RN7SL756P
pseudogene in the species Homo sapiens
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RN7SL756P
Summary
RN7SL756P is a pseudogene[1].
Key Facts
- RN7SL756P's instance of is recorded as pseudogene[2].
- RN7SL756P's instance of is recorded as gene[3].
- RN7SL756P is a type of pseudogene[4].
- RN7SL756P's genomic start is recorded as 67457023[5].
- RN7SL756P's genomic end is recorded as 67457290[6].
- RN7SL756P's found in taxon is recorded as Homo sapiens[7].
- RN7SL756P's chromosome is recorded as human chromosome 17[8].
- RN7SL756P's strand orientation is recorded as reverse strand[9].
- RN7SL756P's exact match is recorded as http://identifiers.org/ncbigene/106481128[10].
- RN7SL756P's cytogenetic location is recorded as 17q24.2[11].
- RN7SL756P's expressed in is recorded as sural nerve[12].
- RN7SL756P's expressed in is recorded as bone marrow cell[13].
- RN7SL756P's expressed in is recorded as human kidney[14].
- RN7SL756P's expressed in is recorded as epithelium of colon[15].
- RN7SL756P's expressed in is recorded as urinary bladder[16].
- RN7SL756P's expressed in is recorded as liver[17].
- RN7SL756P's expressed in is recorded as renal cortex[18].
- RN7SL756P's expressed in is recorded as islet of Langerhans[19].
- RN7SL756P's expressed in is recorded as monocyte[20].
- RN7SL756P's expressed in is recorded as blood[21].