RN7SL622P
pseudogene in the species Homo sapiens
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RN7SL622P
Summary
RN7SL622P is a pseudogene[1].
Key Facts
- RN7SL622P's instance of is recorded as pseudogene[2].
- RN7SL622P's instance of is recorded as gene[3].
- RN7SL622P is a type of pseudogene[4].
- RN7SL622P's genomic start is recorded as 67977698[5].
- RN7SL622P's genomic end is recorded as 67977972[6].
- RN7SL622P's found in taxon is recorded as Homo sapiens[7].
- RN7SL622P's chromosome is recorded as human chromosome 17[8].
- RN7SL622P's strand orientation is recorded as forward strand[9].
- RN7SL622P's exact match is recorded as http://identifiers.org/ncbigene/106481092[10].
- RN7SL622P's cytogenetic location is recorded as 17q24.2[11].
- RN7SL622P's expressed in is recorded as testicle[12].
- RN7SL622P's expressed in is recorded as prefrontal cortex[13].
- RN7SL622P's expressed in is recorded as lymph node[14].
- RN7SL622P's expressed in is recorded as stromal cell of endometrium[15].
- RN7SL622P's expressed in is recorded as placenta[16].
- RN7SL622P's expressed in is recorded as islet of Langerhans[17].
- RN7SL622P's expressed in is recorded as lactiferous gland[18].
- RN7SL622P's expressed in is recorded as bone marrow[19].
- RN7SL622P's expressed in is recorded as right coronary artery[20].
- RN7SL622P's expressed in is recorded as blood[21].