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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Ring finger protein 32

The protein encoded by this gene contains two RING ring finger motifs. RING finger motifs are present in a variety of functionally distinct proteins and are known to be involved in protein-DNA or protein-protein interactions. This gene was found to be expressed during spermatogenesis, most likely in spermatocytes and/or in spermatids. Several alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2011] (from NCBI)
Top mentioned proteins: Lmbr1, HB9, Shh, CIs, PPD
Papers on RNF32
RING finger proteins are involved in the progression of barrett esophagus to esophageal adenocarcinoma: a preliminary study.
Fang et al., Chongqing, China. In Gut Liver, 2014
Among these proteins, the RNF32 and RNF121 expression in BE was 20.3-fold and 16.4-fold higher, respectively, than that in NE, and the expression of RNF24, RNF130, RNF141, RNF139, RNF11, RNF14, and RNF159 was upregulated more than 2-fold compared with NE.
Comparative genomic analysis of the false killer whale (Pseudorca crassidens) LMBR1 locus.
Park et al., Taej┼Ćn, South Korea. In Genome, 2010
We sequenced two false killer whale BAC clones, corresponding to 156 kb and 144 kb, respectively, harboring the tightly linked RNF32, LMBR1, and NOM1 genes.
Mutation analysis of a large Chinese pedigree with congenital preaxial polydactyly.
Zhang et al., Kunming, China. In Eur J Hum Genet, 2009
We directly sequenced the candidate loci in this linked region, including the coding regions of the five genes (HLXB9, LMBR1, NOM1, RNF32 and C7orf13), the regulatory element (ZRS) of shh, the whole intron 5 of LMBR1 which contained the ZRS, and 18 conserved noncoding sequences (CNSs).
A single C to T transition in intron 5 of LMBR1 gene is associated with triphalangeal thumb-polysyndactyly syndrome in a Chinese family.
Kong et al., Shanghai, China. In Biochem Biophys Res Commun, 2007
By using a fine mapping study and a haplotype analysis, we narrowed the affected region to 1.7cM between markers D7S2465 and D7S2423, which contains four candidate genes: HLXB9, LMBR1, NOM1, and RNF32.
High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.
Beverloo et al., Rotterdam, Netherlands. In Genes Chromosomes Cancer, 2006
The 7q36 genes NOM1, LMBR1, RNF32, and SHH were equally expressed among t(7;12)-positive AML versus t(7;12)-negative AML, t(7;12)-negative ALL, or normal bone marrow.
A double RING-H2 domain in RNF32, a gene expressed during sperm formation.
Heutink et al., Rotterdam, Netherlands. In Biochem Biophys Res Commun, 2002
molecular cloning of a RING domain protein expressed during sperm formation
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