RN7SL817P
pseudogene in the species Homo sapiens
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RN7SL817P
Summary
RN7SL817P is a pseudogene[1].
Key Facts
- RN7SL817P's instance of is recorded as pseudogene[2].
- RN7SL817P's instance of is recorded as gene[3].
- RN7SL817P is a type of pseudogene[4].
- RN7SL817P's genomic start is recorded as 46448224[5].
- RN7SL817P's genomic end is recorded as 46448511[6].
- RN7SL817P's found in taxon is recorded as Homo sapiens[7].
- RN7SL817P's chromosome is recorded as human chromosome 2[8].
- RN7SL817P's strand orientation is recorded as reverse strand[9].
- RN7SL817P's exact match is recorded as http://identifiers.org/ncbigene/106481144[10].
- RN7SL817P's cytogenetic location is recorded as 2p21[11].
- RN7SL817P's expressed in is recorded as testicle[12].
- RN7SL817P's expressed in is recorded as urinary bladder[13].
- RN7SL817P's expressed in is recorded as myometrium[14].
- RN7SL817P's expressed in is recorded as blood[15].
- RN7SL817P's expressed in is recorded as placenta[16].
- RN7SL817P's expressed in is recorded as monocyte[17].
- RN7SL817P's expressed in is recorded as renal cortex[18].
- RN7SL817P's expressed in is recorded as smooth muscle tissue[19].
- RN7SL817P's expressed in is recorded as bone marrow[20].
- RN7SL817P's expressed in is recorded as islet of Langerhans[21].