RN7SL788P
pseudogene in the species Homo sapiens
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RN7SL788P
Summary
RN7SL788P is a pseudogene[1].
Key Facts
- RN7SL788P's instance of is recorded as pseudogene[2].
- RN7SL788P's instance of is recorded as gene[3].
- RN7SL788P is a type of pseudogene[4].
- RN7SL788P's genomic start is recorded as 52150104[5].
- RN7SL788P's genomic end is recorded as 52150419[6].
- RN7SL788P's found in taxon is recorded as Homo sapiens[7].
- RN7SL788P's chromosome is recorded as human chromosome 1[8].
- RN7SL788P's strand orientation is recorded as forward strand[9].
- RN7SL788P's exact match is recorded as http://identifiers.org/ncbigene/106481135[10].
- RN7SL788P's cytogenetic location is recorded as 1p32.3[11].
- RN7SL788P's expressed in is recorded as testicle[12].
- RN7SL788P's expressed in is recorded as bone marrow cell[13].
- RN7SL788P's expressed in is recorded as skeletal muscle tissue[14].
- RN7SL788P's expressed in is recorded as epithelium of colon[15].
- RN7SL788P's expressed in is recorded as monocyte[16].
- RN7SL788P's expressed in is recorded as tonsil[17].
- RN7SL788P's expressed in is recorded as lymph node[18].
- RN7SL788P's expressed in is recorded as islet of Langerhans[19].
- RN7SL788P's expressed in is recorded as liver[20].
- RN7SL788P's expressed in is recorded as cervix[21].