Ring finger protein 157

RNF157
Identifiers
Aliases	RNF157, ring finger protein 157
External IDs	MGI: 2442484; GeneCards: RNF157
Enzyme activity
Gene location (Human)
Chr.	Chromosome 17 (human)
End	76,240,493 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	116,303,858 bp
RNA expression pattern
	Top expressed in
	lateral nuclear group of thalamus; ; right frontal lobe; ; cingulate gyrus; ; anterior cingulate cortex; ; dorsolateral prefrontal cortex; ; Brodmann area 9; ; pars compacta; ; prefrontal cortex; ; pars reticulata; ; gastrocnemius muscle;
	Top expressed in
	motor neuron; ; facial motor nucleus; ; trigeminal ganglion; ; substantia nigra; ; dentate gyrus of hippocampal formation granule cell; ; Region I of hippocampus proper; ; superior frontal gyrus; ; visual cortex; ; primary visual cortex; ; retinal pigment epithelium;
	More reference expression data
	n/a
Gene ontology
Molecular function	metal ion binding; transferase activity; 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
Databases	NCBI: entry; OMA: entry
	114804
	217340
	ENSG00000141576
	ENSMUSG00000052949
	Q96PX1
	Q3TEL6
	NM_052916; NM_001330501
	NM_027258
	NP_001317430; NP_443148
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

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

References

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

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.