Symbol: |
AMMECR1
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Description: |
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 [Source:HGNC Symbol;Acc:467]
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Location: |
ChrX:109437414-109683461[-]
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CRmiRSNP:
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Records:null
Compound |
CRmiRSNP |
SNP_sig |
Model |
Molecule |
Mol_sig |
Type |
Model : M1-Allele, M2-Recessive, M3-Additive, M4-Dominant
Total:0 Current:1
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Compound:
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Records:66
Gene |
Compound |
Gen_sig |
Exp_pattern |
AMMECR1 |
5-Hydroxy-3,7-dimethoxy-3',4'-methylenedioxyflavone |
0.032 |
Down |
AMMECR1 |
NSC 680417 |
0.039 |
Down |
AMMECR1 |
1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline,methionine deriv. |
0.03 |
Down |
AMMECR1 |
NSC 681776 |
0.037 |
Up |
AMMECR1 |
Propanoic acid, 3,3,3-trifluoro- 2-[(4-fluorophenyl)amino]-2-[[(ethoxy)carbonyl]amino]-, ethyl ester |
0.042 |
Down |
AMMECR1 |
NSC 691243 |
0.039 |
Down |
AMMECR1 |
NSC 694977 |
0.046 |
Up |
AMMECR1 |
Bassic acid |
0.029 |
Up |
AMMECR1 |
NSC 696990 |
0.029 |
Down |
AMMECR1 |
NSC 698276 |
0.023 |
Up |
AMMECR1 |
NSC 699926 |
0.014 |
Up |
AMMECR1 |
NSC 699928 |
0.029 |
Up |
AMMECR1 |
NSC 699934 |
0.035 |
Up |
AMMECR1 |
NSC 700128 |
0.016 |
Up |
AMMECR1 |
NSC 700424 |
0.038 |
Up |
Expression pattern: Sensitivity / Resistance
Total:5 Current:3
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SNP:
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Records:28
Total:2 Current:1
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miRNA:
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Records:6
Gene |
Gen_transcript |
miRNA |
miR_location |
AMMECR1 |
ENST00000372057 |
hsa-mir-192-3p |
Chr11:64658631-64658652[-] |
AMMECR1 |
ENST00000262844 |
hsa-mir-200b-3p |
Chr1:1102540-1102561[+] |
AMMECR1 |
ENST00000372057 |
hsa-mir-200b-3p |
Chr1:1102540-1102561[+] |
AMMECR1 |
ENST00000372059 |
hsa-mir-200b-3p |
Chr1:1102540-1102561[+] |
AMMECR1 |
ENST00000262844 |
hsa-mir-338-5p |
Chr17:79099723-79099744[-] |
AMMECR1 |
ENST00000372057 |
hsa-mir-618 |
Chr12:81329575-81329597[-] |
Total:1 Current:1
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