Genes | GeDiPNet - Gene Disease Pathway & Associations

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11981 to 11990 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11981	946	SIGLEC6	Sialic acid binding Ig like lectin 6	CD327, CD33L, CD33L1, CD33L2, CDW327, OBBP1	Atherosclerosis, Systemic lupus erythematosus, Rheumatoid arthritis
11982	27181	SIGLEC8	Sialic acid binding Ig like lectin 8	SAF2, SIGLEC-8, SIGLEC8L	Chagas cardiomyopathy
11983	10280	SIGMAR1	Sigma non-opioid intracellular receptor 1	ALS16, DSMA2, HMNR2, OPRS1, SIG-1R, SR-BP, SR-BP1, SRBP, hSigmaR1, sigma1R	Amnesia, Amyotrophic lateral sclerosis, Distal spinal muscular atrophy, Charcot-marie-tooth disease, Distal hereditary motor neuropathy, Learning disorders, Memory disorders, Mood disorder, Schizophrenia, Seizures, Spinal muscular atrophy
11984	150094	SIK1	Salt inducible kinase 1	DEE30, MSK, SIK, SIK-1, SIK1B, SNF1LK	Alzheimer disease, Juvenile arthritis, Asthma, Dilated cardiomyopathy, Developmental and epileptic encephalopathy, Myoclonic encephalopathy, Generalized epilepsy, Global developmental delay, Hypertension, Juvenile idiopathic arthritis, Language development disorders, Oligoarticular juvenile idiopathic arthritis, West syndrome
11985	23235	SIK2	Salt inducible kinase 2	LOH11CR1I, QIK, SIK-2, SNF1LK2	Asthma, Eczema, Breast cancer, Hepatocellular carcinoma, Coronary artery disease, Hypertension, Prostate cancer, Respiratory system disease, Sclerosing cholangitis
11986	23387	SIK3	SIK family kinase 3	L19, QSK, SEMDK, SIK-3	Eczema, Atrial fibrillation, Autism, Breast cancer, Cancer, Color vision deficiency, Coronary artery disease, Diabetes mellitus, Digestive system disease, Diverticular disease, Hearing impairment, Hearing loss, Heart failure, Hypothyroidism, Metabolic syndrome View all (5 more)
11987	80143	SIKE1	Suppressor of IKBKE 1	SIKE	Schizophrenia
11988	64374	SIL1	SIL1 nucleotide exchange factor	BAP, MSS, ULG5	Alzheimer disease, Apraxia, Atrial fibrillation, Blepharoptosis, Cataract, Cerebellar atrophy, Global developmental delay, Insomnia, Marinesco-sjogren syndrome, Prostatic neoplasms, Strabismus
11989	6492	SIM1	SIM bHLH transcription factor 1	bHLHe14	Androgenetic alopecia, Atrial fibrillation, Bipolar disorder, Breast neoplasms, Venous insufficiency, Neurodevelopmental disorder, Erectile dysfunction, Heart failure, Hyperglycemia, Insomnia, Irritable bowel syndrome, Major depressive disorder, Metabolic syndrome, Neurotic disorder, Non-specific syndromic intellectual disability View all (4 more)
11990	6493	SIM2	SIM bHLH transcription factor 2	HMC13F06, HMC29C01, SIM, bHLHe15	Asthma, Cleft palate, Craniofacial abnormalities, Prostate cancer, Seasonal allergic rhinitis, Testicular carcinoma

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