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
2991 to 3000 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2991
Corticotropin releasing hormone receptor 1
CRF-R, CRF-R-1, CRF-R1, CRF1, CRFR-1, CRFR1, CRH-R-1, CRH-R1, CRHR, CRHR1L
Anhedonia, Anorexia, Anxiety disorder, Asthma, Autism, Bipolar disorder, Breast cancer, Breast neoplasms, Obstructive airway disease, Contact dermatitis, Major depressive disorder, Hyperalgesia, Hyperkinesia, Mood disorder, Neurotic disorder
View all (8 more)

2992
Corticotropin releasing hormone receptor 2
CRF-RB, CRF2, CRFR2, HM-CRF
Anhedonia, Anorexia, Anxiety disorder, Asthma, Astrocytoma, Bipolar disorder, Major depressive disorder, Diabetes mellitus, Hypertension, Lung disease, Mood disorder, Diabetes mellitus type 2

2993
Cysteine rich transmembrane BMP regulator 1
CRIM-1, S52
Atrial fibrillation, Obstructive pulmonary disease, Colobomatous macrophthalmia microcornea syndrome, Metabolic syndrome, Neuroblastoma, Oligodendroglioma, Diabetes mellitus type 2

2994
Cysteine rich protein 3
CRP-3, TLP, TLP-A, h6LIMo
Gout, Hearing loss, Hypertension, Diabetes mellitus type 2

2995
CXXC repeat containing interactor of PDZ3 domain
HSPC139, RTS3, SSMDF
Central nervous system cancer, Color vision deficiency, Desbuquois syndrome, Glioblastoma, Glioma, Hypertensive nephropathy, Metabolic syndrome, Pituitary dwarfism, Rothmund-thomson syndrome, Diabetes mellitus type 2

2996
Cripto, EGF-CFC family member
CR, CR-1, CRGF, TDGF1
Congenital heart defects, Congenital heart disease, Heterotaxy syndrome, Holoprosencephaly, Microform holoprosencephaly, Syntelencephaly, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Tetralogy of fallot

2997
Cripto, EGF-CFC family member 3
CR-3, CRIPTO, CRIPTO-3, TDGF1P3, TDGF2, TDGF3
Coronary artery disease, Hemorrhoid, Open angle glaucoma, Diabetes mellitus type 2

2998
Cysteine rich secretory protein 2
CRISP-2, CT36, GAPDL5, TPX1, TSP1
Carotid artery disease

2999
Cysteine rich secretory protein LCCL domain containing 1
CRISP-10, CRISP10, LCRISP1
Colorectal cancer, Colonic neoplasms, Oligodendroglioma, Parkinson disease

3000
Cysteine rich secretory protein LCCL domain containing 2
CRISP11, LCRISP2, LGL1
Asthma, Central nervous system cancer, Digestive system disease, Diverticular disease, Glioblastoma, Glioma, Liver disease, Lung disease, Male reproductive organ cancer, Obesity, Pelvic organ prolapse