Source: MGD

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: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C0220708
Disease: VATER Association
VATER Association
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C0311245
Disease: Congenital cystic kidney disease
Congenital cystic kidney disease
disease 0.200 None 0 0
Entrez Id: 221322
Gene Symbol: TBC1D32
TBC1D32
TBC1 domain family member 32 0.743 0.462 8.0E-27
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
disease 0.200 None 0 0