Source: CLINVAR

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: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		disease 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0518656
Disease: Chronic fatigue
Chronic fatigue 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C1845155
Disease: Exercise-induced myoglobinuria
Exercise-induced myoglobinuria 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C1846672
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I 		disease 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C1850438
Disease: Postural hypotension with compensatory tachycardia
Postural hypotension with compensatory tachycardia 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C4022858
Disease: Elevated aldolase level
Elevated aldolase level 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0233794
Disease: Memory impairment
Memory impairment 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0013404
Disease: Dyspnea
Dyspnea 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0027092
Disease: Myopia
Myopia 		disease 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0030193
Disease: Pain
Pain 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0030252
Disease: Palpitations
Palpitations 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0030554
Disease: Paresthesia
Paresthesia 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0035410
Disease: Rhabdomyolysis
Rhabdomyolysis 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		disease 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0040264
Disease: Tinnitus
Tinnitus 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C0042571
Disease: Vertigo
Vertigo 		phenotype 0.100 None 0 1
Entrez Id: 29888
Gene Symbol: STRN4
STRN4 		striatin 4 0.792 0.346 0.99
CUI: C4024883
Disease: Hyperextensible skin of face
Hyperextensible skin of face 		phenotype 0.100 None 0 1