RNF222
protein-coding gene in the species Homo sapiens
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RNF222
Summary
RNF222 is a gene[1].
Key Facts
- RNF222's instance of is recorded as gene[2].
- RNF222 is a type of protein-coding gene[3].
- RNF222's HomoloGene ID is recorded as 18544[4].
- RNF222's genomic start is recorded as 8294022[5].
- RNF222's genomic start is recorded as 8390702[6].
- RNF222's genomic end is recorded as 8301144[7].
- RNF222's genomic end is recorded as 8397827[8].
- RNF222's ortholog is recorded as Rnf222[9].
- RNF222's ortholog is recorded as Rnf222[10].
- RNF222's ortholog is recorded as rnf222[11].
- RNF222's encodes is recorded as Ring finger protein 222[12].
- RNF222's found in taxon is recorded as Homo sapiens[13].
- RNF222's chromosome is recorded as human chromosome 17[14].
- RNF222's strand orientation is recorded as reverse strand[15].
- RNF222's exact match is recorded as http://identifiers.org/ncbigene/643904[16].
- RNF222's cytogenetic location is recorded as 17p13.1[17].
- RNF222's expressed in is recorded as skin of leg[18].
- RNF222's expressed in is recorded as skin of abdomen[19].
- RNF222's expressed in is recorded as vagina[20].
- RNF222's expressed in is recorded as tonsil[21].
- RNF222's expressed in is recorded as placenta[22].
- RNF222's expressed in is recorded as bone marrow[23].
- RNF222's expressed in is recorded as ectocervix[24].
- RNF222's expressed in is recorded as blood[25].
- RNF222's expressed in is recorded as minor salivary glands[26].