Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "K"

101 to 110 of 320 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
101	319101	KRT73	Keratin 73	CK-73, IRT6IRS3, K6IRS3, K73, KRT6IRS3	Colorectal cancer, Creutzfeldt-jakob disease
102	337975	KRTAP20-1	Keratin associated protein 20-1	KAP20.1	Breast cancer
103	337977	KRTAP21-1	Keratin associated protein 21-1	KAP21.1	Breast cancer
104	338653	KCNQ1-AS1	KCNQ1 antisense RNA 1	-	Hyperuricemia, Jervell-lange nielsen syndrome, Long qt syndrome
105	339855	KY	Kyphoscoliosis peptidase	MFM7	Acquired kyphoscoliosis, Congenital clubfoot, Congenital kyphoscoliosis, Congenital myopathy, Developmental delay, Dysphagia, Elbow flexion contracture, Facial paralysis, Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome, Kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome, Limb amyotrophy, Mental retardation, Myofibrillar myopathy, Spastic paraplegia
106	343450	KCNT2	Potassium sodium-activated channel subfamily T member 2	DEE57, EIEE57, KCa4.2, KNa1.2, SLICK, SLO2.1	Absence seizure, Breast cancer, Developmental delay, Developmental regression, Epilepsy, Epileptic encephalopathy, Exudative macular degeneration, Geographic atrophy, Hypoplasia of corpus callosum, Age-related macular degeneration, Myoclonic seizures
107	353219	KAAG1	Kidney associated DCDC2 antisense RNA 1	RU2AS	Nephronophthisis, Sclerosing cholangitis
108	354	KLK3	Kallikrein related peptidase 3	APS, KLK2A1, PSA, hK3	Asthma, Benign prostatic hyperplasia, Malignant prostate phyllodes tumor, Prostatic neoplasms, Prostate cancer, Prostatic adenoma, Prostatic hyperplasia, Prostatic hypertrophy
109	3735	KARS1	Lysyl-tRNA synthetase 1	CMTRIB, DEAPLE, DFNB89, KARS, KARS2, KRS, LEPID	Cerebellar ataxia, Charcot-marie-tooth disease, Congenital sensorineural hearing loss, Deafness, Developmental delay, Hearing loss, Hypothyroidism, Mental retardation, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Optic neuropathy, Acoustic neuroma
110	3736	KCNA1	Potassium voltage-gated channel subfamily A member 1	AEMK, EA1, HBK1, HUK1, KV1.1, MBK1, MK1, RBK1	Acquired kyphoscoliosis, Autism, Cerebellar atrophy, Choreoathetosis, Clonic seizures, Congenital diaphragmatic hernia, Congenital exomphalos, Congenital kyphoscoliosis, Continuous muscle fiber activity, Developmental delay, Developmental regression, Dysarthria, Dyskinetic syndrome, Dyssomnia, Epileptic encephalopathy View all (27 more)

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