LncRNAWiki:OtherDisease

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Disease LncRNAs
abdominal aortic aneurysm CDKN2B-AS1
acute kidney injury MGAT3-AS1
acute lymphoblastic leukemia CDKN2B-AS1, LOH12CR2
adolescent idiopathic scoliosis CCDC18-AS1
affective disorders DISC2
AIDS NRON, 7SK, 7SL
alcoholic liver disease AIRN
alveolar capillary dysplasia with misalignment of pulmonary veins LINC01081, LINC01082
Alzheimer's disease SNHG3, LINC01616, LINC01080, BACE1-AS, BCYRN1, HAR1A, SOX2-OT
amnestic mild cognitive impairment LINC01080
anorexia nervosa LINC00235
autism spectrum disorder DISC2, LINC00942, FOXG1-AS1
autoimmune disease GAS5
autoimmune thyroid disease ZFAT-AS1
Beckwith-Wiedemann syndrome KCNQ1OT1
bipolar disorder DISC2, DAOA-AS1
blepharophimosis syndrome BPESC1, PISRT1
bone diseases DANCR
cardiac hypertrophy 7SK
cardiometabolic disease ABHD15-AS1, CDKN2B-AS1, MIR222HG, NPSR1-AS1
cat eye syndrome CECR3, CECR5-AS1, CECR7, CECR9
chronic lymphocytic leukemia DLEU1MIR155HG
chronic myeloid leukemia MEG3
chronic nonalcoholic liver disease AIRN
congenital hyperinsulinism H19
coronary heart disease CDKN2B-AS1
depression DISC2, PWAR4
dermatomyositis 7SL
diabetes CDKN2B-AS1, MALAT1, MEG3, LINC00673, LINC01512, LINC01574, TUNAR, IGF2-AS, PVT1
DiGeorge syndrome DGCR11, DGCR12, DGCR10, DGCR5, DGCR9
Duchenne muscular dystrophy LINCMD1
endometriosis CDKN2B-AS1
facioscapulohumeral muscular dystrophy DBET
growth restriction H19
heart failure FENDRR, MT-LIPCAR
heart pathological hypertrophy MHRT
spinocerebellar ataxia type 8 ATXN8OS
Huntington's disease HAR1A, TUG1, MEG3, NOP14-AS1, HTT-AS, BDNF-AS, HAR1B
infertility H19, NEAT1
influenza A virus (IAV) infection NRAV
intervertebral disc degeneration LINC00917, LINC01562
intracranial aneurism CDKN2B-AS1
ischemic stroke CDKN2B-AS1
kawasaki disease THRIL
keloid CACNA1G-AS1
keratolytic winter erythema LINC00529
Klinefelter's syndrome XIST
leukemia BGLT3, TCL, LAMP5-AS1
liver cirrhosis APTR
lymphocytic leukemia DLEU2
macrosomia LINC00237
macrocephaly LINC00237
malaria MIF-AS1
Marek's disease H19
Mullerian aplasia H19
multiple sclerosis IFNG-AS1
myelodysplastic syndrome MEG3, SNHG4
myeloid leukemia MIR99AHG, MIR100HG
myeloproliferative polycythaemia vera H19
myocardial infarction CDKN2B-AS1, MIAT
narcolepsy LINC00165
neural tube defects H19
neurodevelopmental syndromes SOX2-OT
obesity H19, BDNF-AS, SNHG11, LINC00237
pancreaticobiliary maljunction UCA1
periodontitis CDKN2B-AS1
Prader-Willi syndrome MKRN3-AS1, SNHG14, PWRN1, PWRN2, IPW, PWARSN, MKRN3-AS1, H19, MEG8
pre-eclampsia H19
preterm birth LIFR-AS1
primary spontaneous pneumothorax LINC00977
pseudohypoparathyroidism type Ib GNAS-AS1
psoriasis PTCSC3, PRINS,LINC01185
psychiatric disease BDNF-AS
rheumatoid arthritis HOTAIR
schizophrenia DISC2, HAR1A, DAOA-AS1, BDNF-AS, HAR1B, DLG2-AS1, MIR137HG
scleroderma TSIX
Sézary syndrome DNM3OS
Silver-Russell syndrome H19, MESTIT1
skeletal myogenesis YAM1
Smith-Magenis syndrome SMCR6
spinocerebellar ataxia SCAANT1, ATXN8OS
syndromic developmental defect MIR17HG
systemic lupus erythaematosus GAS5, LINC01420
Usher syndrome type 3 CLRN1-AS1
ventricular septal defects SMAD1-AS1
West Syndrome LINC00581
Wiedemann-Beckwith syndrome H19