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EntrezGene:6102

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Symbol:RP2
Description:retinitis pigmentosa 2 (X-linked recessive)
Synonyms:DELXp11.3, NME10, TBCCD2, XRP2
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:6102
HGNC:10274
MIM:300757
Ensembl:ENSG00000102218
HPRD:02424
Vega:OTTHUMG00000021430
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:6102
LocusTag:-
chromosome:X
map location:Xp11.3
type of gene:protein-coding
Symbol from
nomenclature authority:
RP2
Full name from
nomenclature authority:
retinitis pigmentosa 2 (X-linked recessive)
Nomenclature status:O
Other designations:protein XRP2
Modification date:08.01.2012