RNF130
protein-coding gene in the species Homo sapiens
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RNF130
Summary
RNF130 is a gene[1].
Key Facts
- RNF130's instance of is recorded as gene[2].
- RNF130 is a type of protein-coding gene[3].
- RNF130's HomoloGene ID is recorded as 41267[4].
- RNF130's genomic start is recorded as 179911651[5].
- RNF130's genomic start is recorded as 179338651[6].
- RNF130's genomic end is recorded as 179499118[7].
- RNF130's genomic end is recorded as 180072113[8].
- RNF130's ortholog is recorded as Rnf130[9].
- RNF130's ortholog is recorded as Rnf130[10].
- RNF130's ortholog is recorded as rnf130[11].
- RNF130's encodes is recorded as Ring finger protein 130[12].
- RNF130's found in taxon is recorded as Homo sapiens[13].
- RNF130's chromosome is recorded as human chromosome 5[14].
- RNF130's genetic association is recorded as coronary artery disease[15].
- RNF130's strand orientation is recorded as reverse strand[16].
- RNF130's exact match is recorded as http://identifiers.org/ncbigene/55819[17].
- RNF130's cytogenetic location is recorded as 5q35.3[18].
- RNF130's expressed in is recorded as monocyte[19].
- RNF130's expressed in is recorded as C1 segment[20].
- RNF130's expressed in is recorded as corpus callosum[21].
- RNF130's expressed in is recorded as granulocyte[22].
- RNF130's expressed in is recorded as blood[23].
- RNF130's expressed in is recorded as olfactory bulb[24].
- RNF130's expressed in is recorded as tibial nerve[25].
- RNF130's expressed in is recorded as inferior ganglion of vagus nerve[26].