RN7SL666P
pseudogene in the species Homo sapiens
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RN7SL666P
Summary
RN7SL666P is a pseudogene[1].
Key Facts
- RN7SL666P's instance of is recorded as pseudogene[2].
- RN7SL666P's instance of is recorded as gene[3].
- RN7SL666P is a type of pseudogene[4].
- RN7SL666P's genomic start is recorded as 43222206[5].
- RN7SL666P's genomic end is recorded as 43222509[6].
- RN7SL666P's found in taxon is recorded as Homo sapiens[7].
- RN7SL666P's chromosome is recorded as human chromosome 20[8].
- RN7SL666P's strand orientation is recorded as forward strand[9].
- RN7SL666P's exact match is recorded as http://identifiers.org/ncbigene/106481854[10].
- RN7SL666P's cytogenetic location is recorded as 20q13.11[11].
- RN7SL666P's expressed in is recorded as testicle[12].
- RN7SL666P's expressed in is recorded as gonad[13].
- RN7SL666P's expressed in is recorded as sural nerve[14].
- RN7SL666P's expressed in is recorded as bone marrow[15].
- RN7SL666P's expressed in is recorded as placenta[16].
- RN7SL666P's expressed in is recorded as Achilles tendon[17].
- RN7SL666P's expressed in is recorded as prefrontal cortex[18].
- RN7SL666P's expressed in is recorded as monocyte[19].
- RN7SL666P's expressed in is recorded as primary visual cortex[20].
- RN7SL666P's expressed in is recorded as islet of Langerhans[21].