|
351
|
|
|
Integrin subunit beta 1 binding protein 1 |
ICAP-1A, ICAP-1B, ICAP-1alpha, ICAP1, ICAP1A, ICAP1B |
|
|
352
|
|
|
Integral membrane protein 2B |
ABRI, BRI, BRI2, BRICD2B, E25B, E3-16, FBD, RDGCA, imBRI2 |
|
|
353
|
|
|
Immediate early response 2 |
CHX1, ETR101 |
|
|
354
|
|
|
ISG15 ubiquitin like modifier |
G1P2, IFI15, IMD38, IP17, UCRP, hUCRP |
|
|
355
|
|
|
Inhibitor of nuclear factor kappa B kinase subunit epsilon |
IKK-E, IKK-i, IKKE, IKKI |
|
|
356
|
|
|
IQ motif containing B1 |
NPHP5, PIQ, SLSN5 |
Cataract, Ciliopathies, Congenital cerebral hernia, Congenital hepatic fibrosis, Developmental delay, Disorder of eye, Dwarfism, Hemiplegia/hemiparesis, Hypertension, Keratoconus, Kidney disease, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Multiple sclerosis, Nephronophthisis, Nystagmus, Premature menopause, Renal dysplasia and retinal aplasia, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Senior-loken syndromeView all (8 more) |
|
357
|
|
|
Intraflagellar transport 140 |
CED5, MZSDS, PKD9, RP80, SRTD9, WDTC2, c305C8.4, c380F5.1, gs114 |
Anemia, Anetoderma, Asphyxiating thoracic dystrophy, Brachydactyly, Cataract, Cholestasis, Congenital cerebral hernia, Congenital hypoplasia of penis, Cranioectodermal dysplasia, Developmental delay, Diabetes mellitus, Dwarfism, Foot polydactyly, Frontal bossing, Glaucoma, Hearing loss, Hemiplegia/hemiparesis, High palate, Hyperinsulinism, Hypogonadism, Jeune syndrome, Jeune thoracic dystrophy, Joubert syndrome with jeune asphyxiating thoracic dystrophy, Keratoconus, Kidney disease, Leber congenital amaurosis, Liver fibrosis, Macroglossia, Macrostomia, Majewski syndrome, Malformation of cortical development, Mental retardation, Microdontia, Micromelia, Nephronophthisis, Nystagmus, Obesity, Optic atrophy, Osteochondrodysplasia, Polydactyly, Renal cyst, Renal dysplasia, Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia, Renal insufficiency, Retinitis pigmentosa, Rod-cone dystrophy, Saldino-mainzer syndrome, Scaphocephaly, Short rib-polydactyly syndrome, Skeletal dysplasia, Syndactyly of the toes, Trigonocephaly, Postaxial hand polydactylyView all (38 more) |
|
358
|
|
|
IST1 factor associated with ESCRT-III |
CHMP8, OLC1 |
|
|
359
|
|
|
IQ motif and Sec7 domain ArfGEF 1 |
ARF-GEP100, ARFGEP100, BRAG2, GEP100, IDDSSBA |
|
