RNF169
protein-coding gene in the species Homo sapiens
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RNF169
Summary
RNF169 is a gene[1].
Key Facts
- RNF169's instance of is recorded as gene[2].
- RNF169 is a type of protein-coding gene[3].
- RNF169's HomoloGene ID is recorded as 47510[4].
- RNF169's genomic start is recorded as 74459913[5].
- RNF169's genomic start is recorded as 74748849[6].
- RNF169's genomic end is recorded as 74842413[7].
- RNF169's genomic end is recorded as 74553458[8].
- RNF169's ortholog is recorded as Rnf169[9].
- RNF169's ortholog is recorded as Rnf169[10].
- RNF169's ortholog is recorded as rnf169[11].
- RNF169's encodes is recorded as Ring finger protein 169[12].
- RNF169's found in taxon is recorded as Homo sapiens[13].
- RNF169's chromosome is recorded as human chromosome 11[14].
- RNF169's strand orientation is recorded as forward strand[15].
- RNF169's exact match is recorded as http://identifiers.org/ncbigene/254225[16].
- RNF169's cytogenetic location is recorded as 11q13.4[17].
- RNF169's expressed in is recorded as pancreatic epithelial cell[18].
- RNF169's expressed in is recorded as amniotic fluid[19].
- RNF169's expressed in is recorded as skin of arm[20].
- RNF169's expressed in is recorded as cartilage tissue[21].
- RNF169's expressed in is recorded as epithelium of nasopharynx[22].
- RNF169's expressed in is recorded as Achilles tendon[23].
- RNF169's expressed in is recorded as trabecular bone[24].
- RNF169's expressed in is recorded as oral cavity[25].
- RNF169's expressed in is recorded as Skeletal muscle tissue of rectus abdominis[26].