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
6161 to 6170 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

6161
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)

6162
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)

6163
Intraflagellar transport 25
C1orf41, CFAP232, FAP232, HSPB11, HSPCO34, PP25
Renal agenesis

6164
Intraflagellar transport 27
BBS19, CFAP156, FAP156, RABL4, RAYL
Bardet-biedl syndrome, Bipolar disorder, Ciliopathy, Jeune thoracic dystrophy, Optic atrophy, Retinitis pigmentosa

6165
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)

6166
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

6167
Intraflagellar transport 56
BRENS, DYF13, TTC26, dyf-13
Biliary-renal-neuro-skeletal syndrome, Caroli disease, Color vision deficiency, Hydrocephalus, Pelvic organ prolapse

6168
Intraflagellar transport 57
ESRRBL1, HIPPI, MHS4R2, OFD18
Bardet-biedl syndrome, Insomnia, Metabolic syndrome, Orofaciodigital syndrome, Schizophrenia, Diabetes mellitus type 2

6169
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)

6170
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)