TUBGCP6, tubulin gamma complex associated protein 6, 85378
N. diseases: 48; N. variants: 16
Source: ALL
Disease | Type | Disease Class | Semantic Type | N. genes d | N. SNPs d | Score gda | EL gda | EI gda | N. PMIDs | N. SNPs gda | First Ref. | Last Ref. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 152 | 6 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 60 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 429 | 29 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | Congenital Abnormality | 180 | 101 | 0.100 | None | 0 | ||||||||
|
phenotype | Finding | 58 | 5 | 0.100 | None | 0 | |||||||||
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group | Eye Diseases | Disease or Syndrome | 219 | 227 | 0.100 | None | 0 | ||||||||
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disease | Mental or Behavioral Dysfunction | 1825 | 553 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 149 | 5 | 0.100 | None | 0 | |||||||||
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phenotype | Finding | 215 | 5 | 0.100 | None | 0 | |||||||||
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disease | Disease or Syndrome | 271 | 13 | 0.100 | None | 0 | |||||||||
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disease | Anatomical Abnormality | 21 | 0.100 | None | 0 | ||||||||||
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group | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Mental or Behavioral Dysfunction | 2165 | 159 | 0.100 | None | 0 | ||||||||
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phenotype | Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | Finding | 422 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 116 | 5 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 1010 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 39 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 39 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 779 | 0.100 | None | 0 | ||||||||||
|
phenotype | Finding | 98 | 4 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 1127 | 292 | 0.100 | None | 0 | |||||||||
|
disease | Musculoskeletal Diseases | Disease or Syndrome | 850 | 135 | 0.100 | None | 0 | ||||||||
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disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases | Congenital Abnormality | 1261 | 77 | 0.100 | None | 0 |