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EntrezGene:9949

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Symbol:AMMECR1
Description:Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Synonyms:AMMERC1
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:9949
HGNC:467
MIM:300195
Ensembl:ENSG00000101935
HPRD:02182
Vega:OTTHUMG00000022197
Associated motifs:NA
Transcripton Factor?: No

TSS regions




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TSS expression






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ENCODE TF ChIP-seq peak enrichment analysis Analyst: Erik Arner <br>Summary: For each TF and each co-expression cluster, the number of promoters with ENCODE TF ChIP signal was compared with the rest of promoters from the robust set using Fisher's exact test. Clusters with significant ChIP enrichment (q <= 0.05) after Benjamini-Hochberg correction were retained. <br><br><br>link to source dataset.<br>data


No analysis results for this cluster

Details<b>Summary:</b>It includes sequences from the international sequence collaboration, Swiss-Prot, and RefSeq. The RefSeq subset of this file is also available as gene2refseq.<br><br>links to source dataset.<br>human <br>mouse


GeneID:9949
LocusTag:RP13-360B22.1
chromosome:X
map location:Xq22.3
type of gene:protein-coding
Symbol from
nomenclature authority:
AMMECR1
Full name from
nomenclature authority:
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Nomenclature status:O
Other designations:AMME syndrome candidate gene 1 protein
Modification date:18.11.2011