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
2641 to 2650 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2641
Calmin
-
Alzheimer disease, Venous thromboembolism

2642
CXADR like cell adhesion molecule
ACAM, ASAM, CSBM, CSBS
Breast cancer, Central nervous system cancer, Colorectal cancer, Congenital short bowel syndrome, Glaucoma, Glioblastoma, Glioma, Hemorrhoid, Intestinal obstruction, Oligodendroglioma, Partial epilepsy, Post-operative acute kidney injury

2643
CLN3 lysosomal/endosomal transmembrane protein, battenin
BTN1, BTS, JNCL, SLC29B1
Asthma, Bipolar disorder, Bullous pemphigoid, Neuronal ceroid lipofuscinosis, Cone-rod dystrophy, Crohn disease, Progressive myoclonic epilepsy, Hypothyroidism, Inflammatory bowel disease, Intellectual developmental disorder, Retinitis pigmentosa, Stomach neoplasms, Diabetes mellitus type 1, Diabetes mellitus type 2, Visual disorder

2644
CLN5 lysosomal BMP synthase
-
Neuronal ceroid lipofuscinosis, Neurodevelopmental disorder, Pontocerebellar hypoplasia, Visual disorder

2645
CLN6 transmembrane ER protein
CLN4A, CLN6A, HsT18960, nclf
Atrophy, Neuronal ceroid lipofuscinosis, Congenital neurologic anomalies, Cystic fibrosis, Motor skills disorder, Neurodevelopmental disorder, Spastic ataxia, Visual disorder

2646
CLN8 transmembrane ER and ERGIC protein
C8orf61, EPMR, TLCD6
Autism, Neuronal ceroid lipofuscinosis, Gaucher disease, Intellectual developmental disorder, Major depressive disorder

2647
Cytokine dependent hematopoietic cell linker
MIST
Autoimmune thyroid disease, Esophageal disease, Esophageal ulcer, Gout, Hyperuricemia, Hypothyroidism, Osteonecrosis of the femoral head, Psychiatric disorders, Rheumatoid arthritis, Sclerosing cholangitis, Systemic lupus erythematosus, Thyroid disease, Hypertension, Vitiligo

2648
Chloride nucleotide-sensitive channel 1A
CLCI, CLNS1B, ICln
Alzheimer disease, Melanoma

2649
Clock circadian regulator
KAT13D, bHLHe8
Alzheimer disease, Androgenetic alopecia, Bipolar disorder, Coronary artery disease, Major depressive disorder, Mood disorder, Schizophrenia, Seasonal affective disorder, Depression

2650
Cleavage factor polyribonucleotide kinase subunit 1
HEAB, hClp1
Congenital pontocerebellar hypoplasia, Major depressive disorder, Pontocerebellar hypoplasia