RNU7-52P
pseudogene in the species Homo sapiens
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RNU7-52P
Summary
RNU7-52P is a pseudogene[1].
Key Facts
- RNU7-52P's instance of is recorded as pseudogene[2].
- RNU7-52P's instance of is recorded as gene[3].
- RNU7-52P's subclass of is recorded as pseudogene[4].
- RNU7-52P's Entrez Gene ID is recorded as 100151648[5].
- RNU7-52P's HGNC gene symbol is recorded as RNU7-52P[6].
- RNU7-52P's HGNC ID is recorded as 34148[7].
- RNU7-52P's Ensembl gene ID is recorded as ENSG00000251981[8].
- RNU7-52P's genomic start is recorded as 62383104[9].
- RNU7-52P's genomic end is recorded as 62383166[10].
- RNU7-52P's found in taxon is recorded as Homo sapiens[11].
- RNU7-52P's Ensembl transcript ID is recorded as ENST00000516172[12].
- RNU7-52P's chromosome is recorded as human chromosome 17[13].
- RNU7-52P's strand orientation is recorded as forward strand[14].
- RNU7-52P's exact match is recorded as http://identifiers.org/ncbigene/100151648[15].
- RNU7-52P's UMLS CUI is recorded as C2678728[16].
- RNU7-52P's cytogenetic location is recorded as 17q23.2[17].
- RNU7-52P's expressed in is recorded as blood[18].
- RNU7-52P's expressed in is recorded as monocyte[19].
- RNU7-52P's expressed in is recorded as ascending aorta[20].
- RNU7-52P's expressed in is recorded as tibial arteries[21].
- RNU7-52P's expressed in is recorded as thyroid gland[22].
- RNU7-52P's expressed in is recorded as left testis[23].