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EntrezGene:167691

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Symbol:LCA5
Description:Leber congenital amaurosis 5
Synonyms:C6orf152
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:167691
HGNC:31923
MIM:611408
Ensembl:ENSG00000135338
HPRD:10791
Vega:OTTHUMG00000015080
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:167691
LocusTag:-
chromosome:6
map location:6q14.1
type of gene:protein-coding
Symbol from
nomenclature authority:
LCA5
Full name from
nomenclature authority:
Leber congenital amaurosis 5
Nomenclature status:O
Other designations:Lebercilin, leber congenital amaurosis 5 protein, Lebercilin;;leber congenital amaurosis 5 protein
Modification date:12.12.2011