Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3081 to 3090 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3081
Centriolar satellite-associated tubulin polyglutamylase complex regulator 1
C11orf49
Alzheimer disease, Major depressive disorder, Mood disorder, Peripheral vascular disease, Diabetes mellitus type 2, Vascular disease, Venous thromboembolism

3082
Cancer/testis antigen 55
BJHCC20A, CXorf48, SPGFX7
Male infertility single gene azoospermia, Spermatogenic failure, x-linked

3083
Cutaneous T cell lymphoma-associated antigen 1
CT21.1, CT21.2, CTAGE, CTAGE-1, CTAGE-2
Benign prostatic hyperplasia, Obstructive pulmonary disease, Endometrial cancer, Endometrial neoplasms, Oligodendroglioma

3084
C-terminal binding protein 1
BARS, HADDTS
Attention deficit hyperactivity disorder, Colorectal neoplasms, Intellectual developmental disorder, Substance abuse, Diabetes mellitus type 2, Wolff-parkinson-white syndrome

3085
C-terminal binding protein 2
-
Congenital pulmonary artery atresia, Hearing loss, Hemorrhoid, Metabolic syndrome, Prostate cancer, Prostatic neoplasms, Diabetes mellitus type 2

3086
CST telomere replication complex component 1
AAF-132, AAF132, C17orf68, CRMCC, tmp494178
Bone disease, Brain disease, Calcinosis, Cerebroretinal microangiopathy with calcifications and cysts, Coats plus syndrome, Dyskeratosis congenita, Interstitial lung disease, Metabolic bone disorder, Parkinson disease

3087
CCCTC-binding factor
CFAP108, FAP108, MRD21
Alzheimer disease, Neurodevelopmental disorder, Hypothyroidism, Intellectual developmental disorder, Intellectual developmental disorder growth microcephaly, Intellectual developmental disorder dysmorphic microcephaly, Oligodendroglioma, Schizophrenia

3088
CCCTC-binding factor like
BORIS, CT27, CTCF-T, HMGB1L1, dJ579F20.2
Obesity

3089
CTD phosphatase subunit 1
CCFDN, FCP1
Charcot-marie-tooth disease, Congenital cataract facial dysmorphism neuropathy syndrome, Insomnia, Schizophrenia

3090
CTD small phosphatase 1
NIF3, NLI-IF, NLIIF, SCP1
Amyotrophic lateral sclerosis