RN7SL778P
pseudogene in the species Homo sapiens
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RN7SL778P
Summary
RN7SL778P is a pseudogene[1].
Key Facts
- RN7SL778P's instance of is recorded as pseudogene[2].
- RN7SL778P's instance of is recorded as gene[3].
- RN7SL778P is a type of pseudogene[4].
- RN7SL778P's genomic start is recorded as 130310180[5].
- RN7SL778P's genomic end is recorded as 130310476[6].
- RN7SL778P's found in taxon is recorded as Homo sapiens[7].
- RN7SL778P's chromosome is recorded as human chromosome 11[8].
- RN7SL778P's strand orientation is recorded as forward strand[9].
- RN7SL778P's exact match is recorded as http://identifiers.org/ncbigene/106479504[10].
- RN7SL778P's cytogenetic location is recorded as 11q24.3[11].
- RN7SL778P's expressed in is recorded as testicle[12].
- RN7SL778P's expressed in is recorded as human kidney[13].
- RN7SL778P's expressed in is recorded as sural nerve[14].
- RN7SL778P's expressed in is recorded as bone marrow cell[15].
- RN7SL778P's expressed in is recorded as muscle of thigh[16].
- RN7SL778P's expressed in is recorded as muscle tissue[17].
- RN7SL778P's expressed in is recorded as skeletal muscle tissue[18].
- RN7SL778P's expressed in is recorded as ganglionic eminence[19].
- RN7SL778P's expressed in is recorded as liver[20].
- RN7SL778P's expressed in is recorded as prefrontal cortex[21].