RN7SL416P
pseudogene in the species Homo sapiens
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RN7SL416P
Summary
RN7SL416P is a pseudogene[1].
Key Facts
- RN7SL416P's instance of is recorded as pseudogene[2].
- RN7SL416P's instance of is recorded as gene[3].
- RN7SL416P is a type of pseudogene[4].
- RN7SL416P's genomic start is recorded as 100530362[5].
- RN7SL416P's genomic end is recorded as 100530659[6].
- RN7SL416P's found in taxon is recorded as Homo sapiens[7].
- RN7SL416P's chromosome is recorded as human chromosome 7[8].
- RN7SL416P's strand orientation is recorded as reverse strand[9].
- RN7SL416P's exact match is recorded as http://identifiers.org/ncbigene/106481037[10].
- RN7SL416P's cytogenetic location is recorded as 7q22.1[11].
- RN7SL416P's expressed in is recorded as sural nerve[12].
- RN7SL416P's expressed in is recorded as epithelium of colon[13].
- RN7SL416P's expressed in is recorded as muscle tissue[14].
- RN7SL416P's expressed in is recorded as liver[15].
- RN7SL416P's expressed in is recorded as monocyte[16].
- RN7SL416P's expressed in is recorded as skeletal muscle tissue[17].
- RN7SL416P's expressed in is recorded as human kidney[18].
- RN7SL416P's expressed in is recorded as bone marrow cell[19].
- RN7SL416P's expressed in is recorded as superior frontal gyrus[20].
- RN7SL416P's expressed in is recorded as islet of Langerhans[21].