Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "I"
71 to 80 of 438 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

71
Interferon lambda receptor 1
CRF2/12, IFNLR, IL-28R1, IL28RA, LICR2
Ankylosing spondylitis, Eczema, Crohn disease, Inflammatory skin disease, Psoriasis, Psoriasis vulgaris, Sclerosing cholangitis, Systemic lupus erythematosus, Diabetes mellitus type 2, Ulcerative colitis

72
Interferon omega 1
-
Central nervous system cancer, Color vision deficiency, Glioblastoma, Glioma

73
Interferon related developmental regulator 1
PC4, TIS7
Amyotrophic lateral sclerosis, Charcot-marie-tooth disease, Liver cirrhosis, Spinocerebellar ataxia

74
Intraflagellar transport 122
CED, CED1, CFAP80, FAP80, SPG, WDR10, WDR10p, WDR140
Systemic scleroderma, Asthma, Ciliary dyskinesia, Connective tissue disease, Craniodiaphyseal dysplasia, Craniosynostosis, Desbuquois syndrome, Edema, Eye abnormalities, Hydrocephalus, Kidney disease, Rod-cone dystrophy, Short rib dysplasia-polydactyly syndrome

75
Intraflagellar transport 140
CED5, MZSDS, PKD9, RP80, SRTD9, WDTC2, c305C8.4, c380F5.1, gs114
Jeune syndrome, Eczema, Polycystic kidney disease, Axenfeld-rieger syndrome, Coronary artery disease, Craniodiaphyseal dysplasia, Desbuquois syndrome, Anterior segment dysgenesis, Jeune thoracic dystrophy, Joubert syndrome, Kidney disease, Leber congenital amaurosis, Mainzer-saldino disease, Nephronophthisis, Optic atrophy
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76
Intraflagellar transport 172
BBS20, NPHP17, RP71, SLB, SRTD10, osm-1, wim
Jeune syndrome, Bardet-biedl syndrome, Ciliopathy, Desbuquois syndrome, Aplasia of the vermis, Gastrointestinal stromal tumor, Jeune thoracic dystrophy, Mainzer-saldino disease, Majewski syndrome, Metabolic syndrome, Nephronophthisis, Neurodevelopmental disorder, Nonalcoholic fatty liver disease, Optic atrophy, Psoriasis
View all (5 more)

77
Intraflagellar transport 25
C1orf41, CFAP232, FAP232, HSPB11, HSPCO34, PP25
Renal agenesis

78
Intraflagellar transport 27
BBS19, CFAP156, FAP156, RABL4, RAYL
Bardet-biedl syndrome, Bipolar disorder, Ciliopathy, Jeune thoracic dystrophy, Optic atrophy, Retinitis pigmentosa

79
Intraflagellar transport 43
C14orf179, CED3, RP81, SRTD18
Angioedema, Astrocytoma, Central nervous system cancer, Obstructive pulmonary disease, Ciliopathy, Connective tissue disease, Craniodiaphyseal dysplasia, Desbuquois syndrome, Glioblastoma, Glioma, Jeune thoracic dystrophy, Migraine, Open angle glaucoma, Retinitis pigmentosa, Scoliosis
View all (4 more)

80
Intraflagellar transport 52
C20orf9, CGI-53, NGD2, NGD5
Jeune syndrome, Craniodiaphyseal dysplasia, Desbuquois syndrome, Gastrointestinal stromal tumor, Jeune thoracic dystrophy, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia, Diabetes mellitus type 2