RN7SL496P
pseudogene in the species Homo sapiens
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RN7SL496P
Summary
RN7SL496P is a pseudogene[1].
Key Facts
- RN7SL496P's instance of is recorded as pseudogene[2].
- RN7SL496P's instance of is recorded as gene[3].
- RN7SL496P is a type of pseudogene[4].
- RN7SL496P's genomic start is recorded as 39888375[5].
- RN7SL496P's genomic end is recorded as 39888664[6].
- RN7SL496P's found in taxon is recorded as Homo sapiens[7].
- RN7SL496P's chromosome is recorded as human chromosome 7[8].
- RN7SL496P's strand orientation is recorded as forward strand[9].
- RN7SL496P's exact match is recorded as http://identifiers.org/ncbigene/106481058[10].
- RN7SL496P's cytogenetic location is recorded as 7p14.1[11].
- RN7SL496P's expressed in is recorded as testicle[12].
- RN7SL496P's expressed in is recorded as sural nerve[13].
- RN7SL496P's expressed in is recorded as liver[14].
- RN7SL496P's expressed in is recorded as epithelium of colon[15].
- RN7SL496P's expressed in is recorded as human kidney[16].
- RN7SL496P's expressed in is recorded as stomach[17].
- RN7SL496P's expressed in is recorded as right lobe of thyroid gland[18].
- RN7SL496P's expressed in is recorded as monocyte[19].
- RN7SL496P's expressed in is recorded as left coronary artery[20].
- RN7SL496P's expressed in is recorded as blood[21].