Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "K"

11 to 20 of 320 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11	102723508	KANTR	KANTR integral membrane protein	LINC01155, Spasm	Common variable immunodeficiency
12	10300	KATNB1	Katanin regulatory subunit B1	KAT, LIS6	Developmental delay, Hypoplasia of corpus callosum, Impaired cognition, Lissencephaly with microcephaly, Microcephaly, Microlissencephaly, Neuronal heterotopia, Pachygyria, Partial agenesis of corpus callosum, Polymicrogyria
13	10324	KLHL41	Kelch like family member 41	KBTBD10, Krp1, SARCOSIN	Arthrogryposis multiplex congenita, Cardiomyopathy, Pulmonary hypoplasia, Congenital nemaline myopathy, Congenital pectus excavatum, Dysphagia, High palate, Hypospadias, Limb muscle atrophy, Micrognathism, Motor delay, Myopathy, Nemaline myopathy, Hypotonia, Neuromuscular dysphagia View all (5 more)
14	10365	KLF2	KLF transcription factor 2	LKLF	Colorectal cancer, Colorectal neoplasms, Lung diseases, Multiple myeloma
15	10524	KAT5	Lysine acetyltransferase 5	ESA1, HTATIP, HTATIP1, NEDFASB, PLIP, TIP, TIP60, ZC2HC5, cPLA2	Gout, Gouty arthritis
16	10661	KLF1	KLF transcription factor 1	CDAN4A, CDAN4B, EKLF, EKLF/KLF1	Anemia, Congenital dyserythropoietic anemia, Dwarfism, Erythroid hyperplasia, Hematological disease, Hemoglobinopathy, Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome, Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome, Hydrops fetalis, Hyperbilirubinemia
17	10749	KIF1C	Kinesin family member 1C	LTXS1, SATX2, SAX2, SPAX2, SPG58	Ataxia, Cerebellar atrophy, Cerebral atrophy, Developmental delay, Distal amyotrophy, Dwarfism, Dysarthria, Horizontal nystagmus, Hypodontia, Mental retardation, Microcephaly, Nervous system diseases, Spastic ataxia, Ataxia, spastic with optic atrophy and mental retardation, Spastic paraplegia
18	10765	KDM5B	Lysine demethylase 5B	CT31, JARID1B, MRT65, PLU-1, PLU1, PPP1R98, PUT1, RBBP2H1A, RBP2-H1	Absence of septum pellucidum, Astigmatism, Atrial septal defect, Autism, Central visual impairment, Cerebral atrophy, Colonic neoplasms, Cortical dysplasia, Cryptorchidism, Developmental delay, Dolichocephaly, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Hypospadias View all (13 more)
19	10945	KDELR1	KDEL endoplasmic reticulum protein retention receptor 1	ERD2, ERD2.1, HDEL, PM23	Prostatic neoplasms, Prostate cancer
20	109729127	KRT7-AS	KRT7 antisense RNA 1	-	Asthma

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