RN7SL504P
pseudogene in the species Homo sapiens
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RN7SL504P
Summary
RN7SL504P is a pseudogene[1].
Key Facts
- RN7SL504P's instance of is recorded as pseudogene[2].
- RN7SL504P's instance of is recorded as gene[3].
- RN7SL504P is a type of pseudogene[4].
- RN7SL504P's genomic start is recorded as 51872178[5].
- RN7SL504P's genomic end is recorded as 51872464[6].
- RN7SL504P's found in taxon is recorded as Homo sapiens[7].
- RN7SL504P's chromosome is recorded as human chromosome 3[8].
- RN7SL504P's strand orientation is recorded as forward strand[9].
- RN7SL504P's exact match is recorded as http://identifiers.org/ncbigene/106480515[10].
- RN7SL504P's cytogenetic location is recorded as 3p21.2[11].
- RN7SL504P's expressed in is recorded as sural nerve[12].
- RN7SL504P's expressed in is recorded as bone marrow[13].
- RN7SL504P's expressed in is recorded as lymph node[14].
- RN7SL504P's expressed in is recorded as monocyte[15].
- RN7SL504P's expressed in is recorded as liver[16].
- RN7SL504P's expressed in is recorded as corpus callosum[17].
- RN7SL504P's expressed in is recorded as right coronary artery[18].
- RN7SL504P's expressed in is recorded as blood[19].
- RN7SL504P's expressed in is recorded as islet of Langerhans[20].
- RN7SL504P's expressed in is recorded as gallbladder[21].