RN7SL89P
pseudogene in the species Homo sapiens
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RN7SL89P
Summary
RN7SL89P is a pseudogene[1].
Key Facts
- RN7SL89P's instance of is recorded as pseudogene[2].
- RN7SL89P's instance of is recorded as gene[3].
- RN7SL89P is a type of pseudogene[4].
- RN7SL89P's genomic start is recorded as 105293664[5].
- RN7SL89P's genomic end is recorded as 105293946[6].
- RN7SL89P's found in taxon is recorded as Homo sapiens[7].
- RN7SL89P's chromosome is recorded as human chromosome 4[8].
- RN7SL89P's strand orientation is recorded as forward strand[9].
- RN7SL89P's exact match is recorded as http://identifiers.org/ncbigene/106479256[10].
- RN7SL89P's cytogenetic location is recorded as 4q24[11].
- RN7SL89P's expressed in is recorded as testicle[12].
- RN7SL89P's expressed in is recorded as gonad[13].
- RN7SL89P's expressed in is recorded as sural nerve[14].
- RN7SL89P's expressed in is recorded as skeletal muscle tissue[15].
- RN7SL89P's expressed in is recorded as muscle of thigh[16].
- RN7SL89P's expressed in is recorded as primary visual cortex[17].
- RN7SL89P's expressed in is recorded as bone marrow[18].
- RN7SL89P's expressed in is recorded as monocyte[19].
- RN7SL89P's expressed in is recorded as urinary bladder[20].
- RN7SL89P's expressed in is recorded as lymph node[21].