| 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
|
