RN7SL656P
pseudogene in the species Homo sapiens
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RN7SL656P
Summary
RN7SL656P is a pseudogene[1].
Key Facts
- RN7SL656P's instance of is recorded as pseudogene[2].
- RN7SL656P's instance of is recorded as gene[3].
- RN7SL656P is a type of pseudogene[4].
- RN7SL656P's genomic start is recorded as 46319679[5].
- RN7SL656P's genomic end is recorded as 46319959[6].
- RN7SL656P's found in taxon is recorded as Homo sapiens[7].
- RN7SL656P's chromosome is recorded as human chromosome 17[8].
- RN7SL656P's strand orientation is recorded as forward strand[9].
- RN7SL656P's exact match is recorded as http://identifiers.org/ncbigene/106481760[10].
- RN7SL656P's cytogenetic location is recorded as 17q21.31[11].
- RN7SL656P's expressed in is recorded as gonad[12].
- RN7SL656P's expressed in is recorded as testicle[13].
- RN7SL656P's expressed in is recorded as corpus callosum[14].
- RN7SL656P's expressed in is recorded as bone marrow cell[15].
- RN7SL656P's expressed in is recorded as skeletal muscle tissue[16].
- RN7SL656P's expressed in is recorded as apex of heart[17].
- RN7SL656P's expressed in is recorded as blood[18].
- RN7SL656P's expressed in is recorded as monocyte[19].
- RN7SL656P's expressed in is recorded as Achilles tendon[20].
- RN7SL656P's expressed in is recorded as primary visual cortex[21].