Ring finger protein 157

Ring finger protein 157 is a protein that in humans is encoded by the RNF157 gene. [5]

RNF157
Identifiers
Aliases	RNF157, ring finger protein 157
External IDs	MGI: 2442484 HomoloGene: 28235 GeneCards: RNF157
Gene location (Human) Chr. Chromosome 17 (human)[1] Band 17q25.1 Start 76,142,465 bp[1] End 76,240,493 bp[1]
Gene location (Mouse) Chr. Chromosome 11 (mouse)[2] Band 11|11 E2 Start 116,336,353 bp[2] End 116,413,032 bp[2]
Gene ontology Molecular function • metal ion binding • transferase activity • GO:1904264, GO:1904822, GO:0090622, GO:0090302 ubiquitin protein ligase activity Cellular component • cytoplasm • cell body Biological process • protein ubiquitination • negative regulation of apoptotic process • protein autoubiquitination • positive regulation of dendrite extension Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	114804	217340
Ensembl	ENSG00000141576	ENSMUSG00000052949
UniProt	Q96PX1	Q3TEL6
RefSeq (mRNA)	NM_052916 NM_001330501	NM_027258
RefSeq (protein)	NP_001317430 NP_443148	n/a
Location (UCSC)	Chr 17: 76.14 – 76.24 Mb	Chr 11: 116.34 – 116.41 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. GRCh38: Ensembl release 89: ENSG00000141576 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000052949 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. "Entrez Gene: Ring finger protein 157". Retrieved 2018-06-29.

Further reading

• Talmud PJ, et al. (November 2009). "Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip". Am. J. Hum. Genet. 85 (5): 628–42. doi:10.1016/j.ajhg.2009.10.014. PMC 2775832. PMID 19913121.
• Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Mol. Med. 16 (7–8): 247–53. doi:10.2119/molmed.2009.00159. PMC 2896464. PMID 20379614.
• Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S (October 2010). "Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study". Diabetes Care. 33 (10): 2250–3. doi:10.2337/dc10-0452. PMC 2945168. PMID 20628086.
• Flachsbart F, Franke A, Kleindorp R, Caliebe A, Blanché H, Schreiber S, Nebel A (December 2010). "Investigation of genetic susceptibility factors for human longevity - a targeted nonsynonymous SNP study". Mutat. Res. 694 (1–2): 13–9. doi:10.1016/j.mrfmmm.2010.08.006. PMID 20800603.