Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C3278481
Disease: MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1
MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1 		disease 0.400 strong 1.000 0 7 2012 2012
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C0025958
Disease: Microcephaly
Microcephaly 		disease 0.110 None 1.000 0 0 2019 2019
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C0162701
Disease: Polysomnography
Polysomnography 		phenotype 0.100 None 1.000 1 1 2012 2012
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		disease 0.100 None 1.000 1 6 2017 2017
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C0024966
Disease: Maximal Midexpiratory Flow Rate
Maximal Midexpiratory Flow Rate 		phenotype 0.100 None 1.000 1 1 2013 2013
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1855285
Disease: Protruding ear
Protruding ear 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1844505
Disease: Pointed chin
Pointed chin 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C2675111
Disease: Abnormal eyelash morphology
Abnormal eyelash morphology 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C2749675
Disease: Cortical gyral simplification
Cortical gyral simplification 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		disease 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		disease 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		disease 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation 		phenotype 0.100 None 0 0
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		tubulin gamma complex associated protein 6 0.695 0.308 2.6E-31
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		group 0.100 None 0 0