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 658284 |
0.038 |
Down |
AMMECR1 |
NSC 665700 |
0.04 |
Down |
AMMECR1 |
NSC 665961 |
0.047 |
Down |
AMMECR1 |
NSC 668578 |
0.024 |
Down |
AMMECR1 |
NSC 672141 |
0.022 |
Down |
AMMECR1 |
NSC 672434 |
0.006 |
Down |
AMMECR1 |
NSC 674462 |
0.026 |
Down |
AMMECR1 |
NSC 674587 |
0.048 |
Up |
AMMECR1 |
NSC 675773 |
0.039 |
Up |
AMMECR1 |
2-Naphthacenecarboxamide, N-[(6,7-dihydro-7-oxo-v-triazolo[4,5-d]pyrimidin-5-ylamino)methyl]-4-dimethylamino-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo- |
0.03 |
Down |
AMMECR1 |
NSC 676154 |
0.041 |
Down |
AMMECR1 |
10H-Phenothiazine, 1,3,4-trifluoro-2-nitro- |
0.038 |
Up |
AMMECR1 |
NSC 676819 |
0.021 |
Down |
AMMECR1 |
Methanone, (tricyclo[3.3.1.1(3,7)]decan-1-yl) [3-(3-nitrophenyl)-2-oxiranyl]- |
0.04 |
Down |
AMMECR1 |
NSC 678047 |
0.038 |
Down |
Expression pattern: Sensitivity / Resistance
Total:5 Current:2
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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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