TSSC3 Products

Description

GenBank Accession Number - NP_003302. TSSC3 in encoded in the imprinted gene domain of 11p15.5 which is considered to be an important tumor suppressor gene region. Alterations in this region may be associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. Studies of the mouse gene, however, which is also located in an imprinted gene domain, have shown that the product of this gene regulates placental growth.

Bioinformatics

Entrez	7262 Human
Uniprot	NM_003311 Human NP_003302 Human NP_003302. Human Q53GA4 Human
Product By Gene ID	7262
Alternate Names	Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene C protein BWR1Cp17-Beckwith-Wiedemann region 1 C HLDA2BRW1C Imprinted in placenta and liver protein IPLp17-BWR1C pleckstrin homology-like domain family A member 2 pleckstrin homology-like domain, family A, member 2 TSSC3p17-Beckwith-Wiedemann region 1C tumor suppressing subchromosomal transferable fragment cDNA 3 tumor suppressing subtransferable candidate 3 Tumor-suppressing STF cDNA 3 protein Tumor-suppressing subchromosomal transferable fragment candidate gene 3 protein tumor-supressing STF cDNA 3

Research Areas for TSSC3

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Apoptosis