Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6621 to 6630 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6621
Potassium voltage-gated channel subfamily H member 6
ERG-2, ERG2, HERG2, Kv11.2, hERG-2
Non-organic psychosis, Psychotic disorders, Schizophrenia

6622
Potassium voltage-gated channel subfamily H member 7
ERG3, HERG3, Kv11.3
Ankylosing spondylitis, Eczema, Autoimmune disease, Breast cancer, Coronary artery disease, Diabetic neuropathy, Epilepsy, Estrogen-receptor negative breast cancer, Eye disease, Hypothyroidism, Inflammatory skin disease, Internet addiction disorder, Lipoma, Neurotic disorder, Ocular sarcoidosis
View all (5 more)

6623
Potassium voltage-gated channel subfamily H member 8
ELK, ELK1, Kv12.1, elk3, hElk-1
Alzheimer disease, Cerebral amyloid angiopathy, Venous insufficiency, Dementia, Major depressive disorder, Migraine

6624
Potassium voltage-gated channel interacting protein 1
KCHIP1, VABP
Attention deficit hyperactivity disorder, Behcet disease, Obstructive pulmonary disease, Resistant hypertension, Epilepsy, Multiple sclerosis, Sclerosing cholangitis

6625
Potassium voltage-gated channel interacting protein 3
CSEN, DREAM, KCHIP3
Parkinson disease

6626
Potassium voltage-gated channel interacting protein 4
CALP, KCHIP4
Colorectal cancer, Deficiency anemia, Diverticular disease, Insomnia, Learning disorders, Metabolic syndrome, Myopathy, Myositis, Neurotic disorder, Obesity, Osteoarthritis, Parkinson disease, Rheumatoid arthritis, Sarcoidosis, Scoliosis
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6627
Potassium inwardly rectifying channel subfamily J member 1
KIR1.1, ROMK, ROMK1
Bartter syndrome, Hypertension

6628
Potassium inwardly rectifying channel subfamily J member 10
BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME
Nonsyndromic hearing loss, Cerebellar ataxia, Congenital neurologic anomalies, Deafness, East syndrome, Intellectual developmental disorder, Littles disease, Multiple sclerosis, Paroxysmal dystonic choreoathetosis, Paroxysmal dyskinesia, Pendred syndrome, Peripheral neuropathy, Seizures, tonic-clonic, photosensitive

6629
Potassium inwardly rectifying channel subfamily J member 11
BIR, HHF2, IKATP, KIR6.2, MODY13, PHHI, PNDM2, TNDM3
Hyperinsulinism, Congenital hyperinsulinism, Coronary artery disease, Dend syndrome, Atopic dermatitis, Diabetes mellitus, Diabetes mellitus type 1, Diabetes mellitus type 2, Permanent neonatal diabetes mellitus, Transient neonatal diabetes mellitus, Diazoxide-resistant focal hyperinsulinism due to kir6.2 deficiency, Hyperinsulinemic hypoglycemia, Hypertrichosis, Hypoglycemia, Maturity-onset diabetes of the young (mody)
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6630
Potassium inwardly rectifying channel subfamily J member 12
IRK-2, IRK2, KCNJN1, Kir2.2, hIRK, hIRK1, hkir2.2x, kcnj12x
Hypertension, Lymphatic metastasis, Metabolic syndrome, Diabetes mellitus type 2, Urinary bladder neoplasms