KIAA0753, KIAA0753, 9851

N. diseases: 82; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4310701
Disease: OROFACIODIGITAL SYNDROME XV
OROFACIODIGITAL SYNDROME XV
0.500 Biomarker disease GENOMICS_ENGLAND Mutations in KIAA0753 cause Joubert syndrome associated with growth hormone deficiency. 28220259 2017
CUI: C4310701
Disease: OROFACIODIGITAL SYNDROME XV
OROFACIODIGITAL SYNDROME XV
0.500 Biomarker disease GENOMICS_ENGLAND OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome. 26643951 2016
CUI: C4310701
Disease: OROFACIODIGITAL SYNDROME XV
OROFACIODIGITAL SYNDROME XV
0.500 Biomarker disease CTD_human
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
0.430 GeneticVariation disease BEFREE In addition to these, KIAA0753 variants were recently described in seven patients with Jeune asphyxiating thoracic dystrophy (ATD) (two first cousins, one unrelated patient and one fetus), Joubert syndrome (two siblings) and orofaciodigital syndrome type 6 (one patient). 31816441 2019
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
0.430 CausalMutation disease CLINVAR Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies. 29138412 2017
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
0.430 Biomarker disease GENOMICS_ENGLAND KIAA0753 (OFIP) is a centrosome and pericentriolar satellite protein, previously not known to cause Joubert syndrome. 28220259 2017
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
0.430 GeneticVariation disease BEFREE We identified the causative gene in 94% of the families; 126 (27 novel) unique potentially pathogenic variants were found in 20 genes, including KIAA0753 and CELSR2, which had not previously been associated with JS. 28125082 2017
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
0.430 Biomarker disease BEFREE KIAA0753 (OFIP) is a centrosome and pericentriolar satellite protein, previously not known to cause Joubert syndrome. 28220259 2017
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
0.430 Biomarker disease GENOMICS_ENGLAND OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome. 26643951 2016
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
0.430 GeneticVariation disease CLINVAR
CUI: C2745997
Disease: OROFACIODIGITAL SYNDROME VI
OROFACIODIGITAL SYNDROME VI
0.310 GeneticVariation disease BEFREE In addition to these, KIAA0753 variants were recently described in seven patients with Jeune asphyxiating thoracic dystrophy (ATD) (two first cousins, one unrelated patient and one fetus), Joubert syndrome (two siblings) and orofaciodigital syndrome type 6 (one patient). 31816441 2019
CUI: C2745997
Disease: OROFACIODIGITAL SYNDROME VI
OROFACIODIGITAL SYNDROME VI
0.310 GermlineCausalMutation disease ORPHANET OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome. 26643951 2016
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy
0.110 GeneticVariation disease BEFREE In addition to these, KIAA0753 variants were recently described in seven patients with Jeune asphyxiating thoracic dystrophy (ATD) (two first cousins, one unrelated patient and one fetus), Joubert syndrome (two siblings) and orofaciodigital syndrome type 6 (one patient). 31816441 2019
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy
0.110 CausalMutation disease CLINVAR Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies. 29138412 2017
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy
0.110 GeneticVariation disease CLINVAR
CUI: C0003578
Disease: Apnea
Apnea
0.100 Biomarker phenotype HPO
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker phenotype HPO
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
0.100 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism
0.100 Biomarker disease HPO
CUI: C0014877
Disease: Esotropia
Esotropia
0.100 Biomarker disease HPO
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
0.100 Biomarker disease HPO
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
0.100 Biomarker disease HPO
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.100 Biomarker group HPO
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
0.100 Biomarker disease HPO
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0.100 Biomarker phenotype HPO