RN7SL426P
pseudogene in the species Homo sapiens
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RN7SL426P
Summary
RN7SL426P is a pseudogene[1].
Key Facts
- RN7SL426P's instance of is recorded as pseudogene[2].
- RN7SL426P's instance of is recorded as gene[3].
- RN7SL426P is a type of pseudogene[4].
- RN7SL426P's genomic start is recorded as 21229334[5].
- RN7SL426P's genomic end is recorded as 21229628[6].
- RN7SL426P's found in taxon is recorded as Homo sapiens[7].
- RN7SL426P's chromosome is recorded as human chromosome 17[8].
- RN7SL426P's strand orientation is recorded as reverse strand[9].
- RN7SL426P's exact match is recorded as http://identifiers.org/ncbigene/106481842[10].
- RN7SL426P's cytogenetic location is recorded as 17p11.2[11].
- RN7SL426P's expressed in is recorded as bone marrow cell[12].
- RN7SL426P's expressed in is recorded as lymph node[13].
- RN7SL426P's expressed in is recorded as monocyte[14].
- RN7SL426P's expressed in is recorded as placenta[15].
- RN7SL426P's expressed in is recorded as ganglionic eminence[16].
- RN7SL426P's expressed in is recorded as islet of Langerhans[17].
- RN7SL426P's expressed in is recorded as fundus[18].
- RN7SL426P's expressed in is recorded as blood[19].
- RN7SL426P's expressed in is recorded as liver[20].
- RN7SL426P's expressed in is recorded as primary visual cortex[21].