RN7SL766P
pseudogene in the species Homo sapiens
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RN7SL766P
Summary
RN7SL766P is a pseudogene[1].
Key Facts
- RN7SL766P's instance of is recorded as pseudogene[2].
- RN7SL766P's instance of is recorded as gene[3].
- RN7SL766P is a type of pseudogene[4].
- RN7SL766P's genomic start is recorded as 21790537[5].
- RN7SL766P's genomic end is recorded as 21790845[6].
- RN7SL766P's found in taxon is recorded as Homo sapiens[7].
- RN7SL766P's chromosome is recorded as human chromosome 13[8].
- RN7SL766P's strand orientation is recorded as forward strand[9].
- RN7SL766P's exact match is recorded as http://identifiers.org/ncbigene/106479501[10].
- RN7SL766P's cytogenetic location is recorded as 13q12.11[11].
- RN7SL766P's expressed in is recorded as muscle tissue[12].
- RN7SL766P's expressed in is recorded as testicle[13].
- RN7SL766P's expressed in is recorded as gonad[14].
- RN7SL766P's expressed in is recorded as ganglionic eminence[15].
- RN7SL766P's expressed in is recorded as lymph node[16].
- RN7SL766P's expressed in is recorded as prefrontal cortex[17].
- RN7SL766P's expressed in is recorded as bone marrow[18].
- RN7SL766P's expressed in is recorded as gallbladder[19].
- RN7SL766P's expressed in is recorded as placenta[20].
- RN7SL766P's expressed in is recorded as monocyte[21].