RNF168
protein-coding gene in the species Homo sapiens
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RNF168
Summary
RNF168 is a gene[1].
Key Facts
- RNF168's instance of is recorded as gene[2].
- RNF168 is a type of protein-coding gene[3].
- RNF168's HomoloGene ID is recorded as 87044[4].
- RNF168's genomic start is recorded as 196468783[5].
- RNF168's genomic start is recorded as 196195654[6].
- RNF168's genomic end is recorded as 196503768[7].
- RNF168's genomic end is recorded as 196230639[8].
- RNF168's ortholog is recorded as Rnf168[9].
- RNF168's ortholog is recorded as Rnf168[10].
- RNF168's encodes is recorded as Ring finger protein 168[11].
- RNF168's found in taxon is recorded as Homo sapiens[12].
- RNF168's chromosome is recorded as human chromosome 3[13].
- RNF168's genetic association is recorded as RIDDLE syndrome[14].
- RNF168's strand orientation is recorded as reverse strand[15].
- RNF168's exact match is recorded as http://identifiers.org/ncbigene/165918[16].
- RNF168's cytogenetic location is recorded as 3q29[17].
- RNF168's expressed in is recorded as sperm[18].
- RNF168's expressed in is recorded as tendon of biceps brachii[19].
- RNF168's expressed in is recorded as pancreatic epithelial cell[20].
- RNF168's expressed in is recorded as parietal pleura[21].
- RNF168's expressed in is recorded as visceral pleura[22].
- RNF168's expressed in is recorded as Achilles tendon[23].
- RNF168's expressed in is recorded as epithelium of nasopharynx[24].
- RNF168's expressed in is recorded as germinal epithelium[25].
- RNF168's expressed in is recorded as gonad[26].