| Name
|
Transcript ID
|
Alias
|
Description
|
Disease
|
| 7SL
|
lnc-LRR1-1:1
|
"7S RNA, SRP RNA, 4.5S SRP RNA, 4.5S RNA, RN7SL1 RNA, ENSG00000258486"
|
"RNA, 7SL, cytoplasmic 1"
|
AIDS,dermatomyositis
|
| BDNF-AS
|
ENST00000499008.3
|
BDNF antisense RNA
|
"BT2A, BT2B,BT2C,BT2D,NCRNA00049,BDNF-AS1, NCRNA00049"
|
Huntington's disease, psychiatric disease, schizophrenia, obesity
|
| BCYRN1
|
lnc-EPCAM-1:2
|
"BC200,BC200a, NCRNA00004, LINC00004"
|
"BCYRN1, brain cytoplasmic RNA 1"
|
Alzheimer's disease,breast cancer,cervical cancer, lung cancer,oesophagus cancer, ovarian cancer, parotid cancer,tongue cancer
|
| DBET
|
NONHSAT099821
|
"DBE-T, DUX4L30"
|
D4Z4 binding element transcript (non-protein coding)
|
Pancreatic ductal adenocarcinoma, Facioscapulohumeral muscular dystrophy
|
| DHFR upstream transcripts
|
NONHSAT102417
|
"DHFR minor transcript 5'-UTR, ENSG00000228716"
|
N/A
|
_
|
| PWRN1
|
NONHSAT040920
|
NCRNA00198
|
Prader-Willi region non-protein coding RNA 1
|
Prader-Willi syndrome
|
| PWRN2
|
NONHSAT040875
|
NCRNA00199
|
Prader-Willi region non-protein coding RNA 2
|
Prader-Willi syndrome
|
| SCAANT1
|
SCAANT1
|
SCA7/ATXN7 antisense RNA 1
|
ATXN7-AS1
|
Spinocerebellar ataxia type 7
|
| 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
|
| HAR1A
|
lnc-BIRC7-2:1
|
"HAR1F, ENSG00000238820"
|
highly accelerated region 1A
|
Alzheimer's disease,Huntington's disease, schizophrenia
|
| HAR1B
|
ENST00000447910.2
|
"HAR1R, ENSG00000231133"
|
highly accelerated region 1B
|
Huntington's disease, schizophrenia
|
| IPW
|
NONHSAT041063
|
NCRNA00002
|
imprinted in Prader-Willi syndrome
|
Prader-Willi syndrome
|
| MEG3
|
NONHSAT039745
|
"Gtl2, ENSG00000214548"
|
maternally expressed 3 (non-protein coding)
|
bladder cancer, breast cancer, chronic myeloid leukemia, colon cancer, gastric cancer, glioma, hepatocelluar carcinoma, heroin abuse, Huntington's disease, kidney cancer, lung cancer, Meningioma, myelodysplastic syndrome, nonfunctioning pituitary adenomas, Pituitary adenoma, prostate cancer, type 1 diabetes
|
| MEG8
|
ENST00000553584.1
|
"Bsr, ""Imprinted RNA near Meg3/Gtl2"", Irm, LINC00024, ""long intergenic non-protein coding RNA 24"", NCRNA00024, ""non-protein coding RNA 24"", Rian, ""RNA Imprinted and Accumulated in Nucleus"", ENSG00000258399"
|
Rian: RNA Imprinted and Accumulated in Nucleus;Irm: Imprinted RNA near Meg3/Gtl2;MEG8: Maternally expressed gene 8
|
Prader-Willi/Angelman syndrome
|
| ATXN8OS
|
NONHSAT034251
|
"NCRNA00003, ""non-protein coding RNA 3"", ATXN8OS, KLHL1AS, SCA8, ENSG00000230223"
|
Spinocerebellar ataxia 8 (SCA8) RNA;KLHL1AS: kelch-like 1 (Drosophila) antisense;ATXN8OS: ataxin 8 opposite strand
|
human spinocerebellar ataxia type 8,Spinocerebellar ataxia type 8
|
| SNHG3
|
lnc-OR10H5-1:1
|
"U17HG, linc1343, ENSG00000242125"
|
Small nucleolar RNA host gene 3
|
Alzheimer's disease
|
| IFNG-AS1
|
ENST00000538665.1
|
"LincR-Ifng-3'AS, NEST, "Theiler's murine encephalomyelitis virus persistence candidate gene 1", Tmevpg1, ENSG00000255733"
|
IFNG antisense RNA 1
|
multiple sclerosis
|
| TUG1
|
NONHSAT084827
|
ENSG00000253352
|
taurine up-regulated gene 1
|
