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
3151 to 3160 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3151
Cut like homeobox 2
CDP2, CUTL2, DEE67, EIEE67
Alzheimer disease, Atrial fibrillation, Bipolar disorder, Breast cancer, Cardiac arrhythmia, Kidney disease, Color vision deficiency, Colorectal cancer, Coronary artery disease, Developmental and epileptic encephalopathy, Epilepsy, Esophageal cancer, Esophageal disease, Gastric cancer, Gastroesophageal reflux disease
View all (13 more)

3152
CUB and zona pellucida like domains 1
ERG-1, ERG1, ITMAP1, UO-44
Schizophrenia

3153
CWC15 spliceosome associated protein
AD002, C11orf5, Cwf15, HSPC148, ORF5
Attention deficit hyperactivity disorder, Conduct disorder, Scoliosis

3154
CWC22 spliceosome associated protein
EIF4GL, NCM, fSAPb
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Colorectal cancer, Essential tremor, Female infertility, Gout, Major depressive disorder, Metabolic syndrome, Obesity, Ovarian cancer, Pelvic organ prolapse, Prostate cancer, Schizophrenia
View all (3 more)

3155
CWC25 spliceosome associated protein
CCDC49
Alzheimer disease, Major depressive disorder

3156
CWC27 spliceosome associated cyclophilin
NY-CO-10, RPSKA, SDCCAG-10, SDCCAG10
Brachydactyly-short stature-retinits pigmentosa syndrome, Central nervous system cancer, Color vision deficiency, Diverticular disease, Diverticulitis, Glioblastoma, Glioma, Heart failure, Metaphyseal chondrodysplasia with retinitis pigmentosa, Obesity, Optic atrophy, Osteoarthritis, Osteonecrosis, Retinitis pigmentosa, Retinitis pigmentosa with or without skeletal anomalies
View all (2 more)

3157
CWF19 like cell cycle control factor 1
C19L1, SCAR17, hDrn1
Spinocerebellar ataxia, Cerebellar ataxia, Intellectual developmental disorder, Nonalcoholic fatty liver disease, Psoriasis, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm

3158
CWF19 like cell cycle control factor 2
-
Cardiovascular disease, Coronary artery disease, Hypertension, Large artery stroke

3159
Cell wall biogenesis 43 C-terminal homolog
CWH43-C, PGAP2IP
Interstitial lung disease, Lung neoplasms, Metabolic syndrome, Diabetes mellitus type 2, Uterine fibroid

3160
C-X3-C motif chemokine ligand 1
ABCD-3, C3Xkine, CXC3, CXC3C, NTN, NTT, SCYD1, fractalkine, neurotactin
Cor pulmonale, Hypersensitivity, Myocardial ischemia, Peripheral neuropathy, Prostatic neoplasms, Systemic lupus erythematosus