Epithelial-Mesenchymal Transition, human (Scheel, 2011)
Name | miRBASE accession |
---|---|
hsa-miR-129-5p
|
MIMAT0000242 |
Promoter | Score | Transcript | Gene | Gene Info |
---|---|---|---|---|
chr22_+_40390930 | 0.00 |
ENST00000333407.6 |
FAM83F |
family with sequence similarity 83, member F |
chr4_-_170924888 | 0.00 |
ENST00000502832.1 ENST00000393704.3 |
MFAP3L |
microfibrillar-associated protein 3-like |
chr6_+_21593972 | 0.00 |
ENST00000244745.1 ENST00000543472.1 |
SOX4 |
SRY (sex determining region Y)-box 4 |
chr7_-_92463210 | 0.00 |
ENST00000265734.4 |
CDK6 |
cyclin-dependent kinase 6 |
chr5_-_78809950 | 0.00 |
ENST00000334082.6 |
HOMER1 |
homer homolog 1 (Drosophila) |
chr2_+_168725458 | 0.00 |
ENST00000392690.3 |
B3GALT1 |
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 1 |
chr6_+_117996621 | 0.00 |
ENST00000368494.3 |
NUS1 |
nuclear undecaprenyl pyrophosphate synthase 1 homolog (S. cerevisiae) |
chr3_+_142720366 | 0.00 |
ENST00000493782.1 ENST00000397933.2 ENST00000473835.2 ENST00000493598.2 |
U2SURP |
U2 snRNP-associated SURP domain containing |
chr4_+_26862400 | 0.00 |
ENST00000467011.1 ENST00000412829.2 |
STIM2 |
stromal interaction molecule 2 |
chr12_+_2162447 | 0.00 |
ENST00000335762.5 ENST00000399655.1 |
CACNA1C |
calcium channel, voltage-dependent, L type, alpha 1C subunit |
chr10_+_111967345 | 0.00 |
ENST00000332674.5 ENST00000453116.1 |
MXI1 |
MAX interactor 1, dimerization protein |
chr4_-_153457197 | 0.00 |
ENST00000281708.4 |
FBXW7 |
F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase |
chr8_-_81787006 | 0.00 |
ENST00000327835.3 |
ZNF704 |
zinc finger protein 704 |
chr3_-_119813264 | 0.00 |
ENST00000264235.8 |
GSK3B |
glycogen synthase kinase 3 beta |
chr17_-_27278304 | 0.00 |
ENST00000577226.1 |
PHF12 |
PHD finger protein 12 |
chr3_-_87040233 | 0.00 |
ENST00000398399.2 |
VGLL3 |
vestigial like 3 (Drosophila) |
chr4_-_74847800 | 0.00 |
ENST00000296029.3 |
PF4 |
platelet factor 4 |
chr19_-_16738984 | 0.00 |
ENST00000600060.1 ENST00000263390.3 |
MED26 |
mediator complex subunit 26 |
chr13_-_107187462 | 0.00 |
ENST00000245323.4 |
EFNB2 |
ephrin-B2 |
chr21_-_40685477 | 0.00 |
ENST00000342449.3 |
BRWD1 |
bromodomain and WD repeat domain containing 1 |
chr14_-_51562745 | 0.00 |
ENST00000298355.3 |
TRIM9 |
tripartite motif containing 9 |
chr2_-_174830430 | 0.00 |
ENST00000310015.6 ENST00000455789.2 |
SP3 |
Sp3 transcription factor |
chr1_-_20812690 | 0.00 |
ENST00000375078.3 |
CAMK2N1 |
calcium/calmodulin-dependent protein kinase II inhibitor 1 |
chr12_+_51985001 | 0.00 |
ENST00000354534.6 |
SCN8A |
sodium channel, voltage gated, type VIII, alpha subunit |
chr3_+_181429704 | 0.00 |
ENST00000431565.2 ENST00000325404.1 |
SOX2 |
SRY (sex determining region Y)-box 2 |
chr10_-_94003003 | 0.00 |
ENST00000412050.4 |
CPEB3 |
cytoplasmic polyadenylation element binding protein 3 |
chr4_-_105416039 | 0.00 |
ENST00000394767.2 |
CXXC4 |
CXXC finger protein 4 |
chr12_+_52203789 | 0.00 |
ENST00000599343.1 |
AC068987.1 |
HCG1997999; cDNA FLJ33996 fis, clone DFNES2008881 |
chr15_-_51058005 | 0.00 |
ENST00000261854.5 |
SPPL2A |
signal peptide peptidase like 2A |
chrX_-_109561294 | 0.00 |
ENST00000372059.2 ENST00000262844.5 |
AMMECR1 |
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 |
chr8_+_12803176 | 0.00 |
ENST00000524591.2 |
KIAA1456 |
KIAA1456 |
chr6_-_90121938 | 0.00 |
ENST00000369415.4 |
RRAGD |
Ras-related GTP binding D |
chr1_-_78444776 | 0.00 |
ENST00000370767.1 ENST00000421641.1 |
FUBP1 |
far upstream element (FUSE) binding protein 1 |