Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "I"
71 to 80 of 436 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

71
Interferon related developmental regulator 1
PC4, TIS7
Amyotrophic lateral sclerosis, Charcot-marie-tooth disease, Spinocerebellar ataxia

72
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

73
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
View all (7 more)

74
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)

75
Intraflagellar transport 25
C1orf41, CFAP232, FAP232, HSPB11, HSPCO34, PP25
Renal agenesis

76
Intraflagellar transport 27
BBS19, CFAP156, FAP156, RABL4, RAYL
Bardet-biedl syndrome, Bipolar disorder, Ciliopathy, Jeune thoracic dystrophy, Optic atrophy, Retinitis pigmentosa

77
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)

78
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

79
Intraflagellar transport 56
BRENS, DYF13, TTC26, dyf-13
Biliary-renal-neuro-skeletal syndrome, Caroli disease, Color vision deficiency, Hydrocephalus, Pelvic organ prolapse

80
Intraflagellar transport 57
ESRRBL1, HIPPI, MHS4R2, OFD18
Bardet-biedl syndrome, Insomnia, Metabolic syndrome, Orofaciodigital syndrome, Schizophrenia, Diabetes mellitus type 2