Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2521 to 2530 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2521
Calcium and integrin binding family member 2
DFNB48, KIP2, USH1J
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss, Retinitis pigmentosa, Usher syndrome

2522
Calcium and integrin binding family member 3
KIP3
Lymphocytic leukemia, Hodgkin lymphoma, Multiple myeloma

2523
CBY1 interacting BAR domain containing 1
BARMR1, FAM92A, FAM92A1, PAPA9
Ciliopathy, Polydactyly, Postaxial polydactyly, Syndactyly

2524
CBY1 interacting BAR domain containing 2
FAM92B
Color vision deficiency, Crohn disease

2525
Capicua transcriptional repressor
MRD45
Androgenetic alopecia, Attention deficit hyperactivity disorder, Autism, Nonsyndromic intellectual disability, Cerebral folate deficiency, Neurodevelopmental disorder, Dias-logan syndrome, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Ocular hypotension, Spinocerebellar ataxia

2526
Cell death inducing DFFA like effector a
CIDE-A
Attention deficit hyperactivity disorder, Congestive heart failure, Heart failure, Liver neoplasms, Obesity

2527
Cell death inducing DFFA like effector b
-
Anorectal malformation

2528
Cell death inducing DFFA like effector c
CIDE-3, CIDE3, FPLD5, FSP27
Familial partial lipodystrophy, Allergic contact dermatitis, Partial lipodystrophy, Lipodystrophy

2529
Class II major histocompatibility complex transactivator
C2TA, CIITAIV, MHC2D1, MHC2TA, NLRA
Rheumatoid arthritis, Asthma, Eczema, Bare lymphocyte syndrome, Celiac disease, Crohn disease, Gastro-entero-pancreatic neuroendocrine tumor, Inflammatory bowel disease, Juvenile idiopathic arthritis, Systemic lupus erythematosus, Multiple sclerosis, Myocardial infarction, Nasopharyngeal neoplasms, Oligoarticular juvenile idiopathic arthritis, Ulcerative colitis

2530
Ciliogenesis associated kinase 1
ECO, EJM10, ICK, LCK2, MRK, hICK
Attention deficit hyperactivity disorder, Congenital ocular coloboma, Craniodiaphyseal dysplasia, Desbuquois syndrome, Dysgenesis of corpus callosum, Juvenile myoclonic epilepsy, Myoclonic epilepsy, Microphthalmos, Short rib dysplasia-polydactyly syndrome, Substance abuse