RN7SL681P
pseudogene in the species Homo sapiens
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RN7SL681P
Summary
RN7SL681P is a pseudogene[1].
Key Facts
- RN7SL681P's instance of is recorded as pseudogene[2].
- RN7SL681P's instance of is recorded as gene[3].
- RN7SL681P is a type of pseudogene[4].
- RN7SL681P's genomic start is recorded as 87386883[5].
- RN7SL681P's genomic end is recorded as 87387174[6].
- RN7SL681P's found in taxon is recorded as Homo sapiens[7].
- RN7SL681P's chromosome is recorded as human chromosome 4[8].
- RN7SL681P's strand orientation is recorded as reverse strand[9].
- RN7SL681P's exact match is recorded as http://identifiers.org/ncbigene/106479471[10].
- RN7SL681P's cytogenetic location is recorded as 4q22.1[11].
- RN7SL681P's expressed in is recorded as lymph node[12].
- RN7SL681P's expressed in is recorded as blood[13].
- RN7SL681P's expressed in is recorded as urinary bladder[14].
- RN7SL681P's expressed in is recorded as monocyte[15].
- RN7SL681P's expressed in is recorded as liver[16].
- RN7SL681P's expressed in is recorded as corpus callosum[17].
- RN7SL681P's expressed in is recorded as placenta[18].
- RN7SL681P's expressed in is recorded as tonsil[19].
- RN7SL681P's expressed in is recorded as duodenum[20].
- RN7SL681P's expressed in is recorded as Brodmann area 9[21].