B-cell neoplasms, bladder cancer, Huntington's disease, non-small cell lung cancer
|
| CDKN2B-AS1
|
NONHSAT130421,
lnc-C9orf53-2:1
|
"ANRIL, p15AS, ENSG00000240498"
|
CDKN2B antisense RNA 1
|
abdominal aortic aneurysm,acute lymphoblastic leukemia,basal cell carcinoma,breast cancer,cardiovascular disease,coronary artery disease,coronary heart disease,Diabetes,endometriosis,Esophageal squamous cell cancer,gastric cancer,glioma,hereditary cutaneous malignant melanoma,intracranial aneurism,ischemic stroke,melanoma,myocardial infarction,nasopharyngeal carcinoma,neural system tumors syndrome,Neurofibromatosis type 1,periodontitis,prostate cancer,
|
| BACE1-AS
|
NONHSAT024403,lnc-RNF214-1:2
|
"BACE1AS,NCRNA00177; FJ573250"
|
BACE1 antisense RNA
|
Alzheimer's disease,
|
| Beta-globin transcripts
|
NONHSAT017676,
NONHSAT017675,
NONHSAT017674
|
N/A
|
N/A
|
_
|
| LINC00581
|
lnc-PRL-6:2,
lnc-PRL-6:1
|
"BX118339,Hs.112750, linc-MBOAT1-4: TCONS_00012107, linc-MBOAT1-4: TCONS_00012678"
|
long intergenic non-protein coding RNA 581
|
West Syndrome
|
| CAR Intergenic 10
|
NONHSAT016928,
lnc-FANK1-3:1
|
"Intergenic10, CR611911, AK055628"
|
Chromatin Associated RNA 10
|
_
|
| CLRN1-AS1
|
CLRN1-AS1
|
UCRP
|
CLRN1 antisense RNA 1
|
Usher syndrome type 3
|
| HTT-AS
|
HTT-AS
|
HTTAS
|
HTT antisense RNA (head to head)
|
Huntington's disease
|
| LINC00165
|
LINC00165
|
NLC1-B
|
long intergenic non-protein coding RNA 165
|
narcolepsy
|
| LINC01080
|
LINC01080
|
TCONSN/A00021856
|
long intergenic non-protein coding RNA 1080
|
Alzheimer's disease ;amnestic mild cognitive impairment
|
| LINC01616
|
LINC01616
|
n341006
|
long intergenic non-protein coding RNA 1616
|
Alzheimer's disease
|
| LINCMD1
|
LINCMD1
|
N/A
|
"long intergenic non-protein coding RNA, muscle differentiation 1"
|
Duchenne muscular dystrophy
|
| MIR17HG
|
MIR17HG
|
"FLJ14178, MIRH1, MIHG1, NCRNA00048, miR-17-92, LINC00048"
|
miR-17-92a-1 cluster host gene
|
lymphoma, syndromic developmental defect
|
| MKRN3-AS1
|
MKRN3-AS1
|
"FNZ127, NCRNA00009, ZNF127-AS"
|
MKRN3 antisense RNA 1
|
Prader-Willi syndrome ;Angelman syndromes
|
| NOP14-AS1
|
NOP14-AS1
|
RES4-24
|
NOP14 antisense RNA 1
|
Huntington disease
|
| PWARSN
|
PWARSN
|
"PAR-SN, PARSN"
|
"Prader Willi/Angelman region RNA, SNRPN neighbor"
|
Prader-Willi syndrome
|
| SNHG14
|
SNHG14
|
"NCRNA00214, UBE3A-AS"
|
small nucleolar RNA host gene 14
|
Prader-Willi
|
| SOX2-OT
|
SOX2-OT
|
"DKFZp761J1324, NCRNA00043"
|
SOX2 overlapping transcript
|
Esophageal squamous cell cancer, Alzheimer's disease,Neurodevelopmental syndromes associated with the SOX2 locus
|
| DM1-AS
|
DM1-AS
|
N/A
|
DM1 locus antisense RNA
|
Myotonic dystrophy type 1
|
| DSCR4
|
DSCR4
|
DCRB
|
Down syndrome critical region 4
|
Down syndrome
|
| DSCR8
|
DSCR8
|
C21orf65, MTAG2, CT25.1a, CT25.1b, MMA-1a, MMA-1b
|
Down syndrome critical region 8 (non-protein coding)
|
Down syndrome, melanoma
|
| LINC01772
|
ENST00000457898.1
|
ENSG00000226029
|
long intergenic non-protein coding RNA 1772
|
alzheimer's disease, ovarian cancer, pancreatic cancer,gastric cancer
|
| MAPT-AS1
|
MAPT-AS1
|
N/A
|
MAPT antisense RNA 1
|
Parkinson's Disease
|
