71
|
|
|
Inturned planar cell polarity protein |
CPLANE4, INT, OFD17, PDZD6, PDZK6, SRTD20 |
Atrioventricular septal defect, Brachycephaly, Clinodactyly, Congenital duplication of uterus, Pulmonary hypoplasia, Dwarfism, Frontal bossing, Agenesis of gallbladder, Imperforate anus, Laryngeal hypoplasia, Micrognathism, Microphthalmos, Microtia, Mohr syndrome, Nephronophthisis, Orofaciodigital syndrome, Penis agenesis, Polydactyly, Radial polydactyly, Renal hypoplasia, Short rib-polydactyly syndrome, Tetralogy of fallotView all (7 more) |
72
|
|
|
Interleukin 17C |
CX2, IL-17C |
|
73
|
|
|
Interferon lambda 3 |
IFN-lambda-3, IFN-lambda-4, IL-28B, IL-28C, IL28B, IL28C |
|
74
|
|
|
Immunoglobulin heavy variable 4-61 |
IGHV461, VH |
|
75
|
|
|
Immunoglobulin heavy variable 4-34 |
IGHV434, VH |
|
76
|
|
|
Immunoglobulin heavy variable 3-21 |
IGHV321, VH |
|
77
|
|
|
IQ motif containing M |
- |
|
78
|
|
|
Immunoglobulin like domain containing receptor 1 |
DFNB42, ILDR1alpha, ILDR1alpha', ILDR1beta |
|
79
|
|
|
Immunoglobulin lambda variable 10-54 |
IGLV1054, V1-20 |
|
80
|
|
|
Intraflagellar transport 81 |
CDV-1, CDV-1R, CDV1, CDV1R, DV1, SRTD19 |
Ambiguous genitalia, Brachydactyly, Pulmonary hypoplasia, Congenital hypoplasia of radius, Congenital omphalocele, Dolichocephaly, Jeune thoracic dystrophy, Macrocephaly, Micromelia, Polydactyly, Proptosis, Respiratory failure, Short rib-polydactyly syndrome, Short-rib thoracic dysplasia without polydactyly, Syndactyly, Thoracic hypoplasia, Ventricular septal defectView all (2 more) |