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EntrezGene:123606

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Symbol:NIPA1
Description:non imprinted in Prader-Willi/Angelman syndrome 1
Synonyms:FSP3, SPG6
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:123606
HGNC:17043
MIM:608145
Ensembl:ENSG00000170113
HPRD:10487
Vega:OTTHUMG00000129099
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:123606
LocusTag:-
chromosome:15
map location:15q11.2
type of gene:protein-coding
Symbol from
nomenclature authority:
NIPA1
Full name from
nomenclature authority:
non imprinted in Prader-Willi/Angelman syndrome 1
Nomenclature status:O
Other designations:magnesium transporter NIPA1, non-imprinted in Prader-Willi/Angelman syndrome 1, non-imprinted in Prader-Willi/Angelman syndrome region protein 1, spastic paraplegia 6 protein, magnesium transporter NIPA1;;non-imprinted in Prader-Willi/Angelman syndrome 1;;non-imprinted in Prader-Willi/Angelman syndrome region protein 1;;spastic paraplegia 6 protein
Modification date:12.12.2011