Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6671 to 6680 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6671
Potassium sodium-activated channel subfamily T member 1
DEE14, EIEE14, ENFL5, KCa4.1, KNa1.1, SLACK, Slo2.2, bA100C15.2
Nocturnal frontal lobe epilepsy, Childhood-onset epilepsy syndrome, Color vision deficiency, Colorectal cancer, Developmental and epileptic encephalopathy, Developmental disability, Partial epilepsy, Epilepsy of infancy with migrating focal seizures, Frontal lobe epilepsy, Rolandic epilepsy, Gastrointestinal disease, Hydrocephalus, Malignant migrating partial seizures of infancy, Neurodevelopmental disorder, Schizophrenia
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6672
Potassium sodium-activated channel subfamily T member 2
DEE57, EIEE57, KCa4.2, KNa1.2, SLICK, SLO2.1
Atrophic macular degeneration, Color vision deficiency, Developmental and epileptic encephalopathy, Macular degeneration, Major depressive disorder, Scoliosis, Age-related macular degeneration

6673
Potassium calcium-activated channel subfamily U member 1
KCNMC1, KCa5, KCa5.1, Kcnma3, SPGF79, Slo3
Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Contracture, Corneal astigmatism, Diabetes mellitus, Diabetes mellitus type 2, Estrogen-receptor negative breast cancer, Gastric cancer, Schizophrenia, Spermatogenic failure, Substance abuse

6674
Potassium voltage-gated channel modifier subfamily V member 1
HNKA, KCNB3, KV2.3, KV8.1
Color vision deficiency, Diabetic neuropathy, Diabetes mellitus type 2

6675
Potassium voltage-gated channel modifier subfamily V member 2
KV11.1, Kv8.2, RCD3B
Autoimmune thrombocytopenic purpura, Cone dystrophy, Cone-rod dystrophy, Congenital neurologic anomalies, Nystagmus, Obesity, Optic atrophy, Retinal cone dystrophy, Retinitis pigmentosa, Stargardt disease

6676
Kielin cysteine rich BMP regulator
CRIM2, KCP1, NET67
Autoimmune disease, Gout, Hypertrophic cardiomyopathy, Psoriasis, Rheumatoid arthritis, Sjogren syndrome, Systemic lupus erythematosus, Systemic sclerosis

6677
Potassium channel tetramerization domain containing 1
C18orf5
Androgenetic alopecia, Astrocytoma, Breast cancer, Ocular sarcoidosis

6678
Potassium channel tetramerization domain containing 10
BTBD28, MSTP028, ULRO61, hBACURD3
Coronary artery disease, Hearing loss, Insomnia, Neurotic disorder

6679
Potassium channel tetramerization domain containing 12
C13orf2, PFET1, PFETIN
Autism, Bipolar disorder, Cerebral amyloid angiopathy, Kidney disease, Major depressive disorder, Mood disorder, Schizophrenia, Scoliosis, Hypertension, Upper aerodigestive tract neoplasm

6680
Potassium channel tetramerization domain containing 14
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Pelvic organ prolapse