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 |
NSC 147358 |
0.02 |
Down |
AMMECR1 |
NSC 148201 |
0.021 |
Down |
AMMECR1 |
NSC 164887 |
0.036 |
Down |
AMMECR1 |
L-Aspartic acid, N-[4-[[(2-amino-4-hydroxy-6-quinazolinyl)methyl]amino]benzoyl]-, monohydrate |
0.03 |
Down |
AMMECR1 |
5-CHLORO-6-[[(3,4-DICHLOROPHENYL)AMINO]METHYL]-2,4-QUINOZOLINEDIAMINE |
0.047 |
Down |
AMMECR1 |
2,4-Pyrimidinediamine, 5-(4-chloro-3-nitrophenyl)-6-ethyl- |
0.04 |
Down |
AMMECR1 |
7H-Pyrrolo[3,2-f]quinazoline-1,3-diamine, 7-[(4-aminophenyl)methyl]-, dihydrochloride |
0.046 |
Down |
AMMECR1 |
Clonixin |
0.006 |
Down |
AMMECR1 |
CHAETOCHROMIN |
0.002 |
Down |
AMMECR1 |
NSC 401101 |
0.021 |
Up |
AMMECR1 |
RAPAMYCIN PRODRUG |
0.016 |
Down |
AMMECR1 |
Dichlorobis[1-(4-nitrophenyl)-3-phenylpropane-1,3-dionato]-titanium(IV) |
0.013 |
Down |
AMMECR1 |
VIRIDENOMYCIN |
0.039 |
Down |
AMMECR1 |
NSC 649821 |
0.048 |
Up |
AMMECR1 |
NSC 656471 |
0.048 |
Up |
Expression pattern: Sensitivity / Resistance
Total:5 Current:1
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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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