Leukemia, Localized skin lesion, Lymphoma, Malignant neoplasm of the central nervous system, Medulloblastoma, Mode of inheritance, Morphological abnormality of the central nervous system, Neoplasm, Neoplasm by anatomical site, Neoplasm by histology, Neoplasm of striated muscle, Neoplasm of the central nervous system, Neoplasm of the nervous system, Neoplasm of the skin, Neuroblastic tumors, Neuroblastoma, Phenotypic abnormality, Rhabdomyosarcoma, Sarcoma.
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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