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EntrezGene:5311

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Symbol:PKD2
Description:polycystic kidney disease 2 (autosomal dominant)
Synonyms:APKD2, PC2, PKD4, Pc-2, TRPP2
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:5311
HGNC:9009
MIM:173910
Ensembl:ENSG00000118762
HPRD:01437
Vega:OTTHUMG00000160982
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:5311
LocusTag:-
chromosome:4
map location:4q22.1
type of gene:protein-coding
Symbol from
nomenclature authority:
PKD2
Full name from
nomenclature authority:
polycystic kidney disease 2 (autosomal dominant)
Nomenclature status:O
Other designations:R48321, autosomal dominant polycystic kidney disease type II protein, polycystin-2, polycystwin, transient receptor potential cation channel, subfamily P, member 2, R48321;;autosomal dominant polycystic kidney disease type II protein;;polycystin-2;;polycystwin;;transient receptor potential cation channel, subfamily P, member 2
Modification date:08.01.2012