RN7SL596P
pseudogene in the species Homo sapiens
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RN7SL596P
Summary
RN7SL596P is a pseudogene[1].
Key Facts
- RN7SL596P's instance of is recorded as pseudogene[2].
- RN7SL596P's instance of is recorded as gene[3].
- RN7SL596P is a type of pseudogene[4].
- RN7SL596P's genomic start is recorded as 63797784[5].
- RN7SL596P's genomic end is recorded as 63798071[6].
- RN7SL596P's found in taxon is recorded as Homo sapiens[7].
- RN7SL596P's chromosome is recorded as human chromosome 11[8].
- RN7SL596P's strand orientation is recorded as reverse strand[9].
- RN7SL596P's exact match is recorded as http://identifiers.org/ncbigene/106481085[10].
- RN7SL596P's cytogenetic location is recorded as 11q13.1[11].
- RN7SL596P's expressed in is recorded as testicle[12].
- RN7SL596P's expressed in is recorded as sural nerve[13].
- RN7SL596P's expressed in is recorded as bone marrow[14].
- RN7SL596P's expressed in is recorded as skeletal muscle tissue[15].
- RN7SL596P's expressed in is recorded as blood[16].
- RN7SL596P's expressed in is recorded as lymph node[17].
- RN7SL596P's expressed in is recorded as primary visual cortex[18].
- RN7SL596P's expressed in is recorded as gallbladder[19].
- RN7SL596P's expressed in is recorded as monocyte[20].
- RN7SL596P's expressed in is recorded as islet of Langerhans[21].