RNF111
protein-coding gene in the species Homo sapiens
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RNF111
Summary
RNF111 is a gene[1].
Key Facts
- RNF111's instance of is recorded as gene[2].
- RNF111 is a type of protein-coding gene[3].
- RNF111's HomoloGene ID is recorded as 9741[4].
- RNF111's genomic start is recorded as 58865175[5].
- RNF111's genomic start is recorded as 59157374[6].
- RNF111's genomic end is recorded as 59097419[7].
- RNF111's genomic end is recorded as 59389618[8].
- RNF111's ortholog is recorded as Rnf111[9].
- RNF111's ortholog is recorded as Rnf111[10].
- RNF111's ortholog is recorded as rnf111[11].
- RNF111's encodes is recorded as Ring finger protein 111[12].
- RNF111's found in taxon is recorded as Homo sapiens[13].
- RNF111's chromosome is recorded as human chromosome 15[14].
- RNF111's strand orientation is recorded as forward strand[15].
- RNF111's exact match is recorded as http://identifiers.org/ncbigene/54778[16].
- RNF111's cytogenetic location is recorded as 15q22.1-q22.2[17].
- RNF111's expressed in is recorded as secondary oocyte[18].
- RNF111's expressed in is recorded as endothelial cell[19].
- RNF111's expressed in is recorded as monocyte[20].
- RNF111's expressed in is recorded as ganglionic eminence[21].
- RNF111's expressed in is recorded as Epithelium of choroid plexus[22].
- RNF111's expressed in is recorded as ventricular zone[23].
- RNF111's expressed in is recorded as epithelium of colon[24].
- RNF111's expressed in is recorded as stromal cell of endometrium[25].
- RNF111's expressed in is recorded as tonsil[26].