LncRNAWiki:Congenital, Hereditary, and Neonatal Diseases and Abnormalities

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Name Transcript ID Alias Description Disease
H19 NONHSAT017465 "Q96MK8,ENSG00000130600" "H19, imprinted maternally expressed transcript (non-protein coding)" bladder cancer, breast cancer, cervical cancer, choricarcinoma, colon cancer, Congenital hyperinsulinism, Esophageal squamous cell cancer, gastric cancer, germ cell tumor, gestational choriocarcinoma, glioblastoma, glioma, growth restriction, hematopoiesis, infertility, kidney cancer, liver cancer, lung cancer, Marek's disease, Medulloblastoma, melanoma, Meningioma, Mullerian aplasia, myeloproliferative polycythaemia vera, neural tube defects, neuroblastoma, obesity, ovarian cancer, pheochromocytoma, pituitary adenoma, Prader-Willi syndrome, pre-eclampsia, prostate cancer, Silver-Russell syndrome, Wiedemann-Beckwith syndrome, Wilms' tumor
XIST NONHSAT137541 ENSG00000229807 X inactive-specific transcript Trisomy 21, bladder cancer, breast cancer, Klinefelter's syndrome, testicular cancer
CECR3 CECR3 N/A "cat eye syndrome chromosome region, candidate 3 (non-protein coding)" cat eye syndrome
CECR5-AS1 CECR5-AS1 NCRNA00017 CECR5 antisense RNA 1 cat eye syndrome
CECR7 CECR7 SAHL1 "cat eye syndrome chromosome region, candidate 7 (non-protein coding)" cat eye syndrome
CECR9 CECR9 N/A "cat eye syndrome chromosome region, candidate 9 (non-protein coding)" cat eye syndrome
CLRN1-AS1 CLRN1-AS1 UCRP CLRN1 antisense RNA 1 Usher syndrome type 3
DGCR10 DGCR10 DGS-B DiGeorge syndrome critical region gene 10 (non-protein coding) DiGeorge syndrome
DGCR11 DGCR11 DGS-D DiGeorge syndrome critical region gene 11 (non-protein coding) DiGeorge and velo-cardio-facial syndrome
DGCR12 DGCR12 DGS-E DiGeorge syndrome critical region gene 12 (non-protein coding) DiGeorge and velo-cardio-facial syndrome
DGCR5 DGCR5 "NCRNA00037, LINC00037" DiGeorge syndrome critical region gene 5 (non-protein coding) DiGeorge syndrome
DGCR9 DGCR9 "DGS-A, POM121L5P" DiGeorge syndrome critical region gene 9 (non-protein coding) DiGeorge syndrome
LINCMD1 LINCMD1 N/A "long intergenic non-protein coding RNA, muscle differentiation 1" Duchenne muscular dystrophy
MESTIT1 MESTIT1 "NCRNA00040, MEST-AS1" "MEST intronic transcript 1, antisense RNA" _
MIR17HG MIR17HG "FLJ14178, MIRH1, MIHG1, NCRNA00048, miR-17-92, LINC00048" miR-17-92a-1 cluster host gene lymphoma, syndromic developmental defect
SMAD1-AS1 SMAD1-AS1 ENST00000513542 SMAD1 antisense RNA 1 Ventricular septal defects
SMCR6 SMCR6 N/A "Smith-Magenis syndrome chromosome region, candidate 6 (non-protein coding)" Smith-Magenis syndrome
DM1-AS DM1-AS N/A DM1 locus antisense RNA Myotonic dystrophy type 1
HDHD5-AS1 HDHD5-AS1 CECR4, CECR5-AS1, NCRNA00017 HDHD5 antisense RNA 1 cat eye syndrome
LINC00862 LINC00862 C1orf98, SMIM16 long intergenic non-protein coding RNA 862 Cystic Fibrosis
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