Motif ID: AACGGAA

Z-value: 0.496


Mature miRNA associated with seed AACGGAA:

NamemiRBase Accession
hsa-miR-191 MIMAT0000440



Activity profile for motif AACGGAA.

activity profile for motif AACGGAA


Sorted Z-values histogram for motif AACGGAA

Sorted Z-values for motif AACGGAA



Network of associatons between targets according to the STRING database.



First level regulatory network of AACGGAA

PNG image of the network

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Top targets:


Showing 1 to 20 of 33 entries
PromoterScoreRefseqGene SymbolGene Name
chr11_-_27681195 11.104 NM_001143816
NM_170735
 BDNF

brain-derived neurotrophic factor

chr11_-_27743604 10.957 NM_170731
 BDNF
brain-derived neurotrophic factor
chr11_-_27721179 10.728 NM_170734
 BDNF
brain-derived neurotrophic factor
chr11_-_27741192 10.377 NM_001143807
 BDNF
brain-derived neurotrophic factor
chr11_-_27722599 10.314 NM_001143808
NM_001143809
NM_001143810
NM_001143811
 BDNF



brain-derived neurotrophic factor



chr11_-_27721975 10.228 NM_001143813
NM_001143814
NM_001709
 BDNF


brain-derived neurotrophic factor


chr11_-_27742224 10.151 NM_001143805
NM_001143806
NM_170732
 BDNF


brain-derived neurotrophic factor


chr11_-_27722446 10.075 NM_001143812
 BDNF
brain-derived neurotrophic factor
chr11_-_27723061 9.889 NM_170733
 BDNF
brain-derived neurotrophic factor
chrX_-_109683457 5.045 NM_001171689
 AMMECR1
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
chrX_-_109561314 3.798 NM_001025580
NM_015365
 AMMECR1

Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1

chr3_+_115342150 2.006 NM_001130064
NM_002045
 GAP43

growth associated protein 43

chr20_+_44650260 1.581 NM_001134771
 SLC12A5
solute carrier family 12 (potassium/chloride transporter), member 5
chr5_+_149887673 1.537 NM_001543
 NDST1
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
chr1_-_33841142 1.421 NM_198040
 PHC2
polyhomeotic homolog 2 (Drosophila)
chr10_+_114709963 1.310 NM_001146274
NM_001146283
NM_001146284
NM_001146285
NM_001146286
NM_001198525
NM_001198526
NM_001198527
NM_001198528
NM_001198529
NM_001198530
NM_001198531
NM_030756
 TCF7L2












transcription factor 7-like 2 (T-cell specific, HMG-box)












chr20_+_44657812 1.101 NM_020708
 SLC12A5
solute carrier family 12 (potassium/chloride transporter), member 5
chr3_-_10547267 1.088 NM_001001331
NM_001683
 ATP2B2

ATPase, Ca++ transporting, plasma membrane 2

chr10_-_81205091 0.998 NM_153367
 ZCCHC24
zinc finger, CCHC domain containing 24
chr19_-_15560761 0.864 NM_021241
 WIZ
widely interspaced zinc finger motifs

Gene Ontology Analysis

Gene overrepresentation in process category:

Showing 1 to 1 of 1 entries
enrichment   p-value GO term description
4.90 1.19e-02 GO:0007399 nervous system development

Nothing significant found in compartment category.

Nothing significant found in function category.