RN7SL862P
pseudogene in the species Homo sapiens
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RN7SL862P
Summary
RN7SL862P is a pseudogene[1].
Key Facts
- RN7SL862P's instance of is recorded as pseudogene[2].
- RN7SL862P's instance of is recorded as gene[3].
- RN7SL862P is a type of pseudogene[4].
- RN7SL862P's genomic start is recorded as 9830330[5].
- RN7SL862P's genomic end is recorded as 9830627[6].
- RN7SL862P's found in taxon is recorded as Homo sapiens[7].
- RN7SL862P's chromosome is recorded as human chromosome 18[8].
- RN7SL862P's strand orientation is recorded as reverse strand[9].
- RN7SL862P's exact match is recorded as http://identifiers.org/ncbigene/106479535[10].
- RN7SL862P's cytogenetic location is recorded as 18p11.22[11].
- RN7SL862P's expressed in is recorded as testicle[12].
- RN7SL862P's expressed in is recorded as skeletal muscle tissue[13].
- RN7SL862P's expressed in is recorded as sural nerve[14].
- RN7SL862P's expressed in is recorded as bone marrow cell[15].
- RN7SL862P's expressed in is recorded as white blood cell[16].
- RN7SL862P's expressed in is recorded as lymph node[17].
- RN7SL862P's expressed in is recorded as monocyte[18].
- RN7SL862P's expressed in is recorded as blood[19].
- RN7SL862P's expressed in is recorded as gallbladder[20].
- RN7SL862P's expressed in is recorded as liver[21].