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: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1850127
Disease: Osteopetrosis, Autosomal Recessive 1
Osteopetrosis, Autosomal Recessive 1 		disease 0.900 strong 1.000 18 43 1985 2015
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1859966
Disease: Neutropenia, Severe Congenital, Autosomal Dominant 1
Neutropenia, Severe Congenital, Autosomal Dominant 1 		disease 0.400 None 1.000 1 1 2014 2014
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0029454
Disease: Osteopetrosis
Osteopetrosis 		disease 0.200 None 1.000 0 0 2002 2019
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0340970
Disease: Congenital neutropenia
Congenital neutropenia 		disease 0.120 None 1.000 1 1 2014 2016
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		disease 0.110 None 1.000 0 0 2006 2006
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C3203102
Disease: Idiopathic pulmonary arterial hypertension
Idiopathic pulmonary arterial hypertension 		disease 0.110 None 1.000 0 0 2009 2009
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1846546
Disease: Recurrent sinopulmonary infections
Recurrent sinopulmonary infections 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1850134
Disease: Sandwich appearance of vertebral bodies
Sandwich appearance of vertebral bodies 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1843331
Disease: Generalized osteosclerosis
Generalized osteosclerosis 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1842083
Disease: Abnormality of the ribs
Abnormality of the ribs 		disease 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1832160
Disease: Abnormality of temperature regulation
Abnormality of temperature regulation 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1384666
Disease: hearing impairment
hearing impairment 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0242567
Disease: Opsoclonus
Opsoclonus 		disease 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0266052
Disease: Precocious exfoliation of primary tooth
Precocious exfoliation of primary tooth 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0271344
Disease: Compression of optic nerve
Compression of optic nerve 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0423798
Disease: Increased tendency to bruise
Increased tendency to bruise 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0426790
Disease: Narrow thorax
Narrow thorax 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0427543
Disease: Increased blood monocyte number
Increased blood monocyte number 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0456070
Disease: Growth delay
Growth delay 		phenotype 0.100 None 0 0
Entrez Id: 10312
Gene Symbol: TCIRG1
TCIRG1 		T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 0.565 0.692 2.4E-13
CUI: C0456909
Disease: Blindness
Blindness 		phenotype 0.100 None 0 0