RNF216
protein-coding gene in the species Homo sapiens
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RNF216
Summary
RNF216 is a gene[1].
Key Facts
- RNF216's instance of is recorded as gene[2].
- RNF216 is a type of protein-coding gene[3].
- RNF216's HomoloGene ID is recorded as 19442[4].
- RNF216's genomic start is recorded as 5620047[5].
- RNF216's genomic start is recorded as 5659678[6].
- RNF216's genomic end is recorded as 5821370[7].
- RNF216's genomic end is recorded as 5781696[8].
- RNF216's ortholog is recorded as Rnf216[9].
- RNF216's ortholog is recorded as Rnf216[10].
- RNF216's ortholog is recorded as rnf216[11].
- RNF216's encodes is recorded as Ring finger protein 216[12].
- RNF216's found in taxon is recorded as Homo sapiens[13].
- RNF216's chromosome is recorded as human chromosome 7[14].
- RNF216's genetic association is recorded as Gordon-Holmes syndrome[15].
- RNF216's strand orientation is recorded as reverse strand[16].
- RNF216's exact match is recorded as http://identifiers.org/ncbigene/54476[17].
- RNF216's cytogenetic location is recorded as 7p22.1[18].
- RNF216's expressed in is recorded as testicle[19].
- RNF216's expressed in is recorded as right testis[20].
- RNF216's expressed in is recorded as left testis[21].
- RNF216's expressed in is recorded as saphenous vein[22].
- RNF216's expressed in is recorded as sperm[23].
- RNF216's expressed in is recorded as stromal cell of endometrium[24].
- RNF216's expressed in is recorded as oocyte[25].
- RNF216's expressed in is recorded as granulocyte[26].