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: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		group 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		disease 0.200 None 0 0