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EntrezGene:79152

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Symbol:FA2H
Description:fatty acid 2-hydroxylase
Synonyms:FAAH, FAH1, FAXDC1, SCS7, SPG35
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:79152
HGNC:21197
MIM:611026
Ensembl:ENSG00000103089
HPRD:16873
Vega:OTTHUMG00000137603
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:79152
LocusTag:-
chromosome:16
map location:16q23
type of gene:protein-coding
Symbol from
nomenclature authority:
FA2H
Full name from
nomenclature authority:
fatty acid 2-hydroxylase
Nomenclature status:O
Other designations:fatty acid alpha-hydroxylase, fatty acid hydroxylase domain containing 1, spastic paraplegia 35 (autosomal recessive), fatty acid alpha-hydroxylase;;fatty acid hydroxylase domain containing 1;;spastic paraplegia 35 (autosomal recessive)
Modification date:26.12.2011