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"
81 to 90 of 438 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

81
Intraflagellar transport 56
BRENS, DYF13, TTC26, dyf-13
Biliary-renal-neuro-skeletal syndrome, Caroli disease, Color vision deficiency, Hydrocephalus, Pelvic organ prolapse

82
Intraflagellar transport 57
ESRRBL1, HIPPI, MHS4R2, OFD18
Bardet-biedl syndrome, Insomnia, Metabolic syndrome, Orofaciodigital syndrome, Schizophrenia, Diabetes mellitus type 2

83
Intraflagellar transport 74
BBS22, CCDC2, CMG-1, CMG1, JBTS40, SPGF58
Autism, Bardet-biedl syndrome, Ciliary dyskinesia, Ciliopathy, Congenital brain malformation, Congenital hypoplasia of part of brain, Aplasia of the vermis, Hydranencephaly, Joubert syndrome, Jeune thoracic dystrophy, Lissencephaly, Macrogyria, Majewski syndrome, Male infertility large polyploid spermatozoa, Microgyria
View all (3 more)

84
Intraflagellar transport 80
ATD2, CFAP167, FAP167, SRTD2, WDR56
Asphyxia, Jeune syndrome, Beemer-langer syndrome, Bone disease, Clonal hematopoiesis, Connective tissue disease, Cystic kidney disease, Desbuquois syndrome, Jeune thoracic dystrophy, Kidney disease, Majewski syndrome, Polydactyly, Retinal degeneration, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia
View all (1 more)

85
Intraflagellar transport 81
CDV-1, CDV-1R, CDV1, CDV1R, DV1, SRTD19
Alzheimer disease, Atrial fibrillation, Bipolar disorder, Obstructive pulmonary disease, Ciliopathy, Cone-rod dystrophy, Crohn disease, Dementia, Desbuquois syndrome, Esophageal cancer, Iga nephropathy, Inflammatory bowel disease, Jeune thoracic dystrophy, Major depressive disorder, Myocardial infarction
View all (4 more)

86
Intraflagellar transport 88
D13S1056E, DAF19, TG737, TTC10, hTg737
Polycystic kidney disease, Bipolar disorder, Basal cell carcinoma, Gastrointestinal stromal tumor, Insomnia, Jeune thoracic dystrophy, Liver neoplasms, Major depressive disorder, Polydactyly, Retinitis pigmentosa, Rod-cone dystrophy

87
Intraflagellar transport associated protein
C11orf74, HEPIS, NWC
Color vision deficiency, Coronary artery disease, Dementia, Dilated cardiomyopathy, Hemolytic anemia, Machado-joseph disease, Omenn syndrome, Parkinson disease, Scoliosis, Severe combined immunodeficiency, Diabetes mellitus type 2

88
Immunoglobulin binding protein 1
ALPHA-4, IBP1, MRXS28, alpha4
Breast neoplasms, Hepatocellular carcinoma, Corpus callosum agenesis with intellectual disability, coloboma, micrognathia, Corpus callosum agenesis with intellectual disability, ocular coloboma, micrognathia, Lung neoplasms

89
IGBP1 family member C
IGBP1P2
Diabetes mellitus type 2

90
Immunoglobulin superfamily DCC subclass member 4
DDM36, NOPE
Alzheimer disease