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EntrezGene:2188

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Symbol:FANCF
Description:Fanconi anemia, complementation group F
Synonyms:FAF
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:2188
HGNC:3587
MIM:613897
Ensembl:ENSG00000183161
HPRD:04589
Vega:OTTHUMG00000166070
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:2188
LocusTag:-
chromosome:11
map location:11p15
type of gene:protein-coding
Symbol from
nomenclature authority:
FANCF
Full name from
nomenclature authority:
Fanconi anemia, complementation group F
Nomenclature status:O
Other designations:Fanconi anemia group F protein
Modification date:08.01.2012